RECOMBINANT REVERSE TRANSCRIPTASE VARIANTS

REFERENCE TO SEQUENCE LISTING, TABLE OR COMPUTER PROGRAM

The Sequence Listing concurrently submitted herewith via EFS-Web as file name CX9-213US1_ST26.xml, created on Oct. 14, 2022 and having a file size of 1.47 Mbytes, is incorporated by reference herein.

TECHNICAL FIELD

The present disclosure provides recombinant reverse transcriptase polypeptides and compositions thereof, polynucleotides encoding the recombinant reverse transcriptase polypeptides, and methods for use of the recombinant reverse transcriptase polypeptides and compositions thereof for diagnostic, molecular biological tools, and other purposes.

BACKGROUND

Reverse transcriptase (RT), also referred to as an RNA-directed DNA polymerase, catalyzes the synthesis of a DNA copy of an RNA target template. RT enzymes were initially identified from RNA tumor viruses, such as murine leukemia virus and Rous sarcoma virus, in their role in the replication of such viruses. Because of RT's ability to synthesize DNA copies from an RNA template, RTs have become essential tools in diagnostics and research.

For example, RTs are used with polymerase chain reaction, a technique called RT-PCR, for detection of RNA molecules, including for detecting gene expression and RNA of pathogens such as HIV and Covid-19. A variation of RT-PCR is quantitative RT-qPCR which is a quantitative analysis of RNA levels where levels of amplified cDNA are measured in real time during the exponential phase of amplification. The amplification level is used as a basis to quantitate the original targets within the RNA population. As a molecular biological tool, applications of RTs include generation of cDNA from mRNA, such as for generating cDNA libraries; rapid amplification of cDNA ends (RACE) for determining sequences at the 5′ and 3′ ends of cDNAs; and sequencing of RNA.

Reverse transcriptases used as tools in biotechnology and diagnostics include RTs of avian myeloblastosis virus (AMV) and moloney murine leukemia virus (M-MLV). A variant M-MLV reverse transcriptase having a point mutation resulting in reduction of RNase H activity displays enhanced thermostability compared to the wild-type enzyme. Robust RNAseH activity is an advantage in RT-PCR, whereas lower RNAseH activity is beneficial for cDNA cloning, particularly when long mRNA transcripts are reverse transcribed. Other known reverse transcriptases include RTs of human immunodeficiency virus-1 (HIV-1) and telomerase reverse transcriptase.

SUMMARY

The present disclosure provides recombinant reverse transcriptase polypeptides and compositions thereof, polynucleotides encoding the recombinant reverse transcriptase polypeptides, and methods for use of the recombinant reverse transcriptase and compositions thereof for molecular biological tools, diagnostic, and other purposes.

In one aspect, the present disclosure provides a recombinant reverse transcriptase, or a functional fragment thereof, comprising a polypeptide sequence having at least 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity to a reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 2, 24, 94, or 352, or to a reference sequence corresponding to SEQ ID NO: 2, 24, 94, or 352, wherein the polypeptide sequence comprises one or more substitutions relative to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 2, 24, 94, or 352, or to the reference sequence corresponding to SEQ ID NO: 2, 24, 94, or 352.

In some embodiments, the recombinant reverse transcriptases, or a functional fragment thereof, comprises a polypeptide sequence having at least 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 2, or to the reference sequence corresponding to SEQ ID NO: 2, wherein the polypeptide sequence comprises one or more substitutions relative to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 2, or to the reference sequence corresponding to SEQ ID NO: 2.

In some embodiments, the recombinant reverse transcriptases, or a functional fragment thereof, comprises a polypeptide sequence having at least 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 24, 94, or 352, or to the reference sequence corresponding to SEQ ID NO: 24, 94, or 352, wherein the polypeptide sequence comprises one or more substitutions relative to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 2, or to the reference sequence corresponding to SEQ ID NO: 2.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution at amino acid position 18, 25, 49, 63, 68, 69, 72, 74, 78, 81, 83, 84, 85, 89, 90, 92, 94, 98, 102, 113, 114, 118, 119, 129, 130, 132, 134, 163, 167, 171, 173, 178, 196, 199, 205, 209, 210, 212, 216, 242, 258, 260, 261, 266, 294, 297, 298, 300, 303, 305, 307, 308, 309, 310, 311, 314, 317, 319, 321, 329, 331, 333, 338, 342, 343, 349, 356, 370, 403, 444, 447, 454, 464, 465, 466, 474, 479, 508, 509, 519, 536, 537, 554, 574, 576, 583, 595, 598, 606, 638, 639, or 662, or combinations thereof, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 2.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution 18E, 25E, 49G, 63L/P, 68S, 69R, 72M, 74K/M/P, 78V, 81K, 83E/A/C/R/W, 84N, 85R, 89A/M, 90I, 92T, 94L, 98S, 102C, 113G/T, 114G/K, 118R, 119Y, 129L, 130R/S, 132F, 134F/P, 163P, 167Y, 171L, 173A, 178L, 196C/H, 199L, 205M, 209A, 210L, 212K/N/V, 216R, 242A, 258T, 260G, 261N, 266V, 294Q, 297W, 298E/R, 3001, 303G/Q, 305P/S, 307K/N, 308G, 309E/P/T, 310R, 311A/I/P, 314A/K/M, 317C, 319C/G/S, 321A, 329S, 331E, 333V, 338V, 342W, 343A/V, 349G, 356P, 370G, 403H, 444L, 447G/L/R, 454A, 464L, 465S, 466K, 474A, 479D, 508L, 509E, 519P, 536E/A/N, 537W, 554T, 574D/Q, 576I, 583K, 595N, 598S, 606K/Q, 638H, 639H, or 662R, or combinations thereof, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO:2

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution or substitution set at amino acid position 114/210/307, 114/309, 49, 63/68/216/258/261, 63/68/216/261, 63/209/314/665, 447/665, 331, 90/307/349, 114/173/331, or 266, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 2.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution or substitution set at amino acid position 454/508, 536/574, 309, 49/173/309/331, 90/331, 63/90/309/574/650, 90/173/209/210/321/574/598, 508/519, 49/63/90/216/309/321/536/574, 49/114/307/309/536, 307/321/536/574/650, 309/331/536/574/598/650, 173/331/536/574/598, 49/300/403, 74/242, 242/298/508/662, 260/509, 102/370/509, 49/173/216/349/536/598, 49/114/216/307/309/331, 49/90/173/216/307, 63/68/81/167/314/447/574, 49/210/307/309/321/536/574/650, 63/90/307/321/331/537/598, 370/464/465/509/554/576, 49/114/173/216/321/574/598, 90/216/321/650, 574/650, 49/209/210/307/309/536/598, 216/536/574, 49/173/210/309/321/536/598, 331/536/598, 321/574, 173/321/331/349/574, 49/307/536, 216/309/574/650, 94/370/474/576, 90/209/210/309/321/574, 49/63/90/173, 298, 49/300/454/662, 68/81/167/298/536, 49/454, 81, 49/114/173/309/349/536/574/650, 167/261/303/536, 18/102/554, 171/173/307/331/536, 173/216/536, 18/370/464/509, 49/114, 90/216/309/536/574, 444, 90/321/349/536/598/650, 49/163/309/321/536/574/650, 49/63/90/173/307/331/536/598/650, 68/81/167/258/447/466/536, 90/331/574, 49/321, 94/509, 90/173/321/536, 167/298/447/466, 173/216/307/309/536, 216/321, 49/90/173/209/309/331, 261/298/303/447/574, 171/298/444/519, 90/536/574/598/650, 49/63/90/210/307/321/598/650, 90/216/307/536/574, 18/94/102/260/370/464/554, 18/423/465/474, 167/261/447/536, 114/173/209/210, 307/309/536/574/598, 102/260/370/576, 574, 173/209/210/307/536, 216/309/536, 349, 447/536/606, 310/454/479/519/662, 49/90/209/598, 314/536, 171/300/454/479/508/662, 171/242/300/508/662, 49/331/536, 173/216/309/536/574/598, 536/598, 167/261/298/303/447/466/574, 173/536/598, 49/114/309/536/574/598, 49/114/309/349/536, 63/68/81/303/466, 63/90/209/216/307/309/321/349/536/574/598/650, 216, 173/210/307/598/650, 25/102/370/423, 68/261/298/303, 423/474, 94/423/474/554/576, 63/298/447/574, 49/63/90/173/307/321/331/574/595/650, 49/90/536/574, 508, 63/81/167/258/261/298/303/447, 114/331, 212/298/583/606, 49/173/536/574, 49/242/298/300/310/444/454/479, 49/309/321/536/598, 63/68/261/536, 300/444/508, or 298, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 2.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution or substitution set at amino acid position 134, 74, 83, 319, 92, 329, 343,311,338,196,69,72,294,83,134,130,305,319,113,297,319,114,308,309,342,205,212, 199,83,303,309,78,113,132,311,119,83,98,314,129,343,196,74,356,89,212, 444/508/509/574, 63/260/298/300/331/444/509, 63/90/209/444/508/574, 298/444/509, 63/90/508/509/574/595, 83, 311, 89, 130, 178, 118, or combinations thereof, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 2.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution or substitution set at amino acid position 309/342, 309, 129, 574, 85, 98/119/129/132/196, 98/317/343/356, 205/212/309/319/342, 78/132/314, 78/83/98, 78/83/119/132/196, 78/83, 78/83/356, 78, 119/129/132, 178/303/331/338/508, 311/314, 63/297/303/305, 63/178/209/260/574, 63/300/338, 83/294, 83/92/343/574, 83/92/134/574, 83/196/329/343, 83/196, 83/134/196/294/305/311/319/329/343/574, 83, 83/309, 83/319/342, 83/205, 83/114, 83/114/309, 83/114/319, 83/199/212/309/319/639, 83/199, 83/342, 83/308/309/595/638, 83/113/114/205/212, 83/130, 114/309, 114/212/309/342/639, 114/205, 114, 114/130/319, 114/130/212/342, 114/130/309, 199/309, 199/205, 342, 343/595, 74, 74/129, 74/83/129/132/212, 74/83/92/343, 74/83/134/294/574, 74/83, 74/329/574, 74/92/196/294/329, 92, 72, 72/294/311/329/343, 72/294, 72/294/311/329, 72/83/343, 72/74/294, 72/74/83/319/329, 72/74/83/84, 72/74/83/134/196/294, 72/74, 72/74/92/294/329, 72/74/92, 72/74/92/134/343, 72/74/134/196/319/329, 72/196/311/329/574, 72/134/196, 118/178/338, 69/89/178/303/305/338/574, 113, 113/178/260, 113/309, 113/212/309, 113/342, 113/114, 113/114/212, 113/114/205/319/342, 113/114/342, 113/114/130, 130/205/333, 134, or 134/294, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO:2.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution or substitution set 266V/454A/508L, 266V/536E/574Q, 266V/309P, 49G/173A/266V/309P/331E, 90I/266V/331E, 63L/90I/266V/309P/574D/650G, 90I/173A/209A/210L/266V/321A/574D/5985, 266V/508L/519P, 49G/63L/90I/216R/266V/309P/321A/536E/574D, 49G/114K/266V/307N/309P/536E, 266V/307K/321A/536E/574D/650G, 266V/309P/331E/536E/574Q/598S/650G, 173A/266V/331E/536E/574D/598S, 49G/266V/300I/403H, 74K/242A/266V, 242A/266V/298E/508L/662R, 260G/266V/509E, 102C/266V/370G/509E, 49G/173A/216R/266V/349G/536E/5985, 49G/114K/216R/266V/307K/309P/331E, 49G/90I/173A/216R/266V/307K, 63P/68S/81K/167Y/266V/314A/447G/574Q, 49G/210L/266V/307K/309P/321A/536E/574D/650G, 63L/90I/266V/307K/321A/331E/537W/598S, 266V/370G/464L/465S/509E/554T/576I, 49G/114K/173A/216R/266V/321A/574D/598S, 90I/216R/266V/321A/650G, 266V/574D/650G, 49G/209A/210L/266V/307K/309P/536E/598S, 216R/266V/536E/574Q, 49G/173A/210L/266V/309P/321A/536E/5985, 266V/331E/536E/598S, 266V/321A/574D, 173A/266V/321A/331E/349G/574D, 49G/266V/307K/536E, 216R/266V/309P/574D/650G, 94L/266V/370G/474A/576I, 90I/209A/210L/266V/309P/321A/574D, 49G/63L/90I/173A/266V, 266V/298E, 49G/266V/300I/454A/662R, 68S/81K/167Y/266V/298R/536N, 49G/266V/454A, 81K/266V, 49G/114K/173A/266V/309P/349G/536E/574D/650G, 167Y/261N/266V/303Q/536N, 18E/102C/266V/554T, 171L/173A/266V/307K/331E/536E, 173A/216R/266V/536E, 18E/266V/370G/464L/509E, 49G/114K/266V, 90I/216R/266V/309P/536G/574D, 266V/444L, 90I/266V/321A/349G/536G/598S/650G, 49G/163P/266V/309P/321A/536E/574D/650G, 49G/63L/90I/173A/266V/307K/331E/536E/598S/650G, 68S/81K/167Y/258T/266V/447G/466K/536N, 90I/266V/331E/574D, 49G/266V/321A, 94L/266V/509E, 90I/173A/266V/321A/536E, 167Y/266V/298R/447G/466K, 173A/216R/266V/307K/309P/536E, 216R/266V/321A, 49G/90I/173A/209A/266V/309P/331E, 261N/266V/298R/303Q/447R/574Q, 171P/266V/298E/444L/519P, 90I/266V/536E/574D/598S/650G, 49G/63L/90I/210L/266V/307K/321A/598S/650G, 90I/216R/266V/307K/536E/574D, 18E/94L/102C/260G/266V/370G/464L/554T, 18E/266V/423R/465S/474A, 167Y/261N/266V/447G/536G, 114K/173A/209A/210L/266V, 266V/307K/309P/536E/574D/598S, 102C/260G/266V/370G/576I, 266V/574D, 173A/209A/210L/266V/307K/536E, 216R/266V/309P/536E, 266V/349G, 266 V/447L/536A/606Q, 266V/310R/454A/479D/519P/662R, 49G/90I/209A/266V/598S, 266V/314K/536N, 171P/266V/300I/454A/479D/508L/662R, 171P/242A/266V/300I/508L/662R, 49G/266V/331E/536E, 173A/216R/266V/309P/536E/574D/598S, 266V/536E/598S, 167Y/261N/266V/298R/303Q/447R/466K/574Q, 173A/266V/536E/598S, 49G/114K/266V/309P/536E/574D/598S, 49G/114K/266V/309P/349G/536E, 63P/68S/81K/266V/303Q/466K, 63L/90I/209A/216R/266V/307K/309P/321A/349G/536E/574D/598S/650G, 216R/266V, 173A/210L/266V/307K/598S/650G, 25E/102C/266V/370G/423R, 68S/261N/266V/298R/303Q, 266V/423R/474A, 94L/266V/423R/474A/554T/576I, 63P/266V/298R/447R/574Q, 49G/63L/90I/173A/266V/307K/321A/331E/574D/595N/650G, 49G/90I/266V/536E/574D, 266V/508L, 63P/81K/167Y/258T/266V/261N/298R/303Q/447G, 114K/266V/331E, 212N/266V/298E/583K/606K, 49G/173A/266V/536E/574Q, 49G/242A/266V/298E/300I/310R/444L/454A/479D, 49G/266V/309P/321A/536E/598S, 63P/68S/261N/266V/536G, 266V/300I/444L/508L, or 266V/298R, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO:2.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution or substitution set 49G/134P/266V/307K/536E, 49G/74P/266V/307K/536E, 49G/83A/266V/307K/536E, 49G/266V/307K/319G/536E, 49G/92T/266V/307K/536E, 49G/266V/307K/329S/536E, 49G/266V/307K/343A/536E, 49G/266V/307K/311P/536E, 49G/266V/307K/338V/536E, 49G/196C/266V/307K/536E, 49G/69R/266V/307K/536E, 49G/72M/266V/307K/536E, 49G/266V/294Q/307K/536E, 49G/83W/266V/294Q/307K/536E, 49G/134F/266V/307K/536E, 49G/130S/266V/307K/536E, 49G/266V/305P/307K/536E, 49G/266V/307K/319S/536E, 49G/113T/266V/307K/536E, 49G/266V/297W/307K/536E, 49G/266V/307K/319C/536E, 49G/114G/266V/307K/536E, 49G/266V/307K/308G/536E, 49G/266V/307K/309E/536E, 49G/266V/307K/342W/536E, 49G/205M/266V/307K/536E, 49G/212K/266V/307K/536E, 49G/199L/266V/307K/536E, 49G/83C/266V/307K/536E, 49G/266V/303G/307K/536E, 49G/266V/307K/309T/536E, 49G/78V/266V/307K/536E, 49G/113G/266V/307K/536E, 49G/132F/266V/307K/536E, 49G/266V/307K/311I/536E, 49G/119Y/266V/307K/536E, 49G/83E/266V/307K/536E, 49G/98S/266V/307K/536E, 49G/266V/307K/314M/536E, 49G/129L/266V/307K/536E, 49G/266V/307K/343V/536E, 49G/196H/266V/307K/536E, 49G/74M/266V/307K/536E, 49G/266V/307K/356P/536E, 49G/89A/266V/307K/536E, 49G/212V/266V/307K/536E, 49G/266V/307K/444L/508L/509E/536E/574D, 49G/63L/260G/266V/298R/300I/307K/331E/444L/509E/536E , 49G/63L/90I/209A/266V/307K/444L/508L/536E/574Q, 49G/266V/298R/307K/444L/509E/536E, 49G/63L/90I/266V/307K/508L/509E/536E/574Q/595N, 49G/83R/266V/307K/536E, 49G/266V/307K/311A/536E, 49G/89M/266V/307K/536E, 49G/130R/266V/307K/536E, 49G/178L/266V/307K/536E, or 49G/118R/266V/307K/536E, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO:2.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution or substitution set 49G/266V/298R/307K/309E/342W/444L/509E/536E, 49G/266V/298R/307K/309T/444L/509E/536E, 49G/129L/266V/307K/444L/509E/536E, 49G/266V/298R/307K/444L/536E/574Q, 49G/85R/266V/298R/307K/444L/509E/536E, 49G/985/119Y/129L/132F/196H/266V/307K/444L/509E/536E, 49G/985/266V/307K/317C/343V/356P/444L/509E/536E, 49G/205M/212K/266V/307K/309E/319S/342W/444L/536E, 49G/266V/298R/307K/509E/536E, 49G/78V/132F/266V/298R/307K/314M/444L/509E/536E, 49G/78V/83E/98S/266V/298R/307K/444L/509E/536E, 49G/78V/83E/119Y/132F/196H/266V/298R/307K/509E/536E, 49G/78V/83E/266V/307K/444L/509E/536E, 49G/78V/83E/266V/307K/444L/536E, 49G/78V/83E/266V/307K/356P/444L/509E/536E, 49G/78V/266V/307K/509E/536E, 49G/119Y/129L/132F/266V/298R/307K/444L/509E/536E, 49G/178L/266V/303G/307K/331E/338V/444L/508L/509E/536E, 49G/266V/298R/307K/311I/314M/444L/509E/536E, 49G/63L/266V/297W/298R/303G/305P/307K/509E/536E, 49G/63L/178L/209A/260G/266V/298R/307K/444L/509E/536E/574Q, 49G/63L/266V/298R/300I/307K/338V/444L/509E/536E, 49G/83A/266V/294Q/298R/307K/444L/509E/536E, 49G/83A/92T/266V/307K/343A/444L/509E/536E/574Q, 49G/83A/92T/134P/266V/298R/307K/509E/536E/574Q, 49G/83A/196C/266V/298R/307K/329S/343A/444L/509E/536E, 49G/83A/196C/266V/307K/444L/536E, 49G/83A/134F/196C/294Q/266V/305S/307K/311P/319G/329S/343A/509E/536E/574Q, 49G/83C/266V/298R/307K/444L/509E/536E, 49G/83C/266V/298R/307K/309T/444L/509E/536E, 49G/83C/266V/298R/307K/319S/342W/444L/536E, 49G/83C/205M/266V/298R/307K/509E/536E, 49G/83C/266V/298R/307K/509E/536E, 49G/83C/114G/266V/298R/307K/444L/509E/536E, 49G/83C/114G/266V/298R/307K/309T/444L/536E, 49G/83C/114G/266V/307K/319C/444L/509E/536E, 49G/83C/199L/212K/266V/307K/309E/319C/509E/536E/639H, 49G/83C/199L/266V/298R/307K/444L/536E, 49G/83C/266V/307K/444L/509E/536E, 49G/83C/266V/307K/342W/444L/509E/536E, 49G/83C/266V/298R/307K/308G/309E/444L/509E/536E/595N/638H, 49G/83C/113T/114G/205M/212K/266V/298R/307K/444L/509E/536E, 49G/83C/130S/266V/307K/509E/536E, 49G/114G/266V/298R/307K/309E/444L/509E/536E, 49G/114G/266V/298R/307K/309E/444L/536E, 49G/114G/212K/266V/298R/307K/309E/342W/444L/509E/536E/639H, 49G/114G/205M/266V/298R/307K/509E/536E, 49G/114G/266V/307K/444L/509E/536E, 49G/114G/1305S/266V/298R/307K/319S/509E/536E, 49G/114G/130S/212K/266V/307K/342W/444L/509E/536E, 49G/114G/130S/266V/307K/309E/444L/509E/536E, 49G/199L/266V/298R/307K/309T/444L/509E/536E, 49G/199L/205M/266V/298R/307K/509E/536E, 49G/266V/307K/444L/509E/536E, 49G/266V/307K/342W/444L/509E/536E, 49G/266V/307K/444L/536E, 49G/266V/307K/343A/509E/536E/595N, 49G/74M/266V/298R/307K/444L/509E/536E, 49G/74M/129L/266V/307K/509E/536E, 49G/74M/83E/129L/132F/212V/266V/298R/307K/444L/536E, 49G/74P/83A/92T/266V/307K/343A/444L/536E, 49G/74P/83A/134P/266V/294Q/307 K/444L/509E/536E/574Q, 49G/74P/83W/266V/298R/307K/536E, 49G/74P/266V/307K/329S/509E/536E/574Q, 49G/74P/92T/196C/266V/294Q/298R/307K//329S/444L/509E/536E, 49G/92T/266V/307K/444L/536E, 49G/72M/266V/298R/307K/444L/509E/536E, 49G/72M/266V/294Q/298R/307K/311A/329S/343A/509E/536E, 49G/72M/266V/294Q/307K/509E/536E, 49G/72M/266V/294Q/307K/311A/329S/509E/536E, 49G/72M/266V/298R/307K/444L/536E, 49G/72M/83A/266V/307K/343A/509E/536E, 49G/266V/72M/74P/294Q/307K/509E/536E, 49G/72M/74P/83A/266V/298R/307K/319G/329S/444L/536E, 49G/72M/74P/83A/84N/266V/298R/307K/509E/536E, 49G/72M/74P/83A/134F/196C/266V/294Q/307K/444L/509E/536E, 49G/72M/74P/266V/307K/444L/536E, 49G/72M/74P/92T/266V/294Q/307K/329S/444L/509E/536E, 49G/72M/74P/92T/266V/307K/444L/509E/536E, 49G/72M/74P/92T/134P/266V/307K/343A/509E/536E, 49G/72M/74P/134F/196C/266V/307K/319G/329S/444L/536E, 49G/72M/196C/266V/298R/307K/311A/329S/444L/509E/536E/574Q, 49G/72M/134P/196C/266V/307K/444L/509E/536E, 49G/118R/178L/266V/298R/307K/338V/444L/509E/536E, 49G/69R/89A/178L/266V/298R/303G/305P/307K/338V/444L/509E/536E/574Q, 49G/113G/266V/298R/307K/444L/509E/536E, 49G/113G/178L/260G/266V/298R/307K/444L/509E/536E, 49G/113T/266V/298R/307K/309E/444L/509E/536E, 49G/113T/212K/266V/298R/307K/309E/444L/509E/536E, 49G/113T/266V/298R/307K/342W/444L/509E/536E, 49G/113T/114G/266V/298R/307K/444L/509E/536E, 49G/113T/114G/212K/266V/298R/307K/444L/509E/536E, 49G/113T/114G/205M/266V/298R/307K/319C/342W/444L/509E/536E, 49G/113T/114G/266V/307K/342W/444L/509E/536E, 49G/113T/114G/1305S/266V/298R/307K/444L/509E/536E, 49G/113T/266V/307K/444L/509E/536E, 49G/113T/266V/298R/307K/309E/509E/536E, 49G/130S/205M/266V/298R/307K/333V/509E/536E, 49G/134P/266V/298R/307K/444L/509E/536E, or 49G/134P/266V/294Q/298R/307K/536E, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO:2.

In some embodiments, a recombinant reverse transcriptase of the present disclosure comprises a polypeptide sequence having at least 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity to a reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 24, 94, or 352, or to a reference sequence corresponding to SEQ ID NO: 24, 94, or 352.

In some embodiments, a recombinant reverse transcriptase comprises a polypeptide sequence having at least 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity to a reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 24, 94, or 352, or to a reference sequence corresponding to SEQ ID NO: SEQ ID NO: 24, 94, or 352, wherein the polypeptide sequence comprises one or more substitutions relative to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 24, 94, or 352, or to the reference sequence corresponding to SEQ ID NO: 24, 94, or 352.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution at amino acid position 18, 25, 49, 63, 68, 69, 72, 74, 78, 81, 83, 89, 90, 92, 94, 98, 102, 113, 114, 118, 119, 129, 130, 132, 134, 163, 167, 171, 173, 178, 196, 199, 205, 209, 210, 212, 216, 242, 258, 260, 261, 266, 294, 297, 298, 300, 303, 305, 307, 308, 309, 310, 311, 314, 319, 321, 329, 331, 338, 342, 343, 349, 356, 370, 403, 423, 444, 447, 454, 464, 465, 466, 474, 479, 508, 509, 519, 536, 537, 554, 574, 576, 583, 595, 598, 606, 650, 662, or 665, or combinations thereof, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 24, 94, or 352.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least an amino acid residue 18E, 25E, 49G, 63L/P, 68S, 69R, 72M, 74K/M/P, 78V, 81K, 83E/A/C/R/W, 89A/M, 90I, 92T, 94L, 98S, 102C, 113G/T, 114G/K, 118R, 119Y, 129L, 130R/S, 132F, 134F/P, 163P, 167Y, 171L, 173A, 178L, 196C/H, 199L, 205M, 209A, 210L, 212K/NN, 216R, 242A, 258T, 260G, 261N, 266V, 294Q, 297W, 298E/R, 3001, 303G/Q, 305P, 307K/N, 308G, 309E/P/T, 310R, 311A/I/P, 314A/K/M, 319C/G/S, 321A, 329S, 331E, 338V, 342W, 343A/V, 349G, 356P, 370G, 403H, 444L, 447G/L/R, 454A, 464L, 465S, 466K, 474A, 479D, 508L, 509E, 519P, 536E/A/N, 537W, 554T, 574D/Q, 576I, 583K, 595N, 598S, 606K/Q, or 662R, or combinations thereof, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 24, 94, or 352.

the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution at amino acid position 49, 266, 298, 307, 444, 509, or 536, or combinations thereof, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 24, 94, or 352.

In some embodiments, a recombinant reverse transcriptase comprises a polypeptide sequence having at least 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity to a reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 24, or to a reference sequence corresponding to SEQ ID NO: 24, wherein the polypeptide sequence comprises one or more substitutions relative to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 24, or to the reference sequence corresponding to SEQ ID NO: 24.

In some embodiments, a recombinant reverse transcriptase comprises a polypeptide sequence having at least 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity to a reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 94, or to a reference sequence corresponding to SEQ ID NO: 94, wherein the polypeptide sequence comprises one or more substitutions relative to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 94, or to the reference sequence corresponding to SEQ ID NO: 94.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution or substitution set at amino acid position 134, 74, 83, 319, 92, 329, 343, 311, 338, 196, 69, 72, 294, 83, 134, 130, 305, 319, 113, 297, 319, 114, 308, 309, 342, 205, 212, 199, 83, 303, 309, 78, 113, 132, 311, 119, 83, 98, 314, 129, 343, 196, 74, 356, 89, 212, 444/508/509/574, 63/260/298/300/331/444/509, 63/90/209/444/508/574, 298/444/509, 63/90/508/509/574/595, 83, 311, 89, 130, 178, or 118, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 94.

The recombinant reverse transcriptase of claim 20, comprising a polypeptide sequence having at least 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity to a reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 352, or to a reference sequence corresponding to SEQ ID NO: 352, wherein the polypeptide sequence comprises one or more substitutions relative to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 352, or to the reference sequence corresponding to SEQ ID NO: 352.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution or substitution set at amino acid position 309/342, 309, 129/298, 509/574, 85, 98/119/129/132/196/298, 98/298/317/343/356, 205/212/298/309/319/342/509, 444, 78/132/314, 78/83/98, 78/83/119/132/196/444, 78/83/298, 78/83/298/509, 78/83/298/356, 78/298/444, 119/129/132, 178/298/303/331/338/508, 311/314, 63/297/303/305/444, 63/178/209/260/574, 63/300/338, 83/294, 83/92/298/343/574, 83/92/134/444/574, 83/196/329/343, 83/196/298/509, 83/134/196/294/298/305/311/319/329/343/444/574, 83, 83/309, 83/319/342/509, 83/205/444, 83/444, 83/114, 83/114/309/509, 83/114/298/319, 83/199/212/298/309/319/444/639, 83/199/509, 83/298, 83/298/342, 83/308/309/595/638, 83/113/114/205/212, 83/130/298/444, 114/309, 114/309/509, 114/212/309/342/639, 114/205/444, 114/298, 114/130/319/444, 114/130/212/298/342, 114/130/298/309, 199/309, 199/205/444, 298, 298/342, 298/509, 298/343/444/595, 74, 74/129/298/444, 74/83/129/132/212/509, 74/83/92/298/343/509, 74/83/134/294/298/574, 74/83/444/509, 74/298/329/444/574, 74/92/196/294/329, 92/298/509, 72, 72/294/311/329/343/444, 72/294/298/444, 72/294/298/311/329/444, 72/509, 72/83/298/343/444, 72/74/294/298/444, 72/74/83/319/329/509, 72/74/83/84/444, 72/74/83/134/196/294/298, 72/74/298/509, 72/74/92/294/298/329, 72/74/92/298, 72/74/92/134/298/343/444, 72/74/134/196/298/319/329/509, 72/196/311/329/574, 72/134/196/298, 118/178/338/444, 69/89/178/303/305/338/444/574, 113, 113/178/260, 113/309, 113/212/309, 113/342, 113/114, 113/114/212, 113/114/205/319/342, 113/114/298/342, 113/114/130, 113/298, 113/298/309/444, 130/205/333/444, 134, or 134/294/444/509, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO:352.

In some embodiments, the recombinant reverse transcriptase comprises a polypeptide sequence comprising residues 12 to 687 of an even-numbered sequence of SEQ ID NOS: 4-566, wherein the polypeptide sequence optionally has 1, 2, 3, 4, 5, 6, 7, 8, 9, or up to 10 substitutions in the polypeptide sequence.

In some embodiments, the recombinant reverse transcriptase comprises a polypeptide sequence comprising an even-numbered sequence of SEQ ID NOS: 4-566, wherein the polypeptide sequence optionally has 1, 2, 3, 4, 5, 6, 7, 8, 9, or up to 10 substitutions in the polypeptide sequence.

In some embodiments, the recombinant reverse transcriptase comprises a polypeptide sequence comprising residues 12 to 687 of SEQ ID NO: 4, 24, 94, or 352, or a sequence comprising SEQ ID NO: 4, 24, 94, or 352.

In some embodiments, the recombinant reverse transcriptase has reverse transcriptase activity. In some embodiments, the recombinant reverse transcriptase has DNA polymerase activity with a RNA or DNA template. In some embodiments, the recombinant reverse transcriptase has at least one improved property as compared to a reference reverse transcriptase. In some embodiments, the recombinant reverse transcriptase has at least one improved property selected from increased activity, increased product yield, increased thermostability, increased salt tolerance, increased RNA template sensitivity, increased processivity, increased fidelity, and increased product yield in a coupled PCR reaction (e.g., RT-qPCR) with a DNA polymerase compared to a reference reverse transcriptase. In some embodiments, the reference reverse transcriptase has the sequence corresponding to residues 12 to 687 of SEQ ID NO: 2, 24, 94, or 352, or a sequence corresponding to SEQ ID NO: 2, 24, 94, or 352. In some embodiments, the reference reverse transcriptase has the sequence corresponding to residues 12 to 687 of SEQ ID NO: 2, or a sequence corresponding to SEQ ID NO: 2.

In some further embodiments, the recombinant reverse transcriptase is purified. In some embodiments, the recombinant reverse transcriptase is provided in solution, or is immobilized on a substrate, such as surfaces of solid substrates or membranes or particles.

In another aspect, the present disclosure provides recombinant polynucleotides encoding the recombinant reverse transcriptases provided herein. In some embodiments, the recombinant polynucleotide encodes a recombinant reverse transcriptase, or a functional fragment thereof, comprising a polypeptide sequence having at least 75%, 80%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity to a reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 2, 24, 94, or 352, or to a reference sequence corresponding to SEQ ID NO: 2, 24, 94, or 352, wherein the polypeptide sequence comprises one or more substitutions relative to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 2, 24, 94, or 352, or to the reference sequence corresponding to SEQ ID NO: 2, 24, 94, or 352.

In some embodiments, the recombinant polynucleotide encodes a recombinant reverse transcriptase, or a functional fragment thereof, comprising a polypeptide sequence having at least 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 2, or to the reference sequence corresponding to SEQ ID NO: 2, wherein the polypeptide sequence comprises one or more substitutions relative to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 2, or to the reference sequence corresponding to SEQ ID NO: 2.

In some embodiments, the recombinant polynucleotide comprises a sequence having at least 75%, 80%, 81%, 82%, 83%, 84%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity to a reference polynucleotide sequence corresponding to residues 34 to 2061 of SEQ ID NO: 1, 23, 93, or 351, or to a reference polynucleotide sequence corresponding to SEQ ID NO: 1, 23, 93, or 351, wherein the recombinant polynucleotide encodes a recombinant reverse transcriptase. In some embodiments, the reverse transcriptase polynucleotide encodes a recombinant reverse transcriptase or a functional fragment thereof, wherein the recombinant reverse transcriptase comprises at least one substitution at one or more amino acid positions relative to the reference polypeptide sequence of SEQ ID NO: 2.

In some embodiments, the recombinant polynucleotide comprises a sequence having at least 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity to a reference polynucleotide sequence corresponding to nucleotide residues 34 to 2061 of an odd numbered polynucleotide sequence of SEQ ID NOS: 3-565, wherein the polynucleotide encodes a recombinant reverse transcriptase.

In some embodiments, the recombinant polynucleotide comprises a sequence having at least 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity to a reference polynucleotide sequence comprising an odd numbered polynucleotide sequence of SEQ ID NOS: 3-565, wherein the polynucleotide encodes a recombinant reverse transcriptase.

In some embodiments, the recombinant polynucleotide comprises a sequence comprising nucleotide residues 34 to 2061 of an odd numbered polynucleotide sequence of SEQ ID NOS: 3-565. In some embodiments, the recombinant polynucleotide comprises a sequence comprising an odd numbered polynucleotide sequence of SEQ ID NOS: 3-565.

In some embodiments, the recombinant polynucleotide encoding a recombinant reverse transcriptase is codon optimized for expression in a cell, for example bacterial cell or mammalian cell.

In a further aspect, the present disclosure provides expression vectors comprising at least one recombinant polynucleotide provided herein encoding a recombinant reverse transcriptase. In some embodiments, the recombinant polynucleotide encoding a recombinant reverse transcriptase in the expression vector is operably linked to a control sequence. In some embodiments, the control sequence comprises a promoter, for example a heterologous promoter.

In another aspect, the present disclosure also provides host cells transformed with at least one recombinant polynucleotide encoding the recombinant reverse transcriptase or an expression vector provided herein. In some embodiments, the host cell is a prokaryotic or eukaryotic cell. In some embodiments, the host cell is a bacterial cell, such as E. coli. or B. subtilis.

In a further aspect, the present disclosure provides methods of producing a recombinant reverse transcriptase polypeptide in a host cell, the method comprising culturing a host cell provided herein, under suitable culture conditions, such that at least one recombinant reverse transcriptase is produced. In some embodiments, the method further comprises recovering the recombinant reverse transcriptase from the culture and/or host cells. In some embodiments, the method further comprises the step of purifying the recombinant reverse transcriptase.

In another aspect, the present disclosure provides compositions comprising at least one recombinant reverse transcriptase provided herein. In some embodiments, the composition comprises one or more of a buffer, nucleotide substrates, and/or oligonucleotide primer substrate. In some embodiments, the composition further comprises a second DNA polymerase, such as a thermostable DNA polymerase, e.g., Tag or Pfu DNA polymerase.

In a further aspect, the present disclosure provides uses of the recombinant reverse transcriptase in methods of preparing a complementary DNA (cDNA) copy of a target RNA, whole or in part. In some embodiments, the present disclosure provides a method of preparing a complementary DNA of a target RNA, comprising contacting a target RNA with a recombinant reverse transcriptase described herein in presence of appropriate substrates under conditions suitable for reverse transcriptase mediated production of a DNA complementary to the target RNA.

In some embodiments, the recombinant reverse transcriptase is used to detect a target RNA, the method comprising contacting a sample suspected of containing a target RNA with a recombinant reverse transcriptase of the present disclosure in presence of appropriate substrates under conditions suitable for reverse transcriptase mediated production of a DNA complementary to the target RNA, whole or in part, and detecting presence of the complementary DNA. In some embodiments, the sample is a biological or environmental sample. In some embodiments, detecting the complementary DNA is by amplifying the complementary DNA product, such as by polymerase chain reaction (PCR) or LAMP.

In a further aspect, the present disclosure also provides kits comprising at least one recombinant reverse transcriptase of the present disclosure. In some embodiments, the kits can further comprise one or more of a buffer, nucleotide substrate, and/or oligonucleotide primer substrate. In some embodiments, the kits further includes a second DNA polymerase, for example a thermostable DNA polymerase.

DETAILED DESCRIPTION

The present disclosure provides recombinant reverse transcriptase polypeptides and compositions thereof, as well as polynucleotides encoding the recombinant reverse transcriptase polypeptides. The present disclosure also provides methods of using the recombinant reverse transcriptase polypeptides, including compositions thereof, for diagnostic and other purposes. In some embodiments, the recombinant reverse transcriptase polypeptides are optimized to provide enhanced polymerization activity with high replication fidelity and processivity, particularly under conditions involving low concentrations of RNA input or for high-throughput analysis.

In a further aspect, the present disclosure provides methods and compositions comprising the recombinant reverse transcriptases, for example for diagnostic and research purposes. In some embodiments, the recombinant reverse transcriptases are used in preparing a complementary DNA of a target RNA. In some embodiments, the recombinant reverse transcriptases are used in diagnostic and research applications using small amounts of RNA, for example from biological samples, RNA isolated from virally infected cells, single cells isolated by FACS (fluorescence activated cell sorting), laser-capture microscopy, microfluidic devices, or any other suitable sample.

Abbreviations and Definitions

Unless defined otherwise, all technical and scientific terms used herein generally have the same meaning as commonly understood by one of ordinary skill in the art to which this invention pertains. Generally, the nomenclature used herein and the laboratory procedures of cell culture, molecular genetics, microbiology, organic chemistry, analytical chemistry and nucleic acid chemistry described below are those well-known and commonly employed in the art. Such techniques are well-known and described in numerous texts and reference works well known to those of skill in the art. Standard techniques, or modifications thereof, are used for chemical syntheses and chemical analyses.

Although any suitable methods and materials similar or equivalent to those described herein find use in the practice of the present invention, some methods and materials are described herein. It is to be understood that this invention is not limited to the particular methodology, protocols, and reagents described, as these may vary, depending upon the context they are used by those of skill in the art. Accordingly, the terms defined immediately below are more fully described by reference to the application as a whole.

As used herein, the singular “a”, “an,” and “the” include the plural references, unless the context clearly indicates otherwise.

As used herein, the term “comprising” and its cognates are used in their inclusive sense (i.e., equivalent to the term “including” and its corresponding cognates).

It is to be further understood that where description of embodiments use the term “comprising” and its cognates, the embodiments can also be described using language “consisting essentially of” or “consisting of.”

Numeric ranges are inclusive of the numbers defining the range. Thus, every numerical range disclosed herein is intended to encompass every narrower numerical range that falls within such broader numerical range, as if such narrower numerical ranges were all expressly written herein. It is also intended that every maximum (or minimum) numerical limitation disclosed herein includes every lower (or higher) numerical limitation, as if such lower (or higher) numerical limitations were expressly written herein.

As used herein, the term “about” means an acceptable error for a particular value. In some instances “about” means within 0.05%, 0.5%, 1.0%, or 2.0%, of a given value range. In some instances, “about” means within 1, 2, 3, or 4 standard deviations of a given value.

Furthermore, the headings provided herein are not limitations of the various aspects or embodiments of the invention which can be had by reference to the application as a whole. Accordingly, the terms defined immediately below are more fully defined by reference to the application as a whole. Nonetheless, in order to facilitate understanding of the invention, a number of terms are defined below.

Unless otherwise indicated, nucleic acids are written left to right in 5′ to 3′ orientation; amino acid sequences are written left to right in amino to carboxy orientation, respectively.

As used herein, the “EC” number refers to the Enzyme Nomenclature of the Nomenclature Committee of the International Union of Biochemistry and Molecular Biology (NC-IUBMB). The IUBMB biochemical classification is a numerical classification system for enzymes based on the chemical reactions they catalyze.

As used herein, “ATCC” refers to the American Type Culture Collection whose biorepository collection includes genes and strains.

As used herein, “NCBI” refers to National Center for Biological Information and the sequence databases provided therein.

As used herein, the term “DNA” refers to deoxyribonucleic acid.

As used herein, the term “RNA” refers to ribonucleic acid.

As used herein, the terms “fusion protein,” and “chimeric protein” and “chimera” refer to hybrid proteins created through the joining of two or more genes that originally encoded separate proteins. In some embodiments, fusion proteins are created by recombinant technology (e.g., molecular biology techniques known in the art).

As used herein, the term “polymerase” refers to a class of enzymes that polymerize nucleoside triphosphates. Polymerases use a template nucleic acid strand to synthesize a complementary nucleic acid strand. The template strand and synthesized nucleic acid strand can independently be either DNA or RNA. Polymerases known in the art include but are not limited to DNA polymerases (e.g., E. coli DNA poll, T. aquaticus DNA polymerase (Taq), DNA-dependent RNA polymerases, and reverse transcriptases). As used herein, the polymerase is a polypeptide or protein containing sufficient amino acids to carry out a desired enzymatic function of the polymerase. In some embodiments, the polymerase does not contain all of the amino acids found in the native enzyme, but only those which are sufficient to allow the polymerase to carry out a desired catalytic activity, including but not limited to 5′-3′ polymerization, 5′-3′ exonuclease, and 3′-5′ exonuclease activities.

As used herein, the term “reverse transcriptase” refers to enzymes that are capable of generating DNA using an RNA template. Thus, the term “reverse transcriptase activity” refers to the function of reverse transcriptase enzymes to produce DNA from RNA starting material. In addition, some reverse transcriptase enzymes have RNase activity that degrades the RNA strand in the RNA-DNA hybrid after transcription. In some qPCR reactions, an RNaseH is added to improve efficiency of the reaction.

As used herein, “quantitative reverse transcription polymerase chain reaction,” “quantitative reverse transcription PCR,” and “RT-qPCR,” refer to a polymerase chain reaction assay in which the starting material is RNA. In this method, the starting RNA, e.g., either total RNA or messenger RNA (mRNA) is first transcribed into complementary DNA (i.e., “cDNA” by a reverse transcriptase). The cDNA produced is then used as the template for the quantitative PCR reaction. RT-qPCR finds use in various applications, including gene expression analysis, RNAi validation, microarray validation, pathogen detection, genetic testing, disease research, and other settings. RT-qPCR may be conducted as a one-step or a two-step process. In the one-step process, reverse transcription and PCR are conducted in a single tube and buffer containing a reverse transcriptase and a DNA polymerase. In the process, only sequence-specific primers are used. In contrast, in the two-step methods, the reverse transcription and PCR steps are conducted separately, each reaction containing buffers, reactions, and primers optimized for each enzyme activity.

As used herein, the term “DNA polymerase activity,” “synthetic activity,” and “polymerase activity” are used interchangeably herein, and refer to the ability of an enzyme to synthesize new DNA strands by the incorporation of deoxynucleoside triphosphates. In some embodiments, a DNA polymerase can use DNA and/or RNA as a template.

As used herein, the terms “duplex” and “ds” refer to a double-stranded nucleic acid (e.g., DNA) molecule comprised of two single-stranded polynucleotides that are complementary in their sequence (A pairs to T, C pairs to G), arranged in an antiparallel 5′ to 3′ orientation, and held together by hydrogen bonds between the nucleobases (i.e., adenine [A], guanine [G], cytosine [C], and thymine [T]).

As used herein, the terms “protein,” “polypeptide,” and “peptide” are used interchangeably herein to denote a polymer of at least two amino acids covalently linked by an amide bond, regardless of length or post-translational modification (e.g., glycosylation or phosphorylation).

As used herein, the term “amino acids” are referred to by either their commonly known three-letter symbols or by the one-letter symbols recommended by IUPAC-IUB Biochemical Nomenclature Commission. Nucleotides, likewise, may be referred to by their commonly accepted single letter codes. The abbreviations used for the genetically encoded amino acids are conventional and are as follows: alanine (Ala or A), arginine (Arg or R), asparagine (Asn or N), aspartate (Asp or D), cysteine (Cys or C), glutamate (Glu or E), glutamine (Gln or Q), glycine (Gly or G), histidine (His or H), isoleucine (Ile or I), leucine (Leu or L), lysine (Lys or K), methionine (Met or M), phenylalanine (Phe or F), proline (Pro or P), serine (Ser or S), threonine (Thr or T), tryptophan (Trp or W), tyrosine (Tyr or Y), and valine (Val or V). When the three-letter abbreviations are used, unless specifically preceded by an “L” or a “D” or clear from the context in which the abbreviation is used, the amino acid may be in either the L- or D-configuration about α-carbon (C_α). For example, whereas “Ala” designates alanine without specifying the configuration about the α-carbon, “D-Ala” and “L-Ala” designate D-alanine and L-alanine, respectively. When the one-letter abbreviations are used, upper case letters designate amino acids in the L-configuration about the a-carbon and lower case letters designate amino acids in the D-configuration about the a-carbon. For example, “A” designates L-alanine and “a” designates D-alanine. When polypeptide sequences are presented as a string of one-letter or three-letter abbreviations (or mixtures thereof), the sequences are presented in the amino (N) to carboxy (C) direction in accordance with common convention.

The abbreviations used for the genetically encoding nucleosides are conventional and are as follows: adenosine (A); guanosine (G); cytidine (C); thymidine (T); and uridine (U). Unless specifically delineated, the abbreviated nucleosides may be either ribonucleosides or 2′-deoxyribonucleosides. The nucleosides may be specified as being either ribonucleosides or 2′-deoxyribonucleosides on an individual basis or on an aggregate basis. When nucleic acid sequences are presented as a string of one-letter abbreviations, the sequences are presented in the 5′ to 3′ direction in accordance with common convention, and the phosphates are not indicated.

As used herein, the terms “engineered,” “recombinant,” “non-naturally occurring,” and “variant,” when used with reference to a cell, a polynucleotide or a polypeptide refers to a material or a material corresponding to the natural or native form of the material that has been modified in a manner that would not otherwise exist in nature or is identical thereto but produced or derived from synthetic materials and/or by manipulation using recombinant techniques.

As used herein, “wild-type” and “naturally-occurring” refer to the form found in nature. For example a wild-type polypeptide or polynucleotide sequence is a sequence present in an organism that can be isolated from a source in nature and which has not been intentionally modified by human manipulation.

As used herein, “coding sequence” refers to that part of a nucleic acid (e.g., a gene) that encodes an amino acid sequence of a protein.

As used herein, the term “percent (%) sequence identity” refers to comparisons among polynucleotides and polypeptides, and are determined by comparing two optimally aligned sequences over a comparison window, wherein the portion of the polynucleotide or polypeptide sequence in the comparison window may comprise additions or deletions (i.e. , gaps) as compared to the reference sequence for optimal alignment of the two sequences. The percentage may be calculated by determining the number of positions at which the identical nucleic acid base or amino acid residue occurs in both sequences to yield the number of matched positions, dividing the number of matched positions by the total number of positions in the window of comparison and multiplying the result by 100 to yield the percentage of sequence identity. Alternatively, the percentage may be calculated by determining the number of positions at which either the identical nucleic acid base or amino acid residue occurs in both sequences or a nucleic acid base or amino acid residue is aligned with a gap to yield the number of matched positions, dividing the number of matched positions by the total number of positions in the window of comparison and multiplying the result by 100 to yield the percentage of sequence identity. Those of skill in the art appreciate that there are many established algorithms available to align two sequences. Optimal alignment of sequences for comparison can be conducted, e.g., by the local homology algorithm of Smith and Waterman (Smith and Waterman, Adv. Appl. Math., 1981, 2:482), by the homology alignment algorithm of Needleman and Wunsch (Needleman and Wunsch, J. Mol. Biol., 1970, 48:443), by the search for similarity method of Pearson and Lipman (Pearson and Lipman, Proc. Natl. Acad. Sci. USA, 1988, 85:2444), by computerized implementations of these algorithms (e.g., GAP, BESTFIT, FASTA, and TFASTA in the GCG Wisconsin Software Package), or by visual inspection, as known in the art. Examples of algorithms that are suitable for determining percent sequence identity and sequence similarity include, but are not limited to the BLAST and BLAST 2.0 algorithms (See e.g., Altschul et al., J. Mol. Biol., 1990, 215:403-410; and Altschul et al., Nucleic Acids Res., 1977, 3389-3402). Software for performing BLAST analyses is publicly available through the National Center for Biotechnology Information website. This algorithm involves first identifying high scoring sequence pairs (HSPs) by identifying short words of length “W” in the query sequence, which either match or satisfy some positive-valued threshold score “T,” when aligned with a word of the same length in a database sequence. T is referred to as the neighborhood word score threshold (See, Altschul et al, supra). These initial neighborhood word hits act as seeds for initiating searches to find longer HSPs containing them. The word hits are then extended in both directions along each sequence for as far as the cumulative alignment score can be increased. Cumulative scores are calculated using, for nucleotide sequences, the parameters “M” (reward score for a pair of matching residues; always >0) and “N” (penalty score for mismatching residues; always <0). For amino acid sequences, a scoring matrix is used to calculate the cumulative score. Extension of the word hits in each direction are halted when: the cumulative alignment score falls off by the quantity “X” from its maximum achieved value; the cumulative score goes to zero or below, due to the accumulation of one or more negative-scoring residue alignments; or the end of either sequence is reached. The BLAST algorithm parameters W, T, and X determine the sensitivity and speed of the alignment. The BLASTN program (for nucleotide sequences) uses as defaults a wordlength (W) of 11, an expectation (E) of 10, M=5, N=-4, and a comparison of both strands. For amino acid sequences, the BLASTP program uses as defaults a wordlength (W) of 3, an expectation (E) of 10, and the BLOSUM62 scoring matrix (See e.g., Henikoff and Henikoff, Proc. Natl. Acad. Sci. USA, 1989, 89:10915). Exemplary determination of sequence alignment and % sequence identity can employ the BESTFIT or GAP programs in the GCG Wisconsin Software package (Accelrys, Madison Wis.), using default parameters provided.

As used herein, “reference sequence” refers to a defined sequence used as a basis for a sequence comparison. A reference sequence may be a subset of a larger sequence, for example, a segment of a full-length gene or polypeptide sequence. Generally, a reference sequence is at least 20 nucleotide or amino acid residues in length, at least 25 residues in length, at least 50 residues in length, at least 100 residues in length or the full length of the nucleic acid or polypeptide. Since two polynucleotides or polypeptides may each (1) comprise a sequence (i.e., a portion of the complete sequence) that is similar between the two sequences, and (2) may further comprise a sequence that is divergent between the two sequences, sequence comparisons between two (or more) polynucleotides or polypeptide are typically performed by comparing sequences of the two polynucleotides or polypeptides over a “comparison window” to identify and compare local regions of sequence similarity. In some embodiments, a “reference sequence” can be based on a primary amino acid sequence, where the reference sequence is a sequence that can have one or more changes in the primary sequence. For instance, the phrase “a reference sequence based on SEQ ID NO: 2, having a glycine at the residue corresponding to X49” (or “a reference sequence based on SEQ ID NO: 2, having a glycine at the residue corresponding to position 49”) refers to a reference sequence in which the corresponding residue at position X49 in SEQ ID NO: 2 (e.g., an alanine), has been changed to glycine.

As used herein, “comparison window” refers to a conceptual segment of at least about 20 contiguous nucleotide positions or amino acids residues wherein a sequence may be compared to a reference sequence of at least 20 contiguous nucleotides or amino acids and wherein the portion of the sequence in the comparison window may comprise additions or deletions (i.e., gaps) of 20 percent or less as compared to the reference sequence (which does not comprise additions or deletions) for optimal alignment of the two sequences. The comparison window can be longer than 20 contiguous residues, and includes, optionally 30, 40, 50, 100, or longer windows.

As used herein, “corresponding to”, “reference to,” and “relative to” when used in the context of the numbering of a given amino acid or polynucleotide sequence refer to the numbering of the residues of a specified reference sequence when the given amino acid or polynucleotide sequence is compared to the reference sequence. In other words, the residue number or residue position of a given polymer is designated with respect to the reference sequence rather than by the actual numerical position of the residue within the given amino acid or polynucleotide sequence. For example, a given amino acid sequence, such as that of a recombinant reverse transcriptase, can be aligned to a reference sequence by introducing gaps to optimize residue matches between the two sequences. In these cases, although the gaps are present, the numbering of the residue in the given amino acid or polynucleotide sequence is made with respect to the reference sequence to which it has been aligned. In some embodiments, the sequence is tagged (e.g., with a histidine tag).

As used herein, “mutation” refers to the alteration of a nucleic acid sequence. In some embodiments, mutations result in changes to the encoded polypeptide sequence (i.e., as compared to the original sequence without the mutation). In some embodiments, the mutation comprises a substitution, such that a different amino acid is produced (e.g., substitution of an aspartic acid with tryptophan). In some alternative embodiments, the mutation comprises an addition, such that an amino acid is added to the original polypeptide sequence. In some further embodiments, the mutation comprises a deletion, such that an amino acid is deleted from the original polypeptide sequence. Any number of mutations may be present in a given sequence.

As used herein, “amino acid difference” and “residue difference” refer to a difference in the amino acid residue at a position of a polypeptide sequence relative to the amino acid residue at a corresponding position in a reference sequence. The positions of amino acid differences generally are referred to herein as “Xn,” where n refers to the corresponding position in the reference sequence upon which the residue difference is based. For example, a “residue difference at position X18 as compared to SEQ ID NO: 2” (or a “residue difference at position 18 as compared to SEQ ID NO: 2”) refers to a difference of the amino acid residue at the polypeptide position corresponding to position 18 of SEQ ID NO: 2. Thus, if the reference polypeptide of SEQ ID NO: 2 has an aspartic acid at position 18, then a “residue difference at position X18 as compared to SEQ ID NO: 2” refers to an amino acid substitution of any residue other than aspartic acid at the position of the polypeptide corresponding to position 18 of SEQ ID NO: 2. In some instances herein, the specific amino acid residue difference at a position is indicated as “XnY” where “Xn” specified the corresponding residue and position of the reference polypeptide (as described above), and “Y” is the single letter identifier of the amino acid found in the engineered polypeptide (i.e., the different residue than in the reference polypeptide). In some instances (e.g., in the Tables in the Examples), the present disclosure also provides specific amino acid differences denoted by the conventional notation “AnB”, where A is the single letter identifier of the residue in the reference sequence, “n” is the number of the residue position in the reference sequence, and B is the single letter identifier of the residue substitution in the sequence of the engineered polypeptide. In some instances, a polypeptide of the present disclosure can include one or more amino acid residue differences relative to a reference sequence, which is indicated by a list of the specified positions where residue differences are present relative to the reference sequence. In some embodiments, where more than one amino acid can be used in a specific residue position of a polypeptide, the various amino acid residues that can be used are separated by a “/” (e.g., X447G/X447L, X447G/L, or I447G/L or 447G/L). The present disclosure includes engineered polypeptide sequences comprising one or more amino acid differences that include either/or both conservative and non-conservative amino acid substitutions, as well as insertions and deletions of amino acids in the sequence.

As used herein, the terms “amino acid substitution set” and “substitution set” refers to a group of amino acid substitutions within a polypeptide sequence. In some embodiments, substitution sets comprise 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, or more amino acid substitutions. In some embodiments, a substitution set refers to the set of amino acid substitutions that is present in any of the variant Reverse transcriptase polypeptides listed in any of the Tables in the Examples. In these substitution sets, the individual substitutions are separated by a semicolon (“;”; e.g., R114K; I210L; T307K) or slash (“/”; e.g., R114K/I210L/T307K or 114K/210L/307K). In some embodiments, the “substitution” comprises the deletion of an amino acid.

As used herein, “conservative amino acid substitution” refers to a substitution of a residue with a different residue having a similar side chain, and thus typically involves substitution of the amino acid in the polypeptide with amino acids within the same or similar defined class of amino acids. By way of example and not limitation, an amino acid with an aliphatic side chain may be substituted with another aliphatic amino acid (e.g., alanine, valine, leucine, and isoleucine); an amino acid with hydroxyl side chain is substituted with another amino acid with a hydroxyl side chain (e.g., serine and threonine); an amino acids having aromatic side chains is substituted with another amino acid having an aromatic side chain (e.g., phenylalanine, tyrosine, tryptophan, and histidine); an amino acid with a basic side chain is substituted with another amino acid with a basis side chain (e.g., lysine and arginine); an amino acid with an acidic side chain is substituted with another amino acid with an acidic side chain (e.g., aspartic acid or glutamic acid); and a hydrophobic or hydrophilic amino acid is replaced with another hydrophobic or hydrophilic amino acid, respectively.

As used herein, “non-conservative substitution” refers to substitution of an amino acid in the polypeptide with an amino acid with significantly differing side chain properties. Non-conservative substitutions may use amino acids between, rather than within, the defined groups and affect: (a) the structure of the peptide backbone in the area of the substitution (e.g., proline for glycine); (b) the charge or hydrophobicity; and/or (c) the bulk of the side chain. By way of example and not limitation, exemplary non-conservative substitutions include an acidic amino acid substituted with a basic or aliphatic amino acid; an aromatic amino acid substituted with a small amino acid; and a hydrophilic amino acid substituted with a hydrophobic amino acid.

As used herein, “deletion” refers to modification to the polypeptide by removal of one or more amino acids from the reference polypeptide. Deletions can comprise removal of 1 or more amino acids, 2 or more amino acids, 5 or more amino acids, 10 or more amino acids, 15 or more amino acids, or 20 or more amino acids, up to 10% of the total number of amino acids, or up to 20% of the total number of amino acids making up the reference enzyme while retaining enzymatic activity and/or retaining the improved properties of an engineered polymerase enzyme. Deletions can be directed to the internal portions and/or terminal portions of the polypeptide. In various embodiments, the deletion can comprise a continuous segment or can be discontinuous. Deletions are indicated by “-”, and may be present in substitution sets.

As used herein, “insertion” refers to modification to the polypeptide by addition of one or more amino acids from the reference polypeptide. Insertions can be in the internal portions of the polypeptide, or to the carboxy or amino terminus. Insertions as used herein include fusion proteins as is known in the art. The insertion can be a contiguous segment of amino acids or separated by one or more of the amino acids in the naturally occurring polypeptide.

As used herein, “functional fragment” and “biologically active fragment” are used interchangeably herein, to refer to a polypeptide that has an amino-terminal and/or carboxy-terminal deletion(s) and/or internal deletions, but where the remaining amino acid sequence is identical to the corresponding positions in the sequence to which it is being compared (e.g., a full length engineered reverse transcriptase of the present invention) and that retains substantially all of the activity of the full-length polypeptide.

As used herein, “isolated polypeptide” refers to a polypeptide which is substantially separated from other contaminants that naturally accompany it (e.g., protein, lipids, and polynucleotides). The term embraces polypeptides which have been removed or purified from their naturally-occurring environment or expression system (e.g., host cell or in vitro synthesis). The recombinant reverse transcriptase polypeptides may be present within a cell, present in the cellular medium, or prepared in various forms, such as lysates or isolated preparations. As such, in some embodiments, the recombinant reverse polymerase polypeptides provided herein are isolated polypeptides.

As used herein, “substantially pure polypeptide” refers to a composition in which the polypeptide species is the predominant species present (i.e., on a molar or weight basis it is more abundant than any other individual macromolecular species in the composition), and is generally a substantially purified composition when the object species comprises at least about 50 percent of the macromolecular species present by mole or % weight. Generally, a substantially pure DNA polymerase composition will comprise about 60% or more, about 70% or more, about 80% or more, about 90% or more, about 95% or more, and about 98% or more of all macromolecular species by mole or % weight present in the composition. In some embodiments, the object species is purified to essential homogeneity (i.e., contaminant species cannot be detected in the composition by conventional detection methods) wherein the composition consists essentially of a single macromolecular species. Solvent species, small molecules (<500 Daltons), and elemental ion species are not considered macromolecular species. In some embodiments, the isolated recombinant reverse transcriptase polypeptides are substantially pure polypeptide compositions.

As used herein, “improved enzyme property” refers to a recombinant reverse transcriptase polypeptide that exhibits an improvement in any enzyme property as compared to a reference reverse transcriptase polypeptide, such as a wild-type reverse transcriptase polypeptide (e.g., the reverse transcriptase of SEQ ID NO: 2) or another reference recombinant reverse transcriptase polypeptide. Improved properties include but are not limited to such properties as increased protein expression, increased thermoactivity, increased thermostability, increased salt tolerance, increased stability, increased enzymatic activity, increased substrate specificity and/or affinity, increased specific activity, increased resistance to substrate and/or end-product inhibition, increased chemical stability, improved solvent stability, increased tolerance to acidic pH, increased tolerance to proteolytic activity (i.e., reduced sensitivity to proteolysis), increased solubility, increased processivity, increased fidelity, and altered temperature profile.

As used herein, “increased enzymatic activity” and “enhanced catalytic activity” refer to an improved property of the recombinant reverse transcriptase polypeptides, which can be represented by an increase in specific activity (e.g., product produced/time/weight protein) and/or an increase in percent conversion of the substrate to the product (e.g., percent conversion of starting amount of substrate to product in a specified time period using a specified amount of reverse transcriptase) as compared to the reference reverse transcriptase enzyme (e.g., wild-type reverse transcriptase and/or another recombinant reverse transcriptase). Exemplary methods to determine enzyme activity are provided in the Examples. Any property relating to enzyme activity may be affected, including the classical enzyme properties of K_m, V_maxor k_cat, changes of which can lead to increased enzymatic activity. Improvements in enzyme activity can be from about 1.1 fold the enzymatic activity of the corresponding wild-type enzyme, to as much as 2-fold, 5-fold, 10-fold, 20-fold, 25-fold, 50-fold, 75-fold, 100-fold, 150-fold, 200-fold or more enzymatic activity than the naturally occurring reverse transcriptase or another recombinant reverse transcriptase from which the reverse transcriptase polypeptides were derived.

As used herein, “conversion” refers to the enzymatic conversion (or biotransformation) of substrate(s) to the corresponding product(s). “Percent conversion” refers to the percent of the substrate that is converted to the product within a period of time under specified conditions. Thus, the “enzymatic activity” or “activity” of a reverse transcriptase polypeptide can be expressed as “percent conversion” of the substrate to the product in a specific period of time. In some embodiments, in context of a polymerase “conversion” can relate to the amount of nucleotide substrate incorporated into a DNA polymer.

As used herein, “hybridization stringency” relates to hybridization conditions, such as washing conditions, in the hybridization of nucleic acids. Generally, hybridization reactions are performed under conditions of lower stringency, followed by washes of varying but higher stringency. The term “moderately stringent hybridization” refers to conditions that permit target-DNA to bind a complementary nucleic acid that has about 60% identity, preferably about 75% identity, about 85% identity to the target DNA, with greater than about 90% identity to target-polynucleotide. Exemplary moderately stringent conditions are conditions equivalent to hybridization in 50% formamide, 5× Denhart's solution, 5×SSPE, 0.2% SDS at 42° C., followed by washing in 0.2×SSPE, 0.2% SDS, at 42° C. “High stringency hybridization” refers generally to conditions that are about 10° C. or less from the thermal melting temperature T_mas determined under the solution condition for a defined polynucleotide sequence. In some embodiments, a high stringency condition refers to conditions that permit hybridization of only those nucleic acid sequences that form stable hybrids in 0.018M NaCl at 65° C. (i.e., if a hybrid is not stable in 0.018M NaCl at 65° C., it will not be stable under high stringency conditions, as contemplated herein). High stringency conditions can be provided, for example, by hybridization in conditions equivalent to 50% formamide, 5× Denhart's solution, 5× SSPE, 0.2% SDS at 42° C., followed by washing in 0.1× SSPE, and 0.1% SDS at 65° C. Another high stringency condition comprises hybridizing in conditions equivalent to hybridizing in 5× SSC containing 0.1% (w:v) SDS at 65° C. and washing in 0.1× SSC containing 0.1% SDS at 65° C. Other high stringency hybridization conditions, as well as moderately stringent conditions, are described in the references cited above.

As used herein, “codon optimized” refers to changes in the codons of the polynucleotide encoding a protein to those preferentially used in a particular organism such that the encoded protein is more efficiently expressed in that organism. Although the genetic code is degenerate, in that most amino acids are represented by several codons, called “synonyms” or “synonymous” codons, it is well known that codon usage by particular organisms is nonrandom and biased towards particular codon triplets. This codon usage bias may be higher in reference to a given gene, genes of common function or ancestral origin, highly expressed proteins versus low copy number proteins, and the aggregate protein coding regions of an organism's genome. In some embodiments, the polynucleotides encoding the DNA polymerase enzymes are codon optimized for optimal production from the host organism selected for expression.

As used herein, “control sequence” refers herein to include all components that are necessary or advantageous for the expression of a polynucleotide and/or polypeptide of the present disclosure. Each control sequence may be native or foreign to the nucleic acid sequence encoding the polypeptide. Such control sequences include, but are not limited to, leaders, polyadenylation sequences, propeptide sequences, promoter sequences, signal peptide sequences, initiation sequences, and transcription terminators. At a minimum, the control sequences include a promoter, and transcriptional and translational stop signals. In some embodiments, the control sequences are provided with linkers for the purpose of introducing specific restriction sites facilitating ligation of the control sequences with the coding region of the nucleic acid sequence encoding a polypeptide.

As used herein, “operably linked” is defined herein as a configuration in which a control sequence is appropriately placed (i.e., in a functional relationship) at a position relative to a polynucleotide of interest such that the control sequence directs or regulates the expression of the polynucleotide encoding a polypeptide of interest.

As used herein, “promoter sequence” refers to a nucleic acid sequence that is recognized by a host cell for expression of a polynucleotide of interest, such as a coding sequence. The promoter sequence contains transcriptional control sequences that mediate the expression of a polynucleotide of interest. The promoter may be any nucleic acid sequence which shows transcriptional activity in the host cell of choice including mutant, truncated, and hybrid promoters, and may be obtained from genes encoding extracellular or intracellular polypeptides either homologous or heterologous to the host cell.

As used herein, “substrate” in context of reverse transcriptase refers to any substrate used by reverse transcriptase in producing a DNA from a template, either RNA or DNA. In some embodiments, the substrate comprises nucleotides, e.g., nucleotide triphosphates, including non-naturally occurring nucleotides, used by reverse transcriptase. In some embodiments, the substrate is a polynucleotide/oligonucleotide primer, where the primer is used by the reverse transcriptase in initiation polymerization.

As used herein, “target RNA” refers to an RNA that is the RNA of interest to act as a template for a reverse transcriptase. Exemplary “target RNA” includes, without limitation, mRNA, ribosomal RNA (rRNA), micro RNA (miRNA), small nuclear RNA (snRNA), non-coding RNA, cell-free RNA (cfRNA), viral RNA, bacterial RNA, yeast RNA, and iRNA. The “target” refers to all or a portion of the RNA.

As used herein, “suitable reaction conditions” or “suitable conditions” refers to those conditions in the enzymatic conversion reaction solution (e.g., ranges of enzyme loading, substrate loading, temperature, pH, buffers, co-solvents, etc.) under which a reverse transcriptase polypeptide of the present disclosure is capable of converting a substrate to the desired product compound. Exemplary “suitable reaction conditions” are provided herein (see, the Examples).

As used herein, “loading”, such as in “compound loading” or “enzyme loading” refers to the concentration or amount of a component in a reaction mixture at the start of the reaction. “Substrate” in the context of an enzymatic conversion reaction process refers to the compound or molecule acted on by the reverse transcriptase polypeptide.

As used herein, “product” in the context of an enzymatic conversion process refers to the compound or molecule resulting from the action of the reverse transcriptase polypeptide on a template, e.g., RNA template.

As used herein, “culturing” refers to the growing of a population of microbial cells under suitable conditions using any suitable medium (e.g., liquid, gel, or solid).

Recombinant polypeptides (e.g., reverse transcriptase variants) can be produced using any suitable methods known the art. For example, there is a wide variety of different mutagenesis techniques well known to those skilled in the art. In addition, mutagenesis kits are also available from many commercial molecular biology suppliers. Methods are available to make specific substitutions at defined amino acids (site-directed), specific or random mutations in a localized region of the gene (regio-specific), or random mutagenesis over the entire gene (e.g., saturation mutagenesis). Numerous suitable methods are known to those in the art to generate enzyme variants, including but not limited to site-directed mutagenesis of single-stranded DNA or double-stranded DNA using PCR, cassette mutagenesis, gene synthesis, error-prone PCR, shuffling, and chemical saturation mutagenesis, or any other suitable method known in the art. Non-limiting examples of methods used for DNA and protein engineering are provided in the following patents: US Pat. Nos. 6,117,679; 6,420,175; 6,376,246; 6,586,182; 7,747,391; 7,747,393; 7,783,428; and 8,383,346. After the variants are produced, they can be screened for any desired property (e.g., high or increased activity, or low or reduced activity, increased thermal activity, increased thermal stability, increased fidelity, increased processivity, and/or pH stability, etc.). In some embodiments, “recombinant reverse transcriptase polypeptides” (also referred to herein as “recombinant reverse transcriptase polypeptides,” “recombinant reverse transcriptases,” “variant DNA polymerase enzymes,” and “DNA polymerase variants”) find use in diagnostics and molecular biological tools.

As used herein, a “vector” is a DNA construct for introducing a DNA sequence into a cell. In some embodiments, the vector is an expression vector that is operably linked to a suitable control sequence capable of effecting the expression in a suitable host of the polypeptide encoded in the DNA sequence. In some embodiments, an “expression vector” has a promoter sequence operably linked to the DNA sequence (e.g., transgene) to drive expression in a host cell, and in some embodiments, also comprises a transcription terminator sequence.

As used herein, the term “expression” includes any step involved in the production of the polypeptide including, but not limited to, transcription, post-transcriptional modification, translation, and post-translational modification. In some embodiments, the term also encompasses secretion of the polypeptide from a cell.

As used herein, the term “produces” refers to the production of proteins and/or other compounds by cells. It is intended that the term encompass any step involved in the production of polypeptides including, but not limited to, transcription, post-transcriptional modification, translation, and post-translational modification. In some embodiments, the term also encompasses secretion of the polypeptide from a cell.

As used herein, an amino acid or nucleotide sequence (e.g., a promoter sequence, signal peptide, terminator sequence, etc.) is “heterologous” to another sequence with which it is operably linked if the two sequences are not associated in nature.

As used herein, the terms “host cell” and “host strain” refer to suitable hosts for expression vectors comprising DNA provided herein (e.g., a polynucleotide sequences encoding at least one DNA polymerase variant). In some embodiments, the host cells are prokaryotic or eukaryotic cells that have been transformed or transfected with vectors constructed using recombinant DNA techniques as known in the art.

As used herein, the term “analogue” means a polypeptide having more than 70% sequence identity but less than 100% sequence identity (e.g., more than 75%, 78%, 80%, 83%, 85%, 88%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% sequence identity) with a reference polypeptide. In some embodiments, analogues include non-naturally occurring amino acid residues including, but not limited, to homoarginine, ornithine and norvaline, as well as naturally occurring amino acids. In some embodiments, analogues also include one or more D-amino acid residues and non-peptide linkages between two or more amino acid residues.

As used herein, the term “effective amount” means an amount sufficient to produce the desired result. One of general skill in the art may determine what the effective amount by using routine experimentation.

The terms “isolated” and “purified” are used to refer to a molecule (e.g., an isolated nucleic acid, polypeptide, etc.) or other component that is removed from at least one other component with which it is naturally associated. The term “purified” does not require absolute purity, rather it is intended as a relative definition.

As used herein, “cell-free RNA” or “cfRNA” refers to RNA circulating freely in the bloodstream and is not contained by or associated with cells. In some embodiments, cell-free RNA comprises RNA originally derived and released from normal somatic or germ line cells, cancer cells, fetal cells, microbial cells, or viruses.

As used herein, “amplification” refers to nucleic acid replication. In some embodiments, the term refers to replication of specific template nucleic acid.

As used herein, “polymerase chain reaction” and “PCR” refer to the methods described in U.S. Pat. Nos. 4,683,195 and 4,6884,202, hereby incorporated by reference. These methods find use in increasing the concentration of a segment of a target sequence or an entire target sequence in a mixture or purified DNA, without cloning or purification being required. The sequence of denaturation, annealing and extension constitute a “cycle.” The steps of denaturing, primer annealing, and polymerase extension can be repeated many times (i.e., multiple cycles are used), to obtain a high concentration of amplified DNA. The process is well-known in the art and numerous variations have been developed over the years since the method was first described. With PCR, it is possible to amplify a single copy of a specific target sequence to a level that is detectable by several different methodologies, including but not limited to hybridization with a labeled probe, incorporation of biotinylated primers followed by avidin-enzyme conjugate detection, incorporation of ³²P-labeled deoxyribonucleotide triphosphates (e.g., dCTP or dATP) into the amplified segment, etc. In addition to genomic DNA, any oligonucleotide sequence amenable to amplification can be copies using PCR with an appropriate set of primers. PCR products can also serve as templates for amplification.

As used herein, “target” in context of methods of using a DNA polymerase refers to the region of nucleic acid bounded by the primers used in the method. The “target” is sorted out from other nucleic acids present in the sample used the method. In some embodiments, a “segment” is a region of nucleic acid within the target sequence.

As used herein, “target RNA” when used in context of a reverse transcriptase refers to the RNA, all or a portion thereof, that is the object for preparation of a complementary DNA copy. As noted, the target RNA can be the whole of the RNA sequence or a portion thereof, such as a segment of the RNA sequence.

As used herein, “sample template” refers to nucleic acid originating from a sample which is analyzed for the presence of target nucleic acid. In contrast, “background template” refers to nucleic acid other than sample template that may or may not be present within a sample. Background template may be inadvertently included in the sample, it may result from carryover, or may be due to the presence of nucleic acid contaminants from which the target nucleic acid is purified. For example, in some embodiments, nucleic acids from organisms other than those to be detected may be present as background in a test sample. However, it is not intended that the present invention be limited to any specific nucleic acid samples or templates.

As used herein, “amplifiable nucleic acid” is used in reference to nucleic acids which may be amplified by any amplification method, including but not limited to PCR. In most embodiments, amplifiable nucleic acids comprise sample templates.

As used herein, “PCR product”, “PCR fragment,” and “amplification product” refer to the resultant compounds obtained after two or more cycles of PCR amplification (or other amplification method, as indicated by the context), typically comprising the steps of denaturation, annealing, and extension. The terms encompass the situation wherein there has been amplification of one or more segments of one or more target sequences.

As used herein, “amplification reagents” and “PCR reagents” refer to those reagents (e.g., deoxyribonucleotide triphosphates, buffer, etc.), needed for amplification except for the primers, nucleic acid template, and the amplification enzyme. Typically, amplification reagents, along with other reaction components are placed and contained in a reaction vessel (e.g., test tube, microwell, etc.). It is not intended that the present invention be limited to any specific amplification reagents, as any suitable reagents find use in the present invention.

As used herein, “primer” refers to an oligonucleotide or polynucleotide (i.e., a sequence of nucleotides), whether occurring naturally or produced synthetically, recombinantly, or by amplification, which is capable of acting as a point of initiation of nucleic acid synthesis, when placed under conditions in which synthesis of a primer extension product that is complementary to a nucleic acid strand is induced (i.e., in the presence of nucleotides and an inducing agent such as reverse transcriptase, and at a suitable temperature and pH). In most embodiments, primers are single-stranded, but in some embodiments, they are double-stranded. In some embodiments, the primers are of sufficient length to prime the synthesis of extension products in the presence of a reverse transcriptase or DNA polymerase. The exact primer length depends upon many factors, as known to those skilled in the art. In some embodiments, the primers can be sequence specific primers or random primers.

As used herein, “probe” refers to an oligonucleotide (i.e., a sequence of nucleotides), whether occurring naturally or produced synthetically, recombinantly, or by amplification, which is capable of hybridizing to another oligonucleotide of interest. Probes find use in the detection, identification, and/or isolation of particular gene sequences of interest. In some embodiments, probes are labeled with a “reporter molecule” (also referred to as a “label”) that aids in the detection of the probe in a suitable detection system (e.g., fluorescent, radioactive, luminescent, enzymatic, and other systems). It is not intended that the present invention be limited to any particular detection system or label. Primers, deoxyribonucleotides, and deoxyribonucleosides may contain labels. Indeed, it is not intended that the labeled composition of the present invention be limited to any particular component. Illustrative labels include, but are not limited to ³²P, ³⁵S, and fluorescent molecules (e.g., fluorescent dyes, including but not limited to green fluorescent protein).

As used herein, “fidelity,” when used in reference to a polymerase, including a reverse transcriptase, is intended to refer to the accuracy of template-directed incorporation of complementary bases in a synthesized DNA strand relative to the template strand. Typically, fidelity is measured based on the frequency of incorporation of incorrect bases in the newly synthesized nucleic acid strand. The incorporation of incorrect bases can result in point mutations, insertions, or deletions. Fidelity can be calculated according to any method known in the art (See e.g., Tindall and Kunkel, Biochem., 1988, 27:6008-6013; and Barnes, Gene, 1992, 112:29-35). A reverse transcriptase, polymerase or variants thereof can exhibit either high fidelity or low fidelity. As used herein, “high fidelity” refers to polymerases with a frequency of accurate base incorporation that exceeds a predetermined value. As used herein, the term “low fidelity” refers to polymerases with a frequency of accurate base incorporation that is lower than a predetermined value. In some embodiments, the predetermined value is a desired frequency of accurate base incorporation or the fidelity of a known reverse transcriptase or polymerase (i.e., a reference reverse transcriptase or polymerase).

As used herein, “altered fidelity” refers to the fidelity of a reverse transcriptase, polymerase, or variants thereof that differ from the fidelity of the parent reverse transcriptase or polymerase from which the variant was derived. In some embodiments, the altered fidelity is higher than the fidelity of the parent enzyme, while in some other embodiments, the altered fidelity is lower than the fidelity of the parent enzyme. Altered fidelity can be determined by assaying the parent and variant enzymes and comparing their activities using any suitable assay known in the art.

As used herein, the term “processivity” refers to the ability of a nucleic acid modifying enzyme, such as a DNA polymerase, to remain bound to the template or substrate and perform multiple modification reactions. Processivity is generally measured by the number of catalytic events that take place per binding event.

As used herein, “altered processivity” refers to the processivity of polymerase, or variants thereof that differ from the processivity of the parent polymerase from which the variant was derived. In some embodiments, the altered processivity is higher than the processivity of the parent enzyme, while in some other embodiments, the altered processivity is lower than the processivity of the parent enzyme. Altered processivity can be determined by assaying the parent and variant enzymes and comparing their activities using any suitable assay known in the art.

As used herein, the term “subject” encompasses mammals such as humans, non-human primates, livestock, companion animals, and laboratory animals (e.g., rodents and lagamorphs). It is intended that the term encompass females as well as males. As used herein, the term “patient” means any subject that is being assessed for, treated for, or is experiencing disease.

As used herein, the term “sample” refers to a material or substance for reaction with a reverse transcriptase, for example, such as for detecting presence of a target RNA or preparing a cDNA copy of a target RNA for sequencing or generation of cDNA libraries. In some embodiments, the sample is a “biological sample,” which refers to sample of biological tissue or fluid. Such samples are typically from humans, but include tissues isolated from non-human primates, or rodents, e.g., mice, and rats, and includes sections of tissues such as biopsy and autopsy samples, frozen sections taken for histological purposes, blood, plasma, serum, sputum, stool, tears, mucus, hair, skin, etc. A “biological sample” also refers to a cell or population of cells or a quantity of tissue or fluid from organisms. In some embodiments, the biological sample has been removed from an animal, but the term “biological sample” can also refer to cells or tissue analyzed in vivo, i.e., without removal from the animal. Typically, a “biological sample” will contain cells from the animal or of organisms, but the term can also refer to noncellular biological material, such as noncellular fractions of blood, saliva, or urine. Numerous types of biological samples can be used with the enzymes, compositions, and method in the present disclosure, including, but not limited to, a tissue biopsy, a blood sample, a buccal scrape, a saliva sample, or a nipple discharge. As used herein, a “tissue biopsy” refers to an amount of tissue removed from an animal, preferably a human, for diagnostic analysis. In a patient with cancer, tissue may be removed from a tumor, allowing the analysis of cells within the tumor. “Tissue biopsy” can refer to any type of biopsy, such as needle biopsy, fine needle biopsy, surgical biopsy, etc.

Recombinant Reverse Transcriptase Polypeptides

The present disclosure provides recombinant or engineered reverse transcriptase variants having one or more improved properties. In some embodiments, the recombinant reverse transcriptase polypeptide variants are useful in performing polymerase reactions, including preparing a complementary DNA of an RNA target/template, whole or in part. The recombinant reverse transcriptase variants of the present disclosure find use in the efficient creation of DNA libraries from RNA templates, such as for generating cDNA libraries; sequencing; and diagnostic methods, such as for detecting a target RNA. The reverse transcriptase variants of the disclosure can be used in solution, as well as in immobilized embodiments. In some embodiments, the recombinant reverse transcriptase can prepared and used as non-fusion polypeptides or as fusion polypeptides.

In some embodiments herein, when a particular reverse transcriptase variant (i.e., a recombinant reverse transcriptase polypeptide) is referred to by reference to modification of particular amino acid residues in the sequence of a wild-type reverse transcriptase or reference reverse transcriptase polypeptide, it is to be understood that variants of another reverse transcriptase modified in the equivalent position(s) (as determined from the optional amino acid sequence alignment between the respective amino acid sequences) are encompassed herein. For example, for a substitution at specified amino acid position(s) numbered in reference to SEQ ID: 2, an equivalent amino acid position(s) can be readily ascertained for another reference sequence, such as a reference sequence comprising residues 12 to 687 of SEQ ID NO: 2, 24, 94 or 354, or such as a reference sequence of SEQ ID NO: 24, 94 or 354.

In one aspect, the present disclosure provides a recombinant (engineered) reverse transcriptase, or a functional fragment thereof, comprising a polypeptide sequence having at least 70%, 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity to a reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 2, 24, 94, or 352, or to a reference sequence corresponding to SEQ ID NO: 2, 24, 94, or 352, wherein the polypeptide sequence comprises one or more substitutions relative to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 2, 24, 94, or 352, or to the reference sequence corresponding to SEQ ID NO: 2, 24, 94, or 352.

In some embodiments, a recombinant reverse transcriptase, or functional fragment thereof, comprises a polypeptide sequence having at least 70%, 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 2, or to the reference sequence corresponding to SEQ ID NO: 2, wherein the polypeptide sequence comprises one or more substitutions relative to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 2, or to the reference sequence corresponding to SEQ ID NO: 2.

In some embodiments, the recombinant reverse transcriptase, or a functional fragment thereof, comprises a polypeptide sequence having at least 80% or more sequence identity to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 2, or to the reference sequence corresponding to SEQ ID NO: 2, wherein the polypeptide sequence comprises one or more substitutions relative to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 2, or to the reference sequence corresponding to SEQ ID NO: 2.

In some embodiments, a recombinant reverse transcriptase, or a functional fragment thereof, comprises a polypeptide sequence having at least 70%, 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity to a reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 24, 94, or 352, or to a reference sequence corresponding to SEQ ID NO: 24, 94, or 352, wherein the polypeptide sequence comprises one or more substitutions relative to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 2, or to the reference sequence corresponding to SEQ ID NO: 2.

In some embodiments, the recombinant reverse transcriptase, or a functional fragment thereof, comprises a polypeptide sequence having at least 70%, 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity to a reference sequence corresponding to residues 12 to 687 of a recombinant reverse transcriptase variant set forth in Table 4.1, 5.1, 6.1, and 7.1, or to a reference sequence corresponding to a recombinant reverse transcriptase variant set forth in Table 4.1, 5.1, 6.1, and 7.1, wherein the polypeptide sequence comprises one or more substitutions relative to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 2, or to the reference sequence corresponding to SEQ ID NO: 2.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution 18E, 25E, 49G, 63L/P, 68S, 69R, 72M, 74K/M/P, 78V, 81K, 83E/A/C/R/W, 84N, 85R, 89A/M, 90I, 92T, 94L, 98S, 102C, 113G/T, 114G/K, 118R, 119Y, 129L, 130R/S, 132F, 134F/P, 163P, 167Y, 171L, 173A, 178L, 196C/H, 199L, 205M, 209A, 210L, 212K/N/V, 216R, 242A, 258T, 260G, 261N, 266V, 294Q, 297W, 298E/R, 300I, 303G/Q, 305P/S, 307K/N, 308G, 309E/P/T, 310R, 311A/I/P, 314A/K/M, 317C, 319C/G/S, 321A, 329S, 331E, 333V, 338V, 342W, 343A/V, 349G, 356P, 370G, 403H, 444L, 447G/L/R, 454A, 464L, 465S, 466K, 474A, 479D, 508L, 509E, 519P, 536E/A/N, 537W, 554T, 574D/Q, 576I, 583K, 595N, 598S, 606K/Q, 638H, 639H, or 662R, or combinations thereof, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 2.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution D18E, S25E, A49G, Q63L/P, A68S, T69R, S72M, R74K/M/P, L78V, E81K, Q83E/A/C/R/W, E84N, G85R, H89A/M, V90I, R92T, I94L, I98S, V102C, V113G/T, R114G/K, T118R, N119Y, E129L, V130R/S, K132F, V134F/P, L163P, F167Y, R171L, H173A, P178L, T196C/H, R199L, K205M, T209A, I210L, D212K/N/V, H216R, G242A, E258T, S260G, D261N, A266V, E294Q, K297W, K298E/R, V300I, 1303G/Q, A305P, T307K/N, T308G, A309E/P/T, K310R, Q311A/I/P, E314A/K/M, G317C, A319C/G/S, F321A, F329S, T331E, A333V, P338V, E342W, K343A/V, A349G, F356P, A370G, P403H, I444L, I447G/L/R, N454A, M464L, T465S, N466K, S474A, E479D, H508L, Q509E, K519P, D536E/A/N, G537W, D554T, E574D/Q, M576I, M583K, D595N, Y598S, H606K/Q, L638H, P639H, or Q662R, or combinations thereof, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 2.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution at amino acid position 49, 266, 298, 307, 444, 509, or 536, or combinations thereof, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 2. In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution at amino acid position 49. In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution at amino acid position 266. In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution at amino acid position 298. In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution at amino acid position 307. In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution at amino acid position 444. In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution at amino acid position 509. In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution at amino acid position 536.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution at amino acid positions 49, 307, and 536. In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution at amino acid positions 49, 266, 307, and 536. In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution at amino acid positions 298, 444, and 509. In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution at amino acid positions 266, 298, 444, and 509. In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution at amino acid positions 49, 298, 307, 444, 509, and 536. In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution at amino acid positions 49, 266, 298, 307, 444, 509, and 536.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution 49G, 266V, 298E/R, 307K/N, 444L, 509E, or 536E/A/N, or combinations thereof, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO:2. In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution A49G, A266V, K298E/R, T307K/N, I444L, Q509E, or D536E/A/N, or combinations thereof. In some embodiments, for the recombinant reverse transcriptase comprising one or more substitutions at amino acid positions 49, 266, 298, 307, 444, 509, and/or 536, the substitutions can be selected from the foregoing, e.g., 49G, 266V, 298E/R, 307K/N, 444L, 509E, and 536E/A/N.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution or substitution set 114K/210L/307K, 114K/309P, 49G, 63P/68S/216R/258T/261N, 63P/68S/216R/261N, 63L/209A/314K/665N, 447G/665N, 331E, 90I/307K/349G, 114K/173A/331E, or 266V, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 2.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution or substitution set R114K/I210L/T307K, R114K/A309P, A49G, Q63P/A68S/H216R/E258T/D261N, Q63P/A68S/H216R/D261N, Q63L/T209A/E314K/D665N, I447G/D665N, T331E, V90I/T307K/A349G, R114K/H173A/T331E, or A266V, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 2.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution or substitution set 454A/508L, 536E/574Q, 309P, 49G/173A/309P/331E, 90I/331E, 63L/90I/309P/574D/650G, 90I/173A/209A/210L/321A/574D/598S, 508L/519P, 49G/63L/90I/216R/309P/321A/536E/574D, 49G/114K/307N/309P/536E, 307K/321A/536E/574D/650G, 309P/331E/536E/574Q/598S/650G, 173A/331E/536E/574D/598S, 49G/300I/403H, 74K/242A, 242A/298E/508L/662R, 260G/509E, 102C/370G/509E, 49G/173A/216R/349G/536E/598S, 49G/114K/216R/3071K/309P/331E, 49G/90I/173A/216R/307K, 63P/68S/81K/167Y/314A/447G/574Q, 49G/210L/307K/309P/321A/536E/574D/650G, 63L/90I/307K/321A/331E/537W/598S, 370G/464L/465S/509E/554T/576I, 49G/114K/173A/216R/321A/574D/598S, 90I/216R/321A/650G, 574D/650G, 49G/209A/210L/307K/309P/536E/598S, 216R/536E/574Q, 49G/173A/210L/309P/321A/536E/598S, 331E/536E/598S, 321A/574D, 173A/321A/331E/349G/574D, 49G/307K/536E, 216R/309P/574D/650G, 94L/370G/474A/576I, 90I/209A/210L/309P/321A/574D, 49G/63L/90I/173A, 298E, 49G/300I/454A/662R, 68S/811K/167Y/298R/536N, 49G/454A, 81K, 49G/114K/173A/309P/349G/536E/574D/650G, 167Y/261N/303Q/536N, 18E/102C/554T, 171L/173A/307K/331E/536E, 173A/216R/536E, 18E/370G/464L/509E, 49G/114K, 90I/216R/309P/536G/574D, 444L, 90I/321A/349G/536G/598S/650G, 49G/163P/309P/321A/536E/574D/650G, 49G/63L/90I/173A/307K/331E/536E/598S/650G, 68S/81K/167Y/258T/447G/466K/536N, 90I/331E/574D, 49G/321A, 94L/509E, 90I/173A/321A/536E, 167Y/298R/447G/466K, 173A/216R/307K/309P/536E, 216R/321A, 49G/90I/173A/209A/309P/331E, 261N/298R/303Q/447R/574Q, 171P/298E/444L/519P, 90I/536E/574D/598S/650G, 49G/63L/90I/210L/307K/321A/598S/650G, 90I/216R/307K/536E/574D, 18E/94L/102C/260G/370G/464L/554T, 18E/423R/465S/474A, 167Y/261N/447G/536G, 114K/173A/209A/210L, 307K/309P/536E/574D/598S, 102C/260G/370G/576I, 574D, 173A/209A/210L/307K/536E, 216R/309P/536E, 349G, 447L/536A/606Q, 310R/454A/479D/519P/662R, 49G/90I/209A/598S, 3141K/536N, 171P/300I/454A/479D/508L/662R, 171P/242A/300I/508L/662R, 49G/331E/536E, 173A/216R/309P/536E/574D/598S, 536E/598S, 167Y/261N/298R/303Q/447R/466K/574Q, 173A/536E/598S, 49G/114K/309P/536E/574D/598S, 49G/114K/309P/349G/536E, 63P/68S/81K/303Q/466K, 63L/90I/209A/216R/307K/309P/321A/349G/536E/574D/598S/650G, 216R, 173A/210L/307K/598S/650G, 25E/102C/370G/423R, 68S/261N/298R/303Q, 423R/474A, 94L/423R/474A/554T/576I, 63P/298R/447R/574Q, 49G/63L/90I/173A/307K/321A/331E/574D/595N/650G, 49G/90I/536E/574D, 508L, 63P/81K/167Y/258I/261N/298R/303Q/447G, 114K/331E, 212N/298E/583K/606K, 49G/173A/536E/574Q, 49G/242A/298E/300I/310R/444L/454A/479D, 49G/309P/321A/536E/598S, 63P/68S/261N/536G, 300I/444L/508L, or 298R, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 2.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution or substitution set N454A/H508L, D536E/E574Q, A309P, A49G/H173A/A309P/T331E, V90I/T331E, Q63L/V90I/A309P/E574D/H650G, V90I/H173A/T209A/I210L/F321A/E574D/Y598S, H508L/K519P, A49G/Q63L/V90I/H216R/A309P/F321A/D536E/E574D, A49G/R114K/T307N/A309P/D536E, T307K/F321A/D536E/E574D/H650G, A309P/T331E/D536E/E574Q/Y598S/H650G, H173A/T331E/D536E/E574D/Y598S, A49G/V300I/P403H, R74K/G242A, G242A/K298E/H508L/Q662R, S260G/Q509E, V102C/A370G/Q509E, A49G/H173A/H216R/A349G/D536E/Y598S, A49G/R114K/H216R/T307K/A309P/T331E, A49G/V90I/H173A/H216R/T307K, Q63P/A68S/E81K/F167Y/E314A/I447G/E574Q, A49G/I210L/T307K/A309P/F321A/D536E/E574D/H650G, Q63LN90I/T307K/F321A/T331E/G537W/Y598S, A370G/M464L/T465S/Q509E/D554T/M576I, A49G/R114K/H173A/H216R/F321A/E574D/Y598S, V90I/H216R/F321A/H650G, E574D/H650G, A49G/T209A/I210L/T307K/A309P/D536E/Y598S, H216R/D536E/E574Q, A49G/H173A/I210L/A309P/F321A/D536E/Y598S, T331E/D536E/Y598S, F321A/E574D, H173A/F321A/T331E/A349G/E574D, A49G/T307K/D536E, H216R/A309P/E574D/H650G, I94L/A370G/S474A/M576I, V90I/T209A/I210L/A309P/F321A/E574D, A49G/Q63LN90I/H173A, K298E, A49G/V300I/N454A/Q662R, A68S/E81K/F167Y/K298R/D536N, A49G/N454A, E81K, A49G/R114K/H173A/A309P/A349G/D536E/E574D/H650G, F167Y/D261N/I303Q/D536N, D18E/V102C/D554T, R171L/H173A/T307K/T331E/D536E, H173A/H216R/D536E, D18E/A370G/M464L/Q509E, A49G/R114K, V90I/H216R/A309P/D536G/E574D, I444L, V90I/F321A/A349G/D536G/Y598S/H650G, A49G/L163P/A309P/F321A/D536E/E574D/H650G, A49G/Q63L/V90I/H173A/T307K/T331E/D536E/Y598S/H650G, A68S/E81K/F167Y/E258T/I447G/N466K/D536N, V90I/1331E/E574D, A49G/F321A, I94L/Q509E, V90I/H173A/F321A/D536E, F167Y/K298R/I447G/N466K, H173A/H216R/T307K/A309P/D536E, H216R/F321A, A49GN90I/H173A/T209A/A309P/T331E, D261N/K298R/I303Q/I447R/E574Q, R171P/K298E/I444L/K519P, V90I/D536E/E574D/Y598S/H650G, A49G/Q63L/V90I/I210L/T307K/F321A/Y598S/H650G, V90I/H216R/T307K/D536E/E574D, D18E/I94L/V102C/S260G/A370G/M464L/D554T, D18E/K423R/T465S/S474A, F167Y/D261N/I447G/D536G, R114K/H173A/T209A/I210L, T307K/A309P/D536E/E574D/Y598S, V102C/S260G/A370G/M576I, E574D, H173A/T209A/I210L/T307K/D536E, H216R/A309P/D536E, A349G, I447L/D536A/H606Q, K310R/N454A/E479D/K519P/Q662R, A49GN90I/T209A/Y598S, E314K/D536N, R171P/V300I/N454A/E479D/H508L/Q662R, R171P/G242AN300I/H508L/Q662R, A49G/T331E/D536E, H173A/H216R/A309P/D536E/E574D/Y598S, D536E/Y598S, F167Y/D261N/K298R/I303Q/I447R/N466K/E574Q, H173A/D536E/Y598S, A49G/R114K/A309P/D536E/E574D/Y598S, A49G/R114K/A309P/A349G/D536E, Q63P/A68S/E81K/I303Q/N466K, Q63LN90I/T209A/H216R/T307K/A309P/F321A/A349G/D536E/E574D/Y598S/H650G, H216R, H173A/1210L/T307K/Y598S/H650G, S25E/V102C/A370G/K423R, A68S/D261N/K298R/1303Q, K423R/S474A, 194L/K423R/S474A/D554T/M576I, Q63P/K298R/I447R/E574Q, A49G/Q63L/V90I/H173A/T307K/F321A/T331E/E574D/D595N/H650G, A49G/V90I/D536E/E574D, H508L, Q63P/E81K/F167Y/E258T/D261N/K298R/I303Q/I447G, R114K/T331E, D212N/K298E/R583K/H606K, A49G/H173A/D536E/E574Q, A49G/G242A/K298E/V300I/K310R/I444L/N454A/E479D, A49G/A309P/F321A/D536E/Y598S, Q63P/A68S/D261N/D536G, V300I/I444L/H508L, or K298R, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 2.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution or substitution set at amino acid position 134, 74, 83, 319, 92, 329, 343,311,338,196,69,72,294,83,134,130,305,319,113,297,319,114,308,309,342,205,212, 199,83,303,309,78,113,132,311,119,83,98,314,129,343,196,74,356,89,212, 444/508/509/574, 63/260/298/300/331/444/509, 63/90/209/444/508/574, 298/444/509, 63/90/508/509/574/595, 83, 311, 89, 130, 178, or 118, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 2.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution or substitution set 134P, 74P, 83A, 319G, 92T, 329S, 343A, 311P, 338V, 196C, 69R, 72M, 294Q, 83W, 134F, 130S, 305P, 319S, 113T, 297W, 319C, 114G, 308G, 309E, 342W, 205M, 212K, 199L, 83C, 303G, 309T, 78V, 113G, 132F, 311I, 119Y, 83E, 98S, 314M, 129L, 343V, 196H, 74M, 356P, 89A, 212V, 444L/508L/509E/574D, 63L/260G/298R/300I/331E/444L/509E, 63L/90I/209A/444L/508L/574Q, 298R/444L/509E, 63L/90I/508L/509E/574Q/595N, 83R, 311A, 89M, 130R, 178L, or 118R, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 2.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution or substitution set V134P, R74P, Q83A, A319G, R92T, F329S, K343A, Q311P, P338V, T196C, T69R, S72M, E294Q, Q83W, V134F, V130S, A305P, A319S, V113T, K297W, A319C, R114G, T308G, A309E, E342W, K205M, D212K, R199L, Q83C, I303G, A309T, L78V, V113G, K132F, Q311I, N119Y, Q83E, 198S, E314M, E129L, K343V, T196H, R74M, F356P, H89A, D212V, I444L/H508L/Q509E/E574D, Q63L/5260G/K298RN300I/T331E/I444L/Q509E, Q63LN90I/T209A/I444L/H508L/E574Q, K298R/I444L/Q509E, Q63L/V90I/H508L/Q509E/E574Q/D595N, Q83R, Q311A, H89M, V130R, P178L, or T118R, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 2.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution or substitution set 309E/342W, 309T, 129L, 574Q, 85R, 98S/119Y/129L/132F/196H, 98S/317C/343V/356P, 205M/212K//309E/319S/342W, 78V/132F/314M, 78V/83E/98S, 78V/83E/119Y/132F/196H, 78V/83E, 78V/83E356P, 78V, 119Y/129L/132F, 178L/303G/331E/338V/508L, 311I/314M, 63L/297W/303G/305P, 63L/178L/209A/260G/574Q, 63L/300I/338V, 83A/294Q, 83A/92T/343A/574Q, 83A/92T/134P/574Q, 83A/196C/329S/343A, 83A/196C, 83A/134F/196C/294Q/305S/311P/319G/329S/343A/574Q, 83C, 83C/309T, 83C/319S/342W, 83C/205M, 83C/114G, 83C/114G/309T, 83C/114G/319C, 83C/199L/212K/309E/319C/639H, 83C/199L, 83C/342W, 83C/308G/309E/595N/638H, 83C/113T/114G/205M/212K, 83C/130S, 114G/309E, 114G/212K/309E/342W/639H, 114G/205M, 114G, 114G/130S/319S, 114G/130S/212K/342W, 114G/130S/309E, 199L/309T, 199L/205M, 342W, 343A/595N, 74M, 74M/129L, 74M/83E/129L/132F/212V, 74P/83A/92T/343A, 74P/83A/134P/294Q/574Q, 74P/83W, 74P/329S/574Q, 74P/92T/196C/294Q/329S, 92T, 72M, 72M/294Q/311A/329S/343A, 72M/294Q, 72M/294Q/311A/329S, 72M/83A/343A, 72M/74P/294Q, 72M/74P/83A/319G/329S, 72M/74P/83A/84N, 72M/74P/83A/134F/196C/294Q, 72M/74P, 72M/74P/92T/294Q/329S, 72M/74P/92T, 72M/74P/92T/134P/343A, 72M/74P/134F/196C/319G/329S, 72M/196C/311A/329S/574Q, 72M/134P/196C, 118R/178L/338V, 69R/89A/178L/303G/305P/338V/574Q, 113G, 113G/178L/260G, 113T/309E, 113T/212K/309E, 113T/342W, 113T/114G, 113T/114G/212K, 113T/114G/205M/319C/342W, 113T/114G/342W, 113T/114G/130S, 113T, 130S/205M/333V, 134P, or 134P/294Q, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 2.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution or substitution set A309E/E342W, A309T, E129L, E574Q, G85R, 198S/N119Y/E129L/K132F/T196H, I98S/G317C/K343V/F356P, K205M/D212K/A309E/A319S/E342W, L78V/K132F/E314M, L78V/Q83E/I98S, L78V/Q83E/N119Y/K132F/T196H, L78V/Q83E, L78V/Q83E, L78V/Q83E/F356P, L78V, N119Y/E129L/K132F, P178L/I303G/T331E/P338V/H508L, Q311I/E314M, Q63L/K297W/1303G/A305P, Q63L/P178L/T209A/S260G/E574Q, Q63LN300I/P338V, Q83A/E294Q, Q83A/R92T/K343A/E574Q, Q83A/R92T/V134P/E574Q, Q83A/T196C/F329S/K343A, Q83A/T196C, Q83A/V134F/T196C/E294Q/A305S/Q311P/A319G/F329S/K343A/E574Q, Q83C, Q83C/A309T, Q83C/A319S/E342W, Q83C/K205M, Q83C/R114G, Q83C/R114G/A309T, Q83C/R114G/A319C, Q83C/R199L/D212K/A309E/A319C/P639H, Q83C/R199L, Q83C/E342W, Q83C/T308G/A309E/D595N/L638H, Q83C/V113T/R114G/K205M/D212K, Q83C/V130S, R114G/A309E, R114G/D212K/A309E/E342W/P639H, R114G/K205M, R114G, R114GN130S/A319S, R114G/V130S/D212K/E342W, R114GN130S/A309E, R199L/A309T, R199L/K205M, E342W, K343A/D595N, R74M, R74M/E129L, R74M/Q83E/E129L/K132F/D212V, R74P/Q83A/R92T/K343A, R74P/Q83A/V134P/E294Q/E574Q, R74P/Q83W, R74P/F329S/E574Q, R74P/R92T/T196C/E294Q/F329S, R92T, S72M, S72M/E294Q/Q311A/F329S/K343A, S72M/E294Q, S72M/E294Q/Q311A/F329S, S72M/Q83A/K343A, S72M/R74P/E294Q, S72M/R74P/Q83A/A319G/F329S, S72M/R74P/Q83A/E84N, S72M/R74P/Q83AN134F/T196C/E294Q, S72M/R74P, S72M/R74P/R92T/E294Q/F329S, S72M/R74P/R92T, S72M/R74P/R92T/V134P/K343A, S72M/R74PN134F/T196C/A319G/F329S, S72M/T196C/Q311A/F329S/E574Q, S72MN134P/T196C, T118R/P178L/P338V, T69R/H89A/P178L/I303G/A305P/P338V/E574Q, V113G, V113G/P178L/S260G, V113T/A309E, V113T/D212K/A309E, V113T/E342W, V113T/R114G, V113T/R114G/D212K, V113T/R114G/K205M/A319C/E342W, V113T/R114G/E342W, V113T/R114GN130S, V113T, V130S/K205M/A333V, V134P, or V134P/E294Q, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 2.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution or substitution set 266V/454A/508L, 266V/536E/574Q, 266V/309P, 49G/173A/266V/309P/331E, 90I/266V/331E, 63L/90I/266V/309P/574D/650G, 90I/173A/209A/210L/266V/321A/574D/598S, 266V/508L/519P, 49G/63L/90I/216R/266V/309P/321A/536E/574D, 49G/114K/266V/307N/309P/536E, 266V/307K/321A/536E/574D/650G, 266V/309P/331E/536E/574Q/598S/650G, 173A/266V/331E/536E/574D/598S, 49G/266V/300I/403H, 74K/242A/266V, 242A/266V/298E/508L/662R, 260G/266V/509E, 102C/266V/370G/509E, 49G/173A/216R/266V/349G/536E/598S, 49G/114K/216R/266V/3071K/309P/331E, 49G/90I/173A/216R/266V/307K, 63P/68S/81K/167Y/266V/314A/447G/574Q, 49G/210L/266V/307K/309P/321A/536E/574D/650G, 63L/90I/266V/307K/321A/331E/537W/598S, 266V/370G/464L/465S/509E/554T/576I, 49G/114K/173A/216R/266V/321A/574D/598S, 90I/216R/266V/321A/650G, 266V/574D/650G, 49G/209A/210L/266V/307K/309P/536E/598S, 216R/266V/536E/574Q, 49G/173A/210L/266V/309P/321A/536E/598S, 266V/331E/536E/598S, 266V/321A/574D, 173A/266V/321A/331E/349G/574D, 49G/266V/307K/536E, 216R/266V/309P/574D/650G, 94L/266V/370G/474A/576I, 90I/209A/210L/266V/309P/321A/574D, 49G/63L/90I/173A/266V, 266V/298E, 49G/266V/300I/454A/662R, 68S/81K/167Y/266V/298R/536N, 49G/266V/454A, 811K/266V, 49G/114K/173A/266V/309P/349G/536E/574D/650G , 167Y/261N/266V/303Q/536N, 18E/102C/266V/554T, 171L/173A/266V/307K/331E/536E, 173A/216R/266V/536E, 18E/266V/370G/464L/509E, 49G/114K/266V, 90I/216R/266V/309P/536G/574D, 266V/444L, 90I/266V/321A/349G/536G/598S/650G, 49G/163P/266V/309P/321A/536E/574D/650G, 49G/63L/90I/173A/266V/307K/331E/536E/598S/650G, 68S/81K/167Y/258T/266V/447G/466K/536N, 90I/266V/331E/574D, 49G/266V/321A, 94L/266V/509E, 90I/173A/266V/321A/536E, 167Y/266V/298R/447G/466K, 173A/216R/266V/307K/309P/536E, 216R/266V/321A, 49G/90I/173A/209A/266V/309P/331E, 261N/266V/298R/303Q/447R/574Q, 171P/266V/298E/444L/519P, 90I/266V/536E/574D/598S/650G, 49G/63L/90I/210L/266V/307K/321A/598S/650G, 90I/216R/266V/307K/536E/574D, 18E/94L/102C/260G/266V/370G/464L/554T, 18E/266V/423R/465S/474A, 167Y/261N/266V/447G/536G, 114K/173A/209A/210L/266V, 266V/307K/309P/536E/574D/598S, 102C/260G/266V/370G/576I, 266V/574D, 173A/209A/210L/266V/307K/536E, 216R/266V/309P/536E, 266V/349G, 266 V/447L/536A/606Q, 266V/310R/454A/479D/519P/662R, 49G/90I/209A/266V/598S, 266V/314K/536N, 171P/266V/300I/454A/479D/508L/662R, 171P/242A/266V/300I/508L/662R, 49G/266V/331E/536E, 173A/216R/266V/309P/536E/574D/598S, 266V/536E/598S, 167Y/261N/266V/298R/303Q/447R/466K/574Q, 173A/266V/536E/598S, 49G/114K/266V/309P/536E/574D/598S, 49G/114K/266V/309P/349G/536E, 63P/68S/81K/266V/303Q/466K, 63L/90I/209A/216R/266V/307K/309P/321A/349G/536E/574D/598S/650G, 216R/266V, 173A/210L/266V/307K/598S/650G, 25E/102C/266V/370G/423R, 68S/261N/266V/298R/303Q, 266V/423R/474A, 94L/266V/423R/474A/554T/576I, 63P/266V/298R/447R/574Q, 49G/63L/90I/173A/266V/307K/321A/331E/574D/595N/650G, 49G/90I/266V/536E/574D, 266V/508L, 63P/81K/167Y/258T/266V/261N/298R/303Q/447G, 114K/266V/331E, 212N/266V/298E/583K/606K, 49G/173A/266V/536E/574Q, 49G/242A/266V/298E/300I/310R/444L/454A/479D, 49G/266V/309P/321A/536E/598S, 63P/68S/261N/266V/536G, 266 V/300I/444L/508L, or 266V/298R, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO:2.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution or substitution set 49G/134P/266V/307K/536E, 49G/74P/266V/307K/536E, 49G/83A/266V/307K/536E, 49G/266V/307K/319G/536E, 49G/92T/266V/307K/536E, 49G/266V/307K/329S/536E, 49G/266V/307K/343A/536E, 49G/266V/307K/311P/536E, 49G/266V/307K/338V/536E, 49G/196C/266V/307K/536E, 49G/69R/266V/307K/536E, 49G/72M/266V/307K/536E, 49G/266V/294Q/307K/536E, 49G/83W/266V/294Q/307K/536E, 49G/134F/266V/307K/536E, 49G/130S/266V/307K/536E, 49G/266V/305P/307K/536E, 49G/266V/307K/319S/536E, 49G/113T/266V/307K/536E, 49G/266V/297W/307K/536E, 49G/266V/307K/319C/536E, 49G/114G/266V/307K/536E, 49G/266V/307K/308G/536E, 49G/266V/307K/309E/536E, 49G/266V/307K/342W/536E, 49G/205M/266V/307K/536E, 49G/212K/266V/307K/536E, 49G/199L/266V/307K/536E, 49G/83C/266V/307K/536E, 49G/266V/303G/307K/536E, 49G/266V/307K/309T/536E, 49G/78V/266V/307K/536E, 49G/113G/266V/307K/536E, 49G/132F/266V/307K/536E, 49G/266V/307K/311I/536E, 49G/119Y/266V/307K/536E, 49G/83E/266V/307K/536E, 49G/98S/266V/307K/536E, 49G/266V/307K/314M/536E, 49G/129L/266V/307K/536E, 49G/266V/307K/343V/536E, 49G/196H/266V/307K/536E, 49G/74M/266V/307K/536E, 49G/266V/307K/356P/536E, 49G/89A/266V/307K/536E, 49G/212V/266V/307K/536E, 49G/266V/307K/444L/508L/509E/536E/574D, 49G/63L/260G/266V/298R/300I/307K/331E/444L/509E/536E, 49G/63L/90I/209A/266V/307K/444L/508L/536E/574Q, 49G/266V/298R/307K/444L/509E/536E, 49G/63L/90I/266V/307K/508L/509E/536E/574Q/595N, 49G/83R/266V/307K/536E, 49G/266V/307K/311A/536E, 49G/89M/266V/307K/536E, 49G/130R/266V/307K/536E, 49G/178L/266V/307K/536E, or 49G/118R/266V/307K/536E, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO:2.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution or substitution set 49G/266V/298R/307K/309E/342W/444L/509E/536E, 49G/266V/298R/307K/309T/444L/509E/536E, 49G/129L/266V/307K/444L/509E/536E, 49G/266V/298R/307K/444L/536E/574Q, 49G/85R/266V/298R/307K/444L/509E/536E, 49G/985/119Y/129L/132F/196H/266V/307K/444L/509E/536E, 49G/985/266V/307K/317C/343V/356P/444L/509E/536E, 49G/205M/212K/266V/307K/309E/319S/342W/444L/536E, 49G/266V/298R/307K/509E/536E, 49G/78V/132F/266V/298R/307K/314M/444L/509E/536E, 49G/78V/83E/98S/266V/298R/307K/444L/509E/536E, 49G/78V/83E/119Y/132F/196H/266V/298R/307K/509E/536E, 49G/78V/83E/266V/307K/444L/509E/536E, 49G/78V/83E/266V/307K/444L/536E, 49G/78V/83E/266V/307K/356P/444L/509E/536E, 49G/78V/266V/307K/509E/536E, 49G/119Y/129L/132F/266V/298R/307K/444L/509E/536E, 49G/178L/266V/303G/307K/331E/338V/444L/508L/509E/536E, 49G/266V/298R/307K/311I/314M/444L/509E/536E, 49G/63L/266V/297W/298R/303G/305P/307K/509E/536E, 49G/63L/178L/209A/260G/266V/298R/307K/444L/509E/536E/574Q, 49G/63L/266V/298R/300I/307K/338V/444L/509E/536E, 49G/83A/266V/294Q/298R/307K/444L/509E/536E, 49G/83A/92T/266V/307K/343A/444L/509E/536E/574Q, 49G/83A/92T/134P/266V/298R/307K/509E/536E/574Q, 49G/83A/196C/266V/298R/307K/329S/343A/444L/509E/536E, 49G/83A/196C/266V/307K/444L/536E, 49G/83A/134F/196C/294Q/266V/305S/307K/311P/319G/329S/343A/509E/536E/574Q, 49G/83C/266V/298R/307K/444L/509E/536E, 49G/83C/266V/298R/307K/309T/444L/509E/536E, 49G/83C/266V/298R/307K/319S/342W/444L/536E, 49G/83C/205M/266V/298R/307K/509E/536E, 49G/83C/266V/298R/307K/509E/536E, 49G/83C/114G/266V/298R/307K/444L/509E/536E, 49G/83C/114G/266V/298R/307K/309T/444L/536E, 49G/83C/114G/266V/307K/319C/444L/509E/536E, 49G/83C/199L/212K/266V/307K/309E/319C/509E/536E/639H, 49G/83C/199L/266V/298R/307K/444L/536E, 49G/83C/266V/307K/444L/509E/536E, 49G/83C/266V/307K/342W/444L/509E/536E, 49G/83C/266V/298R/307K/308G/309E/444L/509E/536E/595N/638H, 49G/83C/113T/114G/205M/212K/266V/298R/307K/444L/509E/536E, 49G/83C/130S/266V/307K/509E/536E, 49G/114G/266V/298R/307K/309E/444L/509E/536E, 49G/114G/266V/298R/307K/309E/444L/536E, 49G/114G/212K/266V/298R/307K/309E/342W/444L/509E/536E/639H, 49G/114G/205M/266V/298R/307K/509E/536E, 49G/114G/266V/307K/444L/509E/536E, 49G/114G/1305S/266V/298R/307K/319S/509E/536E, 49G/114G/130S/212K/266V/307K/342W/444L/509E/536E, 49G/114G/130S/266V/307K/309E/444L/509E/536E, 49G/199L/266V/298R/307K/309T/444L/509E/536E, 49G/199L/205M/266V/298R/307K/509E/536E, 49G/266V/307K/444L/509E/536E, 49G/266V/307K/342W/444L/509E/536E, 49G/266V/307K/444L/536E, 49G/266V/307K/343A/509E/536E/595N, 49G/74M/266V/298R/307K/444L/509E/536E, 49G/74M/129L/266V/307K/509E/536E, 49G/74M/83E/129L/132F/212V/266V/298R/307K/444L/536E, 49G/74P/83A/92T/266V/307K/343A/444L/536E, 49G/74P/83A/134P/266V/294Q/307K/444L/509E/536E/574Q, 49G/74P/83W/266V/298R/307K/536E, 49G/74P/266V/307K/329S/509E/536E/574Q, 49G/74P/92T/196C/266V/294Q/298R/307K//329S/444L/509E/536E, 49G/92T/266V/307K/444L/536E, 49G/72M/266V/298R/307K/444L/509E/536E, 49G/72M/266V/294Q/298R/307K/311A/329S/343A/509E/536E, 49G/72M/266V/294Q/307K/509E/536E, 49G/72M/266V/294Q/307K/311A/329S/509E/536E, 49G/72M/266V/298R/307K/444L/536E, 49G/72M/83A/266V/307K/343A/509E/536E, 49G/266V/72M/74P/294Q/307K/509E/536E, 49G/72M/74P/83A/266V/298R/307K/319G/329S/444L/536E, 49G/72M/74P/83A/84N/266V/298R/307K/509E/536E, 49G/72M/74P/83A/134F/196C/266V/294Q/307K/444L/509E/536E, 49G/72M/74P/266V/307K/444L/536E, 49G/72M/74P/92T/266V/294Q/307K/329S/444L/509E/536E, 49G/72M/74P/92T/266V/307K/444L/509E/536E, 49G/72M/74P/92T/134P/266V/307K/343A/509E/536E, 49G/72M/74P/134F/196C/266V/307K/319G/329S/444L/536E, 49G/72M/196C/266V/298R/307K/311A/329S/444L/509E/536E/574Q, 49G/72M/134P/196C/266V/307K/444L/509E/536E, 49G/118R/178L/266V/298R/307K/338V/444L/509E/536E, 49G/69R/89A/178L/266V/298R/303G/305P/307K/338V/444L/509E/536E/574Q, 49G/113G/266V/298R/307K/444L/509E/536E, 49G/113G/178L/260G/266V/298R/307K/444L/509E/536E, 49G/113T/266V/298R/307K/309E/444L/509E/536E, 49G/113T/212K/266V/298R/307K/309E/444L/509E/536E, 49G/113T/266V/298R/307K/342W/444L/509E/536E, 49G/113T/114G/266V/298R/307K/444L/509E/536E, 49G/113T/114G/212K/266V/298R/307K/444L/509E/536E, 49G/113T/114G/205M/266V/298R/307K/319C/342W/444L/509E/536E, 49G/113T/114G/266V/307K/342W/444L/509E/536E, 49G/113T/114G/1305S/266V/298R/307K/444L/509E/536E, 49G/113T/266V/307K/444L/509E/536E, 49G/113T/266V/298R/307K/309E/509E/536E, 49G/130S/205M/266V/298R/307K/333V/509E/536E, 49G/134P/266V/298R/307K/444L/509E/536E, or 49G/134P/266V/294Q/298R/307K/536E, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 2.

In some embodiments, the recombinant reverse transcriptase comprises a polypeptide sequence having at least 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity to a reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 24, 94, or 352, or to a reference sequence corresponding to SEQ ID NO: SEQ ID NO: 24, 94, or 352, wherein the polypeptide sequence comprises one or more substitutions relative to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 24, 94, or 352, or to the reference sequence corresponding to SEQ ID NO: 24, 94, or 352.

In some embodiments, the recombinant reverse transcriptase comprises a polypeptide sequence having at least 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity to a reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 94 or 352, or to a reference sequence corresponding to SEQ ID NO: SEQ ID NO: 94 or 352, wherein the polypeptide sequence comprises one or more substitutions relative to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 24, or to the reference sequence corresponding to SEQ ID NO: 24.

In some embodiments, the recombinant reverse transcriptase comprises a polypeptide sequence having at least 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity to a reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 352, or to a reference sequence corresponding to SEQ ID NO: SEQ ID NO: 352, wherein the polypeptide sequence comprises one or more substitutions relative to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 94, or to the reference sequence corresponding to SEQ ID NO: 94.

In some embodiments of the foregoing, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution at amino acid position 18, 25, 49, 63, 68, 69, 72, 74, 78, 81, 83, 89, 90, 92, 94, 98, 102, 113, 114, 118, 119, 129, 130, 132, 134, 163, 167, 171, 173, 178, 196, 199, 205, 209, 210, 212, 216, 242, 258, 260, 261, 266, 294, 297, 298, 300, 303, 305, 307, 308, 309, 310, 311, 314, 319, 321, 329, 331, 338, 342, 343, 349, 356, 370, 403, 423, 444, 447, 454, 464, 465, 466, 474, 479, 508, 509, 519, 536, 537, 554, 574, 576, 583, 595, 598, 606, 650, 662, or 665, or combinations thereof, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 24, 94, or 352.

In some embodiments of the foregoing, the polypeptide sequence of the recombinant reverse transcriptase comprises at least an amino acid residue 18E, 25E, 49G, 63L/P, 68S, 69R, 72M, 74K/M/P, 78V, 81K, 83E/A/C/R/W, 89A/M, 90I, 92T, 94L, 98S, 102C, 113G/T, 114G/K, 118R, 119Y, 129L, 130R/S, 132F, 134F/P, 163P, 167Y, 171L, 173A, 178L, 196C/H, 199L, 205M, 209A, 210L, 212K/N/V, 216R, 242A, 258T, 260G, 261N, 266V, 294Q, 297W, 298E/R, 300I, 303G/Q, 305P, 307K/N, 308G, 309E/P/T, 310R, 311A/I/P, 314A/K/M, 319C/G/S, 321A, 329S, 331E, 338V, 342W, 343A/V, 349G, 356P, 370G, 403H, 444L, 447G/L/R, 454A, 464L, 465S, 466K, 474A, 479D, 508L, 509E, 519P, 536E/A/N, 537W, 554T, 574D/Q, 576I, 583K, 595N, 598S, 606K/Q, or 662R, or combinations thereof, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 24, 94, or 352.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least an amino acid residue 49G, 266V, 298E/R, 307K/N, 444L, 509E, or 536E/A/N, or combinations thereof, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 24, 94, or 352.

In some embodiments, the recombinant reverse transcriptase comprises a polypeptide sequence having at least 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity to a reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 24, or to a reference sequence corresponding to SEQ ID NO: 24, wherein the polypeptide sequence comprises one or more substitutions relative to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 24, or to the reference sequence corresponding to SEQ ID NO: 24.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution or substitution set 454A/508L, 536E/574Q, 309P, 49G/173A/309P/331E, 90I/331E, 63L/90I/309P/574D/650G, 90I/173A/209A/210L/321A/574D/598S, 508L/519P, 49G/63L/90I/216R/309P/321A/536E/574D, 49G/114K/307N/309P/536E, 307K/321A/536E/574D/650G, 309P/331E/536E/574Q/598S/650G, 173A/331E/536E/574D/598S, 49G/300I/403H, 74K/242A, 242A/298E/508L/662R, 260G/509E, 102C/370G/509E, 49G/173A/216R/349G/536E/598S, 49G/114K/216R/307K/309P/331E, 49G/90I/173A/216R/307K, 63P/68S/81K/167Y/314A/447G/574Q, 49G/210L/307K/309P/321A/536E/574D/650G, 63L/90I/307K/321A/331E/537W/598S, 370G/464L/465S/509E/554T/576I, 49G/114K/173A/216R/321A/574D/598S, 90I/216R/321A/650G, 574D/650G, 49G/209A/210L/307K/309P/536E/598S, 216R/536E/574Q, 49G/173A/210L/309P/321A/536E/598S, 331E/536E/598S, 321A/574D, 173A/321A/331E/349G/574D, 49G/307K/536E, 216R/309P/574D/650G, 94L/370G/474A/576I, 90I/209A/210L/309P/321A/574D, 49G/63L/90I/173A, 298E, 49G/300I/454A/662R, 68S/811K/167Y/298R/536N, 49G/454A, 81K, 49G/114K/173A/309P/349G/536E/574D/650G, 167Y/261N/303Q/536N, 18E/102C/554T, 171L/173A/307K/331E/536E, 173A/216R/536E, 18E/370G/464L/509E, 49G/114K, 90I/216R/309P/536G/574D, 444L, 90I/321A/349G/536G/598S/650G, 49G/163P/309P/321A/536E/574D/650G, 49G/63L/90I/173A/307K/331E/536E/598S/650G, 68S/81K/167Y/258T/447G/466K/536N, 90I/331E/574D, 49G/321A, 94L/509E, 90I/173A/321A/536E, 167Y/298R/447G/466K, 173A/216R/307K/309P/536E, 216R/321A, 49G/90I/173A/209A/309P/331E, 261N/298R/303Q/447R/574Q, 171P/298E/444L/519P, 90I/536E/574D/598S/650G, 49G/63L/90I/210L/307K/321A/598S/650G, 90I/216R/307K/536E/574D, 18E/94L/102C/260G/370G/464L/554T, 18E/423R/465S/474A, 167Y/261N/447G/536G, 114K/173A/209A/210L, 307K/309P/536E/574D/598S, 102C/260G/370G/576I, 574D, 173A/209A/210L/307K/536E, 216R/309P/536E, 349G, 447L/536A/606Q, 310R/454A/479D/519P/662R, 49G/90I/209A/598S, 314K/536N, 171P/300I/454A/479D/508L/662R, 171P/242A/300I/508L/662R, 49G/331E/536E, 173A/216R/309P/536E/574D/598S, 536E/598S, 167Y/261N/298R/303Q/447R/466K/574Q, 173A/536E/598S, 49G/114K/309P/536E/574D/598S, 49G/114K/309P/349G/536E, 63P/68S/81K/303Q/466K, 63L/90I/209A/216R/307K/309P/321A/349G/536E/574D/598S/650G, 216R, 173A/210L/307K/598S/650G, 25E/102C/370G/423R, 68S/261N/298R/303Q, 423R/474A, 94L/423R/474A/554T/576I, 63P/298R/447R/574Q, 49G/63L/90I/173A/307K/321A/331E/574D/595N/650G, 49G/90I/536E/574D, 508L, 63P/81K/167Y/258I/261N/298R/303Q/447G, 114K/331E, 212N/298E/583K/606K, 49G/173A/536E/574Q, 49G/242A/298E/300I/310R/444L/454A/479D, 49G/309P/321A/536E/598S, 63P/68S/261N/536G, 300I/444L/508L, or 298R, wherein the amino acid positions are relative to SEQ ID NO: 24.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution or substitution set N454A/H508L, D536E/E574Q, A309P, A49G/H173A/A309P/T331E, V90I/T331E, Q63LN90I/A309P/E574D/H650G, V90I/H173A/T209A/I210L/F321A/E574D/Y598S, H508L/K519P, A49G/Q63L/V90I/H216R/A309P/F321A/D536E/E574D, A49G/R114K/T307N/A309P/D536E, T307K/F321A/D536E/E574D/H650G, A309P/T331E/D536E/E574Q/Y598S/H650G, H173A/T331E/D536E/E574D/Y598S, A49GN300I/P403H, R74K/G242A, G242A/K298E/H508L/Q662R, S260G/Q509E, V102C/A370G/Q509E, A49G/H173A/H216R/A349G/D536E/Y598S, A49G/R114K/H216R/T307K/A309P/T331E, A49G/V90I/H173A/H216R/T307K, Q63P/A68S/E81K/F167Y/E314A/I447G/E574Q, A49G/I210L/T307K/A309P/F321A/D536E/E574D/H650G, Q63LN90I/T307K/F321A/T331E/G537W/Y598S, A370G/M464L/T465S/Q509E/D554T/M576I, A49G/R114K/H173A/H216R/F321A/E574D/Y598S, V90I/H216R/F321A/H650G, E574D/H650G, A49G/T209A/I210L/T307K/A309P/D536E/Y598S, H216R/D536E/E574Q, A49G/H173A/I210L/A309P/F321A/D536E/Y598S, I331E/D536E/Y598S, F321A/E574D, H173A/F321A/T331E/A349G/E574D, A49G/T307K/D536E, H216R/A309P/E574D/H650G, I94L/A370G/S474A/M576I, V90I/T209A/I210L/A309P/F321A/E574D, A49G/Q63LN90I/H173A, K298E, A49G/V300I/N454A/Q662R, A68S/E81K/F167Y/K298R/D536N, A49G/N454A, E81K, A49G/R114K/H173A/A309P/A349G/D536E/E574D/H650G, F167Y/D261N/I303Q/D536N, D18E/V102C/D554T, R171L/H173A/T307K/T331E/D536E, H173A/H216R/D536E, D18E/A370G/M464L/Q509E, A49G/R114K, V90I/H216R/A309P/D536G/E574D, I444L, V90I/F321A/A349G/D536G/Y598S/H650G, A49G/L163P/A309P/F321A/D536E/E574D/H650G, A49G/Q63L/V90I/H173A/T307K/T331E/D536E/Y598S/H650G, A68S/E81K/F167Y/E258T/I447G/N466K/D536N, V90I/T331E/E574D, A49G/F321A, I94L/Q509E, V90I/H173A/F321A/D536E, F167Y/K298R/I447G/N466K, H173A/H216R/T307K/A309P/D536E, H216R/F321A, A49GN90I/H173A/T209A/A309P/T331E, D261N/K298R/I303Q/I447R/E574Q, R171P/K298E/I444L/K519P, V90I/D536E/E574D/Y598S/H650G, A49G/Q63L/V90I/I210L/T307K/F321A/Y598S/H650G, V90I/H216R/T307K/D536E/E574D, D18E/I94L/V102C/S260G/A370G/M464L/D554T, D18E/K423R/T465S/S474A, F167Y/D261N/I447G/D536G, R114K/H173A/T209A/I210L, T307K/A309P/D536E/E574D/Y598S, V102C/S260G/A370G/M576I, E574D, H173A/T209A/I210L/T307K/D536E, H216R/A309P/D536E, A349G, I447L/D536A/H606Q, K310R/N454A/E479D/K519P/Q662R, A49GN90I/T209A/Y598S, E314K/D536N, R171P/V300I/N454A/E479D/H508L/Q662R, R171P/G242AN300I/H508L/Q662R, A49G/T331E/D536E, H173A/H216R/A309P/D536E/E574D/Y598S, D536E/Y598S, F167Y/D261N/K298R/I303Q/I447R/N466K/E574Q, H173A/D536E/Y598S, A49G/R114K/A309P/D536E/E574D/Y598S, A49G/R114K/A309P/A349G/D536E, Q63P/A68S/E81K/I303Q/N466K, Q63LN90I/T209A/H216R/T307K/A309P/F321A/A349G/D536E/E574D/Y598S/H650G, H216R, H173A/I210L/T307K/Y598S/H650G, S25E/V102C/A370G/K423R, A68S/D261N/K298R/I303Q, K423R/S474A, 194L/K423R/S474A/D554T/M576I, Q63P/K298R/I447R/E574Q, A49G/Q63L/V90I/H173A/T307K/F321A/T331E/E574D/D595N/H650G, A49G/V90I/D536E/E574D, H508L, Q63P/E81K/F167Y/E258T/D261N/K298R/I303Q/1447G, R114K/T331E, D212N/K298E/R583K/H606K, A49G/H173A/D536E/E574Q, A49G/G242A/K298E/V300I/K310R/I444L/N454A/E479D, A49G/A309P/F321A/D536E/Y598S, Q63P/A68S/D261N/D536G, V300I/I444L/H508L, or K298R, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 24.

In some embodiments, the recombinant reverse transcriptase comprises a polypeptide sequence having at least 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity to a reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 94, or to a reference sequence corresponding to SEQ ID NO: 94, wherein the polypeptide sequence comprises one or more substitutions relative to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 94, or to the reference sequence corresponding to SEQ ID NO: 94.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution or substitution set at amino acid position 134, 74, 83, 319, 92, 329, 343, 311, 338, 196, 69, 72, 294, 83, 134, 130, 305, 319, 113, 297, 319, 114, 308, 309, 342, 205, 212, 199, 83, 303, 309, 78, 113, 132, 311, 119, 83, 98, 314, 129, 343, 196, 74, 356, 89, 212, 444/508/509/574, 63/260/298/300/331/444/509, 63/90/209/444/508/574, 298/444/509, 63/90/508/509/574/595, 83, 311, 89, 130, 178, or 118, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 94.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution or substitution set V134P, R74P, Q83A, A319G, R92T, F329S, K343A, Q311P, P338V, T196C, T69R, S72M, E294Q, Q83W, V134F, V1305, A305P, A319S, V113T, K297W, A319C, R114G, T308G, A309E, E342W, K205M, D212K, R199L, Q83C, 1303G, A309T, L78V, V113G, K132F, Q311I, N119Y, Q83E, 198S, E314M, E129L, K343V, T196H, R74M, F356P, H89A, D212V, I444L/H508L/Q509E/E574D, Q63L/S260G/K298RN300I/T331E/I444L/Q509E, Q63L/V90I/T209A/I444L/H508L/E574Q, K298R/I444L/Q509E, Q63L/V90I/H508L/Q509E/E574Q/D595N, Q83R, Q311A, H89M, V130R, P178L, or T118R, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 94.

In some embodiments, the recombinant reverse transcriptase comprises a polypeptide sequence having at least 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity to a reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 352, or to a reference sequence corresponding to SEQ ID NO: 352, wherein the polypeptide sequence comprises one or more substitutions relative to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 352, or to the reference sequence corresponding to SEQ ID NO: 352.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution or substitution set at amino acid position 309/342, 309, 129/298, 509/574, 85, 98/119/129/132/196/298, 98/298/317/343/356, 205/212/298/309/319/342/509, 444, 78/132/314, 78/83/98, 78/83/119/132/196/444, 78/83/298, 78/83/298/509, 78/83/298/356, 78/298/444, 119/129/132, 178/298/303/331/338/508, 311/314, 63/297/303/305/444, 63/178/209/260/574, 63/300/338, 83/294, 83/92/298/343/574, 83/92/134/444/574, 83/196/329/343, 83/196/298/509, 83/134/196/294/298/305/311/319/329/343/444/574, 83, 83/309, 83/319/342/509, 83/205/444, 83/444, 83/114, 83/114/309/509, 83/114/298/319, 83/199/212/298/309/319/444/639, 83/199/509, 83/298, 83/298/342, 83/308/309/595/638, 83/113/114/205/212, 83/130/298/444, 114/309, 114/309/509, 114/212/309/342/639, 114/205/444, 114/298, 114/130/319/444, 114/130/212/298/342, 114/130/298/309, 199/309, 199/205/444, 298, 298/342, 298/509, 298/343/444/595, 74, 74/129/298/444, 74/83/129/132/212/509, 74/83/92/298/343/509, 74/83/134/294/298/574, 74/83/444/509, 74/298/329/444/574, 74/92/196/294/329, 92/298/509, 72, 72/294/311/329/343/444, 72/294/298/444, 72/294/298/311/329/444, 72/509, 72/83/298/343/444, 72/74/294/298/444, 72/74/83/319/329/509, 72/74/83/84/444, 72/74/83/134/196/294/298, 72/74/298/509, 72/74/92/294/298/329, 72/74/92/298, 72/74/92/134/298/343/444, 72/74/134/196/298/319/329/509, 72/196/311/329/574, 72/134/196/298, 118/178/338/444, 69/89/178/303/305/338/444/574, 113, 113/178/260, 113/309, 113/212/309, 113/342, 113/114, 113/114/212, 113/114/205/319/342, 113/114/298/342, 113/114/130, 113/298, 113/298/309/444, 130/205/333/444, 134, 134/294/444/509, or combinations thereof, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 352.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution or substitution set 309E/342W, 309T, 129L/298K, 509Q/574Q, 85R, 98S/119Y/129L/132F/196H/298K, 98S/298K/317C/343V/356P, 205M/212K/298K/309E/319S/342W/509Q, 444I, 78V/132F/314M, 78V/83E/98S, 78V/83E/119Y/132F/196H/444I, 78V/83E/298K, 78V/83E/298K/509Q, 78V/83E/298K/356P, 78V/298K/444I, 119Y/129L/132F, 178L/298K/303G/331E/338V/508L, 311I/314M, 63L/297W/303G/305P/444I, 63L/178L/209A/260G/574Q, 63L/300I/338V, 83A/294Q, 83A/92T/298K/343A/574Q, 83A/92T/134P/444I/574Q, 83A/196C/329S/343A, 83A/196C/298K/509Q, 83A/134F/196C/294Q/298K/3055/311P/319G/329S/343A/444I/574Q, 83C, 83C/309T, 83C/319S/342W/509Q, 83C/205M/444I, 83C/444I, 83C/114G, 83C/114G/309T/509Q, 83C/114G/298K/319C, 83C/199L/212K/298K/309E/319C/444I/639H, 83C/199L/509Q, 83C/298K, 83C/298K/342W, 83C/308G/309E/595N/638H, 83C/113T/114G/205M/212K, 83C/130S/298K/444I, 114G/309E, 114G/309E/509Q, 114G/212K/309E/342W/639H, 114G/205M/444I, 114G/298K, 114G/130S/319S/444I, 114G/130S/212K/298K/342W, 114G/130S/298K/309E, 199L/309T, 199L/205M/444I, 298K, 298K/342W, 298K/509Q, 298K/343A/444I/595N, 74M, 74M/129L/298K/444I, 74M/83E/129L/132F/212V/509Q, 74P/83A/92T/298K/343A/509Q, 74P/83A/134P/294Q/298K/574Q, 74P/83W/444I/509Q, 74P/298K/329S/444I/574Q, 74P/92T/196C/294Q/329S, 92T/298K/509Q, 72M, 72M/294Q/311A/329S/343A/444I, 72M/294Q/298K/444I, 72M/294Q/298K/311A/329S/444I, 72M/509Q, 72M/83A/298K/343A/444I, 72M/74P/294Q/298K/444I, 72M/74P/83A/319G/329S/509Q, 72M/74P/83A/84N/444I, 72M/74P/83A/134F/196C/294Q/298K, 72M/74P/298K/509Q, 72M/74P/92T/294Q/298K/329S, 72M/74P/92T/298K, 72M/74P/92T/134P/298K/343A/444I, 72M/74P/134F/196C/298K/319G/329S/509Q, 72M/196C/311A/329S/574Q, 72M/134P/196C/298K, 118R/178L/338V/444I, 69R/89A/178L/303G/305P/338V/444I/574Q, 113G, 113G/178L/260G, 113T/309E, 113T/212K/309E, 113T/342W, 113I/114G, 113T/114G/212K, 113T/114G/205M/319C/342W, 113T/114G/298K/342W, 113T/114G/130S, 113T/298K, 113T/298K/309E/444I, 130S/205M/333V/444I, 134P, or 134P/294Q/444I/509Q, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO:352.

In some embodiments, the polypeptide sequence of the recombinant reverse transcriptase comprises at least a substitution or substitution set A309E/E342W, A309T, E129L/R298K, E509Q/E574Q, G85R, 198S/N119Y/E129L/K132F/T196H/R298K, 198S/R298K/G317C/K343V/F356P, K205M/D212K/R298K/A309E/A319S/E342W/E509Q, L444I, L78V/K132F/E314M, L78V/Q83E/I98S, L78V/Q83E/N119Y/K132F/T196H/L444I, L78V/Q83E/R298K, L78V/Q83E/R298K/E509Q, L78V/Q83E/R298K/F356P, L78V/R298K/L444I, N119Y/E129L/K132F, P178L/R298K/I303G/T331E/P338V/H508L, Q3111/E314M, Q63L/K297W/I303G/A305P/L444I, Q63L/P178L/T209A/S260G/E574Q, Q63L/V300I/P338V, Q83A/E294Q, Q83A/R92T/R298K/K343A/E574Q, Q83A/R92TN134P/L444I/E574Q, Q83A/T196C/F329S/K343A, Q83A/T196C/R298K/E509Q, Q83A/V134F/T196C/E294Q/R298K/A305S/Q311P/A319G/F329S/K343A/L444I/E574Q, Q83C, Q83C/A309T, Q83C/A319S/E342W/E509Q, Q83C/K205M/L444I, Q83C/L444I, Q83C/R114G, Q83C/R114G/A309T/E509Q, Q83C/R114G/R298K/A319C, Q83C/R199L/D212K/R298K/A309E/A319C/L444I/P639H, Q83C/R199L/E509Q, Q83C/R298K, Q83C/R298K/E342W, Q83C/T308G/A309E/D595N/L638H, Q83CN113T/R114G/K205M/D212K, Q83CN130S/R298K/L444I, R114G/A309E, R114G/A309E/E509Q, R114G/D212K/A309E/E342W/P639H, R114G/K205M/L444I, R114G/R298K, R114GN130S/A319S/L444I, R114GN130S/D212K/R298K/E342W, R114GN130S/R298K/A309E, R199L/A309T, R199L/K205M/L444I, R298K, R298K/E342W, R298K/E509Q, R298K/K343A/L444I/D595N, R74M, R74M/E129L/R298K/L444I, R74M/Q83E/E129L/K132F/D212V/E509Q, R74P/Q83A/R92T/R298K/K343A/E509Q, R74P/Q83AN134P/E294Q/R298K/E574Q, R74P/Q83W/L444I/E509Q, R74P/R298K/F329S/L444I/E574Q, R74P/R92T/T196C/E294Q/F329S, R92T/R298K/E509Q, S72M, S72M/E294Q/Q311A/F329S/K343A/L444I, S72M/E294Q/R298K/L444I, S72M/E294Q/R298K/Q311A/F329S/L444I, S72M/E509Q, S72M/Q83A/R298K/K343A/L444I, S72M/R74P/E294Q/R298K/L444I, S72M/R74P/Q83A/A319G/F329S/E509Q, S72M/R74P/Q83A/E84N/L444I, S72M/R74P/Q83AN134F/T196C/E294Q/R298K, S72M/R74P/R298K/E509Q, S72M/R74P/R92T/E294Q/R298K/F329S, S72M/R74P/R92T/R298K, S72M/R74P/R92T/V134P/R298K/K343A/L444I, S72M/R74P/V134F/T196C/R298K/A319G/F329S/E509Q, S72M/T196C/Q311A/F329S/E574Q, S72M/V134P/T196C/R298K, T118R/P178L/P338V/L444I, T69R/H89A/P178L/I303G/A305P/P338V/L444I/E574Q, V113G, V113G/P178L/S260G, V113T/A309E, V113T/D212K/A309E, V113T/E342W, V113T/R114G, V113T/R114G/D212K, V113T/R114G/K205M/A319C/E342W, V113T/R114G/R298K/E342W, V113T/R114G/V130S, V113T/R298K, V113T/R298K/A309E/L444I, V130S/K205M/A333V/L444I, V134P, or V134P/E294Q/L444I/E509Q, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO:352.

In some embodiments, the recombinant reverse transcriptase comprises a polypeptide sequence comprising a substitution in at least one amino acid position provided in Table 4.1, 5.1, 6.1, and 7.1, wherein the substitution is relative to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 2, 24, 94 or 352, or to the reference sequence of SEQ ID NO: 2, 24, 94 or 352.

In some embodiments, the recombinant reverse transcriptase comprises a polypeptide sequence comprising at least one substitution provided in Table 4.1, 5.1, 6.1, and 7.1, wherein the substitution is relative to the reference sequence comprising residues 12 to 687 of SEQ ID NO: 2, 24, 94 or 352, or to the reference sequence of SEQ ID NO: 2, 24, 94 or 352.

In some embodiments, the recombinant reverse transcriptase comprises a polypeptide sequence comprising at least one substitution or substitution set provided in Table 4.1, 5.1, 6.1, and 7.1, wherein the substitution or substitution set is relative to the reference sequence comprising residues 12 to 687 of SEQ ID NO: 2, 24, 94 or 352, or to the reference sequence of SEQ ID NO: 2, 24, 94 or 352.

In some embodiments, a recombinant reverse transcriptase comprises a polypeptide sequence having at least 75%, 80%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more sequence identity to a reference sequence corresponding to residues 12 to 687 of an even numbered SEQ ID NO. set forth in Table 4.1, 5.1, 6.1, and 7.1, or to a reference sequence of an even numbered SEQ ID NO. set forth in Table 4.1, 5.1, 6.1, and 7.1. In some embodiments, the recombinant reverse transcriptase comprises a polypeptide sequence comprising residues 12 to 687 of an even numbered SEQ ID NO. set forth in Table 4.1, 5.1, 6.1, and 7.1, or a polypeptide sequence comprising an even numbered SEQ ID NO. set forth in Table 4.1, 5.1, 6.1, and 7.1.

In some embodiments, a recombinant reverse transcriptase comprises a polypeptide sequence comprising at least 75%, 80%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more sequence identity to a reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32, 34, 36, 38, 40, 42, 44, 46, 48, 50, 52, 54, 56, 58, 60, 62, 64, 66, 68, 70, 72, 74, 76, 78, 80, 82, 84, 86, 88, 90, 92, 94, 96, 98, 100, 102, 104, 106, 108, 110, 112, 114, 116, 118, 120, 122, 124, 126, 128, 130, 132, 134, 136, 138, 140, 142, 144, 146, 148, 150, 152, 154, 156, 158, 160, 162, 164, 166, 168, 170, 172, 174, 176, 178, 180, 182, 184, 186, 188, 190, 192, 194, 196, 198, 200, 202, 204, 206, 208, 210, 212, 214, 216, 218, 220, 222, 224, 226, 228, 230, 232, 234, 236, 238, 240, 242, 244, 246, 248, 250, 252, 254, 256, 258, 260, 262, 264, 266, 268, 270, 272, 274, 276, 278, 280, 282, 284, 286, 288, 290, 292, 294, 296, 298, 300, 302, 304, 306, 308, 310, 312, 314, 316, 318, 320, 322, 324, 326, 328, 330, 332, 334, 336, 338, 340, 342, 344, 346, 348, 350, 352, 354, 356, 358, 360, 362, 364, 366, 368, 370, 372, 374, 376, 378, 380, 382, 384, 386, 388, 390, 392, 394, 396, 398, 400, 402, 404, 406, 408, 410, 412, 414, 416, 418, 420, 422, 424, 426, 428, 430, 432, 434, 436, 438, 440, 442, 444, 446, 448, 450, 452, 454, 456. 458, 460. 462, 464, 466, 468, 470, 472, 474, 476, 478, 480, 482, 484, 486, 488, 490, 492, 494, 496, 498, 500, 502, 504, 506, 508, 510, 512, 514, 516, 518, 520, 522, 524, 526, 528, 530, 532, 534, 536, 538, 540, 542, 544, 546, 548, 550, 552, 554, 556, 558, 560, 562, 564, or 566.

In some embodiments, the recombinant reverse transcriptase comprises a polypeptide sequence comprising residues 12 to 687 of SEQ ID NO: 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32, 34, 36, 38, 40, 42, 44, 46, 48, 50, 52, 54, 56, 58, 60, 62, 64, 66, 68, 70, 72, 74, 76, 78, 80, 82, 84, 86, 88, 90, 92, 94, 96, 98, 100, 102, 104, 106, 108, 110, 112, 114, 116, 118, 120, 122, 124, 126, 128, 130, 132, 134, 136, 138, 140, 142, 144, 146, 148, 150, 152, 154, 156, 158, 160, 162, 164, 166, 168, 170, 172, 174, 176, 178, 180, 182, 184, 186, 188, 190, 192, 194, 196, 198, 200, 202, 204, 206, 208, 210, 212, 214, 216, 218, 220, 222, 224, 226, 228, 230, 232, 234, 236, 238, 240, 242, 244, 246, 248, 250, 252, 254, 256, 258, 260, 262, 264, 266, 268, 270, 272, 274, 276, 278, 280, 282, 284, 286, 288, 290, 292, 294, 296, 298, 300, 302, 304, 306, 308, 310, 312, 314, 316, 318, 320, 322, 324, 326, 328, 330, 332, 334, 336, 338, 340, 342, 344, 346, 348, 350, 352, 354, 356, 358, 360, 362, 364, 366, 368, 370, 372, 374, 376, 378, 380, 382, 384, 386, 388, 390, 392, 394, 396, 398, 400, 402, 404, 406, 408, 410, 412, 414, 416, 418, 420, 422, 424, 426, 428, 430, 432, 434, 436, 438, 440, 442, 444, 446, 448, 450, 452, 454, 456. 458, 460. 462, 464, 466, 468, 470, 472, 474, 476, 478, 480, 482, 484, 486, 488, 490, 492, 494, 496, 498, 500, 502, 504, 506, 508, 510, 512, 514, 516, 518, 520, 522, 524, 526, 528, 530, 532, 534, 536, 538, 540, 542, 544, 546, 548, 550, 552, 554, 556, 558, 560, 562, 564, or 566, wherein the polypeptide sequence has optionally 1, 2, 3, 4, 5, 6, 7, 8, 9, or up to 10 substitutions in the polypeptide sequence.

In some embodiments, a recombinant reverse transcriptase comprises a polypeptide sequence comprising at least 75%, 80%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more sequence identity to a reference sequence corresponding to SEQ ID NO: 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32, 34, 36, 38, 40, 42, 44, 46, 48, 50, 52, 54, 56, 58, 60, 62, 64, 66, 68, 70, 72, 74, 76, 78, 80, 82, 84, 86, 88, 90, 92, 94, 96, 98, 100, 102, 104, 106, 108, 110, 112, 114, 116, 118, 120, 122, 124, 126, 128, 130, 132, 134, 136, 138, 140, 142, 144, 146, 148, 150, 152, 154, 156, 158, 160, 162, 164, 166, 168, 170, 172, 174, 176, 178, 180, 182, 184, 186, 188, 190, 192, 194, 196, 198, 200, 202, 204, 206, 208, 210, 212, 214, 216, 218, 220, 222, 224, 226, 228, 230, 232, 234, 236, 238, 240, 242, 244, 246, 248, 250, 252, 254, 256, 258, 260, 262, 264, 266, 268, 270, 272, 274, 276, 278, 280, 282, 284, 286, 288, 290, 292, 294, 296, 298, 300, 302, 304, 306, 308, 310, 312, 314, 316, 318, 320, 322, 324, 326, 328, 330, 332, 334, 336, 338, 340, 342, 344, 346, 348, 350, 352, 354, 356, 358, 360, 362, 364, 366, 368, 370, 372, 374, 376, 378, 380, 382, 384, 386, 388, 390, 392, 394, 396, 398, 400, 402, 404, 406, 408, 410, 412, 414, 416, 418, 420, 422, 424, 426, 428, 430, 432, 434, 436, 438, 440, 442, 444, 446, 448, 450, 452, 454, 456. 458, 460. 462, 464, 466, 468, 470, 472, 474, 476, 478, 480, 482, 484, 486, 488, 490, 492, 494, 496, 498, 500, 502, 504, 506, 508, 510, 512, 514, 516, 518, 520, 522, 524, 526, 528, 530, 532, 534, 536, 538, 540, 542, 544, 546, 548, 550, 552, 554, 556, 558, 560, 562, 564, or 566.

In some embodiments, the recombinant reverse transcriptase comprises a polypeptide sequence comprising SEQ ID NO: 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32, 34, 36, 38, 40, 42, 44, 46, 48, 50, 52, 54, 56, 58, 60, 62, 64, 66, 68, 70, 72, 74, 76, 78, 80, 82, 84, 86, 88, 90, 92, 94, 96, 98, 100, 102, 104, 106, 108, 110, 112, 114, 116, 118, 120, 122, 124, 126, 128, 130, 132, 134, 136, 138, 140, 142, 144, 146, 148, 150, 152, 154, 156, 158, 160, 162, 164, 166, 168, 170, 172, 174, 176, 178, 180, 182, 184, 186, 188, 190, 192, 194, 196, 198, 200, 202, 204, 206, 208, 210, 212, 214, 216, 218, 220, 222, 224, 226, 228, 230, 232, 234, 236, 238, 240, 242, 244, 246, 248, 250, 252, 254, 256, 258, 260, 262, 264, 266, 268, 270, 272, 274, 276, 278, 280, 282, 284, 286, 288, 290, 292, 294, 296, 298, 300, 302, 304, 306, 308, 310, 312, 314, 316, 318, 320, 322, 324, 326, 328, 330, 332, 334, 336, 338, 340, 342, 344, 346, 348, 350, 352, 354, 356, 358, 360, 362, 364, 366, 368, 370, 372, 374, 376, 378, 380, 382, 384, 386, 388, 390, 392, 394, 396, 398, 400, 402, 404, 406, 408, 410, 412, 414, 416, 418, 420, 422, 424, 426, 428, 430, 432, 434, 436, 438, 440, 442, 444, 446, 448, 450, 452, 454, 456. 458, 460. 462, 464, 466, 468, 470, 472, 474, 476, 478, 480, 482, 484, 486, 488, 490, 492, 494, 496, 498, 500, 502, 504, 506, 508, 510, 512, 514, 516, 518, 520, 522, 524, 526, 528, 530, 532, 534, 536, 538, 540, 542, 544, 546, 548, 550, 552, 554, 556, 558, 560, 562, 564, or 566, wherein the polypeptide optionally has 1, 2, 3, 4, 5, 6, 7, 8, 9, or up to 10 substitutions in the polypeptide sequence.

In some embodiments, the recombinant reverse transcriptase polypeptide has 1, 2, 3, 4, or up to 5 substitutions in the polypeptide sequence. In some embodiments, the recombinant reverse transcriptase polypeptide has 1, 2, 3, or 4 substitutions in the polypeptide sequence. In some embodiments, the substitutions comprises non-conservative or conservative substitutions. In some embodiments, the substitutions comprises conservative substitutions. In some embodiments, the substitutions comprises non-conservative substitutions. In some embodiments, guidance on non-conservative and conservative substitutions are provided by the variants disclosed herein, including in the Examples.

In some embodiments, the recombinant reverse transcriptase comprises a polypeptide sequence comprising residues 12 to 687 of SEQ ID NO: 2, 24, 94, or 352, wherein the polypeptide sequence has optionally 1, 2, 3, 4, 5, 6, 7, 8, 9, or up to 10 substitutions in the polypeptide sequence. In some embodiments, the recombinant reverse transcriptase comprises a polypeptide sequence comprising SEQ ID NO: 2, 24, 94, or 352, wherein the polypeptide sequence has optionally 1, 2, 3, 4, 5, 6, 7, 8, 9, or up to 10 substitutions in the polypeptide sequence. In some embodiments, the recombinant reverse transcriptase includes 1, 2, 3, 4, up to 5 substitutions in the polypeptide sequence. In some embodiments, the recombinant reverse transcriptase includes 1, 2, 3, or 4 substitutions in the polypeptide sequence.

It will be apparent that the description herein, including the Examples and Tables, provide structural information correlating specific amino acid sequence features with the functional activity of the recombinant reverse transcriptase polypeptides. This structure-function correlation information is provided in the form of specific amino acid residue differences relative to the reference engineered polypeptide of SEQ ID NO: 2, 24, 94 and 352, as well as associated experimentally determined activity data for the exemplary recombinant reverse transcriptase polypeptides. Such information provides guidance and information on substitutions implemented in preparing variants of recombinant reverse transcriptase.

In some embodiments, the recombinant reverse transcriptase of the present disclosure has DNA polymerase activity. In particular, the DNA polymerase activity uses a target RNA as a template. As further discussed herein, the target RNA includes, among others, messenger RNA (mRNA), non-coding RNA (ncRNA), micro-RNA (miRNA), bacterial RNA, fungal RNA, and viral RNA. In some embodiments, the recombinant reverse transcriptase of the present disclosure has DNA polymerase activity, wherein the DNA polymerase activity uses a target DNA template.

In some embodiments, the recombinant reverse transcriptase of the present disclosure has at least one improved property as compared to a reference reverse transcriptase. In some embodiments, the recombinant reverse transcriptases have one or more of improved property selected from increased DNA product yield, increased thermostability, increased salt tolerance, increased processivity, increased fidelity, increased RNA template sensitivity, and/or increased product yield in a coupled PCR reaction with a DNA polymerase (e.g., RT-PCR) compared to a reference reverse transcriptase. In some embodiments, the reference reverse transcriptase has a sequence corresponding to residues 12 to 687 of SEQ ID NO: 2, 24, 94, or 352. In some embodiments, the reference reverse transcriptase has the sequence corresponding to residues 12 to 687 of SEQ ID NO: 2, or the sequence corresponding to SEQ ID NO: 2.

In some embodiments, the recombinant reverse transcriptase polypeptide described herein is an isolated composition. In some embodiments, the recombinant reverse transcriptase polypeptide described herein is a purified composition, as further discussed herein.

In some embodiments, the present disclosure further provides functional fragments or biologically active fragments of recombinant reverse transcriptase polypeptides described herein. Thus, for each and every embodiment herein of a recombinant reverse transcriptase, a functional fragment or biologically active fragment of the recombinant reverse transcriptase is provided herewith. In some embodiments, a functional fragment or biologically active fragments of a recombinant reverse transcriptase comprises at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, or at least about 99% of the activity of the recombinant reverse transcriptase polypeptide from which it was derived (i.e., the parent recombinant reverse transcriptase).

In some embodiments, functional fragments or biologically active fragments comprise at least about 90%, at least about 91%, at least about 92%, at least about 93%, at least about 94%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, or at least about 99% of the parent sequence of the recombinant reverse transcriptase. In some embodiments the functional fragment will be truncated by less than 5, less than 10, less than 15, less than 10, less than 25, less than 30, less than 35, less than 40, less than 45, and less than 50 amino acids.

In some embodiments, a functional fragment of a recombinant reverse transcriptase comprises at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% of the parent sequence of the recombinant reverse transcriptase. In some embodiments the functional fragment will be truncated by less than 5, less than 10, less than 15, less than 10, less than 25, less than 30, less than 35, less than 40, less than 45, less than 50, less than 55, less than 60, less than 65, or less than 70 amino acids.

In some embodiments, the functional fragments or biologically active fragments of the recombinant reverse transcriptase polypeptide described herein include at least a substitution or substitution set in the amino acid sequence of the recombinant reverse transcriptase described herein. Accordingly, in some embodiments, the functional fragments or biologically active fragments of the recombinant reverse transcriptase displays the enhanced or improved property associated with the substitution or substitution set in the parent recombinant reverse transcriptase.

Polynucleotides Encoding Engineered Polypeptides, Expression Vectors and Host Cells

In another aspect, the present disclosure provides recombinant polynucleotides encoding the recombinant reverse transcriptase polypeptides described herein. In some embodiments, the recombinant polynucleotides are operatively linked to one or more heterologous regulatory sequences that control gene expression to create a recombinant polynucleotide capable of expressing the polypeptide. In some embodiments, expression constructs containing at least one heterologous polynucleotide encoding the recombinant reverse transcriptase polypeptide(s) is introduced into appropriate host cells to express the corresponding DNA polymerase polypeptide(s).

As will be apparent to the skilled artisan, availability of a protein sequence and the knowledge of the codons corresponding to the various amino acids provide a description of all the polynucleotides capable of encoding the subject polypeptides. The degeneracy of the genetic code, where the same amino acids are encoded by alternative or synonymous codons, allows an extremely large number of nucleic acids to be made, all of which encode a recombinant reverse transcriptase polypeptide. Thus, the present invention provides methods and compositions for the production of each and every possible variation of recombinant reverse transcriptase polynucleotides that could be made that encode the reverse transcriptase polypeptides described herein by selecting combinations based on the possible codon choices, and all such variations are to be considered specifically disclosed for any polypeptide described herein, including the amino acid sequences presented in the Examples (e.g., in Table 4.1, 5.1, 6.1, and 7.1) and in the Sequence Listing.

In some embodiments, the codons are preferably optimized for utilization by the chosen host cell for protein production. For example, preferred codons used in bacteria are typically used for expression in bacteria, and preferred codons used in mammalian cells are typically used for expression in mammalian cells. Consequently, codon optimized polynucleotides encoding the recombinant reverse transcriptase polypeptides contain preferred codons at about 40%, 50%, 60%, 70%, 80%, 90%, or greater than 90% of the codon positions in the full length coding region.

In some embodiments, the recombinant reverse transcriptase polynucleotide encodes an engineered polypeptide having reverse transcriptase activity, wherein the polypeptide comprises an amino acid sequence having at least at least 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity to a reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 2, 24, 94, or 352, or to a reference sequence corresponding to SEQ ID NO: 2, 24, 94, or 352, wherein the polypeptide sequence comprises one or more substitutions relative to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 2, 24, 94, or 352, or to the reference sequence corresponding to SEQ ID NO: 2, 24, 94, or 352, as described herein.

In some embodiments, the recombinant polynucleotide encodes the recombinant reverse transcriptase comprising a polypeptide acid sequence having at least at least 70%, 75%, 80%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% or more sequence identity to a reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 2, or to a reference sequence corresponding to SEQ ID NO: 2, wherein the polypeptide sequence comprises one or more substitutions relative to a reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 2, or to a reference sequence corresponding to SEQ ID NO: 2, as described herein.

As described above, in some embodiments, the recombinant polynucleotide encodes the recombinant reverse transcriptase comprising a polypeptide acid sequence comprising at least a substitution at amino acid position 18, 25, 49, 63, 68, 69, 72, 74, 78, 81, 83, 84, 85, 89, 90, 92, 94, 98, 102, 113, 114, 118, 119, 129, 130, 132, 134, 163, 167, 171, 173, 178, 196, 199, 205, 209, 210, 212, 216, 242, 258, 260, 261, 266, 294, 297, 298, 300, 303, 305, 307, 308, 309, 310, 311, 314, 317, 319, 321, 329, 331, 333, 338, 342, 343, 349, 356, 370, 403, 444, 447, 454, 464, 465, 466, 474, 479, 508, 509, 519, 536, 537, 554, 574, 576, 583, 595, 598, 606, 638, 639, or 662, or combinations thereof, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 2.

In some embodiments, the recombinant polynucleotide encodes a reverse transcriptase polypeptide comprising a polypeptide sequence comprising at least a substitution at amino acid position 49, 266, 298, 307, 444, 509, or 536, or combinations thereof, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 2.

In some embodiments, the recombinant polynucleotide encodes the reverse transcriptase polypeptide comprising a polypeptide acid sequence comprising at least a substitution or substitution set at amino acid position 114/210/307, 114/309, 49, 63/68/216/258/261, 63/68/216/261, 63/209/314/665, 447/665, 331, 90/307/349, 114/173/331, 266, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 2.

In some embodiments, the recombinant polynucleotide encodes the reverse transcriptase polypeptide comprising a polypeptide acid sequence comprising at least a substitution or substitution set at amino acid position 454/508, 536/574, 309, 49/173/309/331, 90/331, 63/90/309/574/650, 90/173/209/210/321/574/598, 508/519, 49/63/90/216/309/321/536/574, 49/114/307/309/536, 307/321/536/574/650, 309/331/536/574/598/650, 173/331/536/574/598, 49/300/403, 74/242, 242/298/508/662, 260/509, 102/370/509, 49/173/216/349/536/598, 49/114/216/307/309/331, 49/90/173/216/307, 63/68/81/167/314/447/574, 49/210/307/309/321/536/574/650, 63/90/307/321/331/537/598, 370/464/465/509/554/576, 49/114/173/216/321/574/598, 90/216/321/650, 574/650, 49/209/210/307/309/536/598, 216/536/574, 49/173/210/309/321/536/598, 331/536/598, 321/574, 173/321/331/349/574, 49/307/536, 216/309/574/650, 94/370/474/576, 90/209/210/309/321/574, 49/63/90/173, 298, 49/300/454/662, 68/81/167/298/536, 49/454, 81, 49/114/173/309/349/536/574/650, 167/261/303/536, 18/102/554, 171/173/307/331/536, 173/216/536, 18/370/464/509, 49/114, 90/216/309/536/574, 444, 90/321/349/536/598/650, 49/163/309/321/536/574/650, 49/63/90/173/307/331/536/598/650, 68/81/167/258/447/466/536, 90/331/574, 49/321, 94/509, 90/173/321/536, 167/298/447/466, 173/216/307/309/536, 216/321, 49/90/173/209/309/331, 261/298/303/447/574, 171/298/444/519, 90/536/574/598/650, 49/63/90/210/307/321/598/650, 90/216/307/536/574, 18/94/102/260/370/464/554, 18/423/465/474, 167/261/447/536, 114/173/209/210, 307/309/536/574/598, 102/260/370/576, 574, 173/209/210/307/536, 216/309/536, 349, 447/536/606, 310/454/479/519/662, 49/90/209/598, 314/536, 171/300/454/479/508/662, 171/242/300/508/662, 49/331/536, 173/216/309/536/574/598, 536/598, 167/261/298/303/447/466/574, 173/536/598, 49/114/309/536/574/598, 49/114/309/349/536, 63/68/81/303/466, 63/90/209/216/307/309/321/349/536/574/598/650, 216, 173/210/307/598/650, 25/102/370/423, 68/261/298/303, 423/474, 94/423/474/554/576, 63/298/447/574, 49/63/90/173/307/321/331/574/595/650, 49/90/536/574, 508, 63/81/167/258/261/298/303/447, 114/331, 212/298/583/606, 49/173/536/574, 49/242/298/300/310/444/454/479, 49/309/321/536/598, 63/68/261/536, 300/444/508, or 298, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 2.

In some embodiments, In some embodiments, the recombinant polynucleotide encodes the reverse transcriptase polypeptide comprising a polypeptide acid sequence comprising at least a substitution or substitution set at amino acid position 134, 74, 83, 319, 92, 329, 343, 311, 338, 196, 69, 72, 294, 83, 134, 130, 305, 319, 113, 297, 319, 114, 308, 309, 342, 205, 212, 199, 83, 303, 309, 78, 113, 132, 311, 119, 83, 98, 314, 129, 343, 196, 74, 356, 89, 212, 444/508/509/574, 63/260/298/300/331/444/509, 63/90/209/444/508/574, 298/444/509, 63/90/508/509/574/595, 83, 311, 89, 130, 178, or 118, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 2.

In some embodiments, In some embodiments, the recombinant polynucleotide encodes the reverse transcriptase comprising a polypeptide acid sequence comprising at least a substitution or substitution set at amino acid position 309/342, 309, 129, 574, 85, 98/119/129/132/196, 98/317/343/356, 205/212/309/319/342, 78/132/314, 78/83/98, 78/83/119/132/196, 78/83, 78/83/356, 78, 119/129/132, 178/303/331/338/508, 311/314, 63/297/303/305, 63/178/209/260/574, 63/300/338, 83/294, 83/92/343/574, 83/92/134/574, 83/196/329/343, 83/196, 83/134/196/294/305/311/319/329/343/574, 83, 83/309, 83/319/342, 83/205, 83/114, 83/114/309, 83/114/319, 83/199/212/309/319/639, 83/199, 83/342, 83/308/309/595/638, 83/113/114/205/212, 83/130, 114/309, 114/212/309/342/639, 114/205, 114, 114/130/319, 114/130/212/342, 114/130/309, 199/309, 199/205, 342, 343/595, 74, 74/129, 74/83/129/132/212, 74/83/92/343, 74/83/134/294/574, 74/83, 74/329/574, 74/92/196/294/329, 92, 72, 72/294/311/329/343, 72/294, 72/294/311/329, 72/83/343, 72/74/294, 72/74/83/319/329, 72/74/83/84, 72/74/83/134/196/294, 72/74, 72/74/92/294/329, 72/74/92, 72/74/92/134/343, 72/74/134/196/319/329, 72/196/311/329/574, 72/134/196, 118/178/338, 69/89/178/303/305/338/574, 113, 113/178/260, 113/309, 113/212/309, 113/342, 113/114, 113/114/212, 113/114/205/319/342, 113/114/342, 113/114/130, 130/205/333, 134, or 134/294, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 2.

In some embodiments, for each of the foregoing embodiments, the specific amino acid substitutions described herein for the substitution or substitution set can be used for the encoded reverse transcriptase polypeptide.

In some embodiments, the recombinant polynucleotide encodes the recombinant reverse transcriptase comprising a polypeptide sequence comprising at least a substitution or substitution set 266V/454A/508L, 266V/536E/574Q, 266V/309P, 49G/173A/266V/309P/331E, 90I/266V/331E, 63L/90I/266V/309P/574D/650G, 90I/173A/209A/210L/266V/321A/574D/5985, 266V/508L/519P, 49G/63L/90I/216R/266V/309P/321A/536E/574D, 49G/114K/266V/307N/309P/536E, 266V/307K/321A/536E/574D/650G, 266V/309P/331E/536E/574Q/598S/650G, 173A/266V/331E/536E/574D/598S, 49G/266V/300I/403H, 74K/242A/266V, 242A/266V/298E/508L/662R, 260G/266V/509E, 102C/266V/370G/509E, 49G/173A/216R/266V/349G/536E/598S, 49G/114K/216R/266V/307K/309P/331E, 49G/90I/173A/216R/266V/307K, 63P/68S/81K/167Y/266V/314A/447G/574Q, 49G/210L/266V/307K/309P/321A/536E/574D/650G, 63L/90I/266V/307K/321A/331E/537W/598S, 266V/370G/464L/465S/509E/554T/576I, 49G/114K/173A/216R/266V/321A/574D/598S, 90I/216R/266V/321A/650G, 266V/574D/650G, 49G/209A/210L/266V/307K/309P/536E/598S, 216R/266V/536E/574Q, 49G/173A/210L/266V/309P/321A/536E/5985, 266V/331E/536E/598S, 266V/321A/574D, 173A/266V/321A/331E/349G/574D, 49G/266V/307K/536E, 216R/266V/309P/574D/650G, 94L/266V/370G/474A/576I, 90I/209A/210L/266V/309P/321A/574D, 49G/63L/90I/173A/266V, 266V/298E, 49G/266V/300I/454A/662R, 68S/81K/167Y/266V/298R/536N, 49G/266V/454A, 81K/266V, 49G/114K/173A/266V/309P/349G/536E/574D/650G , 167Y/261N/266V/303Q/536N, 18E/102C/266V/554T, 171L/173A/266V/307K/331E/536E, 173A/216R/266V/536E, 18E/266V/370G/464L/509E, 49G/114K/266V, 90I/216R/266V/309P/536G/574D, 266V/444L, 90I/266V/321A/349G/536G/598S/650G, 49G/163P/266V/309P/321A/536E/574D/650G, 49G/63L/90I/173A/266V/307K/331E/536E/598S/650G, 68S/81K/167Y/258T/266V/447G/466K/536N, 90I/266V/331E/574D, 49G/266V/321A, 94L/266V/509E, 90I/173A/266V/321A/536E, 167Y/266V/298R/447G/466K, 173A/216R/266V/307K/309P/536E, 216R/266V/321A, 49G/90I/173A/209A/266V/309P/331E, 261N/266V/298R/303Q/447R/574Q, 171P/266V/298E/444L/519P, 90I/266V/536E/574D/598S/650G, 49G/63L/90I/210L/266V/307K/321A/598S/650G, 90I/216R/266V/307K/536E/574D, 18E/94L/102C/260G/266V/370G/464L/554T, 18E/266V/423R/465S/474A, 167Y/261N/266V/447G/536G, 114K/173A/209A/210L/266V, 266V/307K/309P/536E/574D/598S, 102C/260G/266V/370G/576I, 266V/574D, 173A/209A/210L/266V/307K/536E, 216R/266V/309P/536E, 266V/349G, 266 V/447L/536A/606Q, 266V/310R/454A/479D/519P/662R, 49G/90I/209A/266V/598S, 266V/314K/536N, 171P/266V/300I/454A/479D/508L/662R, 171P/242A/266V/300I/508L/662R, 49G/266V/331E/536E, 173A/216R/266V/309P/536E/574D/598S, 266V/536E/598S, 167Y/261N/266V/298R/303Q/447R/466K/574Q, 173A/266V/536E/598S, 49G/114K/266V/309P/536E/574D/598S, 49G/114K/266V/309P/349G/536E, 63P/68S/81K/266V/303Q/466K, 63L/90I/209A/216R/266V/307K/309P/321A/349G/536E/574D/598S/650G, 216R/266V, 173A/210L/266V/307K/598S/650G, 25E/102C/266V/370G/423R, 68S/261N/266V/298R/303Q, 266V/423R/474A, 94L/266V/423R/474A/554T/576I, 63P/266V/298R/447R/574Q, 49G/63L/90I/173A/266V/307K/321A/331E/574D/595N/650G, 49G/90I/266V/536E/574D, 266V/508L, 63P/81K/167Y/258T/266V/261N/298R/303Q/447G, 114K/266V/331E, 212N/266V/298E/583K/606K, 49G/173A/266V/536E/574Q, 49G/242A/266V/298E/300I/310R/444L/454A/479D, 49G/266V/309P/321A/536E/598S, 63P/68S/261N/266V/536G, 266 V/300I/444L/508L, or 266V/298R, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 2.

In some embodiments, the recombinant polynucleotide encodes the recombinant reverse transcriptase comprising a polypeptide sequence comprising at least a substitution or substitution set 49G/266V/298R/307K/309E/342W/444L/509E/536E, 49G/266V/298R/307K/309T/444L/509E/536E, 49G/129L/266V/307K/444L/509E/536E, 49G/266V/298R/307K/444L/536E/574Q, 49G/85R/266V/298R/307K/444L/509E/536E, 49G/985/119Y/129L/132F/196H/266V/307K/444L/509E/536E, 49G/985/266V/307K/317C/343V/356P/444L/509E/536E, 49G/205M/212K/266V/307K/309E/319S/342W/444L/536E, 49G/266V/298R/307K/509E/536E, 49G/78V/132F/266V/298R/307K/314M/444L/509E/536E, 49G/78V/83E/98S/266V/298R/307K/444L/509E/536E, 49G/78V/83E/119Y/132F/196H/266V/298R/307K/509E/536E, 49G/78V/83E/266V/307K/444L/509E/536E, 49G/78V/83E/266V/307K/444L/536E, 49G/78V/83E/266V/307K/356P/444L/509E/536E, 49G/78V/266V/307K/509E/536E, 49G/119Y/129L/132F/266V/298R/307K/444L/509E/536E, 49G/178L/266V/303G/307K/331E/338V/444L/508L/509E/536E, 49G/266V/298R/307K/311I/314M/444L/509E/536E, 49G/63L/266V/297W/298R/303G/305P/307K/509E/536E, 49G/63L/178L/209A/260G/266V/298R/307K/444L/509E/536E/574Q, 49G/63L/266V/298R/300I/307K/338V/444L/509E/536E, 49G/83A/266V/294Q/298R/307K/444L/509E/536E, 49G/83A/92T/266V/307K/343A/444L/509E/536E/574Q, 49G/83A/92T/134P/266V/298R/307K/509E/536E/574Q, 49G/83A/196C/266V/298R/307K/329S/343A/444L/509E/536E, 49G/83A/196C/266V/307K/444L/536E, 49G/83A/134F/196C/294Q/266V/305S/307K/311P/319G/329S/343A/509E/536E/574Q, 49G/83C/266V/298R/307K/444L/509E/536E, 49G/83C/266V/298R/307K/309T/444L/509E/536E, 49G/83C/266V/298R/307K/319S/342W/444L/536E, 49G/83C/205M/266V/298R/307K/509E/536E, 49G/83C/266V/298R/307K/509E/536E, 49G/83C/114G/266V/298R/307K/444L/509E/536E, 49G/83C/114G/266V/298R/307K/309T/444L/536E, 49G/83C/114G/266V/307K/319C/444L/509E/536E, 49G/83C/199L/212K/266V/307K/309E/319C/509E/536E/639H, 49G/83C/199L/266V/298R/307K/444L/536E, 49G/83C/266V/307K/444L/509E/536E, 49G/83C/266V/307K/342W/444L/509E/536E, 49G/83C/266V/298R/307K/308G/309E/444L/509E/536E/595N/638H, 49G/83C/113T/114G/205M/212K/266V/298R/307K/444L/509E/536E, 49G/83C/130S/266V/307K/509E/536E, 49G/114G/266V/298R/307K/309E/444L/509E/536E, 49G/114G/266V/298R/307K/309E/444L/536E, 49G/114G/212K/266V/298R/307K/309E/342W/444L/509E/536E/639H, 49G/114G/205M/266V/298R/307K/509E/536E, 49G/114G/266V/307K/444L/509E/536E, 49G/114G/1305S/266V/298R/307K/319S/509E/536E, 49G/114G/130S/212K/266V/307K/342W/444L/509E/536E, 49G/114G/130S/266V/307 K/309E/444L/509E/536E, 49G/199L/266V/298R/307K/309T/444L/509E/536E, 49G/199L/205M/266V/298R/307K/509E/536E, 49G/266V/307K/444L/509E/536E, 49G/266V/307K/342W/444L/509E/536E, 49G/266V/307K/444L/536E, 49G/266V/307K/343A/509E/536E/595N, 49G/74M/266V/298R/307K/444L/509E/536E, 49G/74M/129L/266V/307K/509E/536E, 49G/74M/83E/129L/132F/212V/266V/298R/307K/444L/536E, 49G/74P/83A/92T/266V/307K/343A/444L/536E, 49G/74P/83A/134P/266V/294Q/307 K/444L/509E/536E/574Q, 49G/74P/83W/266V/298R/307K/536E, 49G/74P/266V/307K/329S/509E/536E/574Q, 49G/74P/92T/196C/266V/294Q/298R/307K//329S/444L/509E/536E, 49G/92T/266V/307K/444L/536E, 49G/72M/266V/298R/307K/444L/509E/536E, 49G/72M/266V/294Q/298R/307K/311A/329S/343A/509E/536E, 49G/72M/266V/294Q/307K/509E/536E, 49G/72M/266V/294Q/307K/311A/329S/509E/536E, 49G/72M/266V/298R/307K/444L/536E, 49G/72M/83A/266V/307K/343A/509E/536E, 49G/266V/72M/74P/294Q/307K/509E/536E, 49G/72M/74P/83A/266V/298R/307K/319G/329S/444L/536E, 49G/72M/74P/83A/84N/266V/298R/307K/509E/536E, 49G/72M/74P/83A/134F/196C/266V/294Q/307K/444L/509E/536E, 49G/72M/74P/266V/307K/444L/536E, 49G/72M/74P/92T/266V/294Q/307K/329S/444L/509E/536E, 49G/72M/74P/92T/266V/307K/444L/509E/536E, 49G/72M/74P/92T/134P/266V/307K/343A/509E/536E, 49G/72M/74P/134F/196C/266V/307K/319G/329S/444L/536E, 49G/72M/196C/266V/298R/307K/311A/329S/444L/509E/536E/574Q, 49G/72M/134P/196C/266V/307K/444L/509E/536E, 49G/118R/178L/266V/298R/307K/338V/444L/509E/536E, 49G/69R/89A/178L/266V/298R/303G/305P/307K/338V/444L/509E/536E/574Q, 49G/113G/266V/298R/307K/444L/509E/536E, 49G/113G/178L/260G/266V/298R/307K/444L/509E/536E, 49G/113T/266V/298R/307K/309E/444L/509E/536E, 49G/113T/212K/266V/298R/307K/309E/444L/509E/536E, 49G/113T/266V/298R/307K/342W/444L/509E/536E, 49G/113T/114G/266V/298R/307K/444L/509E/536E, 49G/113T/114G/212K/266V/298R/307K/444L/509E/536E, 49G/113T/114G/205M/266V/298R/307K/319C/342W/444L/509E/536E, 49G/113T/114G/266V/307K/342W/444L/509E/536E, 49G/113T/114G/130S/266V/298R/307K/444L/509E/536E, 49G/113T/266V/307K/444L/509E/536E, 49G/113T/266V/298R/307K/309E/509E/536E, 49G/130S/205M/266V/298R/307K/333V/509E/536E, 49G/134P/266V/298R/307K/444L/509E/536E, or 49G/134P/266V/294Q/298R/307K/536E, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 2.

In some embodiments, the recombinant polynucleotide encodes the recombinant reverse transcriptase comprising a polypeptide sequence having at least 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity to the reference sequence comprising residues 12 to 687 of SEQ ID NO: 24, 94, or 352, or to a reference sequence of SEQ ID NO: 24, 94, or 352. In some embodiments, it includes the proviso that the polypeptide sequence does not include a sequence corresponding to residues 12 to 687 of SEQ ID NO: 2.

In some embodiments, the recombinant polynucleotide encodes the recombinant reverse transcriptase comprising a polypeptide sequence comprising at least a substitution at amino acid position 18, 25, 49, 63, 68, 69, 72, 74, 78, 81, 83, 89, 90, 92, 94, 98, 102, 113, 114, 118, 119, 129, 130, 132, 134, 163, 167, 171, 173, 178, 196, 199, 205, 209, 210, 212, 216, 242, 258, 260, 261, 266, 294, 297, 298, 300, 303, 305, 307, 308, 309, 310, 311, 314, 319, 321, 329, 331, 338, 342, 343, 349, 356, 370, 403, 423, 444, 447, 454, 464, 465, 466, 474, 479, 508, 509, 519, 536, 537, 554, 574, 576, 583, 595, 598, 606, 650, 662, or 665, or combinations thereof, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 24, 94, or 352.

In some embodiments, the recombinant polynucleotide encodes the recombinant reverse transcriptase comprising a polypeptide sequence comprising at least a substitution at amino acid position 49, 266, 298, 307, 444, 509, or 536, or combinations thereof, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 24, 94, or 352.

In some embodiments, the recombinant polynucleotide encodes the recombinant reverse transcriptase comprising a polypeptide sequence having at least 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity to a reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 24, or to a reference sequence of SEQ ID NO: 24, wherein the polypeptide sequence comprises one or more substitutions relative to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 24, or to a reference sequence of SEQ ID NO: 24.

In some embodiments, the recombinant polynucleotide encodes the recombinant reverse transcriptase comprising a polypeptide sequence comprising at least a substitution or substitution set at amino acid position 454/508, 536/574, 309, 49/173/309/331, 90/331, 63/90/309/574/650, 90/173/209/210/321/574/598, 508/519, 49/63/90/216/309/321/536/574, 49/114/307/309/536, 307/321/536/574/650, 309/331/536/574/598/650, 173/331/536/574/598, 49/300/403, 74/242, 242/298/508/662, 260/509, 102/370/509, 49/173/216/349/536/598, 49/114/216/307/309/331, 49/90/173/216/307, 63/68/81/167/314/447/574, 49/210/307/309/321/536/574/650, 63/90/307/321/331/537/598, 370/464/465/509/554/576, 49/114/173/216/321/574/598, 90/216/321/650, 574/650, 49/209/210/307/309/536/598, 216/536/574, 49/173/210/309/321/536/598, 331/536/598, 321/574, 173/321/331/349/574, 49/307/536, 216/309/574/650, 94/370/474/576, 90/209/210/309/321/574, 49/63/90/173, 298, 49/300/454/662, 68/81/167/298/536, 49/454, 81, 49/114/173/309/349/536/574/650, 167/261/303/536, 18/102/554, 171/173/307/331/536, 173/216/536, 18/370/464/509, 49/114, 90/216/309/536/574, 444, 90/321/349/536/598/650, 49/163/309/321/536/574/650, 49/63/90/173/307/331/536/598/650, 68/81/167/258/447/466/536, 90/331/574, 49/321, 94/509, 90/173/321/536, 167/298/447/466, 173/216/307/309/536, 216/321, 49/90/173/209/309/331, 261/298/303/447/574, 171/298/444/519, 90/536/574/598/650, 49/63/90/210/307/321/598/650, 90/216/307/536/574, 18/94/102/260/370/464/554, 18/423/465/474, 167/261/447/536, 114/173/209/210, 307/309/536/574/598, 102/260/370/576, 574, 173/209/210/307/536, 216/309/536, 349, 447/536/606, 310/454/479/519/662, 49/90/209/598, 314/536, 171/300/454/479/508/662, 171/242/300/508/662, 49/331/536, 173/216/309/536/574/598, 536/598, 167/261/298/303/447/466/574, 173/536/598, 49/114/309/536/574/598, 49/114/309/349/536, 63/68/81/303/466, 63/90/209/216/307/309/321/349/536/574/598/650, 216, 173/210/307/598/650, 25/102/370/423, 68/261/298/303, 423/474, 94/423/474/554/576, 63/298/447/574, 49/63/90/173/307/321/331/574/595/650, 49/90/536/574, 508, 63/81/167/258/261/298/303/447, 114/331, 212/298/583/606, 49/173/536/574, 49/242/298/300/310/444/454/479, 49/309/321/536/598, 63/68/261/536, 300/444/508, 298, or combinations thereof, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 24.

In some embodiments, the recombinant polynucleotide encodes the recombinant reverse transcriptase comprising a polypeptide sequence having at least 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity to a reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 94, or to a reference sequence of SEQ ID NO: 94, wherein the polypeptide sequence comprises one or more substitutions relative to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 94, or to a reference sequence of SEQ ID NO: 94.

In some embodiments, the recombinant polynucleotide encodes the the recombinant reverse transcriptase comprising a polypeptide sequence comprising at least a substitution or substitution set at amino acid position 134, 74, 83, 319, 92, 329, 343, 311, 338, 196, 69, 72, 294, 83, 134, 130, 305, 319,113,297,319,114,308,309,342,205,212,199,83,303,309,78,113,132,311,119,83,98, 314, 129, 343, 196, 74, 356, 89, 212, 444/508/509/574, 63/260/298/300/331/444/509, 63/90/209/444/508/574, 298/444/509, 63/90/508/509/574/595, 83, 311, 89, 130, 178, or 118, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 94.

In some embodiments, the recombinant polynucleotide encodes the recombinant reverse transcriptase comprising a polypeptide sequence having at least 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity to a reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 352, or to a reference sequence of SEQ ID NO: 352, wherein the polypeptide sequence comprises one or more substitutions relative to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 352, or to a reference sequence of SEQ ID NO: 352.

In some embodiments, the recombinant polynucleotide encodes the recombinant reverse transcriptase comprising a polypeptide sequence comprising at least a substitution or substitution set at amino acid position 309/342, 309, 129/298, 509/574, 85, 98/119/129/132/196/298, 98/298/317/343/356, 205/212/298/309/319/342/509, 444, 78/132/314, 78/83/98, 78/83/119/132/196/444, 78/83/298, 78/83/298/509, 78/83/298/356, 78/298/444, 119/129/132, 178/298/303/331/338/508, 311/314, 63/297/303/305/444, 63/178/209/260/574, 63/300/338, 83/294, 83/92/298/343/574, 83/92/134/444/574, 83/196/329/343, 83/196/298/509, 83/134/196/294/298/305/311/319/329/343/444/574, 83, 83/309, 83/319/342/509, 83/205/444, 83/444, 83/114, 83/114/309/509, 83/114/298/319, 83/199/212/298/309/319/444/639, 83/199/509, 83/298, 83/298/342, 83/308/309/595/638, 83/113/114/205/212, 83/130/298/444, 114/309, 114/309/509, 114/212/309/342/639, 114/205/444, 114/298, 114/130/319/444, 114/130/212/298/342, 114/130/298/309, 199/309, 199/205/444, 298, 298/342, 298/509, 298/343/444/595, 74, 74/129/298/444, 74/83/129/132/212/509, 74/83/92/298/343/509, 74/83/134/294/298/574, 74/83/444/509, 74/298/329/444/574, 74/92/196/294/329, 92/298/509, 72, 72/294/311/329/343/444, 72/294/298/444, 72/294/298/311/329/444, 72/509, 72/83/298/343/444, 72/74/294/298/444, 72/74/83/319/329/509, 72/74/83/84/444, 72/74/83/134/196/294/298, 72/74/298/509, 72/74/92/294/298/329, 72/74/92/298, 72/74/92/134/298/343/444, 72/74/134/196/298/319/329/509, 72/196/311/329/574, 72/134/196/298, 118/178/338/444, 69/89/178/303/305/338/444/574, 113, 113/178/260, 113/309, 113/212/309, 113/342, 113/114, 113/114/212, 113/114/205/319/342, 113/114/298/342, 113/114/130, 113/298, 113/298/309/444, 130/205/333/444, 134, or 134/294/444/509, wherein the amino acid positions are relative to the reference sequence of SEQ ID NO: 352.

In some embodiments, the recombinant polynucleotide encodes a recombinant reverse transcriptase comprising a polypeptide sequence comprising at least one substitution provided in Table 4.1, 5.1, 6.1, and 7.1, wherein the substitution is relative to SEQ ID NO: 2, 24, 94 or 352.

In some embodiments, the recombinant polynucleotide encodes a recombinant reverse transcriptase comprising a polypeptide sequence comprising at least a substitution or substitution set provided in Table 4.1, 5.1, 6.1, and 7.1, wherein the substitution or substitution set is relative to SEQ ID NO: 2, 24, 94 or 352.

In some embodiments, the recombinant polynucleotide encodes a recombinant reverse transcriptase comprising a polypeptide sequence having at least 75%, 80%, 85%, 86%, 887%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more sequence identity to a sequence corresponding to residues 12 to 687 of an even numbered SEQ ID NO. set forth in Table 4.1, 5.1, 6.1, and 7.1. In some embodiments, the recombinant polynucleotide encodes a recombinant reverse transcriptase comprising a polypeptide sequence having at least 75%, 80%, 85%, 86%, 887%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more sequence identity to a sequence of an even numbered SEQ ID NO. set forth in Table 4.1, 5.1, 6.1, and 7.1. In some embodiments, the recombinant polynucleotide encodes a recombinant reverse transcriptase comprising a polypeptide sequence comprising residues 12 to 687 of an even numbered SEQ ID NO. set forth in Table 4.1, 5.1, 6.1, and 7.1. In some embodiments, the recombinant polynucleotide encodes a recombinant reverse transcriptase comprising a polypeptide sequence comprising an even numbered SEQ ID NO. set forth in Table 4.1, 5.1, 6.1, and 7.1.

In some embodiments, the recombinant polynucleotide encodes a recombinant reverse transcriptase comprising a polypeptide sequence comprising residues 12 to 687 of SEQ ID NO: 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32, 34, 36, 38, 40, 42, 44, 46, 48, 50, 52, 54, 56, 58, 60, 62, 64, 66, 68, 70, 72, 74, 76, 78, 80, 82, 84, 86, 88, 90, 92, 94, 96, 98, 100, 102, 104, 106, 108, 110, 112, 114, 116, 118, 120, 122, 124, 126, 128, 130, 132, 134, 136, 138, 140, 142, 144, 146, 148, 150, 152, 154, 156, 158, 160, 162, 164, 166, 168, 170, 172, 174, 176, 178, 180, 182, 184, 186, 188, 190, 192, 194, 196, 198, 200, 202, 204, 206, 208, 210, 212, 214, 216, 218, 220, 222, 224, 226, 228, 230, 232, 234, 236, 238, 240, 242, 244, 246, 248, 250, 252, 254, 256, 258, 260, 262, 264, 266, 268, 270, 272, 274, 276, 278, 280, 282, 284, 286, 288, 290, 292, 294, 296, 298, 300, 302, 304, 306, 308, 310, 312, 314, 316, 318, 320, 322, 324, 326, 328, 330, 332, 334, 336, 338, 340, 342, 344, 346, 348, 350, 352, 354, 356, 358, 360, 362, 364, 366, 368, 370, 372, 374, 376, 378, 380, 382, 384, 386, 388, 390, 392, 394, 396, 398, 400, 402, 404, 406, 408, 410, 412, 414, 416, 418, 420, 422, 424, 426, 428, 430, 432, 434, 436, 438, 440, 442, 444, 446, 448, 450, 452, 454, 456. 458, 460. 462, 464, 466, 468, 470, 472, 474, 476, 478, 480, 482, 484, 486, 488, 490, 492, 494, 496, 498, 500, 502, 504, 506, 508, 510, 512, 514, 516, 518, 520, 522, 524, 526, 528, 530, 532, 534, 536, 538, 540, 542, 544, 546, 548, 550, 552, 554, 556, 558, 560, 562, 564, or 566, wherein the polypeptide sequence has optionally 1, 2, 3, 4, 5, 6, 7, 8, 9, or up to 10 substitutions in the polypeptide sequence.

In some embodiments, the recombinant polynucleotide encodes a recombinant reverse transcriptase comprising a polypeptide sequence comprising SEQ ID NO: 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32, 34, 36, 38, 40, 42, 44, 46, 48, 50, 52, 54, 56, 58, 60, 62, 64, 66, 68, 70, 72, 74, 76, 78, 80, 82, 84, 86, 88, 90, 92, 94, 96, 98, 100, 102, 104, 106, 108, 110, 112, 114, 116, 118, 120, 122, 124, 126, 128, 130, 132, 134, 136, 138, 140, 142, 144, 146, 148, 150, 152, 154, 156, 158, 160, 162, 164, 166, 168, 170, 172, 174, 176, 178, 180, 182, 184, 186, 188, 190, 192, 194, 196, 198, 200, 202, 204, 206, 208, 210, 212, 214, 216, 218, 220, 222, 224, 226, 228, 230, 232, 234, 236, 238, 240, 242, 244, 246, 248, 250, 252, 254, 256, 258, 260, 262, 264, 266, 268, 270, 272, 274, 276, 278, 280, 282, 284, 286, 288, 290, 292, 294, 296, 298, 300, 302, 304, 306, 308, 310, 312, 314, 316, 318, 320, 322, 324, 326, 328, 330, 332, 334, 336, 338, 340, 342, 344, 346, 348, 350, 352, 354, 356, 358, 360, 362, 364, 366, 368, 370, 372, 374, 376, 378, 380, 382, 384, 386, 388, 390, 392, 394, 396, 398, 400, 402, 404, 406, 408, 410, 412, 414, 416, 418, 420, 422, 424, 426, 428, 430, 432, 434, 436, 438, 440, 442, 444, 446, 448, 450, 452, 454, 456. 458, 460. 462, 464, 466, 468, 470, 472, 474, 476, 478, 480, 482, 484, 486, 488, 490, 492, 494, 496, 498, 500, 502, 504, 506, 508, 510, 512, 514, 516, 518, 520, 522, 524, 526, 528, 530, 532, 534, 536, 538, 540, 542, 544, 546, 548, 550, 552, 554, 556, 558, 560, 562, 564, or 566, wherein the polypeptide sequence has optionally 1, 2, 3, 4, 5, 6, 7, 8, 9, or up to 10 substitutions in the polypeptide sequence.

In some embodiments, the encoded recombinant reverse transcriptase polypeptide includes 1, 2, 3, 4, up to 5 substitutions in the polypeptide sequence. In some embodiments, the recombinant reverse transcriptase includes 1, 2, 3, or 4 substitutions in the polypeptide sequence. In some embodiments, the substitutions comprises non-conservative or conservative substitutions. In some embodiments, the substitutions comprises conservative substitutions. In some embodiments, the substitutions comprises non-conservative substitutions. In some embodiments, guidance on non-conservative and conservative substitutions are provided by the variants disclosed herein.

In some embodiments, the recombinant polynucleotide encodes a recombinant reverse transcriptase polypeptide comprising a polypeptide sequence comprising residues 12 to 687 of SEQ ID NO: 4, 24, 94, or 352, wherein the polypeptide sequence has optionally 1, 2, 3, 4, 5, 6, 7, 8, 9, or up to 10 substitutions in the polypeptide sequence. In some embodiments, the recombinant reverse transcriptase includes 1, 2, 3, 4, up to 5 substitutions in the polypeptide sequence. In some embodiments, the recombinant reverse transcriptase includes 1, 2, 3, or 4 substitutions in the polypeptide sequence.

In some embodiments, the recombinant polynucleotide encodes the recombinant reverse transcriptase polypeptide comprising a polypeptide sequence comprising SEQ ID NO: 4, 24, 94, or 352, wherein the polypeptide sequence has optionally 1, 2, 3, 4, 5, 6, 7, 8, 9, or up to 10 substitutions in the polypeptide sequence. In some embodiments, the recombinant reverse transcriptase includes 1, 2, 3, 4, up to 5 substitutions in the polypeptide sequence. In some embodiments, the recombinant reverse transcriptase includes 1, 2, 3, or 4 substitutions in the polypeptide sequence.

In some embodiments, the recombinant polynucleotide comprises a polynucleotide sequence having at least 75%, 80%, 81%, 82%, 83%, 84%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity to the reference polynucleotide sequence comprising nucleotide residues 34 to 2061 of SEQ ID NO: 1, or to a reference polynucleotide sequence of SEQ ID NO: 1, wherein the recombinant polynucleotide encodes a recombinant reverse transcriptase or a functional fragment thereof, wherein the polypeptide sequence of the recombinant reverse transcriptase comprises one or more substitutions at one or more amino acid positions relative to the reference sequence corresponding to residues 12 to 687 of SEQ ID NO: 2, or to the reference sequence of SEQ ID NO: 2.

In some embodiments, a reverse transcriptase polynucleotide comprises at least 75%, 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or more sequence identity to the reference polynucleotide sequence of SEQ ID NO: 1 encoding a recombinant reverse transcriptase or a functional fragment thereof, wherein the recombinant reverse transcriptase comprises at least one substitution at one or more amino acid positions relative to the reference polypeptide sequence of SEQ ID NO: 2.

In some embodiments, the recombinant polynucleotide comprises a polynucleotide sequence having at least 75%, 80%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more sequence identity to a polynucleotide sequence corresponding to nucleotide residues 34 to 2061 of SEQ ID NO: 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 29, 31, 33, 35, 37. 39, 41, 43, 45, 47, 49, 51, 53, 55, 57, 59, 61, 63, 65, 67, 69, 71, 73, 75, 77, 79, 81, 83, 85, 87, 89, 91, 93, 95, 97, 99, 101, 103, 105, 107, 109, 111, 113, 115, 117, 119, 121, 123, 125, 127, 129, 131, 133, 135, 137, 139, 141, 143, 145, 147, 149, 151, 153, 155, 157, 159, 161, 163, 165, 167, 169, 171, 173, 175, 177, 179, 181, 183, 185, 187, 189, 191, 193, 195, 197, 199, 201, 203, 205, 207, 209, 211, 213, 215, 217, 219, 221, 223, 225, 227, 229, 231, 233, 235, 237, 239, 241, 243, 245, 247, 249, 251, 253, 255, 257, 259, 261, 263, 265, 267, 269, 271, 273, 275, 277, 279, 281, 283, 285, 287, 289, 291, 293, 295, 297, 299, 301, 303, 305, 307, 309, 311, 313, 315, 317, 319, 321, 323, 325, 327, 329, 331, 333, 335, 337, 339, 341, 343, 345, 347, 349, 351, 353, 355, 357, 359, 361, 363, 365, 367, 369, 371, 373, 375, 377, 379, 381, 383, 385, 387, 389, 391, 393, 395, 397, 399, 401, 403, 405, 407, 409, 411, 413, 415, 417, 419, 421, 423, 425, 427, 429, 431, 433, 435, 437, 439, 441, 443, 445, 447, 449, 451, 453, 455, 457. 459, 461. 463, 465, 467, 469, 471, 473, 475, 477, 479, 481, 483, 485, 487, 489, 491, 493, 495, 497, 499, 501, 503, 505, 507, 509, 511, 513, 515, 517, 519, 521, 523, 525, 527, 529, 531, 533, 535, 537, 539, 541, 543, 545, 547, 549, 551, 553, 555, 557, 559, 561, 563, or 565, wherein the polynucleotide encodes a reverse transcriptase, as described herein.

In some embodiments, the recombinant polynucleotide comprises a polynucleotide sequence comprising nucleotide residues 34 to 2061 of SEQ ID NO: 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 29, 31, 33, 35, 37.39, 41, 43, 45, 47, 49, 51, 53, 55, 57, 59, 61, 63, 65, 67, 69, 71, 73, 75, 77, 79, 81, 83, 85, 87, 89, 91, 93, 95, 97, 99, 101, 103, 105, 107, 109, 111, 113, 115, 117, 119, 121, 123, 125, 127, 129, 131, 133, 135, 137, 139, 141, 143, 145, 147, 149, 151, 153, 155, 157, 159, 161, 163, 165, 167, 169, 171, 173, 175, 177, 179, 181, 183, 185, 187, 189, 191, 193, 195, 197, 199, 201, 203, 205, 207, 209, 211, 213, 215, 217, 219, 221, 223, 225, 227, 229, 231, 233, 235, 237, 239, 241, 243, 245, 247, 249, 251, 253, 255, 257, 259, 261, 263, 265, 267, 269, 271, 273, 275, 277, 279, 281, 283, 285, 287, 289, 291, 293, 295, 297, 299, 301, 303, 305, 307, 309, 311, 313, 315, 317, 319, 321, 323, 325, 327, 329, 331, 333, 335, 337, 339, 341, 343, 345, 347, 349, 351, 353, 355, 357, 359, 361, 363, 365, 367, 369, 371, 373, 375, 377, 379, 381, 383, 385, 387, 389, 391, 393, 395, 397, 399, 401, 403, 405, 407, 409, 411, 413, 415, 417, 419, 421, 423, 425, 427, 429, 431, 433, 435, 437, 439, 441, 443, 445, 447, 449, 451, 453, 455, 457. 459, 461. 463, 465, 467, 469, 471, 473, 475, 477, 479, 481, 483, 485, 487, 489, 491, 493, 495, 497, 499, 501, 503, 505, 507, 509, 511, 513, 515, 517, 519, 521, 523, 525, 527, 529, 531, 533, 535, 537, 539, 541, 543, 545, 547, 549, 551, 553, 555, 557, 559, 561, 563, or 565.

In some embodiments, the recombinant polynucleotide comprises a polynucleotide sequence having at least 75%, 80%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more sequence identity to a polynucleotide sequence corresponding to SEQ ID NO: 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 29, 31, 33, 35, 37. 39, 41, 43, 45, 47, 49, 51, 53, 55, 57, 59, 61, 63, 65, 67, 69, 71, 73, 75, 77, 79, 81, 83, 85, 87, 89, 91, 93, 95, 97, 99, 101, 103, 105, 107, 109, 111, 113, 115, 117, 119, 121, 123, 125, 127, 129, 131, 133, 135, 137, 139, 141, 143, 145, 147, 149, 151, 153, 155, 157, 159, 161, 163, 165, 167, 169, 171, 173, 175, 177, 179, 181, 183, 185, 187, 189, 191, 193, 195, 197, 199, 201, 203, 205, 207, 209, 211, 213, 215, 217, 219, 221, 223, 225, 227, 229, 231, 233, 235, 237, 239, 241, 243, 245, 247, 249, 251, 253, 255, 257, 259, 261, 263, 265, 267, 269, 271, 273, 275, 277, 279, 281, 283, 285, 287, 289, 291, 293, 295, 297, 299, 301, 303, 305, 307, 309, 311, 313, 315, 317, 319, 321, 323, 325, 327, 329, 331, 333, 335, 337, 339, 341, 343, 345, 347, 349, 351, 353, 355, 357, 359, 361, 363, 365, 367, 369, 371, 373, 375, 377, 379, 381, 383, 385, 387, 389, 391, 393, 395, 397, 399, 401, 403, 405, 407, 409, 411, 413, 415, 417, 419, 421, 423, 425, 427, 429, 431, 433, 435, 437, 439, 441, 443, 445, 447, 449, 451, 453, 455, 457. 459, 461. 463, 465, 467, 469, 471, 473, 475, 477, 479, 481, 483, 485, 487, 489, 491, 493, 495, 497, 499, 501, 503, 505, 507, 509, 511, 513, 515, 517, 519, 521, 523, 525, 527, 529, 531, 533, 535, 537, 539, 541, 543, 545, 547, 549, 551, 553, 555, 557, 559, 561, 563, or 565, wherein the polynucleotide encodes a reverse transcriptase, as described herein.

In some embodiments, the recombinant polynucleotide comprises the sequence comprising SEQ ID NO: 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, 29, 31, 33, 35, 37. 39, 41, 43, 45, 47, 49, 51, 53, 55, 57, 59, 61, 63, 65, 67, 69, 71, 73, 75, 77, 79, 81, 83, 85, 87, 89, 91, 93, 95, 97, 99, 101, 103, 105, 107, 109, 111, 113, 115, 117, 119, 121, 123, 125, 127, 129, 131, 133, 135, 137, 139, 141, 143, 145, 147, 149, 151, 153, 155, 157, 159, 161, 163, 165, 167, 169, 171, 173, 175, 177, 179, 181, 183, 185, 187, 189, 191, 193, 195, 197, 199, 201, 203, 205, 207, 209, 211, 213, 215, 217, 219, 221, 223, 225, 227, 229, 231, 233, 235, 237, 239, 241, 243, 245, 247, 249, 251, 253, 255, 257, 259, 261, 263, 265, 267, 269, 271, 273, 275, 277, 279, 281, 283, 285, 287, 289, 291, 293, 295, 297, 299, 301, 303, 305, 307, 309, 311, 313, 315, 317, 319, 321, 323, 325, 327, 329, 331, 333, 335, 337, 339, 341, 343, 345, 347, 349, 351, 353, 355, 357, 359, 361, 363, 365, 367, 369, 371, 373, 375, 377, 379, 381, 383, 385, 387, 389, 391, 393, 395, 397, 399, 401, 403, 405, 407, 409, 411, 413, 415, 417, 419, 421, 423, 425, 427, 429, 431, 433, 435, 437, 439, 441, 443, 445, 447, 449, 451, 453, 455, 457. 459, 461. 463, 465, 467, 469, 471, 473, 475, 477, 479, 481, 483, 485, 487, 489, 491, 493, 495, 497, 499, 501, 503, 505, 507, 509, 511, 513, 515, 517, 519, 521, 523, 525, 527, 529, 531, 533, 535, 537, 539, 541, 543, 545, 547, 549, 551, 553, 555, 557, 559, 561, 563, or 565.

In some embodiments, the recombinant polynucleotide encodes a reverse transcriptase and hybridizes under highly stringent conditions to a reference polynucleotide sequence described herein encoding a recombinant reverse transcriptase. In some embodiments, the reference sequence corresponds to residues residues 34 to 2061 of SEQ ID NO: 1, 3, 23, 93, or 351, or to the sequence corresponding to SEQ ID NO: 1, 3, 23, 93, or 351, or a complement thereof, or a polynucleotide sequence encoding any of the other recombinant reverse transcriptases provided herein. In some embodiments, the polynucleotide encodes a reverse transcriptase and hybridizes under highly stringent conditions to a reference polynucleotide comprising a sequence corresponding to residues 34 to 2061 of an odd numbered sequence of SEQ ID NOS: 1-565, or to a reference polynucleotide comprising a sequence corresponding to an odd numbered sequence of SEQ ID NOS: 1-565.

In some embodiments, the polynucleotide capable of hybridizing under highly stringent conditions encodes a reverse transcriptase comprising an amino acid sequence that has one or more residue differences as compared to SEQ ID NO: 2, 4, 24, 94, or 352, at residue positions selected from any positions as set forth in Tables 4.1, 5.1, 6.1, and 7.1. In some embodiments, the polynucleotide that hybridizes under highly stringent conditions comprises a polynucleotide having at least 70%, 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more sequence identity to a reference sequence corresponding to residues 34 to 2061 of SEQ ID NO: 1, 3, 23, 93, or 351, or to a reference sequence corresponding to SEQ ID NO: 1, 3, 23, 93, or 351. In some additional embodiments, the polynucleotide hybridizing under highly stringent conditions comprises a sequence having at least 75%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more sequence identity to at least one polynucleotide reference sequence corresponding to residues 34 to 2061 of a polynucleotide sequence provided in Tables 4.1, 5.1, 6.1, and 7.1, or corresponding to a polynucleotide sequence provided in Tables 4.1, 5.1, 6.1, and 7.1.

In some embodiments, an isolated polynucleotide encoding any of the recombinant reverse transcriptase polypeptides herein is manipulated in a variety of ways to facilitate expression of the reverse transcriptase polypeptide. In some embodiments, the polynucleotide encoding a recombinant reverse transcriptase is in an expression vector to express the polynucleotide and/or encoded polypeptide. In some embodiments, the polynucleotide can be operably linked to one or more control sequences to regulate expression of the reverse transcriptase polynucleotides and/or polypeptides. Manipulation of the isolated polynucleotide prior to its insertion into a vector may be desirable or necessary depending on the expression vector utilized. Techniques for modifying polynucleotides and nucleic acid sequences utilizing recombinant DNA methods are well known in the art.

In some embodiments, the control sequences include among others, promoters, leader sequences, polyadenylation sequences, propeptide sequences, signal peptide sequences, and transcription terminators. In some embodiments, suitable promoters are selected based on the host cells selection. For bacterial host cells, suitable promoters for directing transcription of the nucleic acid constructs of the present disclosure, include, but are not limited to promoters obtained from the E. coli lac operon, Streptomyces coelicolor agarase gene (dagA), Bacillus subtilis levansucrase gene (sacB), Bacillus licheniformis alpha-amylase gene (amyL), Bacillus stearothermophilus maltogenic amylase gene (amyM), Bacillus amyloliquefaciens alpha-amylase gene (amyQ), Bacillus licheniformis penicillinase gene (penP), Bacillus subtilis xylA and xylB genes, and prokaryotic beta-lactamase gene (See e.g., Villa-Kamaroff et al., Proc. Natl Acad. Sci. USA, 1978, 75:3727-3731), as well as the tac promoter (See e.g., DeBoer et al., Proc. Natl Acad. Sci. USA, 1983, 80: 21-25). Exemplary promoters for filamentous fungal host cells, include, but are not limited to promoters obtained from the genes for Aspergillus oryzae TAKA amylase, Rhizomucor miehei aspartic proteinase, Aspergillus niger neutral alpha-amylase, Aspergillus niger acid stable alpha-amylase, Aspergillus niger or Aspergillus awamori glucoamylase (glaA), Rhizomucor miehei lipase, Aspergillus oryzae alkaline protease, Aspergillus oryzae triose phosphate isomerase, Aspergillus nidulans acetamidase, and Fusarium oxysporum trypsin-like protease (See e.g., WO 96/00787), as well as the NA2-tpi promoter (a hybrid of the promoters from the genes for Aspergillus niger neutral alpha-amylase and Aspergillus oryzae triose phosphate isomerase), and mutant, truncated, and hybrid promoters thereof. Exemplary yeast cell promoters can be from the genes can be from the genes for Saccharomyces cerevisiae enolase (ENO-1), Saccharomyces cerevisiae galactokinase (GAL1), Saccharomyces cerevisiae alcohol dehydrogenase/glyceraldehyde-3-phosphate dehydrogenase (ADH2/GAP), and Saccharomyces cerevisiae 3-phosphoglycerate kinase. Other useful promoters for yeast host cells are known in the art (See e.g., Romanos et al., Yeast, 1992, 8:423-488).

In some embodiments, the control sequence is also a suitable transcription terminator sequence (i.e., a sequence recognized by a host cell to terminate transcription). In some embodiments, the terminator sequence is operably linked to the 3′ terminus of the nucleic acid sequence encoding the DNA polymerase polypeptide. Any suitable terminator which is functional in the host cell of choice finds use in the present invention. Exemplary transcription terminators for filamentous fungal host cells can be obtained from the genes for Aspergillus oryzae TAKA amylase, Aspergillus niger glucoamylase, Aspergillus nidulans anthranilate synthase, Aspergillus niger alpha-glucosidase, and Fusarium oxysporum trypsin-like protease. Exemplary terminators for yeast host cells can be obtained from the genes for Saccharomyces cerevisiae enolase, Saccharomyces cerevisiae cytochrome C (CYC1), and Saccharomyces cerevisiae glyceraldehyde-3-phosphate dehydrogenase. Other useful terminators for yeast host cells are known in the art (see e.g., Romanos et al., supra).

In some embodiments, the control sequence is also a suitable leader sequence (i.e., a non-translated region of an mRNA that is important for translation by the host cell). In some embodiments, the leader sequence is operably linked to the 5′ terminus of the nucleic acid sequence encoding the DNA polymerase polypeptide. Any suitable leader sequence that is functional in the host cell of choice find use in the present invention. Exemplary leaders for filamentous fungal host cells are obtained from the genes for Aspergillus oryzae TAKA amylase, and Aspergillus nidulans triose phosphate isomerase. Suitable leaders for yeast host cells are obtained from the genes for Saccharomyces cerevisiae enolase (ENO-1), Saccharomyces cerevisiae 3-phosphoglycerate kinase, Saccharomyces cerevisiae alpha-factor, and Saccharomyces cerevisiae alcohol dehydrogenase/glyceraldehyde-3-phosphate dehydrogenase (ADH2/GAP).

In some embodiments, the control sequence is also a polyadenylation sequence (i.e., a sequence operably linked to the 3′ terminus of the nucleic acid sequence and which, when transcribed, is recognized by the host cell as a signal to add polyadenosine residues to transcribed mRNA). Any suitable polyadenylation sequence which is functional in the host cell of choice finds use in the present invention. Exemplary polyadenylation sequences for filamentous fungal host cells include, but are not limited to the genes for Aspergillus oryzae TAKA amylase, Aspergillus niger glucoamylase, Aspergillus nidulans anthranilate synthase, Fusarium oxysporum trypsin-like protease, and Aspergillus niger alpha-glucosidase. Useful polyadenylation sequences for yeast host cells are known (See e.g., Guo and Sherman, Mol. Cell. Biol., 1995, 15:5983-5990).

In some embodiments, the control sequence comprises a 3′ untranslated nucleic acid region and polyadenylation tail nucleic acid sequence, sequences operably linked to the 3′ terminus of the protein coding nucleic acid sequence which mediate binding to proteins involved in mRNA trafficking and translation and mRNA half-life. Any polyadenylation sequence and 3′ UTR which is functional in the host cell of choice may be used in the present invention. Exemplary polyadenylation sequences for filamentous fungal host cells include, but are not limited to those from the genes for Aspergillus oryzae TAKA amylase, Aspergillus niger glucoamylase, Aspergillus nidulans anthranilate synthase, Fusarium oxysporum trypsin-like protease, and Aspergillus niger alpha-glucosidase.

In some embodiments, the control sequence is also a signal peptide (i.e., a coding region that codes for an amino acid sequence linked to the amino terminus of a polypeptide and directs the encoded polypeptide into the cell's secretory pathway). In some embodiments, the 5′ end of the coding sequence of the nucleic acid sequence inherently contains a signal peptide coding region naturally linked in translation reading frame with the segment of the coding region that encodes the secreted polypeptide. Alternatively, in some embodiments, the 5′ end of the coding sequence contains a signal peptide coding region that is foreign to the coding sequence. Any suitable signal peptide coding region which directs the expressed polypeptide into the secretory pathway of a host cell of choice finds use for expression of the engineered polypeptide(s). Effective signal peptide coding regions for bacterial host cells are the signal peptide coding regions include, but are not limited to those obtained from the genes for Bacillus NCIB 11837 maltogenic amylase, Bacillus stearothermophilus alpha-amylase, Bacillus licheniformis subtilisin, Bacillus licheniformis beta-lactamase, Bacillus stearothermophilus neutral proteases (nprT, nprS, nprM), and Bacillus subtilis prsA. Further signal peptides are known in the art (See e.g., Simonen and Palva, Microbiol. Rev., 1993, 57:109-137). In some embodiments, effective signal peptide coding regions for filamentous fungal host cells include, but are not limited to the signal peptide coding regions obtained from the genes for Aspergillus oryzae TAKA amylase, Aspergillus niger neutral amylase, Aspergillus niger glucoamylase, Rhizomucor miehei aspartic proteinase, Humicola insolens cellulase, and Humicola lanuginosa lipase. Useful signal peptides for yeast host cells include, but are not limited to those from the genes for Saccharomyces cerevisiae alpha-factor and Saccharomyces cerevisiae invertase.

In some embodiments, the control sequence is also a propeptide coding region that codes for an amino acid sequence positioned at the amino terminus of a polypeptide. The resultant polypeptide is referred to as a “proenzyme,” “propolypeptide,” or “zymogen.” A propolypeptide can be converted to a mature active polypeptide by catalytic or autocatalytic cleavage of the propeptide from the propolypeptide. The propeptide coding region may be obtained from any suitable source, including, but not limited to the genes for Bacillus subtilis alkaline protease (aprE), Bacillus subtilis neutral protease (nprT), Saccharomyces cerevisiae alpha-factor, Rhizomucor miehei aspartic proteinase, and Myceliophthora thermophila lactase (See e.g., WO 95/33836). Where both signal peptide and propeptide regions are present at the amino terminus of a polypeptide, the propeptide region is positioned next to the amino terminus of a polypeptide and the signal peptide region is positioned next to the amino terminus of the propeptide region.

In some embodiments, regulatory sequences are also utilized. These sequences facilitate the regulation of the expression of the polypeptide relative to the growth of the host cell. Examples of regulatory systems are those that cause the expression of the gene to be turned on or off in response to a chemical or physical stimulus, including the presence of a regulatory compound. In prokaryotic host cells, suitable regulatory sequences include, but are not limited to the lac, tac, and trp operator systems. In yeast host cells, suitable regulatory systems include, but are not limited to the ADH2 system or GAL1 system. In filamentous fungi, suitable regulatory sequences include, but are not limited to the TAKA alpha-amylase promoter, Aspergillus niger glucoamylase promoter, and Aspergillus oryzae glucoamylase promoter.

In view of the foregoing, in another aspect, the present disclosure provides a recombinant expression vector comprising a recombinant polynucleotide encoding a recombinant reverse transcriptase polypeptide described herein, and one or more expression regulating regions such as a promoter and a terminator, a replication origin, etc., depending on the type of hosts into which they are to be introduced. In some embodiments, the various nucleic acid and control sequences described herein are joined together to produce recombinant expression vectors which include one or more convenient restriction sites to allow for insertion or substitution of the nucleic acid sequence encoding the DNA polymerase polypeptide at such sites. Alternatively, in some embodiments, the nucleic acid sequence of the present invention is expressed by inserting the nucleic acid sequence or a nucleic acid construct comprising the sequence into an appropriate vector for expression. In some embodiments involving the creation of the expression vector, the coding sequence is located in the vector so that the coding sequence is operably linked with the appropriate control sequences for expression.

The recombinant expression vector may be any suitable vector (e.g., a plasmid or virus), that can be conveniently subjected to recombinant DNA procedures and bring about the expression of the DNA polymerase polynucleotide sequence. The choice of the vector typically depends on the compatibility of the vector with the host cell into which the vector is to be introduced. The vectors may be linear or closed circular plasmids.

In some embodiments, the expression vector is an autonomously replicating vector (i.e., a vector that exists as an extra-chromosomal entity, the replication of which is independent of chromosomal replication, such as a plasmid, an extra-chromosomal element, a minichromosome, or an artificial chromosome). The vector may contain any means for assuring self-replication. In some alternative embodiments, the vector is one in which, when introduced into the host cell, it is integrated into the genome and replicated together with the chromosome(s) into which it has been integrated. Furthermore, in some embodiments, a single vector or plasmid, or two or more vectors or plasmids which together contain the total DNA to be introduced into the genome of the host cell, and/or a transposon is utilized.

In some embodiments, the expression vector contains one or more selectable markers, which permit easy selection of transformed cells. A “selectable marker” is a gene, the product of which provides for biocide or viral resistance, resistance to heavy metals, prototrophy to auxotrophs, and the like. Examples of bacterial selectable markers include, but are not limited to the dal genes from Bacillus subtilis or Bacillus licheniformis, or markers, which confer antibiotic resistance such as ampicillin, kanamycin, chloramphenicol or tetracycline resistance. Suitable markers for yeast host cells include, but are not limited to ADE2, HIS3, LEU2, LYS2, MET3, TRP1, and URA3. Selectable markers for use in filamentous fungal host cells include, but are not limited to, amdS (acetamidase; e.g., from A. nidulans or A. orzyae), argB (ornithine carbamoyltransferases), bar (phosphinothricin acetyltransferase; e.g., from S. hygroscopicus), hph (hygromycin phosphotransferase), niaD (nitrate reductase), pyrG (orotidine-5′-phosphate decarboxylase; e.g., from A. nidulans or A. orzyae), sC (sulfate adenyltransferase), and trpC (anthranilate synthase), as well as equivalents thereof.

In a further aspect, the present disclosure also provides a host cell comprising at least one polynucleotide encoding at least one recombinant reverse transcriptase polypeptide of the present invention, the polynucleotide(s) being operatively linked to one or more control sequences for expression of the recombinant reverse transcriptase enzyme(s) in the host cell. Host cells suitable for use in expressing the polypeptides encoded by the expression vectors of the present disclosure are well known in the art and include but are not limited to, bacterial cells, such as E. coli, Vibrio fluvialis, Streptomyces and Salmonella typhimurium cells; fungal cells, such as yeast cells (e.g., Saccharomyces cerevisiae or Pichia pastoris (ATCC Accession No. 201178)); insect cells such as Drosophila S2 and Spodoptera Sf9 cells; animal cells such as CHO, COS, BHK, 293, and Bowes melanoma cells; and plant cells. Exemplary host cells also include various Escherichia coli strains (e.g., W3110 (ΔfhuA) and BL21).

In another aspect, the present disclosure provides a method of producing the recombinant reverse transcriptase polypeptides, where the method comprises culturing a host cell capable of expressing a polynucleotide encoding the recombinant reverse transcriptase polypeptide under conditions suitable for expression of the polypeptide. In some embodiments, the methods further comprise the steps of isolating and/or purifying the DNA polymerase polypeptides, as described herein. In some embodiments, the host cell is a bacterial cell, such as E. coli. or B subtilis.

Appropriate culture media and growth conditions for host cells are well known in the art. It is contemplated that any suitable method for introducing polynucleotides for expression of the DNA polymerase polypeptides into cells will find use in the present invention. Suitable techniques include, but are not limited to electroporation, biolistic particle bombardment, liposome mediated transfection, calcium chloride transfection, and protoplast fusion.

Recombinant reverse transcriptase polypeptides with the properties disclosed herein can be obtained by subjecting the polynucleotide encoding the naturally occurring or recombinant reverse transcriptase polypeptide to any suitable mutagenesis and/or directed evolution methods known in the art, and/or as described herein. An exemplary directed evolution technique is mutagenesis and/or DNA shuffling (See e.g., Stemmer, Proc. Natl. Acad. Sci. USA, 1994, 91:10747-10751; WO 95/22625; WO 97/0078; WO 97/35966; WO 98/27230; WO 00/42651; WO 01/75767 and U.S. Pat. 6,537,746). Other directed evolution procedures that can be used include, among others, staggered extension process (StEP), in vitro recombination (See e.g., Zhao et al., Nat. Biotechnol., 1998, 16:258-261), mutagenic PCR (See e.g., Caldwell et al., PCR Methods Appl., 1994, 3:S136-S140), and cassette mutagenesis (See e.g., Black et al., Proc. Natl. Acad. Sci. USA, 1996, 93:3525-3529).

For example, mutagenesis and directed evolution methods can be readily applied to reverse transcriptase-encoding polynucleotides to generate variant libraries that can be expressed, screened, and assayed. Any suitable mutagenesis and directed evolution methods find use in the present invention and are well known in the art (See e.g., U.S. Pat. Nos. 5,605,793, 5,811,238, 5,830,721, 5,834,252, 5,837,458, 5,928,905, 6,096,548, 6,117,679, 6,132,970, 6,165,793, 6,180,406, 6,251,674, 6,265,201, 6,277,638, 6,287,861, 6,287,862, 6,291,242, 6,297,053, 6,303,344, 6,309,883, 6,319,713, 6,319,714, 6,323,030, 6,326,204, 6,335,160, 6,335,198, 6,344,356, 6,352,859, 6,355,484, 6,358,740, 6,358,742, 6,365,377, 6,365,408, 6,368,861, 6,372,497, 6,337,186, 6,376,246, 6,379,964, 6,387,702, 6,391,552, 6,391,640, 6,395,547, 6,406,855, 6,406,910, 6,413,745, 6,413,774, 6,420,175, 6,423,542, 6,426,224, 6,436,675, 6,444,468, 6,455,253, 6,479,652, 6,482,647, 6,483,011, 6,484,105, 6,489,146, 6,500,617, 6,500,639, 6,506,602, 6,506,603, 6,518,065, 6,519,065, 6,521,453, 6,528,311, 6,537,746, 6,573,098, 6,576,467, 6,579,678, 6,586,182, 6,602,986, 6,605,430, 6,613,514, 6,653,072, 6,686,515, 6,703,240, 6,716,631, 6,825,001, 6,902,922, 6,917,882, 6,946,296, 6,961,664, 6,995,017, 7,024,312, 7,058,515, 7,105,297, 7,148,054, 7,220,566, 7,288,375, 7,384,387, 7,421,347, 7,430,477, 7,462,469, 7,534,564, 7,620,500, 7,620,502, 7,629,170, 7,702,464, 7,747,391, 7,747,393, 7,751,986, 7,776,598, 7,783,428, 7,795,030, 7,853,410, 7,868,138, 7,783,428, 7,873,477, 7,873,499, 7,904,249, 7,957,912, 7,981,614, 8,014,961, 8,029,988, 8,048,674, 8,058,001, 8,076,138, 8,108,150, 8,170,806, 8,224,580, 8,377,681, 8,383,346, 8,457,903, 8,504,498, 8,589,085, 8,762,066, 8,768,871, 9,593,326, 9,665,694, 9,684,771, and all related PCT and non-US counterparts; Ling et al., Anal. Biochem., 1997, 254(2):157-78; Dale et al., Meth. Mol. Biol., 1996, 57:369-74; Smith, Ann. Rev. Genet., 1985, 19:423-462; Botstein et al., Science, 1985, 229:1193-1201; Carter, Biochem. J., 1986, 237:1-7; Kramer et al., Cell, 1984, 38:879-887; Wells et al., Gene, 1985, 34:315-323; Minshull et al., Curr. Op. Chem. Biol., 1999, 3:284-290; Christians et al., Nat. Biotechnol., 1999, 17:259-264; Crameri et al., Nature, 1998, 391:288-291; Crameri, et al., Nat. Biotechnol., 1997, 15:436-438; Zhang et al., Proc. Nat. Acad. Sci. U.S.A., 1997, 94:4504-4509; Crameri et al., Nat. Biotechnol., 1996, 14:315-319; Stemmer, Nature, 1994, 370:389-391; Stemmer, Proc. Nat. Acad. Sci. USA, 1994, 91:10747-10751; EP 3 049 973; WO 95/22625; WO 97/0078; WO 97/35966; WO 98/27230; WO 00/42651; WO 01/75767; WO 2009/152336; and WO 2015/048573, all of which are incorporated herein by reference).

In some embodiments, the protein variants obtained following mutagenesis treatment are screened by subjecting the enzyme preparations to a defined temperature (or other assay conditions) and measuring the amount of enzyme activity remaining after heat treatments or other suitable assay conditions. Clones containing a polynucleotide encoding a reverse transcriptase polypeptide are then isolated from the gene, sequenced to identify the nucleotide sequence changes (if any), and used to express the enzyme in a host cell. Measuring reverse transcriptase (e.g., DNA polymerase) activity from the expression libraries can be performed using any suitable methods known in the art (e.g., standard biochemistry and molecular techniques, such as RT-qPCR).

For engineered reverse transcriptase polypeptides of known sequence, the polynucleotides encoding the enzyme can be prepared by standard solid-phase methods, according to known synthetic methods. In some embodiments, fragments of up to about 100 bases can be individually synthesized, then joined (e.g., by enzymatic or chemical ligation methods, or polymerase mediated methods) to form any desired continuous sequence. For example, polynucleotides and oligonucleotides disclosed herein can be prepared by chemical synthesis using the classical phosphoramidite method (See e.g., Beaucage et al., Tet. Lett., 1981, 22:1859-69; and Matthes et al., EMBO J., 1984, 3:801-05), as it is typically practiced in automated synthetic methods. According to the phosphoramidite method, oligonucleotides are synthesized (e.g., in an automatic DNA synthesizer, purified, annealed, ligated and cloned in appropriate vectors).

Accordingly, in some embodiments, a method for preparing the recombinant reverse transcriptase polypeptide can comprise: (a) synthesizing a polynucleotide encoding a polypeptide comprising an amino acid sequence selected from the amino acid sequence of any variant as described herein, and (b) expressing the polypeptide encoded by the polynucleotide. In some embodiments of the method, the amino acid sequence encoded by the polynucleotide can optionally have one or several (e.g., up to 3, 4, 5, or up to 10) amino acid residue deletions, insertions and/or substitutions. In some embodiments, the amino acid sequence has optionally 1-2, 1-3, 1-4, 1-5, 1-6, 1-7, 1-8, 1-9, 1-10, 1-15, 1-20, 1-21, 1-22, 1-23, 1-24, 1-25, 1-30, 1-35, 1-40, 1-45, or 1-50 amino acid residue deletions, insertions and/or substitutions. In some embodiments, the amino acid sequence has optionally 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 30, 30, 35, 40, 45, or 50 amino acid residue deletions, insertions and/or substitutions. In some embodiments, the amino acid sequence has optionally 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 18, 20, 21, 22, 23, 24, or 25 amino acid residue deletions, insertions and/or substitutions. In some embodiments, the substitutions are conservative or non-conservative substitutions.

The expressed recombinant reverse transcriptase polypeptide can be evaluated for any desired improved property or combination of properties (e.g., activity, selectivity, fidelity, processivity, stability, thermostability, tolerance to various pH levels, etc.) using any suitable assay known in the art, including but not limited to the assays and conditions described herein.

In some embodiments, any of the recombinant reverse transcriptase polypeptides expressed in a host cell are recovered from the cells and/or the culture medium using any one or more of the well-known techniques for protein purification, including, among others, lysozyme treatment, sonication, filtration, salting-out, ultra-centrifugation, and chromatography.

Chromatographic techniques for isolation of the DNA polymerase polypeptides include, among others, reverse phase chromatography, high-performance liquid chromatography, ion-exchange chromatography, hydrophobic-interaction chromatography, size-exclusion chromatography, gel electrophoresis, and affinity chromatography. Conditions for purifying a particular enzyme depends, in part, on factors such as net charge, hydrophobicity, hydrophilicity, molecular weight, molecular shape, etc., and will be apparent to those having skill in the art. In some embodiments, affinity techniques may be used to isolate the improved reverse transcriptase enzymes. For affinity chromatography purification, any antibody that specifically binds a reverse transcriptase polypeptide of interest may find use. For the production of antibodies, various host animals, including but not limited to rabbits, mice, rats, etc., are immunized by injection with a reverse transcriptase polypeptide, or a fragment thereof. In some embodiments, the reverse transcriptase polypeptide or fragment is attached to a suitable carrier, such as BSA, by means of a side chain functional group or linkers attached to a side chain functional group.

In some embodiments, the isolated or purified recombinant reverse transcriptase polypeptides are combined with other ingredients and compounds to provide compositions and formulations comprising the recombinant reverse transcriptase polypeptide as appropriate for different applications and uses (e.g., diagnostic methods and compositions). In some embodiments, a composition comprises at least one recombinant reverse transcriptase of the present disclosure. In some embodiments, the composition further comprises a buffer. In some embodiments, the composition further comprises a substrate, such as a nucleotide substrates (e.g., dNTPs) and/or at least one primer, e.g., complementary to a target RNA. In some embodiments, the composition can further comprise a DNA polymerase (e.g., a second DNA polymerase) other than the reverse transcriptase. In some embodiments, the second DNA polymerase is a thermostable DNA polymerase, for example Taq or Pfu polymerase, useful in RT-PCR coupled reactions. In some embodiments, the composition includes a probe or indicator, such as a nucleic acid binding dye (e.g., SYBR® Green), for detecting and/or quantitating the amount of product formed, e.g., in a qRT-PCR reaction.

Uses of Recombinant Reverse Transcriptase Polypeptides and Kits

In another aspect, the present disclosure provides uses of the recombinant reverse transcriptase for diagnostic and molecular biological applications, such as for detecting the presence of a target RNA, preparing cDNA libraries, and direct/indirect sequence of nucleic acids.

In some embodiments, the recombinant reverse transcriptase is used in preparing a complementary DNA of a target RNA. In some embodiments, a method of preparing a complementary DNA of a target RNA comprises contact a target RNA with a recombinant reverse transcriptase described herein in presence of substrates sufficient for producing a complementary DNA under reaction conditions suitable for production of a complementary DNA to all or a portion of the target RNA. As discussed herein and known in the art, substrates include nucleotides (e.g., dNTPs) for DNA polymerase activity and/or oligonucleotide primers. Primers can be to a specific sequence of the target RNA, or random primers, such as for generation of cDNA libraries.

In some embodiments, the target RNA is any RNA appropriate as a template for reverse transcriptase, including, but not limited to, messenger RNA (mRNA), non-coding RNA (ncRNA), micro-RNA (miRNA), bacterial RNA, fungal RNA, or viral RNA.

In some embodiments, the recombinant reverse transcriptase is useful in diagnostic applications, e.g., for detecting the presence of a target RNA. In some embodiments, a method for detecting presence of a target RNA comprises reacting a sample suspected of containing a target RNA with a recombinant reverse transcriptase of described herein in presence of substrates under conditions suitable for reverse transcriptase mediated production of a DNA complementary to all or a portion of the target RNA, and detecting the presence of the complementary DNA. In some embodiments, the target RNA can be messenger RNA (mRNA), non-coding RNA (ncRNA), micro-RNA (miRNA), bacterial RNA, fungal RNA, or viral RNA.

In some embodiments, the sample can be any material or substance suspected of containing a target RNA. In some embodiments, the sample is a biological sample, such as biopsy and autopsy samples, frozen sections taken for histological purposes, blood, plasma, serum, sputum, stool, tears, mucus, hair, skin, etc. In some embodiments, the biological sample are cells or viruses, such as from a bacterial culture, virus culture, or cell culture. In some embodiments, the sample is an environmental sample, such as from water, sewage, surfaces, air, filtrates, etc.

In some embodiments for detecting a target RNA, the detection of the complementary DNA product can be effectuated by known methods in the art. In some embodiments, the complementary DNA is detected by amplifying the complementary DNA, such as by polymerase chain reaction (PCR) or isothermal amplification. In some embodiments, a suitable isothermal amplification is by loop mediated isothermal amplification (LAMP). In some embodiments for detecting the presence of a target RNA, the reverse transcription reaction is conducted separately from the amplification reaction. In some embodiments, where the amplification is by PCR, the reverse transcriptase reaction and the PCR is a one-step RT-PCR (i.e., performed in a single reaction simultaneously). In some embodiments, where the amplification is by PCR, the reverse transcriptase reaction and the PCR is a two-step RT-PCR (i.e., performed separately).

In some embodiments, the recombinant reverse transcriptase is used for sequencing nucleic acids. In some embodiments, the recombinant reverse transcriptase is used for indirectly sequencing a target RNA by preparing a complementary DNA, and sequencing the resulting complementary DNA. Various methods for sequencing DNA, particularly NGS sequencing methods, are well known in the art.

In a further aspect, the present disclosure provides a kit comprising at least one recombinant reverse transcriptase disclosed herein. In some embodiments, the kit further comprises one or more of a buffer, a nucleotide substrate, and/or an oligonucleotide primer. In some embodiments, the kit can include multiple (e.g., two or more) oligonucleotide primers, for example to different portions of a target RNA. In some embodiments, the kit comprises a second DNA polymerase, e.g., for coupled RT-PCR reaction. In some embodiments, the second DNA polymerase comprises a thermostable DNA polymerase, such as a Taq or Pfu DNA polymerase.

EXAMPLES

The following Examples, including experiments and results achieved, are provided for illustrative purposes only and are not to be construed as limiting the present invention.

In the experimental disclosure below, where applicable, the following abbreviations apply: ppm (parts per million); M (molar); mM (millimolar), uM and μM (micromolar); nM (nanomolar); mol (moles); gm and g (gram); mg (milligrams); ug and μg (micrograms); L and 1 (liter); ml and mL (milliliter); cm (centimeters); mm (millimeters); um and μm (micrometers); sec. (seconds); min(s) (minute(s)); h(s) and hr(s) (hour(s)); Ω (ohm); μf (microfarad); U (units); MW (molecular weight); rpm (rotations per minute); CT (critical threshold); rcf (relative centrifugal force); psi and PSI (pounds per square inch); nt (nucleotide); aa (amino acid); ° C. (degrees Centigrade); rt (room temperature); RT (reverse transcriptase); PCR (polymerase chain reaction); NGS (next-generation sequencing); ds (double stranded); ss (single stranded); CDS (coding sequence); RT-qPCR (quantitative reverse transcription PCR); DNA (deoxyribonucleic acid); cDNA (complementary DNA); RNA (ribonucleic acid); E. coli W3110 (commonly used laboratory E. coli strain, available from the Coli Genetic Stock Center [CGSC], New Haven, CT); HTP (high throughput); HPLC (high pressure liquid chromatography); MCYP (microcyp); ddH2O (double distilled water); PBS (phosphate buffered saline); BSA (bovine serum albumin); DTT (dithiothreitol); CAM (chloramphenicol); CAT (chloramphenicol acetyltransferase); IPTG (isopropyl β-D-1-thiogalactopyranoside); GFP (green fluorescent protein); eGFP (enhanced GFP); DsRed (red fluorescent protein isolated from Discosoma sp.); FIOPC (fold improvements over positive control); LB (Luria-Bertani); SPRI (solid phase reversible immobilization); Sigma-Aldrich (Sigma-Aldrich, St. Louis, Mo.); Perkin Elmer (Perkin Elmer, Inc, Waltham, Mass.); Harvard Apparatus (Harvard Apparatus, Holliston, Mass.); Millipore (Millipore, Corp., Billerica Mass.); Covaris (Covaris, Inc., Woburn, Mass.); MagBio (MagBio Genomics, Inc., Gaithersburg, Md.); Qiagen (Qiagen Inc., Germantown, Md.); Illumina (Illumina, Inc., San Diego, Calif.); BD Biosciences (BD Biosciences, San Jose, Calif.); Difco (Difco Laboratories, BD Diagnostic Systems, Detroit, Mich.); Kuhner (Adolf Kuhner, AG, Basel, Switzerland); Zymo (Zymo Research, Irvine, Calif.); Agilent (Agilent Technologies, Inc., Santa Clara, Calif.); Thermo Scientific (part of Thermo Fisher Scientific, Waltham, Mass.); GE Healthcare (GE Healthcare Bio-Sciences, Piscataway, N.J.); and Bio-Rad (Bio-Rad Laboratories, Hercules, Calif.).

Example 1: E. coli Expression Hosts Containing Recombinant Reverse transcriptase (RT) Genes

The initial reverse transcriptase enzyme used to produce the variants of the present invention was SEQ ID NO: 2 cloned into the expression vector pCK110900 (See, FIG. 3 of US Patent Publication No. 2006/0195947) operatively linked to the lac promoter under control of the lacl repressor. The expression vector also contains the P15a origin of replication and the chloramphenicol resistance gene. The resulting plasmids were transformed into E. coli W3110, using standard methods known in the art. The transformants were isolated by subjecting the cells to chloramphenicol selection, as known in the art (see, e.g., U.S. Pat. No. 8,383,346 and WO2010/144103).

Example 2: Preparation of HTP Reverse Transcriptase (RT) -Containing Wet Cell Pellets

E. coli cells containing recombinant RT-encoding genes from monoclonal colonies were inoculated into 180 μl LB containing 1% glucose and 30 μg/mL chloramphenicol (CAM) in the wells of 96-well, shallow-well microtiter plates. The plates were sealed with O₂-permeable seals, and cultures were grown overnight at 30° C., 200 rpm, and 85% humidity. Then, 10 μl of each of the cell cultures were transferred into the wells of 96-well, deep-well plates containing 390 mL TB and 30 μg/mL CAM. The deep-well plates were sealed with O₂-permeable seals and incubated at 30° C., 250 rpm, and 85% humidity until OD₆₀₀0.6-0.8 was reached. The cell cultures were then induced by IPTG to a final concentration of 1 mM and incubated overnight under the same conditions as originally used. The cells were then pelleted using centrifugation at 4,000 rpm for 10 min. The supernatants were discarded, and the pellets were frozen at −80° C. prior to lysis.

Example 3: Preparation of HTP RT -Containing Cell Lysates

First, 200 μl buffer containing 50 mM Tris-HCl pH 7.5 and 20 mM sodium chloride, were added to the cell paste in each well, produced as described in Example 2. The cells were resuspended by shaking on a bench top shaker. Resuspended cells were transferred to a 96 well Hard shell plate and lysed at 80° C. for 60 min. in a thermocycler. The plate was then centrifuged for 15 min at 4,000 rpm and 4° C. The clear supernatants were used in biocatalytic reactions to determine their activity, RNA sensitivity, and thermostability levels.

Example 4: Improvements over SEQ ID NO: 2 in Reverse Transcriptase Activity

The polypeptide of SEQ ID NO: 2 was selected as the parent enzyme after screening wild type reverse transcriptase enzymes in a RT-qPCR assay using Sars-Cov2 RNA fragment and N1 primers and probe from the CDC EUA assay. Libraries of engineered genes were produced using well established techniques (e.g., saturation mutagenesis, recombination of previously identified beneficial mutations). The polypeptides encoded by each gene were produced in HTP as described in Example 2, and the soluble lysate was generated as described in Example 3. Each variant was screened in a 20 μL reaction that comprised 0.05-1 ng/uL SARS-CoV2 RNA fragment containing the transcript of the nucleocapsid gene, 500 nM N1 primers, 125 nM probe (CDC EUA assay, Catalog #2019-nCoVEUA-01), 0.2 mM dNTPs, RT buffer (10 mM Tris-HCl, 50 mM KCl, 1.5 mM MgCl₂), 0.015 vol % RT HTP lysate, incubated at 62.5C for 30 min. After the incubation at 62.5° C. for 30 min, an engineered thermal DNA polymerase (SEQ ID NO: 567) was added to a final concentration of 20 ng/uL and qPCR cycling performed (95° C. 2 min, 95° C. 3 sec, 55° C. 30 sec for 45 cycles) in a CFX384 Touch Real-Time PCR detection System (BioRad).

Activity relative to SEQ ID NO: 2 (Activity Fold Improvement Over Parent or FIOP) was calculated as the inverse of Ct value (critical threshold) formed by the variant over the inverse of Ct value of SEQ ID NO: 2 and shown in Table 4.1.

TABLE 4.1

Activity of Variants Relative to SEO ID NO: 2

Amino Acid Differences
Activity FIOP 1

SEQ ID NO:
(Relative to
(Relative to

(nt/aa)
SEQ ID NO: 2)
SEQ ID NO: 2)

1/2
Wild type
+

3/4
R114K/I210L/T307K
+

5/6
R114K/A309P
+

7/8
A49G
+

9/10
Q63P/A68S/H216R/E258T/D261N
+

11/12
Q63P/A68S/H216R/D261N
+

13/14
Q63L/T209A/E314K/D665N
+

15/16
I447G/D665N
+

17/18
T331E
+

19/20
V90I/T307K/A349G
+

21/22
R114K/H173A/T331E
+

23/24
A266V
+

1 Levels of increased activity were determined relative to the reference polypeptide of SEQ ID NO: 2, and defined as follows: “+” > than 1-fold but less than 2.0-fold increased activity; “++” > than 2.0-fold but less than 4-fold increased activity; and “+++” > than 4-fold increased activity

Example 5: Improvements Over SEQ ID NO: 24 in RNA Sensitivity

SEQ ID NO: 24 was selected as the parent enzyme for this round of directed evolution. Libraries of engineered genes were produced using well established techniques (e.g., saturation mutagenesis, recombination of previously identified beneficial mutations). The polypeptides encoded by each gene were produced in HTP as described in Example 2, and the soluble lysate was generated as described in Example 3. Each variant was screened in a 20 _jut reaction that comprised 0.03 ng/uL SARS-CoV2 RNA fragment containing the transcript of the nucleocapsid gene, 500 nM N1 primers, 125 nM probe (CDC EUA assay, Catalog #2019-nCoVEUA-01), 0.2 mM dNTPs, RT buffer (10 mM Tris-HCl, 50 mM KCl, 1.5 mM MgCl₂), 0.625 vol % RT HTP lysate, 20 ng/uL engineered thermal DNA Polymerase (SEQ ID NO: 568) and RT-qPCR performed by incubation at 62.5° C. for 30 min followed by qPCR cycling (95° C. 2 min, 95° C. 3 sec, 55° C. 30 sec for 45 cycles) in a CFX384 Touch Real-Time PCR detection System (BioRad).

RNA sensitivity relative to SEQ ID NO:24 (Sensitivity FIOP) was calculated as the inverse of Ct value (critical threshold) formed by the variant over the inverse of Ct value of SEQ ID NO:24 and shown in Table 5.1.

TABLE 5.1

RNA sensitivity of Variants Relative to SEQ ID NO: 24

Amino Acid
Amino Acid
Sensitivity

SEQ ID
Differences
Differences
FIOP ¹

NO:
(Relative to
(Relative to
(Relative to

(nt/aa)
SEQ ID NO: 24)
SEQ ID NO: 2)
SEQ ID NO: 24)

25/26
N454A/H508L
A266V/N454A/H508L
++

27/28
D536E/E574Q
A266V/D536E/E574Q
+

29/30
A309P
A266V/A309P
+

31/32
A49G/H173A/A309P/T331E
A49G/H173A/A266V/A309P/
+

T331E

33/34
V90I/T331E
V90I/A266V/T331E
+

35/36
Q63L/V90I/A309P/E574D/
Q63L/V90I/A266V/A309P/
+

H650G
E574D/H650G

37/38
V90I/H173A/T209A/I210L/
V90I/H173A/T209A/I210L/
+

F321A/E574D/Y598S
A266V/F321A/E574D/Y598S

39/40
H508L/K519P
A266V/H508L/K519P
+

41/42
A49G/Q63L/V90I/H216R/
A49G/Q63L/V90I/H216R/
+

A309P/F321A/D536E/E574D
A266V/A309P/F321A/D536E/

E574D

43/44
A49G/R114K/T307N/A309P/
A49G/R114K/A266V/T307N/
+

D536E
A309P/D536E

45/46
T307K/F321A/D536E/E574D/
A266V/T307K/F321A/D536E/
+

H650G
E574D/H650G

47/48
A309P/T331E/D536E/E574Q/
A266V/A309P/T331E/D536E/
+

Y598S/H650G
E574Q/Y598S/H650G

49/50
H173A/T331E/D536E/E574D/
H173A/A266V/T331E/D536E/
+

Y598S
E574D/Y598S

51/52
A49G/V300I/P403H
A49G/A266V/V300I/P403H
+

53/54
R74K/G242A
R74K/G242A/A266V
+

55/56
G242A/K298E/H508L/Q662R
G242A/A266V/K298E/H508L/
+

Q662R

57/58
S260G/Q509E
S260G/A266V/Q509E
+

59/60
V102C/A370G/Q509E
V102C/A266V/A370G/Q509E
+

61/62
A49G/H173A/H216R/A349G/
A49G/H173A/H216R/A266V/
+

D536E/Y598S
A349G/D536E/Y598S

63/64
A49G/R114K/H216R/T307K/
A49G/R114K/H216R/A266V/
+

A309P/T331E
T307K/A309P/T331E

65/66
A49G/V90I/H173A/H216R/
A49G/V90I/H173A/H216R/
+

T307K
A266V/T307K

67/68
Q63P/A68S/E81K/F167Y/
Q63P/A68S/E81K/F167Y/
+

E314A/I447G/E574Q
A266V/E314A/I447G/E574Q

69/70
A49G/I210L/T307K/A309P/
A49G/I210L/A266V/T307K/
+

F321A/D536E/E574D/H650G
A309P/F321A/D536E/E574D/

H650G

71/72
Q63L/V90I/T307K/F321A/
Q63L/V90I/A266V/T307K/
+

T331E/G537W/Y598S
F321A/T331E/G537W/Y598S

73/74
A370G/M464L/T465S/Q509E/
A266V/A370G/M464L/T465S/
+

D554T/M576I
Q509E/D554T/M576I

75/76
A49G/R114K/H173A/H216R/
A49G/R114K/H173A/H216R/
+

F321A/E574D/Y598S
A266V/F321A/E574D/Y598S

77/78
V90I/H216R/F321A/H650G
V90I/H216R/A266V/F321A/
+

H650G

79/80
E574D/H650G
A266V/E574D/H650G
+

81/82
A49G/T209A/I210L/T307K/
A49G/T209A/I210L/A266V/
+

A309P/D536E/Y598S
T307K/A309P/D536E/Y598S

83/84
H216R/D536E/E574Q
H216R/A266V/D536E/E574Q
+

85/86
A49G/H173A/I210L/A309P/
A49G/H173A/I210L/A266V/
+

F321A/D536E/Y598S
A309P/F321A/D536E/Y598S

87/88
T331E/D536E/Y598S
A266V/T331E/D536E/Y598S
+

89/90
F321A/E574D
A266V/F321A/E574D
+

91/92
H173A/F321A/T331E/A349G/
H173A/A266V/F321A/T331E/
+

E574D
A349G/E574D

93/94
A49G/T307K/D536E
A49G/A266V/T307K/D536E
+

95/96
H216R/A309P/E574D/H650G
H216R/A266V/A309P/E574D/
+

H650G

97/98
I94L/A370G/S474A/M576I
I94L/A266V/A370G/S474A/
+

M576I

99/100
V90I/T209A/I210L/A309P/
V90I/T209A/I210L/A266V/
+

F321A/E574D
A309P/F321A/E574D

101/102
A49G/Q63L/V90I/H173A
A49G/Q63L/V90I/H173A/
+

A266V

103/104
K298E
A266V/K298E
+

105/106
A49G/V300I/N454A/Q662R
A49G/A266V/V300I/N454A/
+

Q662R

107/108
A68S/E81K/F167Y/K298R/
A68S/E81K/F167Y/A266V/
+

D536N
K298R/D536N

109/110
A49G/N454A
A49G/A266V/N454A
+

111/112
E81K
E81K/A266V
+

113/114
A49G/R114K/H173A/A309P/
A49G/R114K/H173A/A266V/
+

A349G/D536E/E574D/H650G
A309P/A349G/D536E/E574D/

H650G

115/116
F167Y/D261N/I303Q/D536N
F167Y/D261N/A266V/I303Q/
+

D536N

117/118
D18E/V102C/D554T
D18E/V102C/A266V/D554T
+

119/120
R171L/H173A/T307K/T331E/
R171L/H173A/A266V/T307K/
+

D536E
T331E/D536E

121/122
H173A/H216R/D536E
H173A/H216R/A266V/D536E
+

123/124
D18E/A370G/M464L/Q509E
D18E/A266V/A370G/M464L/
+

Q509E

125/126
A49G/R114K
A49G/R114K/A266V
+

127/128
V90I/H216R/A309P/D536G/
V90I/H216R/A266V/A309P/
+

E574D
D536G/E574D

129/130
I444L
A266V/I444L
+

131/132
V90I/F321A/A349G/D536G/
V90I/A266V/F321A/A349G/
+

Y598S/H650G
D536G/Y598S/H650G

133/134
A49G/L163P/A309P/F321A/
A49G/L163P/A266V/A309P/
+

D536E/E574D/H650G
F321A/D536E/E574D/H650G

135/136
A49G/Q63L/V90I/H173A/
A49G/Q63L/V90I/H173A/A266V/
+

T307K/T331E/D536E/Y598S/
T307K/T331E/D536E/Y598S/

H650G
H650G

137/138
A68S/E81K/F167Y/E258T/
A68S/E81K/F167Y/E258T/
+

I447G/N466K/D536N
A266V/I447G/N466K/D536N

139/140
V90I/T331E/E574D
V90I/A266V/T331E/E574D
+

141/142
A49G/F321A
A49G/A266V/F321A
+

143/144
I94L/Q509E
I94L/A266V/Q509E
+

145/146
V90I/H173A/F321A/D536E
V90I/H173A/A266V/F321A/
+

D536E

147/148
F167Y/K298R/I447G/N466K
F167Y/A266V/K298R/I447G/
+

N466K

149/150
H173A/H216R/T307K/A309P/
H173A/H216R/A266V/T307K/
+

D536E
A309P/D536E

151/152
H216R/F321A
H216R/A266V/F321A
+

153/154
A49G/V90I/H173A/T209A/
A49G/V90I/H173A/T209A/
+

A309P/T331E
A266V/A309P/T331E

155/156
D261N/K298R/I303Q/I447R/
D261N/A266V/K298R/I303Q/
+

E574Q
I447R/E574Q

157/158
R171P/K298E/I444L/K519P
R171P/A266V/K298E/I444L/
+

K519P

159/160
V90I/D536E/E574D/Y598S/
V90I/A266V/D536E/E574D/
+

H650G
Y598S/H650G

161/162
A49G/Q63L/V90I/I210L/
A49G/Q63L/V90I/I210L/A266V/
+

T307K/F321A/Y598S/H650G
T307K/F321A/Y598S/H650G

163/164
V90I/H216R/T307K/D536E/
V90I/H216R/A266V/T307K/
+

E574D
D536E/E574D

165/166
D18E/I94L/V102C/S260G/
D18E/I94L/V102C/S260G/
+

A370G/M464L/D554T
A266V/A370G/M464L/D554T

167/168
D18E/K423R/T465S/S474A
D18E/A266V/K423R/T465S/
+

S474A

169/170
F167Y/D261N/I447G/D536G
F167Y/D261N/A266V/I447G/
+

D536G

171/172
R114K/H173A/T209A/I210L
R114K/H173A/T209A/I210L/
+

A266V

173/174
T307K/A309P/D536E/E574D/
A266V/T307K/A309P/D536E/
+

Y598S
E574D/Y598S

175/176
V102C/S260G/A370G/M576I
V102C/S260G/A266V/A370G/
+

M576I

177/178
E574D
A266V/E574D
+

179/180
H173A/T209A/I210L/T307K/
H173A/T209A/I210L/A266V/
+

D536E
T307K/D536E

181/182
H216R/A309P/D536E
H216R/A266V/A309P/D536E
+

183/184
A349G
A266V/A349G
+

185/186
I447L/D536A/H606Q
A266V/I447L/D536A/H606Q
+

187/188
K310R/N454A/E479D/K519P/
A266V/K310R/N454A/E479D/
+

Q662R
K519P/Q662R

189/190
A49G/V90I/T209A/Y598S
A49G/V90I/T209A/A266V/
+

Y598S

191/192
E314K/D536N
A266V/E314K/D536N
+

193/194
R171P/V300I/N454A/E479D/
R171P/A266V/V300I/N454A/
+

H508L/Q662R
E479D/H508L/Q662R

195/196
R171P/G242A/V300I/H508L/
R171P/G242A/A266V/V300I/
+

Q662R
H508L/Q662R

197/198
A49G/T331E/D536E
A49G/A266V/T331E/D536E
+

199/200
H173A/H216R/A309P/D536E/
H173A/H216R/A266V/A309P/
+

E574D/Y598S
D536E/E574D/Y598S

201/202
D536E/Y598S
A266V/D536E/Y598S
+

203/204
F167Y/D261N/K298R/I303Q/
F167Y/D261N/A266V/K298R/
+

I447R/N466K/E574Q
I303Q/I447R/N466K/E574Q

205/206
H173A/D536E/Y598S
H173A/A266V/D536E/Y598S
+

207/208
A49G/R114K/A309P/D536E/
A49G/R114K/A266V/A309P/
+

E574D/Y598S
D536E/E574D/Y598S

209/210
A49G/R114K/A309P/A349G/
A49G/R114K/A266V/A309P/
+

D536E
A349G/D536E

211/212
Q63P/A68S/E81K/I303Q/
Q63P/A68S/E81K/A266V/
+

N466K
I303Q/N466K

213/214
Q63L/V90I/T209A/H216R/
Q63L/V90I/T209A/H216R/
+

T307K/A309P/F321A/A349G/
A266V/T307K/A309P/F321A/

D536E/E574D/Y598S/H650G
A349G/D536E/E574D/Y598S/

H650G

215/216
H216R
H216R/A266V
+

217/218
H173A/I210L/T307K/Y598S/
H173A/I210L/A266V/T307K/
+

H650G
Y598S/H650G

219/220
S25E/V102C/A370G/K423R
S25E/V102C/A266V/A370G/
+

K423R

221/222
A68S/D261N/K298R/I303Q
A68S/D261N/A266V/K298R/
+

I303Q

223/224
K423R/S474A
A266V/K423R/S474A
+

225/226
I94L/K423R/S474A/D554T/
I94L/A266V/K423R/S474A/
+

M576I
D554T/M576I

227/228
Q63P/K298R/I447R/E574Q
Q63P/A266V/K298R/I447R/
+

E574Q

229/230
A49G/Q63L/V90I/H173A/
A49G/Q63L/V90I/H173A/
+

T307K/F321A/T331E/E574D/
A266V/T307K/F321A/T331E/

D595N/H650G
E574D/D595N/H650G

231/232
A49G/V90I/D536E/E574D
A49G/V90I/A266V/D536E/
+

E574D

233/234
H508L
A266V/H508L
+

235/236
Q63P/E81K/F167Y/E258T/
Q63P/E81K/F167Y/E258T/
+

D261N/K298R/I303Q/I447G
A266V/D261N/K298R/I303Q/

I447G

237/238
R114K/T331E
R114K/A266V/T331E
+

239/240
D212N/K298E/R583K/H606K
D212N/A266V/K298E/R583K/
+

H606K

241/242
A49G/H173A/D536E/E574Q
A49G/H173A/A266V/D536E/
+

E574Q

243/244
A49G/G242A/K298E/V3W
A49G/G242A/A266V/K298E/
+

K310R/I444L/N454A/E479D
V300I/K310R/I444L/N454A/

E479D

245/246
A49G/A309P/F321A/D536E/
A49G/A266V/A309P/F321A/
+

Y598S
D536E/Y598S

247/248
Q63P/A68S/D261N/D536G
Q63P/A68S/D261N/A266V/
+

D536G

249/250
V300I/I444L/H508L
A266V/V300I/I444L/H508L
+

251/252
K298R
A266V/K298R
+

¹Levels of increased activity were determined relative to the reference polypeptide of SEQ ID NO: 24, and defined as follows: “+” > than 1-fold but less than 2.0-fold increased activity; “++” > than 2.0-fold but less than 4-fold increased activity; and “+++” > than 4-fold increased activity.

Example 6: Improvements Over SEQ ID NO: 94 in RNA Sensitivity and Reverse Transcriptase Activity

SEQ ID NO: 94 was selected as the parent enzyme for this round of directed evolution. Libraries of engineered genes were produced using well established techniques (e.g., saturation mutagenesis, recombination of previously identified beneficial mutations). The polypeptides encoded by each gene were produced in HTP as described in Example 2, and the soluble lysate was generated as described in Example 3. Each variant was screened in a 20 μL reaction that comprised 0.00078 ng/uL SARS-CoV2 RNA fragment containing the transcript of the nucleocapsid gene, 500 nM N1 primers, 125 nM probe (CDC EUA assay, Catalog #2019-nCoVEUA-01), 0.2 mM dNTPs, RT buffer (10 mM Tris-HCl, 50 mM KCl, 1.5 mM MgCl₂), 2.5 vol % RT HTP lysate, 20 ng/uL engineered thermal DNA Polymerase (SEQ ID NO: 569) and RT-qPCR performed by incubation at 62.5° C. for 30 min followed by qPCR cycling (95° C. 2 min, 95° C. 3 sec, 55° C. 30 sec for 45 cycles) in a CFX384 Touch Real-Time PCR detection System (BioRad).

RNA sensitivity relative to SEQ ID NO: 94 (Sensitivity FIOP) was calculated as the inverse of Ct value (critical threshold) formed by the variant over the inverse of Ct value of SEQ ID NO: 94 and shown in Table 6.1.

Variants with improved RNA sensitivity were re-screened at the following conditions: each variant was screened in a 20 _jut reaction that comprised 0.25 ng/uL SARS-CoV2 RNA fragment containing the transcript of the nucleocapsid gene, 500 nM N1 primers, 125 nM probe (CDC EUA assay, Catalog #2019-nCoVEUA-01), 0.2 mM dNTPs, RT buffer (10 mM Tris-HCl, 50 mM KCl, 1.5 mM MgCl₂), 0.004 vol % RT HTP lysate, incubated at 62.5° C. for 30 min. After the incubation at 62.5° C. for 30 min, engineered thermal DNA polymerase (SEQ ID NO: 569) was added to a final concentration of 20 ng/uL and qPCR cycling performed (95° C. 2 min, 95° C. 3 sec, 55° C. 30 sec for 45 cycles) in a CFX384 Touch Real-Time PCR detection System (BioRad).

Activity relative to SEQ ID NO: 94 (Activity Fold Improvement Over Parent or FIOP) was calculated as the inverse of Ct value (critical threshold) formed by the variant over the inverse of Ct value of SEQ ID NO: 94 and shown in Table 6.1.

TABLE 6.1

Activity and Stability of Variants Relative to SEQ ID NO: 94

Amino Acid
Amino Acid
RNA sensitivity
Activity

SEQ ID
Differences
Differences
FIOP ¹
FIOP ²

NO:
(Relative to
(Relative to
(Relative to
(Relative to

(nt/aa)
SEQ ID NO: 94)
SEQ ID NO: 2)
SEQ ID NO: 94)
SEQ ID NO: 94)

253/254
V134P
A49G/V134P/A266V/T307K/
+
+

D536E

255/256
R74P
A49G/R74P/A266V/T307K/
+
+

D536E

257/258
Q83A
A49G/Q83A/A266V/T307K/
+
+

D536E

259/260
A319G
A49G/A266V/T307K/A319G/
+
+

D536E

261/262
R92T
A49G/R92T/A266V/T307K/
+
+

D536E

263/264
F329S
A49G/A266V/T307K/F329S/
+
+

D536E

265/266
K343A
A49G/A266V/T307K/K343A/
+
+

D536E

267/268
Q311P
A49G/A266V/T307K/Q311P/
+
+

D536E

269/270
P338V
A49G/A266V/T307K/P338V/
+
+

D536E

271/272
T196C
A49G/T196C/A266V/T307K/
+
+

D536E

273/274
T69R
A49G/T69R/A266V/T307K/
+
+

D536E

275/276
S72M
A49G/S72M/A266V/T307K/
+
+

D536E

277/278
E294Q
A49G/A266V/E294Q/T307K/
+
+

D536E

279/280
Q83W
A49G/Q83W/A266V/E294Q/
+
+

T307K/D536E

281/282
V134F
A49G/V134F/A266V/T307K/
+
+

D536E

283/284
V130S
A49G/V130S/A266V/T307K/
+
+

D536E

285/286
A305P
A49G/A266V/A305P/T307K/
+
+

D536E

287/288
A319S
A49G/A266V/T307K/A319S/
+
+

D536E

289/290
V113T
A49G/V113T/A266V/T307K/
+
+

D536E

291/292
K297W
A49G/A266V/K297W/T307K/
+
+

D536E

293/294
A319C
A49G/A266V/T307K/A319C/
+
+

D536E

295/296
R114G
A49G/R114G/A266V/T307K/
+
+

D536E

297/298
T308G
A49G/A266V/T307K/T308G/
+
+

D536E

299/300
A309E
A49G/A266V/T307K/A309E/
+
+

D536E

301/302
E342W
A49G/A266V/T307K/E342W/
+
+

D536E

303/304
K205M
A49G/K205M/A266V/T307K/
+
+

D536E

305/306
D212K
A49G/D212K/A266V/T307K/
+
+

D536E

307/308
R199L
A49G/R199L/A266V/T307K/
+
+

D536E

309/310
Q83C
A49G/Q83C/A266V/T307K/
+
+

D536E

311/312
I303G
A49G/A266V/I303G/T307K/
+
+

D536E

313/314
A309T
A49G/A266V/T307K/A309T/
+
+

D536E

315/316
L78V
A49G/L78V/A266V/T307K/
+
+

D536E

317/318
V113G
A49G/V113G/A266V/T307K/
+
+

D536E

319/320
K132F
A49G/K132F/A266V/T307K/
+
+

D536E

321/322
Q311I
A49G/A266V/T307K/Q311I/
+
+

D536E

323/324
N119Y
A49G/N119Y/A266V/T307K/
+
+

D536E

325/326
Q83E
A49G/Q83E/A266V/T307K/
+
+

D536E

327/328
I98S
A49G/I98S/A266V/T307K/
+
+

D536E

329/330
E314M
A49G/A266V/T307K/E314M/
+
+

D536E

331/332
E129L
A49G/E129L/A266V/T307K/
+
+

D536E

333/334
K343V
A49G/A266V/T307K/K343V/
+
+

D536E

335/336
T196H
A49G/T196H/A266V/T307K/
+
+

D536E

337/338
R74M
A49G/R74M/A266V/T307K/
+
+

D536E

339/340
F356P
A49G/A266V/T307K/F356P/
+
+

D536E

341/342
H89A
A49G/H89A/A266V/T307K/
+
+

D536E

343/344
D212V
A49G/D212V/A266V/T307K/
+
+

D536E

345/346
I444L/H508L/Q509E/
A49G/A266V/T307K/I444L/
+
+

E574D
H508L/Q509E/D536E/E574D

347/348
Q63L/S260G/K298R/
A49G/Q63L/S260G/A266V/
+
+

V300I/T331E/
K298R/V300I/T307K/T331E/

I444L/Q509E
I444L/Q509E/D536E

349/350
Q63L/V90I/T209A/
A49G/Q63L/V90I/T209A/
+
+

I444L/H508L/
A266V/T307K/I444L/H508L/

E574Q
D536E/E574Q

351/352
K298R/I444L/Q509E
A49G/A266V/K298R/T307K/
+
+

I444L/Q509E/D536E

353/354
Q63L/V90I/H508L/
A49G/Q63L/V90I/A266V/T307K/
+
+

Q509E/E574Q/
H508L/Q509E/D536E/

D595N
E574Q/D595N

355/356
Q83R
A49G/Q83R/A266V/T307K/
+
+

D536E

357/358
Q311A
A49G/A266V/T307K/Q311A/
+
+

D536E

359/360
H89M
A49G/H89M/A266V/T307K/
+
+

D536E

361/362
V130R
A49G/V130R/A266V/T307K/
+
+

D536E

363/364
P178L
A49G/P178L/A266V/T307K/
+
+

D536E

365/366
T118R
A49G/T118R/A266V/T307K/
+
+

D536E

¹Levels of increased RNA sensitivity were determined relative to the reference polypeptide of SEQ ID NO: 94, and defined as follows: “+” > than 1-fold but less than 1.75-fold increased activity; “++” > than 1.75-fold

²Levels of increased activity were determined relative to the reference polypeptide of SEQ ID NO: 94, and defined as follows: “+” > than 1-fold but less than 1.75-fold increased activity; “++” > than 1.75-fold

Example 7: Improvements over SEQ ID NO: 352 in Reverse Transcriptase Processivity

SEQ ID NO: 352 was selected as the parent enzyme for this round of directed evolution. Libraries of engineered genes were produced using well established techniques (e.g., saturation mutagenesis, recombination of previously identified beneficial mutations). The polypeptides encoded by each gene were produced in HTP as described in Example 2, and the soluble lysate was generated as described in Example 3. Each variant was screened in a 20 μL reaction that comprised 0.00078 ng/uL SARS-CoV2.

RNA fragment containing the transcript of the nucleocapsid gene, 500 nM N1 primers, 125 nM probe (CDC EUA assay, Catalog #2019-nCoVEUA-01), 0.2 mM dNTPs, RT buffer (10 mM Tris-HCl, 50 mM KCl, 1.5 mM MgCl₂), 2.5 vol % RT HTP lysate, 20 ng/uL engineered DNA polymerase (SEQ ID NO: 569) and RT-qPCR performed by incubation at 62.5° C. for 5 min followed by qPCR cycling (95° C. 2 min, 95° C. 3 sec, 55° C. 30 sec for 45 cycles) in a CFX384 Touch Real-Time PCR detection System (BioRad).

RNA sensitivity relative to SEQ ID NO: 352 (Processivity FIOP) was calculated as the inverse of Ct value (critical threshold) formed by the variant over the inverse of Ct value of SEQ ID NO:352 and shown in Table 7.1.

TABLE 7.1

Processivity of Variants Relative to SEQ ID NO: 352

Amino Acid
Amino Acid
Processivity

SEQ ID
Differences
Differences
FIOP ¹

NO:
(Relative to
(Relative to
(Relative to

(nt/aa)
SEQ ID NO: 352)
SEQ ID NO: 2)
SEQ ID NO: 352)

367/368
A309E/E342W
A49G/A266V/K298R/T307K/A309E/E342W/
+

I444L/Q509E/D536E

369/370
A309T
A49G/A266V/K298R/T307K/A309T/I444L/
+

Q509E/D536E

371/372
E129L/R298K
A49G/E129L/A266V/T307K/I444L/Q509E/
+

D536E

373/374
E509Q/E574Q
A49G/A266V/K298R/T307K/I444L/D536E/
+

E574Q

375/376
G85R
A49G/G85R/A266V/K298R/T307K/I444L/
+

Q509E/D536E

377/378
I98S/N119Y/E129L/
A49G/I98S/N119Y/E129L/K132F/T196H/
+

K132F/T196H/R298K
A266V/T307K/I444L/Q509E/D536E

379/380
I98S/R298K/G317C/
A49G/I98S/A266V/T307K/G317C/K343V/
+

K343V/F356P
F356P/I444L/Q509E/D536E

381/382
K205M/D212K/R298K/
A49G/K205M/D212K/A266V/T307K/A309E/
+

A309E/A319S/E342W/E509Q
A319S/E342W/I444L/D536E

383/384
L444I
A49G/A266V/K298R/T307K/Q509E/D536E
+

385/386
L78V/K132F/E314M
A49G/L78V/K132F/A266V/K298R/T307K/
+

E314M/I444L/Q509E/D536E

387/388
L78V/Q83E/I98S
A49G/L78V/Q83E/I98S/A266V/K298R/T307K/
+

I444L/Q509E/D536E

389/390
L78V/Q83E/N119Y/
A49G/L78V/Q83E/N119Y/K132F/T196H/
+

K132F/T196H/L444I
A266V/K298R/T307K/Q509E/D536E

391/392
L78V/Q83E/R298K
A49G/L78V/Q83E/A266V/T307K/I444L/
+

Q509E/D536E

393/394
L78V/Q83E/R298K/E509Q
A49G/L78V/Q83E/A266V/T307K/I444L/
+

D536E

395/396
L78V/Q83E/R298K/F356P
A49G/L78V/Q83E/A266V/T307K/F356P/
+

I444L/Q509E/D536E

397/398
L78V/R298K/L444I
A49G/L78V/A266V/T307K/Q509E/D536E
+

399/400
N119Y/E129L/K132F
A49G/N119Y/E129L/K132F/A266V/K298R/
+

T307K/I444L/Q509E/D536E

401/402
P178L/R298K/I303G/
A49G/P178L/A266V/I303G/T307K/T331E/
+

T331E/P338V/H508L
P338V/I444L/H508L/Q509E/D536E

403/404
Q311I/E314M
A49G/A266V/K298R/T307K/Q311I/E314M/
+

I444L/Q509E/D536E

405/406
Q63L/K297W/I303G/
A49G/Q63L/A266V/K297W/K298R/I303G/
+

A305P/L444I
A305P/T307K/Q509E/D536E

407/408
Q63L/P178L/T209A/
A49G/Q63L/P178L/T209A/S260G/A266V/
+

S260G/E574Q
K298R/T307K/I444L/Q509E/D536E/E574Q

409/410
Q63L/V300I/P338V
A49G/Q63L/A266V/K298R/V300I/T307K/
+

P338V/I444L/Q509E/D536E

411/412
Q83A/E294Q
A49G/Q83A/A266V/E294Q/K298R/T307K/
+

I444L/Q509E/D536E

413/414
Q83A/R92T/R298K/
A49G/Q83A/R92T/A266V/T307K/K343A/
+

K343A/E574Q
I444L/Q509E/D536E/E574Q

415/416
Q83A/R92T/V134P/
A49G/Q83A/R92T/V134P/A266V/K298R/
+

L444I/E574Q
T307K/Q509E/D536E/E574Q

417/418
Q83A/T196C/F329S/
A49G/Q83A/T196C/A266V/K298R/T307K/
+

K343A
F329S/K343A/I444L/Q509E/D536E

419/420
Q83A/T196C/R298K/
A49G/Q83A/T196C/A266V/T307K/I444L/
+

E509Q
D536E

421/422
Q83A/V134F/T196C/
A49G/Q83A/V134F/T196C/E294Q/A266V/
+

E294Q/R298K/A305S/
A305S/T307K/Q311P/A319G/F329S/K343A/

Q311P/A319G/
Q509E/D536E/E574Q

F329S/K343A/L444I/

E574Q

423/424
Q83C
A49G/Q83C/A266V/K298R/T307K/I444L/
+

Q509E/D536E

425/426
Q83C/A309T
A49G/Q83C/A266V/K298R/T307K/A309T/
+

I444L/Q509E/D536E

427/428
Q83C/A319S/E342W/
A49G/Q83C/A266V/K298R/T307K/A319S/
+

E509Q
E342W/I444L/D536E

429/430
Q83C/K205M/L444I
A49G/Q83C/K205M/A266V/K298R/T307K/
+

Q509E/D536E

431/432
Q83C/L444I
A49G/Q83C/A266V/K298R/T307K/Q509E/
+

D536E

433/434
Q83C/R114G
A49G/Q83C/R114G/A266V/K298R/T307K/
+

I444L/Q509E/D536E

435/436
Q83C/R114G/A309T/
A49G/Q83C/R114G/A266V/K298R/T307K/
+

E509Q
A309T/I444L/D536E

437/438
Q83C/R114G/R298K/
A49G/Q83C/R114G/A266V/T307K/A319C/
+

A319C
I444L/Q509E/D536E

439/440
Q83C/R199L/D212K/
A49G/Q83C/R199L/D212K/A266V/T307K/
+

R298K/A309E/
A309E/A319C/Q509E/D536E/P639H

A319C/L444I/P639H

441/442
Q83C/R199L/E509Q
A49G/Q83C/R199L/A266V/K298R/T307K/
+

I444L/D536E

443/444
Q83C/R298K
A49G/Q83C/A266V/T307K/I444L/Q509E/
+

D536E

445/446
Q83C/R298K/E342w
A49G/Q83C/A266V/T307K/E342W/I444L/
+

Q509E/D536E

447/448
Q83C/T308G/A309E/
A49G/Q83C/A266V/K298R/T307K/T308G/
+

D595N/L638H
A309E/I444L/Q509E/D536E/D595N/L638H

449/450
Q83C/V113T/R114G/
A49G/Q83C/V113T/R114G/K205M/D212K/
+

K205M/D212K
A266V/K298R/T307K/I444L/Q509E/D536E

451/452
Q83C/V130S/R298K/
A49G/Q83C/V130S/A266V/T307K/Q509E/
+

L444I
D536E

453/454
R114G/A309E
A49G/R114G/A266V/K298R/T307K/A309E/
+

I444L/Q509E/D536E

455/456
R114G/A309E/E509Q
A49G/R114G/A266V/K298R/T307K/A309E/
+

I444L/D536E

457/458
R114G/D212K/A309E/
A49G/R114G/D212K/A266V/K298R/T307K/
+

E342W/P639H
A309E/E342W/I444L/Q509E/D536E/

P639H

459/460
R114G/K205M/L444I
A49G/R114G/K205M/A266V/K298R/T307K/
+

Q509E/D536E

461/462
R114G/R298K
A49G/R114G/A266V/T307K/I444L/Q509E/
+

D536E

463/464
R114G/V130S/A319S/
A49G/R114G/V130S/A266V/K298R/T307K/
+

L444I
A319S/Q509E/D536E

465/466
R114G/V130S/D212K/
A49G/R114G/V130S/D212K/A266V/T307K/
+

R298K/E342W
E342W/I444L/Q509E/D536E

467/468
R114G/V130S/R298K/
A49G/R114G/V130S/A266V/T307K/A309E/
+

A309E
I444L/Q509E/D536E

469/470
R199L/A309T
A49G/R199L/A266V/K298R/T307K/A309T/
+

I444L/Q509E/D536E

471/472
R199L/K205M/
A49G/R199L/K205M/A266V/K298R/T307K/
+

L444I
Q509E/D536E

473/474
R298K
A49G/A266V/T307K/I444L/Q509E/D536E
+

475/476
R298K/E342W
A49G/A266V/T307K/E342W/I444L/Q509E/
+

D536E

477/478
R298K/E509Q
A49G/A266V/T307K/I444L/D536E
+

479/480
R298K/K343A/L444I/
A49G/A266V/T307K/K343A/Q509E/D536E/
+

D595N
D595N

481/482
R74M
A49G/R74M/A266V/K298R/T307K/I444L/
+

Q509E/D536E

483/484
R74M/E129L/R298K/
A49G/R74M/E129L/A266V/T307K/Q509E/
+

L444I
D536E

485/486
R74M/Q83E/E129L/
A49G/R74M/Q83E/E129L/K132F/D212V/
+

K132F/D212V/
A266V/K298R/T307K/I444L/D536E

E509Q

487/488
R74P/Q83A/R92T/
A49G/R74P/Q83A/R92T/A266WT307K/
+

R298K/K343A/
K343A/I444L/D536E

E509Q

489/490
R74P/Q83A/V134P/
A49G/R74P/Q83A/V134P/A266V/E294Q/
+

E294Q/R298K/
T307K/I444L/Q509E/D536E/E574Q

E574Q

491/492
R74P/Q83W/L444I/
A49G/R74P/Q83W/A266V/K298R/T307K/
+

E509Q
D536E

493/494
R74P/R298K/F329S/
A49G/R74P/A266V/T307K/F329S/Q509E/
+

L444I/E574Q
D536E/E574Q

495/496
R74P/R92T/T196C/
A49G/R74P/R92T/T196C/A266V/E294Q/
+

E294Q/F329S
K298R/T307K/F329S/I444L/Q509E/

D536E

497/498
R92T/R298K/E509Q
A49G/R92T/A266V/T307K/I444L/D536E
+

499/500
S72M
A49G/S72M/A266V/K298R/T307K/I444L/
+

Q509E/D536E

501/502
S72M/E294Q/Q311A/
A49G/S72M/A266V/E294Q/K298R/T307K/
+

F329S/K343A/
Q311A/F329S/K343A/Q509E/D536E

L444I

503/504
S72M/E294Q/R298K/
A49G/S72M/A266V/E294Q/T307K/Q509E/
+

L444I
D536E

505/506
S72M/E294Q/R298K/
A49G/S72M/A266V/E294Q/T307K/Q311A/
+

Q311A/F329S/
F329S/Q509E/D536E

L444I

507/508
S72M/E509Q
A49G/S72M/A266V/K298R/T307K/I444L/
+

D536E

509/510
S72M/Q83A/R298K/
A49G/S72M/Q83A/A266V7T307K/K343A/
+

K343A/L444I
Q509E/D536E

511/512
S72M/R74P/E294Q/
A49G/A266V/S72M/R74P/E294Q/T307K/
+

R298K/L444I
Q509E/D536E

513/514
S72M/R74P/Q83A/
A49G/S72M/R74P/Q83A/A266V/K298R/
+

A319G/F329S/
T307K/A319G/F329S/I444L/D536E

E509Q

515/516
S72M/R74P/Q83A/
A49G/S72M/R74P/Q83A/E84N/A266V/
+

E84N/L444I
K298R/T307K/Q509E/D536E

517/518
S72M/R74P/Q83A/
A49G/S72M/R74P/Q83A/V134F/T196C/
+

V134F/T196C/E294Q/
A266V/E294Q/T307K/I444L/Q509E/D536E

R298K

519/520
S72M/R74P/R298K/
A49G/S72M/R74P/A266V/T307K/I444L/
+

E509Q
D536E

521/522
S72M/R74P/R92T/
A49G/S72M/R74P/R92T/A266V/E294Q/
+

E294Q/R298K/F329S
T307K/F329S/I444L/Q509E/D536E

523/524
S72M/R74P/R92T/
A49G/S72M/R74P/R92T/A266V/T307K/
+

R298K
I444L/Q509E/D536E

525/526
S72M/R74P/R92T/
A49G/S72M/R74P/R92T/V134P/A266V/
+

V134P/R298K/K343A/
T307K/K343A/Q509E/D536E

L444I

527/528
S72M/R74P/V134F/
A49G/S72M/R74P/V134F/T196C/A266V/
+

T196C/R298K/A319G/
T307K/A319G/F329S/I444L/D536E

F329S/E509Q

529/530
S72M/T196C/Q311A/
A49G/S72M/T196C/A266V/K298R/T307K/
+

F329S/E574Q
Q311A/F329S/I444L/Q509E/D536E/E574Q

531/532
S72M/V134P/T196C/
A49G/S72M/V134P/T196C/A266V/T307K/
+

R298K
I444I/Q509E/D536E

533/534
T118R/P178L/P338V/
A49G/T118R/P178L/A266V/K298R/T307K/
+

L444I
P338V/I444L/Q509E/D536E

535/536
T69R/H89A/P178L/
A49G/T69R/H89A/P178L/A266V/K298R/
+

I303G/A305P/P338V/
I303G/A305P/T307K/P338V/I444L/Q509E/

L444I/E574Q
D536E/E574Q

537/538
V113G
A49G/V113G/A266V/K298R/T307K/I444L/
+

Q509E/D536E

539/540
V113G/P178L/
A49G/V113G/P178L/S260G/A266V/K298R/
+

S260G
T307K/I444L/Q509E/D536E

541/542
V113T/A309E
A49G/V113T/A266V/K298R/T307K/A309E/
+

I444L/Q509E/D536E

543/544
V113T/D212K/A309E
A49G/V113T/D212K/A266V/K298R/T307K/
+

A309E/I444L/Q509E/D536E

545/546
V113T/E342W
A49G/V113T/A266V/K298R/T307K/E342W/
+

I444L/Q509E/D536E

547/548
V113T/R114G
A49G/V113T/R114G/A266V/K298R/T307K/
+

I444L/Q509E/D536E

549/550
V113T/R114G/
A49G/V113T/R114G/D212K/A266V/K298R/
+

D212K
T307K/I444L/Q509E/D536E

551/552
V113T/R114G/K205M/
A49G/V113T/R114G/K205M/A266V/K298R/
+

A319C/E342W
T307K/A319C/E342W/I444L/Q509E/D536E

553/554
V113T/R114G/R298K/
A49G/V113T/R114G/A266WT307K/E342W/
+

E342W
I444L/Q509E/D536E

555/556
V113T/R114G/V130S
A49G/V113T/R114G/V130S/A266V/K298R/
+

T307K/I444L/Q509E/D536E

557/558
V113T/R298K
A49G/V113T/A266V/T307K/I444L/Q509E/
+

D536E

559/560
V113T/R298K/A309E/
A49G/V113T/A266V/K298R/T307K/A309E/
+

L444I
Q509E/D536E

561/562
V130S/K205M/A333V/
A49G/V130S/K205M/A266V/K298R/T307K/
+

L444I
A333V/Q509E/D536E

563/564
V134P
A49G/V134P/A266V/K298R/T307K/I444L/
+

Q509E/D536E

565/566
V134P/E294Q/L444I/
A49G/V134P/A266V/E294Q/K298R/T307K/
+

E509Q
D536E

¹Levels of increased activity were determined relative to the reference polypeptide of SEQ ID NO: 352 and defined as follows: “+” > than 1-fold but less than 2.0-fold increased activity; “++” > than 2.0-fold but less than 4-fold increased activity; “+++” > than 4-fold increased activity

While the invention has been described with reference to the specific embodiments, various changes can be made and equivalents can be substituted to adapt to a particular situation, material, composition of matter, process, process step or steps, thereby achieving benefits of the invention without departing from the scope of what is claimed.

For all purposes, each and every publication and patent document cited in this disclosure is incorporated herein by reference as if each such publication or document was specifically and individually indicated to be incorporated herein by reference. Citation of publications and patent documents is not intended as an indication that any such document is pertinent prior art, nor does it constitute an admission as to its contents or date.

RECOMBINANT REVERSE TRANSCRIPTASE VARIANTS

Information

Publication Number

Date Filed

Date Published

Inventors

Original Assignees

CPC

International Classifications

Abstract

Description

Claims

CROSS-REFERENCE TO RELATED APPLICATIONS

Provisional Applications (1)