Patent Application
20100261878
None.
This application contains a sequence listing. The nucleotide and amino acid sequences listed in Appendix A, Appendix B and Appendix C are incorporated herein by reference in their entireties.
Histone deacetylase (HDAC) inhibitors are a diverse group of molecules that can induce growth arrest, differentiation, apoptosis and autophagocytic cell death of cancer cells. Hence, HDAC inhibitors are prime agents for the development of novel anticancer drugs. One HDAC inhibitor, Zolinza (vorinostat or suberoylanilide hydroxamic acid—SAHA), was recently approved by the U.S. Food and Drug Administration, and at least nine other HDAC inhibitors, including FK228, are in various stages of clinical trials.
FK228 (C24H36N4O6S2; molecular weight, 540.2) (
Structurally, FK228 is a bicyclic depsipeptide that features a 16-membered macrolactone ring containing an ester linkage and a 17-membered ring containing the same ester linkage and a disulfide bond (
Despite its promise as an anticancer agent, efforts to obtain large quantities of FK228 have been hampered because native production of FK228 from Chromobacterium violaceum No. 968 is relatively limited, and total synthesis of FK228 has proven difficult (Li, Wu et al. 1996). Due to its anticancer activities and novel structural characteristics, FK228 may serve as a molecular scaffold to generate structural analogs, from which additional compounds with therapeutic properties may be developed.
Thus, there is a need in the art for compositions and methods for synthesizing FK228 and FK228 analogs.
In one aspect, isolated polynucleotides are disclosed. The isolated polynucleotides comprise a coding sequence encoding a polypeptide having at least 80% amino acid identity to a protein encoded by depA, depB, depC, depD, depE, depF, depG, depH, depI, depJ, depK, depL, depM, or depN. Other isolated polynucleotides comprise a coding sequence encoding a polypeptide having at least 80% amino acid identity to a protein encoded by tdpA, tdpB, tdpC1, tdpC2, tdpDE1, tdpE2, tdpF, tdpG, tdpH, tdpI, tdpJ, tdpL, or tdpN. The isolated polynucleotides may be operably connected to a promoter.
In another aspect, polypeptides are disclosed, which have at least 80% amino acid identity to DepA, DepB, DepC, DepD, DepE, DepF, DepG, DepH, DepI, DepJ, DepK, DepL, DepM, or DepN. Other polypeptides disclosed have at least 80% amino acid identity to TdpA, TdpB, TdpC1, TdpC2, TdpDE1, TdpE2, TdpF, TdpG, TdpH, TdpI, TdpJ, TdpL, or TdpN. The Tdp polypeptides are homologs of the Dep polypeptides and have homologous activities.
In yet another aspect, Chromobacterium and Burkholderia gene inactivation mutants are disclosed.
In still another aspect, FK228 analog compounds are disclosed. One identified FK228 analog is thailandepsin, which has three forms. In yet another aspect, the compounds are histone deacetylase inhibitors.
In a further aspect, methods of treating a disease associated with increased histone deacetylation are provided. The methods include administering an effective amount of one of the FK228 analog compounds to a subject having the disease.
In a still further aspect, methods of reducing histone deacetylase-mediated inhibition of gene expression in a cell are provided. The methods include contacting the cell with an effective amount of a composition comprising the FK228 analog compounds.
In another aspect, methods of modifying production of FK228 in Chromobacterium violaceum No. 968 and production of thailandepsin in Burkholderia thailandensis E264. The methods include introducing at least one of the polynucleotides of the dep gene cluster into Chromobacterium violaceum No. 968 or introducing at least one of the polynucleotides of the tdp gene cluster into Burkholderia thailandensis E264. The polynucleotides are operably connected to a promoter.
In yet another aspect, methods of producing an FK228 analog comprising growing Burkholderia thailandensis E264 in medium and partially isolating the FK228 analog from the growth medium are provided.
In yet another aspect, methods of making FK228 or thailandepsin analogs in recombinant cells are provided. The methods include growing a recombinant cell comprising polynucleotides encoding proteins encoded by the dep or the tdp gene cluster or homologs thereof under conditions that allow synthesis of FK228 or thailandepsin analogs.
In yet another aspect, methods of making an FK228 or thailandepsin analog are provided. The methods include introducing a polynucleotide into a bacterium to produce a recombinant bacterium. The polynucleotide encodes a polypeptide that is a homolog of at least one of the proteins of the dep gene cluster or of the tdp gene cluster. The polynucleotide is operably connected to a promoter. The recombinant bacterium is then grown under conditions that allow expression of the polynucleotide and production of the FK228 or thailandepsin analog.
In yet another aspect, methods of producing FK228 or FK228 analogs in Chromobacterium violaceum No. 968 are provided. The methods include manipulating at least one of the polynucleotides of the dep gene cluster to produce a mutated polynucleotide and introducing the mutated polynucleotide into Chromobacterium violaceum No. 968. The polynucleotides are operably connected to a promoter.
In yet another aspect, methods of producing thailandepsin or thailandepsin analogs in Burkholderia thailandensis E264 are provided. The methods include manipulating at least one of the polynucleotides of the tdp gene cluster to produce a mutated polynucleotide and introducing the mutated polynucleotide into Burkholderia thailandensis E264. The polynucleotides are operably connected to a promoter.
In a further aspect, a polynucleotide comprising a coding sequence encoding a polypeptide having at least 80% amino acid identity to a protein encoded by ecm 17 is provided. The coding sequence for ecm17 is operably connected to a promoter.
In a still further aspect, methods of forming a disulfide bond in a chemical having at least two free thiol or sulfhydryl groups are provided. The methods include contacting the chemical with a polypeptide having at least 80% amino acid identity to a protein encoded by ecm17, depH or tdpH. The polypeptide catalyzes formation of a disulfide bond between the two thiols.
a depicts the results of a phylogenetic analysis of five disulfide bond formation enzymes, which clearly categorizes Cv_DepH, Bt_TdpH and Sl_Ecm17 into a new group, distinct from the DsbA group of enzymes.
Described herein is an alternative approach to making FK228 and FK228 analogs using pathway engineering, combinatorial biosynthesis, or chemoenzymatic synthesis.
By examining the FK228 structure, we identified the building blocks of three amino acids (D-cysteine, D-valine, and L-valine), an amino acid derivative (2,3-dehydro-2-aminobutanoic acid, Dhb; also called 2,3-dehydrothreonine, Dht) and a complex L-(S,E)-3-hydroxy-7-mercaptohept-4-enoic acid moiety that is likely built from one Cys and two C2 units derived from malonyl coenzyme A (MCoA). Based on this information, we hypothesized that FK228 is a hybrid nonribosomal peptide (NRP)-polyketide (PK)-NRP.
The biosynthetic gene cluster (designated as dep for depsipeptide) responsible for FK228 biosynthesis was identified, cloned and characterized. The candidate biosynthetic genes were identified by a genome scanning approach. A gene replacement system was adapted to create targeted gene-inactivated mutant strains, and the subsequent cloning and characterization of an unusual hybrid nonribosomal peptide synthetase (NRPS)-polyketide synthase (PKS)—NRPS pathway for FK228 biosynthesis in Chromobacterium violaceum No. 968 was elucidated. Acquisition of the dep gene cluster and development of an efficient genetic system will allow FK228 analogs to be generated by engineered biosynthetic strategies.
The FK228 biosynthetic (dep) gene cluster and a proposed model of FK228 biosynthesis are depicted in
The present invention encompasses isolated polynucleotides encoding a polypeptide having at least 80%, 85%, 90%, 95%, or greater amino acid identity to a protein encoded by depA, depB, depC, depD, depE, depF, depG, depH, depl, depJ, depK, depL, depM, or depN. Suitably, the polynucleotides encode DepA, DepB, DepC, DepD, DepE, DepF, DepG, DepH, DepI, DepJ, DepK, DepL, DepM, or DepN. The present invention also includes isolated polypeptides having at least 80%, 85%, 90%, 95%, or greater amino acid identity to DepA, DepB, DepC, DepD, DepE, DepF, DepG, DepH, DepI, DepJ, DepK, DepL, DepM, or DepN and having the activity of DepA, DepB, DepC, DepD, DepE, DepF, DepG, DepH, DepI, DepJ, DepK, DepL, DepM, or DepN, respectively.
In another aspect, the present invention includes constructs comprising a polynucleotide of the invention operably linked to a promoter. Promoters may be any promoter active in the cell and capable of driving gene expression. Promoters include constitutive and inducible promoters. A variety of suitable promoters are known to those of skill in the art. Suitably the promoter is not the promoter natively associated with the polynucleotide. A vector comprising one or more of the polynucleotides or the polynucleotides operably connected to a promoter are also provided. Suitable vectors include, but are not limited to, a plasmid, a cosmid, a transposon, a virus, a phage, a BAC, a YAC or any other vectors known to those of skill in the art or which may be subsequently developed.
Recombinant or transgenic cells comprising one or more of the polynucleotides are provided. Such recombinant cells may be made by introducing the polynucleotides or vectors of the invention into a suitable host cell using any suitable method. Polynucleotides may be introduced into a suitable host cell by any means, including but not limited to, transformation, transduction, conjugation and electroporation. Many suitable host cells are known to those of skill in the art, including but not limited to, eukaryotic cells and prokaryotic cells. For example, recombinant or transgenic cells may be made by introducing the polynucleotides into a bacterium of a genus selected from Chromobacterium, Pseudomonas, Escherichia, Salmonella, Burkholderia, Bifidobacterium, and Clostridium, or in any other bacterium. Suitably the cell is capable of large scale culture or fermentation.
It is envisioned that FK228 biosynthesis by a Chromobacterium violaceum strain natively comprising the FK228 biosynthetic pathway, for example Chromobacterium violaceum No. 968, could be enhanced by introducing exogenous sequences encoding one or more proteins of the FK228 biosynthetic pathway. In other words, using the teachings of this application, one of skill in the art could readily develop Chromobacterium violaceum strains genetically engineered to have increased expression of one or more sequences (i.e., protein or mRNA) of the FK228 biosynthetic pathway, and such strains would reasonably be expected to have advantageous properties, such as increased FK228 biosynthesis. For example, depL is a regulatory gene. One of skill in the art would expect that altering expression of depL would alter expression of other dep constituents.
The FK228 biosynthetic pathway could be reconstituted in a bacterium that does not ordinarily synthesize FK228 analogs. As indicated above, bacteria that do not natively possess the FK228 biosynthetic pathway, for example, Chromobacterium violaceum strains other than Chromobacterium violaceum No. 968, Esherichia coli or Burkholderia thailandensis, may be genetically modified to express polypeptides having at least 80%, 85%, 90%, 95% or greater amino acid identity to one or more of DepA, DepB, DepC, DepD, DepE, DepF, DepG, DepH, DepI, DepJ, DepK, DepL, DepM, and DepN.
In another embodiment, one or more proteins of the FK228 biosynthetic pathway could be expressed in a bacterium in which an FK228 analog is synthesized, with the expectation that such bacteria would produce a unique FK228 analog. One such bacterium is Burkholderia thailandensis E264. As discussed in more detail below, Burkholderia thailandensis E264 makes a FK228 analog, designated as thailandepsin.
It is also envisioned that one or more of the sequences encoding DepA, DepB, DepC, DepD, DepE, DepF, DepG, DepH, DepI, DepJ, DepK, DepL, DepM, or DepN could be modified or genetically manipulated to alter the specificity or activity of the encoded protein. For example, the coding sequences could be modified by site-directed mutagenesis or random mutagenesis to make specific substitutions of one or more amino acids. In another embodiment, sequences encoding specific modules or domains of one or more of the proteins of the FK228 biosynthetic pathway could be replaced with sequences encoding analogous modules or domains from other distinct, but related proteins, including, but not limited to, nonribosomal peptide synthetases (NRPS) or polyketide synthases (PKS), for example. Numerous NRPS and PKS are known in the art. It is envisioned that genetically engineered bacteria expressing such sequences can be used to develop bacterial strains capable of synthesizing FK228 analogs.
Provided herein is an FK228 analog, designated thailandepsin (Tdp), from Burkholderia thailandensis E264, which was elucidated as described in the Examples by its homology to the dep gene cluster. A tdp gene cluster (Table 4,
The coding sequences for proteins involved in biosynthesis of thailandepsin may be isolated from genomic Burkholderia thailandensis E264 DNA or mRNA and further modified or manipulated using standard methods. Accordingly, in yet another aspect, the invention includes an isolated polynucleotide encoding at least one polypeptide having at least 80%, 85%, 90%, 95% or greater amino acid identity to a protein encoded by tdpA, tdpB, tdpC1, tdpC2, tdpDE1, tdpE2, tdpF, tdpG, tdpH, tdpI, tdpJ, tdpL, or tdpN operably connected to a promoter not natively associated with the coding sequence. Suitably, the polynucleotides encode TdpA, TdpB, TdpC1, TdpC2, TdpDE1, TdpE2, TdpF, TdpG, TdpH, TdpI, TdpJ, TdpL, or TdpN. The present invention also includes isolated polypeptides having at least 80%, 85%, 90%, 95%, or greater amino acid identity to TdpA, TdpB, TdpC1, TdpC2, TdpDE1, TdpE2, TdpF, TdpG, TdpH, TdpI, TdpJ, TdpL, or TdpN and having the activity of TdpA, TdpB, TdpC1, TdpC2, TdpDE1, TdpE2, TdpF, TdpG, TdpH, TdpI, TdpJ, TdpL, or TdpN, respectively. The invention also includes vectors and recombinant or transgenic cells comprising one or more of the polynucleotides.
As discussed above for the FK228 biosynthetic pathway, the biosynthetic pathway of thailandepsin could be reconstituted in bacteria that do not natively possess the pathway, i.e., in bacteria other than Burkholderia thailandensis E264. The synthesis of thailandepsin in Burkholderia thailandensis E264 may be enhanced by introducing exogenous sequences expressing one or more polypeptides having least 80%, 85%, 90%, 95% or greater amino acid identity to a protein encoded by tdpA, tdpB, tdpC1, tdpC2, tdpDE1, tdpE2, tdpF, tdpG, tdpH, tdpI, tdpJ, tdpL, or tdpN. Additionally, recombinant Burkholderia thailandensis E264 could be made in the same manner as discussed above for Chromobacterium violaceum No. 968 to produce unique FK228 analogs.
The proposed synthesis scheme for thailandepsin is depicted in
As described more fully in the Examples, FK228 and thailandepsin are synthesized by sequential addition of simple moieties, such as amino acids, amino acid derivatives, or short carboxylic acids to form the backbone of the molecule. FK228 uses cysteine, valine, dehydro-threonine and malonyl coenzyme A (MCoA) as building blocks, while thailandepsins use cysteine, phenylalanine, alanine and/or glycine, and MCoA as building blocks. Based on these four identified species, the general structure of this family of molecules which are FK228 analogs may be depicted as follows:
wherein each of R1, R2 and R3 are an amino acid side chain or a derivative thereof. The amino acid side chains are well-known to those of skill in the art and include, e.g., alanine —CH3; valine —CH(CH3)2; cysteine —CH2SH; leucine —CH2CH(CH3)2; isoleucine —CH(CH3)CH2CH3; and threonine —CH(OH)CH3.
Compounds of Formula (I), Formula (II) and Formula (III) in which each of R1, R2, and R3 are amino acid side chains are provided herein. The compounds may contain the disulfide bond as depicted in Formula (I), or the disulfide bond may be reduced as depicted in
Also encompassed are compounds of formula II or III, reduced forms of the compounds of formula II or III, dehydration products of the compounds of formula II or III, or salts thereof. Each of R1, R2, and R3 are an amino acid side chain or a derivative thereof. Examples of compounds of formula (II) include, but are not limited to, compounds of formula (II) wherein R1 is —CH2-benzyl, wherein R2 is —H, —CH3, or —CH(CH3)2 and wherein R3 is —CH3 or —CH(CH3)2. Also included are thailandepsin A, thailandepsin B, thailandepsin C, formula (II) wherein R1 is —CH2-benzyl, R2 is —CH(CH3)2, and R3 is —CH(CH3)2, formula (II) wherein R1 is —CH2-benzyl, R2 is —CH(CH3)2, and R3 is —CH3, formula (II) wherein R1 is —CH2-benzyl, R2 is —H and R3 is —CH(CH3)2 and formula (II) wherein R1 is —CH2-benzyl, R2 is —CH3 and R3 is CH(CH3)2, formula (III) wherein R1 is —CH2-benzyl, R2 is —CH(CH3)2, and R3 is —CH(CH3)2, formula (III) wherein R1 is —CH2-benzyl, R2 is —CH(CH3)2, and R3 is —CH3, formula (III) wherein R1 is —CH2-benzyl, R2 is —H and R3 is —CH(CH3)2 and formula (III) wherein R1 is —CH2-benzyl, R2 is —CH3 and R3 is CH(CH3)2.
These FK228 and thailandepsin analogs may be made using routine microbial fermentation, bacterial genetics and molecular cloning procedures, such as those known to those of skill in the art, in combination with the disclosure of the dep and tdp gene clusters and structures of the resulting molecules.
The Examples also provide a gene inactivation protocol for Chromobacterium and Burkholderia, by which native sequences in the gene clusters encoding the synthetic apparatus for making FK228 and thailandepsin can be inactivated and non-native sequences can be inserted to produce novel FK228 and thailandepsin analogs. In the Examples, depD was inactivated in C. violaceum No. 968 and TdpA was inactivated in B. thailandensis E264. In both cases, inactivation of the gene resulted in bacteria that no longer made FK228 and thailandepsin, respectively. Similar methods could be used to inactivate any gene of interest, suitably any gene in the dep or tdp gene cluster may be inactivated using these methods.
Bacterial strains capable of synthesizing FK228 analogs may be developed from gene-inactivated mutants of Chromobacterium violaceum No. 968 or Burkholderia thailandensis E264 in which one or more genes involved in the biosynthesis of FK228 is inactivated by genetically manipulating the mutants to express a sequence encoding an analogous protein having a function similar to, but distinct from, that of the protein encoded by the native gene. The sequence encoding the analogous protein could be from a different bacterial genus, e.g., Burkholderia thailandensis E264, from a different species of Chromobacterium, from a different Chromobacterium violaceum isolate, from a different bacterial species, or it could be a chimeric sequence (e.g., a sequence encoding a protein having modules or domains ordinarily found on different proteins).
Provided herein are various methods for making FK228 and FK228 analogs. Notably, similar methods may be used to make thailandepsin and thailandepsin analogs as well. First, methods of making FK228 or an FK228 analog are provided. A recombinant cell comprising polynucleotides encoding proteins encoded by depA, depB, depC, depD, depE, depF, depG, depH, depl, depJ, depK, depL, depM, or depN or a homolog thereof are grown by any suitable method. The polynucleotides are operably connected to a promoter, under conditions that allow synthesis of FK228 or an FK228 analog. Homologs of the proteins encoded by the dep gene cluster include, but are not limited to, proteins that share at least about 40%, 50%, 60%, 70% or more amino acid similarity and/or 25%, 35%, 45%, 55% or more amino acid identity and catalyzing analogous reactions. Homologs may share specific domains within the proteins. For example, candidate homologs for the dep gene cluster may have NRPS, PKS or hybrid NRPS-PKS domains. The polynucleotides may be expressed in any suitable cell. Suitably, the cell is a bacterium of a genus selected from the group consisting of Chromobacterium, Pseudomonas, Escherichia, Salmonella, Burkholderia, Bifidobacterium, or Clostridium.
Alternatively, an FK228 analog can be made by introducing a polynucleotide into Chromobacterium violaceum No. 968 to produce a recombinant bacterium. The introduced polynucleotide encodes a polypeptide that is a homolog of at least one of DepA, DepB, DepC, DepD, DepE, DepF, DepG, DepH, DepI, DepJ, DepK, DepL, DepM, or DepN, and the polynucleotide is operably connected to a promoter. The recombinant bacterium is then grown under conditions that allow expression of the polynucleotide and production of the FK228 analog. In one embodiment the polynucleotide encodes TdpE2. Suitably, the native DepD is inactivated in this embodiment. In another embodiment, the polynucleotide encodes TdpDE1. Suitably the native DepE is inactivated in the recombinant bacterium of this embodiment. Similar methods may be used to make a thailandepsin analog. In one embodiment, the polynucleotide introduced into B. thailandensis encodes DepD. Suitably tdpE2 is inactivated in the recombinant bacterium in this embodiment. In another embodiment, the polynucleotide introduced into B. thailandensis encodes DepE. Suitably tdpDE1 is inactivated in the recombinant bacterium in this embodiment.
In yet another embodiment, methods of producing FK228 or an FK228 analog in Chromobacterium violaceum No. 968 are provided. Analogs may be made by manipulating at least one of the polynucleotides in the dep gene cluster to produce a mutated polynucleotide and then introducing the mutated polynucleotide into Chromobacterium violaceum No. 968. The polynucleotides are operably connected to a promoter such that they are expressed in the recombinant bacteria. Similar methods may be used to make thailandepsin analogs in B. thailandensis E264.
Suitably the FK228 and thailandepsin analogs have histone deacetylase inhibitor activity. Assays for histone deacetylase inhibition are known to those of skill in the art and may be used to assess whether the analogs are active. The FK228 and thailandepsin analogs may be used in pharmaceutical compositions and administered to subjects to treat disease. Pharmaceutically acceptable carriers are well known to those of skill in the art.
The FK228 analogs described herein may be used to treat diseases associated with increased histone deacetylation by administering an effective amount of an FK228 analog to a subject with such a disease. Diseases include, but are not limited to, inflammatory disorders, diabetes, diabetic complication, homozygous thalassemia, fibrosis, cirrhosis, tumor, acute myeloid leukemia (AML), chronic lymphocytic leukemia (CLL), neurodegenerative disease, cognitive disorder, and autoimmune disease. Treatment of a disease includes but is not limited to, prophylaxis of symptoms, reduction in disease severity, or reduction in disease length as compared to an untreated subject.
Administration of an effective amount of a FK228 analog to a subject may be carried out by any means known in the art including, but not limited to intraperitoneal, intravenous, intramuscular, subcutaneous, or transcutaneous injection or oral, nasopharyngeal or transmucosal absorption. Determination of a preferred pharmaceutical formulation and a therapeutically effective dose regimen for a given application is within the skill of the art taking into consideration, for example, the condition and weight of the patient, the extent of desired treatment and the tolerance of the patient for the treatment.
Methods of reducing histone deacetylase-mediated inhibition of gene expression in a cell are also provided. These methods include contacting the cell with an effective amount of a composition comprising an FK228 analog compound. The FK228 analog is capable of inhibiting HDACs. The HDACs are known to inhibit gene expression, thus inhibition of HDACs may result in increased expression of genes. As used herein gene encompasses polynucleotides encoding for polypeptides natively associated with the cell as well as polynucleotides encoding non-native polypeptides. Effects of contacting a cell with a FK228 analog may be evaluated by comparing expression of a polynucleotide in cells treated with the FK228 analog to expression in untreated cells. Expression of a polynucleotide may be assessed by any means known to those of skill in the art, including but not limited to, rtPCR, Northern analysis, and Western analysis.
The yield of FK228 production from its native bacterial strain, C. violaceum No. 968, is low (Ueda, Nakajima et al. 1994). Production of FK228 may be improved using the methods of the invention. The nucleic acid sequence of a regulatory gene, depL, is provided herein. The regulatory genes depL and its B. thailandensis homolog, tdpL, regulate the expression of the entire dep or tdp gene cluster. Thus, genetic manipulation of these genes may improve production of FK228 and thailandepsin. The expression level of depL can be increased by increasing the copy number of the gene by, for example, supplementing the polynucleotide encoding DepL on a multi-copy plasmid or integrating multiple copies of depL into the chromosome, and/or by cloning the intact gene into an expression vector with a strong promoter and subsequently introducing the construct into the wild-type strain or any genetically engineered strains of C. violaceum No. 968. The expression level of depL can also be decreased by design and expression of an anti-sense of depL, and/or by deleting various amounts of the depL gene upstream regulatory elements in the wild-type strain or any genetically altered strains of C. violaceum No. 968. Alternatively, the depL expression level could be abolished by targeted gene inactivation as described for depD in the Examples. The sequence encoding DepL can be further mutated to encode DepL variants with altered activity and/or specificity. FK228 production can be assessed by conventional natural product purification and identification procedures.
Disulfide bonds that link two nonadjacent (in most cases) cysteines often exist in proteins and peptides, and their derived products, such as lantibiotics, toxins, venoms and hormones, to maintain proper folding configuration. Enzymes that are capable of catalyzing protein/peptide disulfide bond formation are members of a large collection of thiol-disulfide oxidoreductases found in all living cells. Many of these enzymes belong to the thioredoxin superfamily, which is defined by an active site containing a CXXC motif (cysteines separated by two amino acids) and by a thioredoxin fold seen in the three-dimensional structure (Kadokura, Katzen et al. 2003). The best studied catalyst of disulfide bond formation is the DsbA and its associated proteins (DsbB, DsbC, and DsbD) in E. coli.
Disulfide bonds are also, however rarely, found in small molecule natural products (e.g. FK228 and thailandepsins, psammaplins (Pina, Gautschi et al. 2003), triostins (precursors of echinomycins), thiocoraline, BE-22179 and SW-163C (Lombo, Velasco et al. 2006; Watanabe, Hotta et al. 2006; Dawson, Malkinson et al. 2007)). In the triostin/echinomycin biosynthetic gene cluster, a gene, ecm17, encodes an FAD-dependent pyridine nucleotide-disulphide oxidoreductase (Sl_Ecm17; accession no. BAE98166) that catalyzes a disulfide bond formation between two cysteine residues (Watanabe, Hotta et al. 2006). Despite a high degree of structural similarity between triostins and thiocoraline, surprisingly, the thiocaroline biosynthetic gene cluster does not contain an apparent gene encoding a disulfide bond formation enzyme (Lombo, Velasco et al. 2006).
In the FK228 biosynthetic gene cluster, a particular gene, depH, was identified that encodes an FAD-dependent pyridine nucleotide-disulphide oxidoreductase (Cheng, Yang et al. 2007). In the thailandepsin biosynthetic gene cluster, a particular gene, tdpH, was identified that encodes an FAD-dependent pyridine nucleotide-disulphide oxidoreductase. See the Examples. The deduced protein sequences of DepH (GenBank accession no. ABP57752) and TdpH (GenBank accession no. ABC38333) have a 72% identity/85% similarity to each other. Either DepH or TdpH sequence has a 32% identity/46% similarity to the deduced Ecm17 protein sequence of ecm17 gene in the triostin/echinolycin biosynthetic gene cluster. DepH, TdpH or Ecm17 sequences have no significant similarity to DsbA of E. coli, except sharing an active site containing a CXXC motif (
In yet another embodiment, methods of catalyzing a disulfide bond in a chemical comprising at least two free thiol or sulfhydryl groups are provided. The chemical is contacted with a polypeptide having at least 80% amino acid identity to a protein encoded by Ecm17, DepH or TdpH. The Ecm17, DepH or TdpH polypeptide catalyzes formation of a disulfide bond between the two free thiols. Suitably the chemical comprises a macrolide ring structure. The chemical may be contacted by the polypeptide using any means known to those of skill in the art. In one embodiment, the chemical is contacted by the polypeptide by introducing a polynucleotide encoding the polypeptide into a cell in which the chemical is synthesized.
A generic formula for the substrate for Ecm17, DepH or TdpH is as follows:
wherein FAD is a cofactor required by the FAD-dependent pyridine nucleotide-disulphide oxidoreductase (DepH, TdpH, or Ecm17) and FADH2 is the reduced form of FAD. X and y represent any number of C—C units in any format. Z represents any number of any type bonds (C—C, C—N, or C—O) in any format. M and n represent any chemical moieties, but preferred ones that form a macrolide ring structure.
Sequences encoding a polypeptide having at least 80% amino acid identity to DepH, TdpH or Ecm17 can be used to form disulfide bonds in drug molecules by (1) cloning the sequence into a suitable expression vector to make an expression construct; (2) introducing the construct into a microorganism that produces a precursor or multiple precursors, according to formula (IV) to produce the desired enzyme, which in turn catalyzes the conversion of the precursor into a disulfide bond product according to formula (V).
Alternatively, sequences encoding a polypeptide having at least 80% amino acid identity to DepH, TdpH or Ecm17 can be used to form disulfide bonds in drug molecules by (1) cloning the sequence into a suitable integrative vector to make an integrative construct; (2) introducing the construct into a microorganism that produces a precursor or multiple precursors, according to formula (IV); and (3) selecting strains with the sequence integrated into the bacterial chromosome, such that the sequence is expressed and produces an enzyme capable of catalyzing the conversion of the precursor into a disulfide bond product according to formula (V).
DepH, TdpH, or Ecm17 protein can be used to catalyze the formation of disulfide bonds in drug molecules in vitro. The protein can be expressed in and purified from a heterologous host, including but not limited to, E. coli, Streptomyces lividans, or yeasts. The purified enzyme is contacted with a precursor according to formula (IV) under suitable conditions of temperature, pressure, pH, cofactors, etc., to catalyze the conversion of the precursor to a disulfide bond-containing product according to formula (V).
The following examples are meant to be illustrative only and are not meant to be limiting upon the invention claimed.
Bacterial strains, culture conditions, and plasmids. The bacterial strains and plasmids used in this study are listed in Table 1. The FK228-producing strain, C. violaceum No. 968, was cultured in nutrient broth (1% Difco nutrient broth and 1% glucose) at 30° C. for genomic DNA preparation and in fermentation medium (nutrient broth supplemented with 5% Diaion HP-20 resin [Supelco, Pennsylvania]) at 30° C. for FK228 production. The vectors pEX18Tc and pPS858, originally developed for Pseudomonas aeruginosa genetics (Hoang, Karkhoff-Schweizer et al. 1998), were adopted and applied successfully in C. violaceum.
Chromobacterium violaceum
Escherichia coli
aThior, thiostrepton resistance.
bIPOD, International Patent Organism Depositary, Tsukuba, Japan.
DNA manipulations, genome library construction, and DNA sequencing. General DNA manipulations, including plasmid preparation, restriction enzyme digestion, agarose gel electrophoresis, subcloning, and bacterial transformation, were done according to standard protocols (Sambrook and Russell 2000) or manufacturer's instructions (New England BioLabs; QIAGEN). Genomic DNA of a C. violaceum wild-type or mutant strain was prepared from an overnight culture with a Genomic-tip 500/G kit (QIAGEN) or with an UltraClean Microbial DNA Isolation kit (MO BIO Labs).
For construction of a genome sampling library (Zazopoulos, Huang et al. 2003), high-molecular-weight C. violaceum genomic DNA was mechanically sheared with a nebulization device (Invitrogen). DNA molecules that were 2 to 4 kb long were recovered from an agarose gel and ends repaired with T4 DNA polymerase and Klenow enzyme in the presence of deoxynucleotide triphosphates (dNTPs; 1 mM each). The ends of resultant DNA molecules were adenylated using Taq DNA polymerase with dATP, ligated to the pGEM-T Easy vector, and transformed into Escherichia coli DH5α cells. Four 96-well plates of clones were subjected to template DNA preparation by PCR amplification and purification with a PerfectPrep PCR Cleanup 96 kit (Eppendorf), and end sequencing with BigDye chemistry and SP6 as primer was performed on an ABI 3730 automated DNA sequencer (Applied Biosystems) at the University of Wisconsin-Madison Biotechnology Center. DNA oligonucleotides were synthesized by Operon Biotechnologies, Inc., and DNA sequencing by primer walking was performed by standard procedures (Sambrook and Russell 2000).
A cosmid library was constructed in the SuperCos 1 vector using previously described procedures (Cheng 2006). Southern blotting, labeling of DNA as a probe, hybridization, and detection were performed according to manufacturer's protocols (Roche). Shotgun sequencing of cosmid 18 and contig assembling were performed by a service company (ACGT Inc.). Local sequence analysis was performed with the Lasergene program package (DNASTAR, Inc.), and by a homology search against the GenBank database using the BLAST algorithms (Altschul, Gish et al. 1990). The domain organization of biosynthetic enzymes was analyzed as described by Ansari et al. (Ansari, Yadav et al. 2004), with manual intervention.
General strategy for the construction of targeted gene-inactivated mutants of C. violaceum No. 968. To mutate a candidate gene by a gene replacement strategy, an internal part of the DNA of a genomic DNA clone (Apr, ampicillin resistant) was replaced by a 1.8-kb FRT cassette (Gmr, gentamycin resistant) from pPS858 to make an intermediate construct (Apr Gmr). The FRT cassette, along with two flanking genomic DNAs for homologous DNA recombination, was excised and subcloned into pEX18Tc to make a final conjugation construct (Gmr and tetracycline resistant —Tcr).
The conjugation construct was introduced into E. coli S17-1 cells and subsequently transferred into C. violaceum cells by conjugation as follows. Two bacterial strains were grown in LB media supplemented with appropriate antibiotics (10 μg/ml Gm and 10 μg/ml Tc for E. coli S17-1 [a conjugation construct] and 200 μg/ml Ap for C. violaceum, which is naturally resistant to Ap) at 37 or 30° C. with shaking until late mid-log phase (6 to 8 h). Cells from 1 ml of each culture were collected by centrifugation at 4,000×g for 15 min at 4° C., and the cell pellets were washed once with 1 ml LB medium. Cells were collected again by centrifugation and resuspended in 100 μl LB medium. Cell suspensions of two bacterial strains were pooled and spread evenly on a wet 0.45-μm nitrocellulose membrane (Whatman) on LB agar supplemented with 10 mM MgSO4. After the plate had been incubated at 30° C. for 12 to 16 h, the membrane seeded with bacteria was used to print several LB agar plates containing 200 μg/ml Ap, 50 μg/ml Gm and 5% sucrose to select for exconjugants.
FK228 production and detection by LC-MS. Wild-type and mutant strains of C. violaceum were grown in 25 ml of fermentation medium at 30° C. for 3 days under constant agitation (200 rpm). Cells and resins were then collected together by centrifugation at 4,000×g for 20 min at the ambient temperature and lyophilized to dryness. A crude FK228 preparation was obtained by eluting the dried cell debris and resins with 10 ml ethyl acetate. Twenty microliters of this preparation was injected into an Agilent 1100 Series LC/MSD Trap mass spectrometer (MS) (Agilent) for detection of the positive ion signals of FK228. The liquid chromatography (LC) program included a linear gradient from buffer A (20% methanol with 0.1% formic acid) to buffer B (80% methanol with 0.1% formic acid) in 15 min and a constant elution in buffer B for 5 min, followed by a linear return to buffer A in 5 min. Samples were fractionated by using a Zorbax Eclipse XDB-C18 column (2.1 by 110 mm; Agilent) with a flow rate of 0.25 ml/min.
Nucleotide sequence accession numbers. The nucleotide sequences of the inserts in pP3-B6, pP4-B4, pP4-G7, and cosmid 18 have been deposited in the GenBank database under accession numbers EF015612, EF015613, EF015614, and EF210776, respectively. The nucleotide sequence of the dep gene cluster is included herein as SEQ ID NO:1. The putative amino acid sequences are also in the appended sequence listing.
Identification of candidate natural product biosynthetic genes in C. violaceum No. 968. The hybrid NRP-PK-NRP nature of FK228 (
For ester bond formation in depsipeptide natural products, the involvement of a discrete D-hydroxyisovalerate dehydrogenase in enniatin biosynthesis by Fusarium sambucinum (Lee, Gorisch et al. 1992), or a novel NRPS module containing an adenylation (A) domain to activate an α-keto acid and an embedded α-ketoreductase (KR) to reduce the tethered substrate into α-hydroxyacyl intermediate (and presumably a downstream condensation [C] domain acting as chiral ester synthase rather than an amide synthase) in cereulide and valinomycin biosynthesis in actinomycetes (Magarvey, Ehling-Schulz et al. 2006), has been experimentally established. However, whether intramolecular disulfide bond formation in natural products (such as FK228) is an enzymatic reaction or a spontaneous chemical oxidation is unknown. Therefore, our search for candidate FK228 biosynthetic genes focused initially on those encoding an obvious NRPS, PKS, or, in particular, hybrid NRPS-PKS or PKS-NRPS system.
Among 360 valid sequence tags obtained from sequencing of the genome sampling library of C. violaceum (See Materials and Methods), three distinctive sequence tags, P3-A6-SP6, P4-B4-SP6, and P4-G7-SP6, were identified to be parts of genes encoding PKS, NRPS, and hybrid PKS-NRPS system, respectively (Table 2). Genes that contain those three tags were considered as candidate natural product biosynthetic genes, possibly involved in FK228 biosynthesis. Further primer walking sequencing revealed the complete sequences of the corresponding inserts in pP3-A6, pP4-B4, and pP4-G7.
The insert in pP3-A6 contains a 2,826-bp DNA that includes a partial PKS gene (not named) and its translated amino acid sequence has homology to the β-ketoacyl synthase (KS) and acyltransferase (AT) domains of type I PKSs (Shen 2003). Three signature motifs (QTRTAQ, GHSYG, and AAFH) were identified within the AT domain, and these motifs are similar to the motifs of ATs using MCoA as a substrate (Reeves, Murli et al. 2001).
The insert in pP4-B4 contains a 3,612-bp DNA that includes a partial gene (designated depD) (Table 3 and
The insert in pP4-G7 contains a 2,599-bp DNA that includes two partial genes (designated depC and depD) (Table 3 and
aSee FIG. 2.
bA superscript I indicates incomplete. KS, β-ketoacyl synthase; E, epimerase.
cNN, not named.
dNA, not available.
150c
C. violaceum ATCC
C. violaceum ATCC
C. violaceum ATCC
Campylobacter coli
C. violaceum ATCC
Pseudomonas
fluorescens Pf-5
Myxococcus xanthus
Lyngbya majuscula
Nostoc sp. ATCC
Pseudomonas
aeruginosa
Microcystis aeruginosa
Pseudomonas putida
Pseudomonas syringae
Pseudomonas
aeruginosa PAO1
Ralstonia
solanacearum UW551
Streptomyces
atroolivaceus S-140
C. violaceum ATCC
C. violaceum ATCC
C. violaceum ATCC
107c
C. violaceum ATCC
aSubscripts indicate the substrate specificities of enzymes. Superscripts indicate inactive (i) or nonfunctional (n). Dhb, 2-3-dehydro-2-aminobutanic acid.
bIncomplete.
cTruncated.
Adaptation of a Pseudomonas aeruginosa genetic system in C. violaceum No. 968 to create targeted gene-inactivated mutant strains. To test whether the identified candidate genes are necessary for FK228 biosynthesis, we inactivated the individual genes (except depC, which has only a very short segment on the insert of pP4-G7) in C. violaceum No. 968. C. violaceum strains belong to the gram-negative β-proteobacterium. Although isolates of C. violaceum produce many products with biotechnological and pharmaceutical utility, and the genome of a type strain, C. violaceum ATCC 12472, has been sequenced (Consortium 2003), a genetic system for targeted gene inactivation in C. violaceum has not been reported. Here, a broad-host-range Flp-FRT recombination system originally developed for P. aeruginosa genetics (Hoang, Karkhoff-Schweizer et al. 1998) was adopted and successfully applied to C. violaceum No. 968.
To inactivate the P4-G7-SP6-associated depD gene (depD was chosen as an example for full description here because it encodes part of a hybrid PKS-NRPS system that is of prime interest) (
Southern analysis (
The same strategy was used to inactivate the P3-A6-SP6-associated gene (not named) and the P4-B4-SP6-associated depD gene (3′-part), to create mutant strains Cv56a/b/c and Cv57a/b/c, respectively, and their genotypes were verified by Southern analyses as well (data not shown).
During the course of method development, two other conjugation systems were also tested. One method used the methylation-deficient E. coli ET12567 (pUZ8002) (MacNeil, Gewain et al. 1992; Kieser, Bibb et al. 2000) and the other used E. coli MT607 (pRK600) (Finan, Kunkel et al. 1986) as donor strains to mobilize a conjugation construct (such as pYC03-58b) into C. violaceum cells. Both systems generated exconjugants, but they were at least 10-fold less efficient than the E. coli S17-1 strain-mediated conjugation between E. coli and C. violaceum cells (data not shown). In addition, it was noticed that, since the FRT cassette contains a functional GFP gene that encodes the green fluorescent protein (GFP), E. coli and C. violaceum colonies or cultures with the FRT cassette present on a replicable plasmid or integrated into chromosome were distinguishable from the wild-type bacteria by a greenish color (data not shown). Therefore, bacterial exconjugants carrying the FRT cassette could be identified by direct observation or by a simple GFP assay. Furthermore, the marker genes (aacC1 and GFP in the FRT cassette) integrated into the mutant chromosome could be excised precisely by a FLP recombinase encoded by pFLP2 plasmid in the Flp-FRT system to create unmarked mutants (Hoang, Karkhoff-Schweizer et al. 1998). Unmarked mutants could be mutated at different loci sequentially to create multiple gene deletions or gene replacements. This feature could be very useful for future pathway engineering and combinatorial biosynthesis studies.
Confirmation of the necessity of the depD gene for FK228 biosynthesis in C. violaceum No. 968. The FK228 productivity of the wild-type and mutant (Cv56a/b/c, Cv57a/b/c and Cv58a/b/c) strains of C. violaceum was examined by fermentation and LC-MS analysis. FK228 does not produce a characteristic UV spectrum because it lacks a chromophore, but its positive ion signals are strong and appeared near 20.8 min under the chromatographic conditions tested (
Cloning, sequencing, and in silico analysis of the FK228 biosynthetic (dep) gene cluster. A series of overlapping cosmid clones were obtained by colony hybridization with digoxigenin-labeled insert DNA of pP4-G7 as a probe. Cosmid end sequencing indicated that, among those clones, cosmid 18 appears to contain the entire dep gene cluster; therefore, the nucleotide sequence of cosmid 18 was determined by shotgun method, which revealed a 40,434-bp contig (
The assembled contig contains 21 apparent genes or open reading frames (ORFs) (two partial sequences at the ends) (Table 3 and
Interestingly, five ATCC 12472 genes (CV—3379 through CV—3383) are seemingly replaced by the dep gene cluster, suggesting that a lateral gene transfer event occurred (Ochman, Lawrence et al. 2000). Further evidence that supports this notion comes from a G+C content analysis. The flanking housekeeping genes have an average G+C content of 62.9%, while the dep gene cluster has a G+C content of 69.0%. C. violaceum No. 968 could have acquired the dep gene cluster from an organism with a higher-G+C genome at the expense of a five-gene deletion of its own.
Cotranscription is common among related genes in bacteria. In the dep gene cluster and flanking regions, orf1 through orf3, orf18 through orf21, depABCDEFGH, and depIJ are very likely organized as operons, respectively, because genes within each putative operon have overlapping stop and start codons. In contrast, genes depK, depL, depM, and depN are separated by variable lengths of intergenic DNA. This analysis facilitated the prediction that depJ is the downstream boundary of the dep gene cluster because orf18 through orf21 are housekeeping genes in a single putative operon.
Model for FK228 biosynthesis by a hybrid NRPS-PKS-NRPS assembly line. Many natural products are often biosynthesized by modular NPRSs, PKSs, or hybrid NRPS-PKS or PKS-NRPS assembly lines in a colinearity model in which the substrate specificity and the number and order of modules dictate the chemical makeup of the products (for recent comprehensive reviews, see references (Finking and Marahiel 2004; Fischbach and Walsh 2006; Hill 2006); meanwhile, variations from the canonical model, including colinearity violation, iterative polymerization (iteration), missing or misplacing domains, module skipping or stuttering, stand-alone domains, alternative chain termination, the presence of unique domains, or trans-acting enzymes, have all been documented in individual biosynthetic pathways [for recent comprehensive reviews, see references (Shen 2003; Wenzel and Muller 2005; Fischbach and Walsh 2006). Based on extensive bioinformatics analyses of the domain and module organization of biosynthetic enzymes encoded by the dep gene cluster, a model for FK228 biosynthesis by a hybrid NRPS-PKS-NRPS assembly line is proposed (
Based on the model, FK228 biosynthesis starts with the activation of a Cysteine by the A domain in module 1 to form a cysteinyl-S—PCP intermediate. DepM (an aminotransferase) is proposed to act in trans to remove an amino group from the intermediate to form 4-mercaptobutanyl-S-PCP. Aminotransferase domains have been found to be an integral part of the PKSs in the biosynthesis of mycosubtilin (Duitman, Hamoen et al. 1999) and iturin A (Tsuge, Akiyama et al. 2001), adding an amino group; no such domain, however, has been found to remove an amino group in a reverse reaction. The C domain in module 1 appears to be nonfunctional because of a lack of a critical catalytic motif, HHXXXDG; a nonfunctional C domain disconnects the possible chemical interaction between the upstream acyl coenzyme A ligase (AL) domain and the downstream A domain.
Next, PKS modules 2 and 3 sequentially extend the growing chain with two C2 units from MCoA. However, module 2 contains only a remnant nonfunctional AT domain that lacks essential motifs (e.g., GHSXG and A[FS]HS), and module 3 lacks an AT domain. The dehydratase (DH) domain in modules 2 and 3 also appear to be nonfunctional because of a lack of a conserved active site motif, HXXXGXXXXP. An unknown stand-alone AT-DH didomain protein (or, alternatively, discrete AT and DH proteins) is proposed to act in trans to compensate the modules in the PKS mode of biosynthesis. Furthermore, since no gene encoding a stand-alone AT-DH didomain is present in the dep gene cluster, it must exist in another region of the genome. Stand-alone AT domains or AT-X didomains (where X is any domain) have been identified in recent years in the biosynthetic pathways of natural products, including leinamycin (Cheng, Tang et al. 2003), pederin (Piel 2002), and many other compounds. A recent molecular cellular study of the bacillaene biosynthetic enzyme complex revealed an amazing interaction between a stand-alone AT-X didomain and the rest of a mega-PKS complex in Bacillus subtilis (Straight, Fischbach et al. 2007).
In addition, DepF, an FadE2-like acyl coenzyme A dehydrogenase, has been proposed to act in trans on module 2 to generate a double bond on the β-hydroxyl-5-mercaptopentanoyl-S-ACP intermediate to form the β-5-mercaptopent-2-enoyl-S-ACP intermediate. If this is true, DepF would be functionally equivalent to an enoylreductase (ER). KR domains in modules 2 and 3, although intact, are proposed to be inactive, probably due to a lack of proper interaction with the putative in trans-acting AT-DH didomain. Modules 4, 5, and 6 extend the growing intermediate chain with activated D-Val, D-Cys, and 2,3-dehydro-2-aminobutanoic acid (Dhb) (2,3-dehydrothreonine—Dht) sequentially in the canonical model of the NRPS mode of biosynthesis. Module 7 is expected to incorporate a Val, but an A domain is completely missing in this module. It is proposed that the A domain in module 4, which specifies a Val, acts in trans to aminoacylate the PCP domain in module 7. Such phenomenon has been observed in the biosynthetic pathways of viomycin (Thomas, Chan et al. 2003), yersiniabactin (Gehring, DeMoll et al. 1998), and other compounds.
Finally, terminal thioesterase (TE) on DepE should catalyze the formation of an ester linkage between a hydroxyl group originated from MCoA and an β-keto group from Val to form a 16-membered macrolactone ring. In addition, a flavin adenine dinucleotide (FAD)-dependent pyridine nucleotide-disulfide oxidoreductase encoded by depH is proposed to bring the free sulfhydryl groups from two Cys residues together and to form an intramolecular disulfide bond. Disulfide bond formation hallmarks the formation of a 17-membered ring structure and brings the FK228 biosynthesis to completion. DepJ, a discrete type II TE, is not drawn into the model, and type II TEs are generally believed to have a proofreading function during chain elongation to ensure smooth biosynthesis by selectively removing misprimed thioesters or shunt-intermediates (Heathcote, Staunton et al. 2001). It is necessary to point out that, in the model described above, several unique features that include the trans-acting DepM, DepF, an unknown stand-alone AT-DH didomain and a trans-acting A domain are speculative and require further experimental validation.
Other genes in the dep gene cluster. There are two apparent resistance genes in the dep gene cluster. An esterase/lipase, encoded by depI, is proposed to hydrolyze the ester linkage and/or the disulfide bond in FK228 to prevent the accumulation of excess concentration of FK228 in cells where FK228 may become toxic. A phosphotransferase, encoded by depG, is proposed to further mask and quench the hydrolyzed FK228 by adding a phosphate group to the freed hydroxyl and/or sulfhydroxyl group(s).
Surprisingly, no gene encoding exportation machinery is found in the dep gene cluster. The depL gene encodes a typical transcriptional regulator that contains a helix-turn-helix motif, indicting its DNA-binding activity. The depK gene encodes a conserved functionally unknown protein. Finally, depN encodes a nonfunctional PCP remnant without a critical serine residue in a conserved motif GX(HD)S, necessary for phosphopantetheinylation and covalent substrate aminoacylation.
Discovery of FK228 Analogs (Thailandepsins) from Burkholderia thailandensis E264
The cloning and characterization of the FK228 biosynthetic gene cluster (Cheng, Yang et al. 2007) lead to the identification of a biosynthetic gene cluster (designated tdp for thailandepsin) in the genome of Burkholderia thailandensis E264 (GenBank accession no. CP000085 and CP000086). The gene and deduced protein organizations of this tdp gene cluster resemble those of the dep gene cluster (
48/58f
31/41g
32/49h
aNumber of amino acids;
babbreviations are defined in text; subscript indicates the substrate specificity of enzymes;
fthe first 1489 aa;
gfirst 1174 aa between TdpC2 and DepC;
hfirst 367 aa of TdpE2 and DepE C-terminal end;
iinactive;
nnonfunctional.
Bacterial strains and plasmids. Burkholderia thailandensis E264 (ATCC 700388; a gram-negative motile rod bacterial species isolated from a rice paddy in Thailand; AmR KmR GmR smR PmR TcS) and E. coli were routinely cultured in Luria-Bertani (LB) broth or on LB agar at 37° C. For the construction of a targeted gene-disruption mutant, a suicide vector, pEX18Tc (TcR oriT* sacB, conjugative), originally developed for Pseudomonas aeruginosa genetics (Hoang, Karkhoff-Schweizer et al. 1998), was adopted and applied successfully in B. thailandensis.
Construction of a targeted gene-disruption mutant of B. thailandensis. General DNA manipulations, including plasmid preparation, restriction enzyme digestion, agarose gel electrophoresis, and bacterial transformation, were performed according to standard protocols (Sambrook and Russell 2000) or the manufacturer's instructions (New England BioLabs). Genomic DNA of the wild-type or mutant strain of B. thailandensis was prepared from an overnight culture with an UltraClean microbial DNA isolation kit (MO BIO Labs). An internal DNA fragment of tdpA was amplified from B. thailandensis genomic DNA with the following PCR primers: TdpA-KO-FP1, 5′-AGGTACCGCCTACGTGATCTTCACG-3′, containing a KpnI site (underlined); and TdpA-KO-RP1, 5′-CTAAGCTTGACCTGGCCGTCCATCC-3′, containing a HindIII site (underlined). Amplified product was purified from the PCR mixture with a QIAGEN PCR Purification kit, double digested with KpnI and HindIII, separated and re-purified from an agarose gel. A final 760-bp KpnI-HindIII product was cloned into the KpnI-HindIII sites of pEX18Tc to yield a gene disruption construct pDZ01-69a6. This construct was first transformed into E. coli S17-1 cells and then transferred into B. thailandensis cells by bacterial interspecies conjugation as follows.
Two bacterial strains, E. coli S17-1 (pDZ01-69a6) and B. thailandensis, were grown separately in 3 ml of LB medium supplemented with appropriate antibiotics (10 μg/ml tetracycline for E. coli S17-1 [pDZ01-69a6] and 50 μg/ml apramycin for B. thailandensis) at 37° C. with shaking until the late mid-log phase (6 to 8 h). Cells from 1 ml of each culture were collected by centrifugation at 4,000×g for 15 min at 4° C., and the cell pellets were washed once with 1 ml LB medium. Each cell pellet was finally resuspended in 100 μl of LB. Cell suspensions of two bacterial strains were then pooled and spread evenly on a wet 0.45-μm nitrocellulose membrane (Whatman) on LB agar supplemented with 10 mM MgSO4. After the plate had been incubated at 30° C. for 12 h to 16 h, the membrane seeded with bacteria was used to print several LB agar plates containing 100 μg/ml tetracycline and 50 μg/ml apramycin to select for vector-integrated mutant strain (designated Bth69a6; tdpA::pEX18Tc; TcR AmR). The correct integration of nonreplicative vector pEX18Tc into the B. thailandensis chromosome via homologous DNA recombination was examined and confirmed by PCR analysis.
Examination of the metabolic differences between wild-type and the Bth69a6 mutant strain of B. thailandensis. Gene tdpA is proposed to be involved in the biosynthesis of thailandepsins (
LC-MS analysis of crude extracts from the fermentation broths of wild-type and the Bth69a6 mutant strain of B. thailandensis revealed that three ion signals ([M+H]+ m/z 548.0, 534.0, and 515.9, respectively) were present in the crude extract of wild-type strain but were absent in the crude extract of Bth69a6 mutant strain (data not shown). This experiment indicated that disruption of tdpA gene resulted in the loss of production of three putative compounds in the mutant strain, and thus established a causal relationship between the genotype (tdpA gene) and the phenotype (production of three putative natural products).
Purification and identification of thailandepsins. Wild-type B. thailandensis E264 strain was fermented in a modified nutrient broth (1.0% glucose, 1.0% Difco nutrient broth, 0.5% NaCl, 0.1% CaCO3, pH 7.0) (8×500 ml) and in a modified YM-254890 medium (2.0% glycerol, 0.5% glucose, 0.5% peptone, 0.1% yeast extract, 0.1% NaCl, pH 7.0) (8×500 ml) at 37° C. for 4 days with shaking (160 rpm). Sterile resins, HP-20 and XAD-4 (for absorbing secreted metabolites), were added to culture to a final concentration of 2.5% (w/v) each at day 2. Resins and cells were collected at the end of fermentation by centrifugation and subsequently freeze-dried for 2 days. The dry mass was extracted with two volumes of methanol (w/v). Methanol extracts from two fermentation media were combined at this point and the solvent was removed under reduced pressure to give a crude extract. The crude extract was redissolved in methanol, fractionated and eluted by methanol through a Sephadex LH20 column, and four parts (B-1, B-2, B-3 and B-4) were collected manually, according to distinctive color zones. Part B-3 was further fractionated and eluted through a Sephadex LH20 column, to yield three fractions (B-3-1, B-3-2 and B-3-3). Fraction B-3-3 was then separated by preparative HPLC through an Rp-18 column (5 μm particles, 35 mm×250 mm) with a linear gradient (180 min from 15% to 60% methanol) and a flow rate of 7 ml/min. UV absorption signals were recorded at 210 nm wavelength by a diode array detection.
Three thailandepsin peaks were collected within 120 to 150 min of elution time window. Solvent was evaporated under reduced pressure and the purified thailandepsin samples were subjected to MS analysis (
This application claims priority to U.S. Provisional Application No. 60/888,851, filed Feb. 8, 2007, which is incorporated herein by reference in its entirety.
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/US2008/053473 | 2/8/2008 | WO | 00 | 8/6/2009 |
| Number | Date | Country | |
|---|---|---|---|
| 60888851 | Feb 2007 | US |
