Patent Grant
7098009
The subject invention relates to newly isolated organisms from nature that produce L(+)-lactic acid at high yield from hexose and pentose sugars. Organisms and processes or methods for the production of lactic acid and other industrially important chemicals are also provided.
Lactic acid is widely used in food, pharmaceutical and textile industries. It is also used as a source of lactic acid polymers which are being used as biodegradable plastics (Brown, S. F., 2003, Fortune, 148:92–94; Datta, R., et al., 1995, FEMS Microbiol. Rev. 16:221–231). The physical properties and stability of polylactides can be controlled by adjusting the proportions of the L(+)- and D(−)-lactides (Tsuji, F., 2002, Polymer 43:1789–1796). Optically pure lactic acid is currently produced by the fermentation of glucose derived from corn starch using various lactic acid bacteria (Carr, F. J., et al., 2002, Crit. Rev. Microbiol. 28:281–370; Hofvendahl, K. and Hahn-Hagerdal, B., 2000, Enz. Microb. Technol. 26:87–107). However, the fastidious lactic acid bacteria have complex nutritional requirements (Chopin, A., 1993, FEMS Microbiol. Rev. 12:21–38) and the use of corn as the feedstock competes directly with the food and feed uses.
Lignocellulosic biomass represents a potentially inexpensive and renewable source of sugars for fermentation (Duff, S. J. B. and Murray, W. D., 1996, Bioresource Technol. 55:1–33; Parajo, J. C., et al., 1996, Process Biochem. 31:271–280; Wyman, C. E., 1999, Ann. Rev. Energy Env. 24:189–226). The hemicellulose portion of biomass contains up to 35% of the total carbohydrate and can be readily hydrolyzed to monomeric sugars by dilute sulfuric acid (Saha, B. and Bothast, R. J., 1999, Appl. Biochem. Biotechnol. 76:65–77). With crop residues and hardwoods, this hemicellulose syrup contains primarily xylose. During acid hydrolysis, an assortment of microbial inhibitors is also produced which must be removed by treatment with lime (Amartey, S. and Jeffries, T., 1996, World J. Microbiol. Biotechnol. 12:281–283; Clark, T. A. and Mackie, K. L., 1984, J. Chem. Technol. Biotechnol. 34B:101–110; Martinez, A., et al., 2001, Biotechnol. Prog. 17:287–293).
Lactobacillus spp. are used extensively in industry for starch-based lactic acid production, the majority of which lack the ability to ferment pentose sugars such as xylose and arabinose (Carr, F. J., et al., 2002, Crit. Rev. Microbiol. 28:281–370). Although, Lactobacillus pentosus, Lb. brevis and Lactococcus lactis ferment pentoses to lactic acid, pentoses are metabolized using the phosphoketolase pathway which is inefficient for lactic acid production (Garde, A., et al., 2002, Bioresource Technol. 81:217–223; Tanaka, K., et al., 2002, Appl. Microbiol. Biotechnol. 60:160–167). In the phosphoketolase pathway, xylulose 5-phosphate is cleaved to glyceraldehyde 3-phosphate and acetyl-phosphate. With this pathway, the maximum theoretical yield of lactic acid is limited to one per pentose (0.6 g lactic acid per g xylose) due to the loss of two carbons to acetic acid.
We have recently isolated new organisms (sometimes referred to herein as “second generation biocatalysts”, “second generation organisms” or “biocatalyst(s)”) from nature that produce L(+) lactic acid at high yield from hexose and pentose sugars. These organisms have the added advantage of performing well under conditions that are optimal for cellulose enzymes (pH of about 5 and temperatures of about 50° C.). As the cost of cellulose enzymes is currently quite high, matching an organism that can produce a desired chemical compound from hexose and pentose sugars with optimal conditions for this enzyme offers the potential for considerable cost savings by reducing the amount of cellulose enzyme needed. Organisms provided by the subject invention can also ferment dilute acid hydrolysates of hemicellulose. Organisms can also ferment hemicellulose and cellulose sugars together in a single unified fermentation. The subject invention also provides organisms and processes or methods for the production of L(+)-lactic acid from cellulose and hemicellulose. Organisms of the subject invention can also be engineered for the production of additional products, such as (and not limited to), 1,3-propanediol, 1,2-propanediol, succinic acid, ethanol, and D(−)-lactic acid. The subject invention also provides polynucleotides and polypeptides encoding D-lactate dehydrogenase (d-ldh; D-LDH). Additionally, the subject invention also provides a DNA fragment that encodes pyruvate formate lyase (pfl; PFL).
These newly isolated organisms, as exemplified by Bacillus sp. strain 17C5, ferment sugars in hemicellulose hydrolysate to L(+)-lactic acid at high yields using a simple salts medium supplemented with 0.5% corn steep liquor. The L(+)-lactate product had an optical purity of greater than 99% and comprised 90% of the sugar weight. These organisms, and genetically modified derivatives thereof, can be used for the conversion of pentose-rich feedstocks such as corn stover, corn fiber, bagasse, rice hulls, rice straw, or other forms of biomass into commodity chemicals such as L(+)-lactic acid.
SEQ ID NOs: 1 and 2 are the polynucleotide and polypeptide sequences encoding D-lactate dehydrogenase (d-ldh; D-LDH).
SEQ ID NOs: 3–39 are nucleic acid sequences encoding 16S rRNA (partial; 525 nucleotides) of various isolates of the subject invention.
SEQ ID NOs: 40–42 are longer length nucleic acid sequences encoding 16S rRNA of isolates 36D1, 17C5 and P4-102B of the subject invention.
Table 1 provides locations from which organisms of the subject invention were isolated.
Table 2 illustrates various properties of organisms isolated according to the subject invention. Where Bacillus coagulans is indicated in the “Identification” column, this isolate is related to B. coagulans based on the first 500 bp of the 16s rRNA sequence; these organisms are not B. coagulans (on the basis of the 16S rRNA sequence analysis). Isolate Y56 is Bacillus smithii while isolate 57H2 is closely related to B. smithii. B. coagulans in the “Isolate” column represents an ATCC culture (ATCC 7050). T and W represent two different colony forms obtained from the culture. Additional legend information: blank space—indicates test not performed; CSL—corn steep liquor; GLU—glucose; HCH—hemicellulose hydrolysate; MS—minimal salts medium; XYL—xylose; YE—yeast extract; and +—denotes positive character for the growth or activity tested. An increase in the number of + signs represents an appropriate increase in the final cell yield of the culture. This same Table legend applies to all other Tables.
Table 3 shows various properties for Bacillus coagulans-like isolates that have been grouped on the basis of 16S rRNA sequences.
Table 4 provides growth and fermentation profiles of selected organisms in 3% glucose.
Table 5 illustrates growth and fermentation profiles of selected isolates in 3% xylose.
Table 6 shows fermentation profiles of various selected isolates in 5% sugars.
Table 7 relates to growth and fermentation profiles of selected isolates in minimal salts medium.
Table 8 provides growth and fermentation profiles of select isolates in hemicellulose hydrolysates.
Table 9 is a fermentation profile of 3% glucose in LB medium and in minimal medium with 1% corn steep liquor at pH 5.0 and 50° C. for isolates 17C5, 36D1, P4-102B, and P4-74B.
Table 10 is a fermentation profile of 3% xylose in LB medium and in minimal medium with 1% corn steep liquor at pH 5.0 and 50° C. for isolates 17C5, 36D1, P4-102B, and P4-74B.
Table 11 provides analysis of the lactic acid produced by isolates 17C5, 36D1, P4-102B, and P4-74B.
Table 12 provides 13C-enrichment ratios for fermentation products produced from 13C1-xylose.
Table 13 is the SSF profile of strain 36D1 in mineral salts medium at different pH and temperature.
Table 14 relates to sugar cane bagasse hemicellulose hydrolysate fermentation by Bacillus sp. strain 17C5.
Bacillus isolates 17C5, 36D1 and P4-102B were deposited with the American Type Culture Collection (10801 University Blvd., Manassas, Va. 20110-2209 USA) on Mar. 2, 2004 and have accession numbers PTA-5826, PTA-5827, and PTA-5828, respectively. In various embodiments, the subject invention provides isolates that have not been genetically modified (e.g., a non-transformed isolate selected from the group consisting of isolates 17C5, 36D1 and P4-102B). Also included within the scope of the subject invention are subclones, progeny, and subcultures of these isolates.
The culture deposited for the purposes of this patent application was deposited under conditions that assure that access to the culture is available during the pendency of this patent application to one determined by the Commissioner of Patents and Trademarks entitled thereto under 37 C.F.R. § 1.14 and 35 U.S.C. § 122. The deposit will be available as required by foreign patent laws in countries wherein counterparts of the subject application, or its progeny, are filed. However, it should be understood that the availability of a deposit does not constitute a license to practice the subject invention in derogation of patent rights granted by government action.
Further, the subject culture deposit will be stored and made available to the public in accord with the provisions of the Budapest Treaty for the deposit of biological materials, i.e., they will be stored with all the care necessary to keep them viable and uncontaminated for a period of at least five years after the most recent request for the furnishing of a sample of the deposit, and in any case, for a period of at least thirty (30) years after the date of deposit or for the enforceable life of any patent which may issue disclosing the culture. The depositor acknowledges the duty to replace the deposit should the depository be unable to furnish a sample when requested, due to the condition of a deposit. All restrictions on the availability to the public of the subject culture deposit will be irrevocably removed upon the granting of a patent disclosing it.
In one embodiment, the subject invention provides novel isolated Gram positive organisms capable of producing L(+) lactic acid at high yield from hexose and pentose sugars. In certain embodiments, the organisms are isolated from nature and have not been modified by recombinant DNA technologies. The organisms of the subject invention also have the added advantage of performing well under conditions that are optimal for cellulose enzymes, growing well in media maintained at a pH of about 5 and temperatures of 50° C.
Accordingly, one aspect of the subject invention provides for novel Gram positive organisms that have not been recombinantly modified, are isolated from nature and comprise at least one of, or any combination of, the following characteristics:
In certain embodiments of the subject invention, the novel organisms of the subject invention have at least two, three, four, five, six, seven, eight, nine, ten, eleven, twelve, or thirteen of the aforementioned characteristics. In other embodiments, the novel organisms of the subject invention have all fourteen of the aforementioned characteristics. As would be apparent to the skilled artisan, the organisms of the subject invention can have any combination of the aforementioned characteristics and the various combinations of these characteristics have not been set forth in this specification in the interests of not unduly lengthening the subject specification. Additionally, any of the aforementioned characteristics can be specifically included or excluded from the characteristics of organisms of the subject invention.
The subject invention also provides methods of isolating these organisms comprising the steps provided in
Thus, in one embodiment, a sample obtained from the environment is added to a composition comprising a sterile mineral salts solution and beads at a pH of about 5 to form a first liquid culture composition. For example, about 3–4 grams of a sample (for example a soil sample) is added to the sterile mineral salt solution and the subsequent incubation of the resulting mixture in a shaker at 50° C. for 3 hours to dislodge the bacteria from particles.
After the bacteria have been dislodged from particles, enrichment for cellulase-positive bacteria is performed according to methods known to the skilled artisan. For example, about 5 ml of the suspended particle sample can be added to 50 ml of a composition comprising mineral salts and yeast extract [mineral salts-yeast extract medium (1 g/L YE)] and a filter paper strip to form a first culture to form a second liquid culture composition. This second culture composition can be incubated in the shaker at 50° C. (100 RPM) and the filter paper structure monitored visually. After filter paper appears to be decomposed, a loopful of medium can be removed and streaked out for the isolation of colonies on complete medium containing 2 g/L Avicel or Sigmacel 50 cellulose. Dilutions, typically ten-fold dilutions, can also be made and the various dilutions plated on complete medium containing 2 g/L Avicel or Sigmacel 50 cellulose, a medium containing carboxymethylcellulose (CMC) and/or cellobiose (0.2%). Incubate all the plates at 50° C. in plastic boxes. Colonies thus isolated are then picked and tested for growth in Sigmacel plates and for filter paper hydrolysis in liquid medium (a third liquid culture composition) in tubes (e.g., 4 ml of medium with one strip of filter paper). After 48 and 96 hours of growth, the OD420 nm and pH of the cultures are determined.
Hemicellulose fermenting organisms can then be isolated using solid and/or liquid medium. Where solid medium is used, remove 1 ml of a sample from the suspended culture (third liquid culture composition) and make serial dilutions (e.g., 10-fold) in mineral salts solution. Spread 0.1 ml samples on xylose medium containing 10 g xylose per liter and incubate the plates at 50° C. overnight. Pick colonies to a new plate and grow overnight at 50° C. Streak the colonies for isolation on xylose medium and pick single colonies from each morphological type to store in glycerol and also patch for routine use. Isolates which are facultative can be tested for growth in the presence of 25% hemicellulose hydrolysate in plates as well as in medium containing overlimed hemicellulose hydrolysate.
When using liquid medium, add nutrients to the third liquid culture medium. In one embodiment, 5 ml of 10% xylose and 1 ml of 1% YE (pH 5, filter sterilized) can be added to 44 ml of the suspended sample in said third liquid culture medium to form a fourth liquid culture medium. Incubate said fourth liquid culture medium for 24 hours at 50° C., shaking. Remove a sample from said fourth liquid culture medium and make serial dilutions (e.g., 10-fold) in mineral salts solution. Spread 0.1 ml samples on xylose medium with 10 g xylose per liter and incubate the plates at 50° C., overnight. Pick colonies to a new plate and grow overnight at 50° C. and streak the colonies for isolation on xylose medium. Pick single colonies from each morphological type and store in glycerol and also patch for routine use.
In the analysis step of the subject method, each isolate can be tested for other properties in complete medium with 10 g/L xylose. These properties include, and are not limited to: 1) growth under aerobic and anaerobic conditions in rich medium as well as in minimal salts medium with or without supplements such as yeast extract or corn steep liquor at a starting pH of 5.0 or 6.8; 2) fermentation profile of facultative organisms; 3) growth in hemicellulose hydrolysate both overlimed as well as not-overlimed, at a starting pH of 5.0; 4) ethanol tolerance; 5) ability to grow at a starting medium pH of less than 5.0; 6) ability to produce xylanase; or 7) ability to hydrolyze crystalline cellulose (e.g., Avicel) as well as amorphous cellulose, carboxymethyl cellulose (CMC). In various embodiments of the subject invention, the organisms isolated according to these methods have at least one of the properties listed in this paragraph. Other embodiments provide for organisms of the subject invention to have any combination of 2, 3, 4, 5 or 6 of the aforementioned properties. Yet other embodiments provide for the identification of organisms, as well as isolated organisms, that all seven of the properties mentioned in this paragraph.
As set forth supra, isolated organisms of the subject invention can, as a characteristic, be classified into the unique phylogenetic group of organisms of the subject invention on the basis of 16S rRNA sequences. In this regard, the organisms are classified on the basis of the sequence of at least 50, 150, 200, 250, 300, 350, 400, 450, 500, 525, 550 or 600 consecutive nucleotides of the 16S rRNA sequence or on the basis of the full length 16S rRNA sequence. In this aspect of the invention, organisms can be compared against the 16S rRNA sequences provided in the appended sequence listing or the Ribosomal Database at web site: rdp.cme.msu.edu/html/citation.html. Organisms within the scope of the subject invention can have a similarity score of 1.00 or a similarity score of at least (or greater than) 0.95, 0.96, 0.97, 0.98, or 0.99. As discussed herein, organisms with a similarity score of 0.99 to 1.00 can be grouped within the same species with confidence. Methods for classifying organisms on the basis of 16S rRNA sequences are well known to those skilled in the art (and one method for such an analysis is provided in the Examples described herein). Specifically excluded from the scope of the instant invention are those organisms that can be, or are, classified as Bacillus coagulans, B. smithii, or B. coagulans, strain IDSp on the basis of the 16S rRNA sequence information.
The subject invention further provides genetically modified organisms useful for the production of industrially useful chemicals. Non-limiting examples of such chemicals include ethanol, 1,3-propanediol, 1,2-propanediol, succinic acid, and D(−)-lactic acid. In this embodiment of the invention, organisms isolated according to the methods taught herein are genetically modified to express those enzymes necessary for the production of a desired chemical. Sources of nucleic acids suitable for the transformation or genetic engineering of organisms of the subject invention can be obtained from the ATCC. “ATCC” refers to the American Type Culture Collection depository (P.O. Box 1549, Manassas, Va. 20108, USA). Alternatively, nucleotide sequences encoding the enzymes discussed in the following paragraphs can be obtained from other sources that include, and are not limited to, GENBANK, EMBL, or the NCBI database (maintained by the National Library of Medicine (USA)).
In one aspect of the invention, the organisms of the subject invention can be engineered to inactivate the L-lactate dehydrogenase (l-ldh) gene via methods known in the art (for example, chromosomal deletion, insertion or inactivation). Other genes may also be inactivated in the construction of recombinant organisms for use in the production of industrially useful chemicals. For example, genes encoding fumarate reductase (frd), alcohol/aldehyde dehydrogenase (adh), pyruvate formate lyase (pfl), acetate kinase gene (ack), and/or the phosphoenolpyruvate carboxylase (ppc) may be, optionally, inactivated. Other aspects of the invention allow for the use of organisms in which the l-ldh gene is, or other genes are, not inactivated; additionally, any of the aforementioned genes can be singly inactivated or any combination of said genes can be inactivated according to methods known in the art. The organisms can then be transformed with various vectors containing those genes necessary for the production of a desired chemical and recombinant organism and vectors are known in the art for the production of chemicals, such as the non-limiting examples provided infra.
For example, U.S. Pat. Nos. 6,136,576 and 6,025,184 (each of which is hereby incorporated by reference in its entirety) are directed to genetically engineered organisms that produce 1,3-propanediol and methods of producing such engineered organisms. Accordingly, isolated organisms of the subject invention can be engineered to produce 1-3-propanediol using the vectors taught therein. Alternatively, new vectors can be constructed that contain genes and/or enzymes taught in these patents that allow for the production of 1,3-propanediol in the organisms of the subject invention. For the production of 1,2-propanediol, vectors, genes, and/or enzymes taught in U.S. Pat. Nos. 6,303,352 and 6,087,140 (each of which is hereby incorporated by reference in its entirety) can be used to engineer organisms of the subject invention.
For the production of 1,3-propanediol, E. coli host cell W1485 harboring plasmids pDT20 and pAH42 (Accession Number ATCC 98188 and deposited in the ATCC under the terms of the Budapest Treaty) can be used as sources of nucleic acids that encode glycerol-3-phosphate dehydrogenase (G3PDH), glycerol-3-phosphatase (G3Phosphatase), glycerol dehydratase (dhaB), and 1,3-propanediol oxidoreductase (dhaT). Alternatively, S. cerevisiae YPH500 (deposited as ATCC 74392 under the terms of the Budapest Treaty) harboring plasmids pMCK10, pMCK17, pMCK30 and pMCK35 containing genes encoding glycerol-3-phosphate dehydrogenase (G3PDH), glycerol-3-phosphatase (G3P phosphatase), glycerol dehydratase (dhaB), and 1,3-propanediol oxidoreductase (dhaT) can be used as a source of genetic material for the production of recombinant organisms capable of producing 1,3-propanediol. Yet another source of readily available genetic material for the production of recombinant organisms capable of producing 1,3-propanediol is E. coli DH5α containing pKP1 which has about 35 kb insert of a Klebsiella genome which contains glycerol dehydratase, protein X and proteins 1, 2 and 3 (deposited with the ATCC under the terms of the Budapest Treaty and designated ATCC 69789); E. coli DH5α cells containing pKP4 comprising a portion of the Klebsiella genome encoding diol dehydratase enzyme, including protein X was deposited with the ATCC under the terms of the Budapest Treaty and was designated ATCC 69790. Preferred enzymes for the production of 1,2-propanediol are aldose reductase, glycerol dehydrogenase, or both. Exemplary sources of these enzymes are rat lens aldose reductase and E. coli glycerol dehydrogenase. Aldose reductase sequences are highly conserved, thus the source of the aldose reductase gene is not critical to the present invention. The source of the glycerol dehydrogenase gene is not critical. Other genes that can be used in the practice of this aspect of the invention include: carbonyl reductase (EC 1.1.1.84), glycerol dehydrogenase (EC 1.1.1.6, EC 1.1.1.156), aldehyde reductase (EC 1.1.1.2), methylglyoxal reductase (also known as 2-oxoaldehyde reductase and lactaldehyde dehydrogenase, EC 1.1.1.78), L-glycol dehydrogenase (EC 1.1.1.185), alcohol dehydrogenase EC 1.1.1.1, EC 1.1.1.2), 1,2-propanediol dehydrogenase, (lactaldehyde reductase, EC 1.1.1.55), and 1,2-propanediol oxidoreductase, (lactaldehyde reductase, EC 1.1.1.77).
Where succinic acid is a contemplated end product for production by recombinant organisms of the subject invention, the methods and materials of U.S. Patent Application Publication No. US 2003/0017559 A1 (which is hereby incorporated by reference in its entirety) can be used in the engineering of organisms provided by the subject invention. The inactivation of genes, such as l-ldh, pta, adh, ack, and pfl of the organisms of the subject invention, can be, optionally, inactivated in the engineered organisms. In one embodiment, pfl and ldh (and, optionally pts) genes are inactivated in the cells provided by the subject invention to redirect the metabolic products into the metabolic pathways that produce succinic acid (succinate). The production of succinic acid can be further enhanced by the optional addition of one or more heterologous genes encoding malic enzyme and/or fumarate reductase to the cells of the invention by recombinant means known to those skilled in the art.
Engineering of D(−)-lactic acid production into organisms of the subject invention can be performed according to the teachings of Zhou et al. ((Applied and Environmental Microbiology, 2003, 69(1):399–407) which is hereby incorporated by reference in its entirety). Briefly, genes encoding L-lactate dehydrogenase (l-ldh), fumarate reductase (frd), alcohol/aldehyde dehydrogenase (adh), and pyruvate formate lyase (pfl) are, optionally, inactivated by chromosomal deletion. In some embodiments, the acetate kinase gene (ack) can be mutated or inactivated to further increase yields. Cells are then engineered with the D-lactate dehydrogenase gene, provided in SEQ ID No: 1.
In the production of ethanol, the organisms of the subject invention can be engineered with nucleic acids, such as those disclosed in U.S. Pat. No. 5,000,000 (which is hereby incorporated by reference in its entirety). In this aspect of the invention, the d-ldh, l-ldh, ppc, ack, pfl genes of organisms provided by the subject invention are, optionally, inactivated. Organisms can then be transformed with the nucleic acids taught in this patent can then be used in methods of producing ethanol. For example, genes coding for the alcohol dehydrogenase II and pyruvate decarboxylase activities together with appropriate regulatory sequences are used to transform host cells provided by the subject invention (the regulatory sequences may consist of promoters, inducers, operators, ribosomal binding sites, terminators, and/or other regulatory sequences).
The subject invention provides methods of making an industrially useful chemical comprising the steps of: a) providing a recombinant or non-recombinant organism having at least one of the characteristics set forth for isolated organisms provided by the subject invention (or any combination of said characteristics); and b) culturing said microorganism in the presence of at least one carbon source capable of being converted to said industrially useful chemical under conditions suitable for the production of said chemical. The method may further comprise the optional step of recovering the industrially useful chemical. Non-limiting examples of chemical compounds that can be produced according to the subject invention include L(+)-lactic acid, 1,3-propanediol, 1,2-propanediol, succinic acid, ethanol and D(−)-lactic acid.
In various aspects of the aforementioned methods of making industrially useful compounds, any variety of carbon sources can be used. In certain aspects of the invention, the carbon source is a hexose or pentose sugar. Non-limiting examples of these sugars include glucose, galactose, mannose, xylose, and arabinose. Optionally, the carbon source can be a disaccharide, such as cellobiose. Other carbon sources useful in the practice of the subject invention include lignocellulose; hemicellulose hydrolysates from sugar cane bagasse, corn fiber, corn stover, straw, or other forms of hardwood, softwood or agricultural residue; and/or crystalline cellulose. Conditions useful in the aforementioned methods include maintaining a pH of between 4 and 6, 4.5 and 5.5, or a pH of about 5 and temperatures ranging from 45° C. to 60° C., 45° C. to 55° C., or temperatures that are maintained at about 50° C. The pH of fermentation systems used in the production of industrially useful chemicals as taught herein can be maintained according to well-known methods in the art (e.g., pH stats).
The subject invention further provides nucleic acid and polypeptide sequence for newly isolated enzyme D-lactate dehydrogenase (d-ldh; D-LDH [see SEQ ID Nos: 1–2]). The subject invention also provides a nucleic acid fragment derived from organisms disclosed herein that encodes a pyruvate formate lyase pfl; PFL). This polynucleotide fragment was derived from isolate P4-102B (ATCC PTA-5828) and was obtained using Sau3A as a restriction enzyme. The fragment is about 4 kilobases in length and has been used to reconstitute PFL activity in a strain of E. coli that is defective in this regard (the plasmid containing this insert was able to complement an E. coli pflB mutant). Of course, other restriction enzymes can be used to obtain polynucleotide fragments encoding PFL and these various polynucleotide fragments can be screened (according to methods known in the art) in organisms that are pfl defective to determine if they are able to reconstitute PFL function. The subject invention also encompasses degenerate polynucleotide sequences that encode the PFL and D-LDH enzymes provided herein. Degenerate polynucleotide sequences for these enzymes can be obtained by inputting the amino acids sequences provided herein into a variety of commercially available software suites. Non-limiting examples of such software suites include: Bio/Chem Lab Assistant (Dundee Scientific Ltd., Dundee Scotland UK) or DNATools (available for download at crc.dk/dnatools/dnatools.htm).
Accordingly, the subject invention further provides:
Nucleotide sequence, polynucleotide or nucleic acid are understood to mean, according to the present invention, either a double-stranded DNA, a single-stranded DNA or products of transcription of the said DNAs (e.g., RNA molecules).
As indicated supra, the subject invention also provides nucleotide sequences complementary to the sequences disclosed herein. Thus, the invention is understood to include any DNA whose nucleotides are complementary to those of the sequence of the invention, and whose orientation is reversed (e.g., anti-sense sequences). These sequences may be complementary over the full length of the nucleic acids that encode the PFL and D-LDH enzymes or over fragments of these nucleic acids.
The present invention further comprises fragments of the sequences of the instant invention as well as fragments of the gene products contained within the polynucleotide sequences provided herein. Representative fragments of the polynucleotide sequences according to the invention will be understood to mean any nucleotide fragment having at least 8 successive nucleotides, preferably at least 12 successive nucleotides, and still more preferably at least 15 or at least 20 successive nucleotides of the sequence from which it is derived. The upper limit for such fragments is the total number of polynucleotides found in the full length sequence (or, in certain embodiments, of the full length open reading frame (ORF) identified herein). It is understood that such fragments refer only to portions of the disclosed polynucleotide sequences that are not listed in a publicly available database.
In some embodiments, the subject invention includes those fragments capable of hybridizing under stringent conditions with a nucleotide sequence according to the invention. Hybridization under conditions of high or intermediate stringency, are defined below. Thus, conditions are chosen such that they allow hybridization to be maintained between two complementary DNA fragments. Hybridization conditions described above for a polynucleotide of about 300 bases in size can be adapted by persons skilled in the art for larger- or smaller-sized oligonucleotides, according to the teaching of Sambrook et al., 1989.
The nucleic acid sequences described herein have other uses as well. For example, the nucleic acids of the subject invention can be useful as probes to identify complementary sequences within other nucleic acid molecules or genomes. Such use of probes can be applied to methods to identify or distinguish organisms. As is well known in the art, probes can be made by labeling the nucleic acid sequences of interest according to accepted nucleic acid labeling procedures and techniques.
Various degrees of stringency of hybridization can be employed. The more severe the conditions, the greater the complimentarily that is required for duplex formation. Severity of conditions can be controlled by temperature, probe concentration, probe length, ionic strength, time, and the like. Preferably, hybridization is conducted under moderate to high stringency conditions by techniques well known in the art, as described, for example, in Keller, G. H., M. M. Manak [1987] DNA Probes, Stockton Press, New York, N.Y., pp. 169–170.
Examples of various stringency conditions are provided herein. Hybridization of immobilized DNA on Southern blots with 32P-labeled gene-specific probes can be performed by standard methods (Maniatis et al. [1982] Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory, New York). In general, hybridization and subsequent washes can be carried out under moderate to high stringency conditions that allow for detection of target sequences with homology to the exemplified polynucleotide sequence. For double-stranded DNA gene probes, hybridization can be carried out overnight at 20–25° C. below the melting temperature (Tm) of the DNA hybrid in 6×SSPE, 5×Denhardt's solution, 0.1% SDS, 0.1 mg/ml denatured DNA. The melting temperature is described by the following formula (Beltz et al. [1983] Methods in Enzymology, R. Wu, L. Grossman and K. Moldave [eds.] Academic Press, New York 100:266–285).
Tm=81.5° C.+16.6 Log[Na+]+0.41(% G+C)−0.61(% formamide)−600/length of duplex in base pairs.
Washes are typically carried out as follows:
For oligonucleotide probes, hybridization can be carried out overnight at 10–20° C. below the melting temperature (Tm) of the hybrid in 6×SSPE, 5×Denhardt's solution, 0.1% SDS, 0.1 mg/ml denatured DNA. Tm for oligonucleotide probes can be determined by the following formula:
Tm (° C.)=2(number T/A base pairs)+4(number G/C base pairs)
(Suggs et al. [1981] ICN-UCLA Symp. Dev. Biol. Using Purified Genes, D. D. Brown [ed.], Academic Press, New York, 23:683–693).
Washes can be carried out as follows:
In general, salt and/or temperature can be altered to change stringency. With a labeled DNA fragment >70 or so bases in length, the following conditions can be used:
By way of another non-limiting example, procedures using conditions of high stringency can also be performed as follows: Pre-hybridization of filters containing DNA is carried out for 8 h to overnight at 65° C. in buffer composed of 6×SSC, 50 mM Tris-HCl (pH 7.5), 1 mM EDTA, 0.02% PVP, 0.02% Ficoll, 0.02% BSA, and 500 μg/ml denatured salmon sperm DNA. Filters are hybridized for 48 h at 65° C., the preferred hybridization temperature, in pre-hybridization mixture containing 100 μg/ml denatured salmon sperm DNA and 5–20×106 cpm of 32P-labeled probe. Alternatively, the hybridization step can be performed at 65° C. in the presence of SSC buffer, 1×SSC corresponding to 0.15M NaCl and 0.05 M Na citrate. Subsequently, filter washes can be done at 37° C. for 1 h in a solution containing 2×SSC, 0.01% PVP, 0.01% Ficoll, and 0.01% BSA, followed by a wash in 0.1×SSC at 50° C. for 45 min. Alternatively, filter washes can be performed in a solution containing 2×SSC and 0.1% SDS, or 0.5×SSC and 0.1% SDS, or 0.1×SSC and 0.1% SDS at 68° C. for 15 minute intervals. Following the wash steps, the hybridized probes are detectable by autoradiography. Other conditions of high stringency which may be used are well known in the art and as cited in Sambrook et al., 1989, Molecular Cloning, A Laboratory Manual, Second Edition, Cold Spring Harbor Press, N.Y., pp. 9.47–9.57; and Ausubel et al., 1989, Current Protocols in Molecular Biology, Green Publishing Associates and Wiley Interscience, N.Y. are incorporated herein in their entirety.
Another non-limiting example of procedures using conditions of intermediate stringency are as follows: Filters containing DNA are pre-hybridized, and then hybridized at a temperature of 60° C. in the presence of a 5×SSC buffer and labeled probe. Subsequently, filters washes are performed in a solution containing 2×SSC at 50° C. and the hybridized probes are detectable by autoradiography. Other conditions of intermediate stringency which may be used are well known in the art and as cited in Sambrook et al., 1989, Molecular Cloning, A Laboratory Manual, Second Edition, Cold Spring Harbor Press, N.Y., pp. 9.47–9.57; and Ausubel et al., 1989, Current Protocols in Molecular Biology, Green Publishing Associates and Wiley Interscience, N.Y. are incorporated herein in their entirety.
Duplex formation and stability depend on substantial complimentarily between the two strands of a hybrid and, as noted above, a certain degree of mismatch can be tolerated. Therefore, the probe sequences of the subject invention include mutations (both single and multiple), deletions, insertions of the described sequences, and combinations thereof, wherein said mutations, insertions and deletions permit formation of stable hybrids with the target polynucleotide of interest. Mutations, insertions and deletions can be produced in a given polynucleotide sequence in many ways, and these methods are known to an ordinarily skilled artisan. Other methods may become known in the future.
It is also well known in the art that restriction enzymes can be used to obtain functional fragments of the subject DNA sequences. For example, Bal31 exonuclease can be conveniently used for time-controlled limited digestion of DNA (commonly referred to as “erase-a-base” procedures). See, for example, Maniatis et al. [1982] Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory, New York; Wei et al. [1983] J. Biol. Chem. 258:13006–13512.
Thus, the subject invention also provides nucleic acid based methods for the identification of the presence of the pfl and d-ldh genes in an organism or a sample. These methods can utilize the nucleic acids of the subject invention and are well known to those skilled in the art (see, for example, Sambrook et al. (1989). Among the techniques useful in such methods are enzymatic gene amplification (or PCR), Southern blots, Northern blots, or other techniques utilizing hybridization for the identification of polynucleotide sequences in a sample.
The subject invention also provides for modified nucleotide sequences. Modified nucleic acid sequences will be understood to mean any nucleotide sequence that has been modified, according to techniques well known to persons skilled in the art, and exhibiting modifications in relation to the native, naturally occurring nucleotide sequences. One non-limiting example of a “modified nucleotide sequences” includes mutations in regulatory and/or promoter sequences of a polynucleotide sequence that result in a modification of the level of expression of the polypeptide. A modified nucleotide sequence will also be understood to mean any nucleotide sequence encoding a modified polypeptide as defined below.
The subject invention also provides detection probes (e.g., fragments of the disclosed polynucleotide sequences) for hybridization with a target sequence or the amplicon generated from the target sequence. Such a detection probe will advantageously have as sequence a sequence of at least 12, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, or 100 nucleotides. The detection probes can also be used as labeled probe or primer in the subject invention. Labeled probes or primers are labeled with a radioactive compound or with another type of label. Alternatively, non-labeled nucleotide sequences may be used directly as probes or primers; however, the sequences are generally labeled with a radioactive element (32P, 33P, 35S, 3H, 125I) or with a molecule such as biotin, acetylaminofluorene, digoxigenin, 5-bromo-deoxyuridine, or fluorescein to provide probes that can be used in numerous applications.
The nucleotide sequences according to the invention may also be used in analytical systems, such as DNA chips. DNA chips and their uses are well known in the art and (see for example, U.S. Pat. Nos. 5,561,071; 5,753,439; 6,214,545; Schena et al., BioEssays, 1996, 18:427–431; Bianchi et al., Clin. Diagn. Virol., 1997, 8:199–208; each of which is hereby incorporated by reference in their entireties) and/or are provided by commercial vendors such as Affymetrix, Inc. (Santa Clara, Calif.).
Another aspect of the invention provides vectors for the cloning and/or the expression of a polynucleotide sequence taught herein. Vectors of this invention can also comprise elements necessary to allow the expression and/or the secretion of the said nucleotide sequences in a given host cell. The vector can contain a promoter, signals for initiation and for termination of translation, as well as appropriate regions for regulation of transcription. In certain embodiments, the vectors can be stably maintained in the host cell and can, optionally, contain signal sequences directing the secretion of translated protein. These different elements are chosen according to the host cell used. Vectors can integrate into the host genome or, optionally, be autonomously-replicating vectors.
The subject invention also provides for the expression of a polypeptide, peptide, derivative, or analog encoded by a polynucleotide sequence disclosed herein. The disclosed sequences can also be regulated by a second nucleic acid sequence so that the protein or peptide is expressed in a host transformed with the recombinant DNA molecule. For example, expression of a protein or peptide may be controlled by any promoter/enhancer element known in the art. Promoters which may be used to control expression include, but are not limited to, the CMV promoter, the SV40 early promoter region (Bemoist and Chambon, 1981, Nature 290:304–310), the promoter contained in the 3′ long terminal repeat of Rous sarcoma virus (Yamamoto, et al., 1980, Cell 22:787–797), the herpes thymidine kinase promoter (Wagner et al., 1981, Proc. Natl. Acad. Sci. U.S.A. 78:1441–1445), the regulatory sequences of the metallothionein gene (Brinster et al, 1982, Nature 296:39–42); prokaryotic vectors containing promoters such as the β-lactamase promoter (Villa-Kamarof, et al., 1978, Proc. Natl. Acad. Sci. U.S.A. 75:3727–3731), or the tac promoter (DeBoer, et al., 1983, Proc. Natl. Acad. Sci. U.S.A. 80:21–25); see also “Useful proteins from recombinant bacteria” in Scientific American, 1980, 242:74–94; plant expression vectors comprising the nopaline synthetase promoter region (Herrera-Estrella et al., 1983, Nature 303:209–213) or the cauliflower mosaic virus 35S RNA promoter (Gardner, et al., 1981,Nucl. Acids Res. 9:2871), and the promoter of the photosynthetic enzyme ribulose bisphosphate carboxylase (Herrera-Estrella et al., 1984, Nature 310:115–120); promoter elements from yeast or fungi such as the Gal 4 promoter, the ADC (alcohol dehydrogenase) promoter, PGK (phosphoglycerol kinase) promoter, and/or the alkaline phosphatase promoter
The vectors according to the invention are, for example, vectors of plasmid or viral origin. In a specific embodiment, a vector is used that comprises a promoter operably linked to a protein or peptide-encoding nucleic acid sequence contained within the disclosed polynucleotide sequences, one or more origins of replication, and, optionally, one or more selectable markers (e.g., an antibiotic resistance gene). Expression vectors comprise regulatory sequences that control gene expression, including gene expression in a desired host cell. Exemplary vectors for the expression of the polypeptides of the invention include the pET-type plasmid vectors (Novagen) or pBAD plasmid vectors (Invitrogen) or those provided in the examples below. Furthermore, the vectors according to the invention are useful for transforming host cells so as to clone or express the nucleotide sequences of the invention.
The invention also encompasses the host cells transformed by a vector according to the invention. These cells may be obtained by introducing into host cells a nucleotide sequence inserted into a vector as defined above, and then culturing the said cells under conditions allowing the replication and/or the expression of the transfected nucleotide sequence.
The host cell may be chosen from eukaryotic or prokaryotic systems, such as for example bacterial cells, (Gram negative or Gram positive), yeast cells, animal cells (such as Chinese hamster ovary (CHO) cells), plant cells, and/or insect cells using baculovirus vectors. In some embodiments, the host cells for expression of the polypeptides include, and are not limited to, those taught in U.S. Pat. Nos. 6,319,691, 6,277,375, 5,643,570, or 5,565,335, each of which is incorporated by reference in its entirety, including all references cited within each respective patent.
Furthermore, a host cell strain may be chosen which modulates the expression of the inserted sequences, or modifies and processes the gene product in the specific fashion desired. Expression from certain promoters can be elevated in the presence of certain inducers; thus, expression of the genetically engineered polypeptide may be controlled. Furthermore, different host cells have characteristic and specific mechanisms for the translational and post-translational processing and modification (e.g., glycosylation, phosphorylation) of proteins. Appropriate cell lines or host systems can be chosen to ensure the desired modification and processing of the foreign protein expressed. For example, expression in a bacterial system can be used to produce an unglycosylated core protein product. Expression in yeast will produce a glycosylated product. Expression in mammalian cells can be used to ensure “native” glycosylation of a heterologous protein. Furthermore, different vector/host expression systems may effect processing reactions to different extents.
The subject invention also provides one or more isolated polypeptides comprising:
The subject invention also provides fragments of at least 5 amino acids of a polypeptide encoded by the polynucleotides of the instant invention. In some embodiments, the polypeptide fragments are reactive with antibodies generated against the full-length polypeptides set forth in the immediately preceding paragraph. In the context of the instant invention, the terms polypeptide, peptide and protein are used interchangeably; however, it should be understood that the invention does not relate to the polypeptides in natural form, that is to say that they are not taken in their natural environment but that they may have been isolated or obtained by purification from natural sources, obtained from host cells prepared by genetic manipulation (e.g., the polypeptides, or fragments thereof, are recombinantly produced by host cells, or by chemical synthesis). Polypeptides according to the instant invention may also contain non-natural amino acids, as will be described below.
A homologous (or modified) polypeptide will be understood to designate a polypeptide exhibiting, in relation to the natural polypeptide, certain modifications. These modifications can include a deletion, addition, or substitution of at least one amino acid, a truncation, an extension, a chimeric fusion, a mutation, or polypeptides exhibiting post-translational modifications. Among the homologous polypeptides, those whose amino acid sequences exhibit between at least (or at least about) 20.00% to 99.99% (inclusive) identity to the native, naturally occurring polypeptide are another aspect of the invention. The aforementioned range of percent identity is to be taken as including, and providing written description and support for, any fractional percentage, in intervals of 0.01%, between 20.00% and, up to, including 99.99%. These percentages are purely statistical and differences between two polypeptide sequences can be distributed randomly and over the entire sequence length.
Homologous polypeptides can, alternatively, have 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87, 88, 89, 90, 91, 92, 93, 94, 95, 96, 97, 98, or 99 percent identity with the polypeptide sequences of the instant invention. The expression equivalent amino acid is intended here to designate any amino acid capable of being substituted for one of the amino acids in the basic structure without, however, essentially modifying the biological activities of the corresponding peptides (e.g., its enzymatic activity).
By way of example, amino acid substitutions can be carried out without resulting in a substantial modification of the biological activity of the corresponding modified polypeptides; for example, the replacement of leucine with valine or isoleucine, of aspartic acid with glutamic acid, of glutamine with asparagine, of arginine with lysine, and the like, the reverse substitutions can be performed without substantial modification of the biological activity of the polypeptides.
In other specific embodiments, the polypeptides, peptides or derivatives, or analogs thereof may be expressed as a fusion, or chimeric protein product (comprising the protein, fragment, analog, or derivative joined via a peptide bond to a heterologous protein sequence (e.g., a different protein)). Such a chimeric product can be made by ligating the appropriate nucleic acid sequences encoding the desired amino acid sequences to each other by methods known in the art, in the proper coding frame, and expressing the chimeric product by methods commonly known in the art. Alternatively, such a chimeric product may be made by protein synthetic techniques, e.g., by use of a peptide synthesizer.
The subject invention further provides antibodies to the polypeptides of SEQ ID NOs 2 or the fragments thereof. These antibodies can be used in any variety of methods including affinity purification of the PFL and D-LDH enzymes (or related enzymes). Other uses for such antibodies including contacting a sample with the antibodies and assaying for the presence of an antigen-antibody complex. In this aspect of the invention, either the antibodies to the PFL and D-LDH enzymes can be directly labeled with a marker or another antibody that is appropriately labeled can be used to detect the presence of an antibody-antigen complex.
The terms “comprising”, “consisting of” and “consisting essentially of” are defined according to their standard meaning. The terms may be substituted for one another throughout the instant application in order to attach the specific meaning associated with each term.
All percentages are by weight and all solvent mixture proportions are by volume unless otherwise noted. It should be understood that the examples and embodiments described herein are for illustrative purposes only and that various modifications or changes in light thereof will be suggested to persons skilled in the art and are to be included within the spirit and purview of this application and the scope of the appended claims. All publications, patents, and/or patent applications cited in this patent application are hereby incorporated by reference in their entireties.
Isolation and Characterization of Organisms
Environmental samples from 77 locations (Table 1) were collected and bacteria which grew in xylose medium at a pH of 5.0 and at 50° C. were isolated. The protocol followed for the enrichment and isolation is presented in
Characteristics analyzed included: 1) Growth under aerobic and anaerobic conditions in rich medium as well as in minimal salts medium (with or without supplements such as yeast extract or corn steep liquor) at a starting pH of 5.0 or 6.8; 2) Fermentation profile of facultative organisms; 3) Growth in hemicellulose hydrolysate (both overlimed and not-overlimed) at a starting pH of 5.0; 4) Ethanol tolerance; 5) Ability to grow at a starting medium pH of less than 5.0; 6) Ability to produce xylanase; and 7) Ability to hydrolyze crystalline cellulose (Avicel) as well as amorphous cellulose, carboxymethyl cellulose (CMC).
Based on the growth characteristics, 100 isolates were found to be strict aerobes when grown at pH 5.0. However, 27 of these 100 isolates grew under anaerobic conditions when the starting pH of the medium was increased to 6.8. This difference could be related to the inability of the isolates to grow when the medium pH dropped below 4.5 since the medium pH of all the isolates decreased from a starting pH of 5.0 to less than 4.5 within 6 hours even during aerobic growth. This decrease in pH is due to the accumulation of lactate in the medium. When cultured in glucose-supplemented medium, all the isolates produced lactate as the main fermentation product. With xylose as the carbon source, lactate was still the major fermentation product but small amounts of acetate, ethanol and, with some isolates, formate were detected. The presence of formate in the spent medium suggests that during xylose-dependent growth, pyruvate formate lyase is also produced by the isolates.
Sixteen of the isolates produced cellulase activity based on hydrolysis of carboxymethyl cellulose. These cellulase-positive isolates did not hydrolyze crystalline cellulose such as Avicel or Sigmacel. All 16 cellulolytic isolates are strict aerobes. Seventeen isolates produced xylanase activity detected as hydrolysis of remazol brilliant blue R-o-xylan (RBB-xylan). Five of the xylanase-positive isolates are also facultative anaerobes.
Based on the growth characteristics of these isolates under anaerobic conditions in a glucose or xylose medium as well as in various other media (Table 2), 44 of the 380 isolates were selected for identification using the sequence of first 500 bases of the DNA coding for the 16S rRNA. 16S rRNA gene sequence was determined by MIDI Labs using their specific protocol for isolating and sequencing 16S rRNA gene from bacteria. Specifically, the 16S rRNA gene was PCR amplified from genomic DNA using primers corresponding to E. coli positions 005 and 531. This PCR product is expected to be about 500 base pairs of the first part of the 16S rRNA gene. The DNA after amplification was sequenced by cycle-sequencing using AmpliTaq FS DNA polymerase and dRhodamine dye terminators. The DNA sequence was obtained after electrophoresis on an ABI Prism DNA sequencer and analyzed using PE/Applied Biosystems DNA editing and assembly software. These sequences are presented in SEQ ID # 3–39.
Similar methods were used to determine 16S rRNA(DNA) sequence of over 1500 bp. The primers used correspond to E. coli positions 005 and 1540 by the MIDI Labs for isolates 17C5 and Bacillus coagulans ATCC 7050 (ATCC type strain for B. coagulans). Sequence of over 1500 bp for 16S rRNA(DNA) for strains 36D1 and P4-102B were determined at the University of Florida, Dept. of Microbiology and Cell Science DNA sequencing facility. Appropriate DNA was PCR-amplified using two primers based on E. coli 16S rRNA sequence; Primer 1, GAGTTTGATCCTGGCTCAG (SEQ ID No: 43); Primer 2, AGAAAGGAGGTGATCCAGCC (SEQ ID No: 44) (Suzuki, T. and Yamasato, K. (1994) Phylogeny of spore-forming lactic acid bacteria based on 16S rRNA gene sequences, FEMS Microbiol. Letters 115:13–18). The amplified product was cloned into vector plasmid PCR-II TOPO (Invitrogen) and sequenced. The DNA insert was also sub-cloned into vector plasmid pUC19 for convenience of sequencing. These three sequences are presented in SEQ ID # 40–42. DNA sequence was analyzed for sequence similarity using the Ribosomal Database Project II (web site rdp.cme.msu.edu/html/citation.html) (Cole J R, Chai B, Marsh T L, Farris R J, Wang Q, Kulam S A, Chandra S, McGarrell D M, Schmidt T M, Garrity G M, Tiedje J M. The Ribosomal Database Project (RDP-II): previewing a new autoaligner that allows regular updates and the new prokaryotic taxonomy. 2003. Nucleic Acids Research 31(1):442–443).
Using the RDP database, the similarity scores between the closest Bacillus organism (B. coagulans IDSP) and three isolates (17C5, 36D1 and P4-102B; SEQ ID# 40–42) were determined. These values are 0.978 (17C5), 0.969 (36D1) and 0.975 (P4-102B). A similarity score between 0.99 and 1.000 would indicate that the two bacteria can be grouped with confidence in the same species. A similarity score of 0.97 or lower suggests that the two bacteria can only be identified at the genus level with confidence. (Suzuki, T. and K. Yamasato. 1994. Phylogeny of spore-forming lactic acid bacteria based on 16S rRNA gene sequences. FEMS Microbiol. Letters 115:13–18). The similarity scores between the current isolates and RDP database entries which are also Bacillus coagulans type strains from various collections vary from 0.87 to 0.95. Thus, it is difficult to group these new isolates at the species level with Bacillus coagulans strictly based on 16S rRNA gene sequence information. It is possible that these new isolates represent a new Bacillus species closely related to Bacillus coagulans. Phylograms representing 38 of the 44 isolates is presented in
An authentic Bacillus coagulans obtained from American Type Culture Collection (ATCC 7050) (Hammer, B. W., 1915. Iowa Agric. Exp. Stn. Res. Bull. 19:119–131) was found to be xylose-negative and also differed in other physiological properties. The 37 B. coagulans-like isolates can be grouped into 12 groups (
Thirty two of the 41 identified isolates completely fermented the 1% glucose or xylose present in the medium within 24 hours in a pH-stat operating at pH 5.0 and at 50° C. (Table 3). Recovery of glucose carbon in products was about 95% with lactate accounting for about 90% to 100% of the fermentation products produced by the glucose cultures. Significant amounts of acetate, formate and ethanol were also produced by these isolates when xylose served as the C-source. For example, isolate 18C2 converted 93% of glucose and 98% of xylose to products when grown in rich medium with 1% sugar. Under these conditions, lactate fraction of the total products was 95% with glucose and 77% with xylose.
Based on the rate of sugar utilization (1%) in the pH-stat, as well as other physiological characteristics, 76 isolates were selected for detailed fermentation analysis. When the sugar concentration in the rich medium was increased to 3%, 7 isolates converted both glucose and xylose to products within 48 hours; isolates 13E1L, 36D1, HCH8, Y40, P4-74B, P4-85 and P4-102B (Tables 4 & 5). When analyzed after 72 hours of growth and fermentation, 5 additional isolates were also found to ferment 3% of glucose and xylose to completion (isolates 3F2, 17C5, HCH7, HCH10 and Y55). These 12 isolates fermented glucose to lactate with a conversion efficiency of about 85–90%. Lactate accounted for more than 95% of the total products produced from glucose. The lactate produced by 15 isolates was found to be L-(+)-lactate by HPLC analysis and the highest amount of lactate produced by these isolates was about 0.30 M (27 g/L lactic acid). When grown with xylose, the lactate fraction of the fermentation products only accounted for about 80% of the total while the remainder included acetate, ethanol, formate and small amounts of succinate.
Fourteen isolates were further tested for their ability to ferment 5% sugar in the same rich medium. Increasing the sugar concentration to 5% also increased the lactate production. With one exception (isolate P4-102B) none of the isolates completely fermented the added sugar (Table 6). The highest level of lactate produced by isolate P4-102B grown in LB+ glucose (5%) was about 0.45 M (40.5 g/L lactic acid). Trace amounts of ethanol and acetate were also detected in the fermentation broths. Most of the other isolates produced varying levels of lactate ranging from 0.25 to 0.4 M. Again, lactate accounted for more than 95% of the products from glucose. The fermentation profile of the isolates grown in 5% xylose was not different from that obtained at lower xylose concentration and the highest amount of lactate detected was about 0.34 M (Table 6).
These isolates were also grown in minimal salts medium supplemented with 1% corn steep liquor with either glucose or xylose (3%) as the C-source (Table 7). Only one isolate, 36D1 fermented both sugars in this medium in about 48 hours. Two other isolates, 17C5 and P4-74B, completely fermented both sugars by about 72–96 hours. These three along with three other isolates (selected on their ability to utilize xylose) were also tested for their ability to ferment the sugars present in hemicellulose hydrolysate (HCH). For these fermentations, either 25% HCH (Batch T6-#5) adjusted to pH 5.0 with Ca(OH)2 or 50% overlimed HCH (Batch BCI-November 99) was used in a minimal salts medium base with 1% corn steep liquor. A number of the isolates completely fermented the sugars present in the HCH (Table 8).
Additional Analysis of Isolates 17C5, 36D1, P4-102B, and P4-74B
Four isolates were selected for further study (isolates 17C5, 36D1, P4-102B, and P4-74B). Isolates 17C5 and 36D1 grew and fermented the sugars in sugar cane bagasse hemicellulose hydrolysate as well as SSF of crystalline cellulose, Solka Floc, in minimal-salts medium with 1% corn steep liquor. Isolate P4-102B was easily transformable by plasmid DNA. Isolate P4-74B was included because of its growth and fermentation characteristics.
Taxonomy of the New Isolates
Based on the sequence of first 500 bp of the 16S rRNA sequence (as discussed in Example 1), 37 of the 39 tested isolates, including the four selected strains, were found to form a unique phylogenetic group with the nearest neighbor being Bacillus coagulans. To confirm these identities, the DNA encoding the entire 16S rRNA from three of the isolates, 17C5, 36D1 and P4-102B, was sequenced and these sequences were compared to other sequences in the rRNA sequence database. Based on full length sequence, isolates 17C5, 36D1 and P4-102B formed a unique phylogenetic group with the nearest neighbor being Bacillus coagulans (see
Fermentation of Glucose
Detailed growth and fermentation profiles of four of the selected second generation isolates on glucose are presented in Table 9 and
After a very short lag (less than 2 hours), LB+glucose cultures grew in a linear manner until the maximal cell density was reached in about 12 hours (
Cell yield of strains 17C5 and P4-74B were significantly higher in rich medium with glucose than the other two strains although the cell density of strains 17C5 and P4-74B decreased significantly when they reached stationary phase (
All four strains grew in glucose-minimal medium supplemented with 1% corn steep liquor with strain P4-74B growing at the highest growth rate (
The main fermentation product of all four strains from glucose was lactate (Table 9). Acetate and ethanol accounted for about 5% of the total products produced irrespective of the medium composition. In rich medium, strains 36D1 and P4-74B had the highest specific glucose consumption rate and corresponding lactate production rate. In minimal medium, the specific rate of glucose consumption and lactate production were about the same for strains 3 6D 1, P4-74B and P4-102B. Total product yield from glucose was about 85%.
Fermentation of Xylose.
Xylose is the primary sugar in the hemicellulose fraction of hardwood and agricultural residues such as sugar cane bagasse, corn fiber, corn stover, straw, and other biomass. All four isolates used in this detailed study, strains 17C5, 36D1, P4-74B and P4-102B, grew and fermented xylose in both rich medium and minimal-salts medium supplemented with corn steep liquor (Table 10;
In minimal medium strain 36D1 was most effective in fermenting xylose converting 30 g/L xylose in less than 48 hours (
Xylose Utilization Pathway
Many of the lactic acid bacteria used at the industrial level do not ferment pentoses such as xylose. The few lactic acid bacteria capable of fermenting pentoses, such as Lactobacillus pentosus, Lb. arabinosus, etc. utilize phosphoketolase pathway for pentose utilization. The key enzyme of this pathway, phosphoketolase, cleaves xylulose-5-phosphate in the presence of inorganic phosphate to one molecule each of glyceraldehyde-3-phosphate and acetyl phosphate. The products of pentose fermentation by these bacteria are an equimolar amount of lactic acid and acetic acid plus ethanol. The loss of ⅖ of the xylose carbons to acetyl phosphate will reduce the amount of xylose carbon that can be channeled to lactic acid or to ethanol in ethanologenic constructs by about 40%.
The main product produced by the isolated second generation biocatalysts is lactic acid (about 80 to 90% of fermentation products). Acetic acid and ethanol represented only 10–20% of the products produced from the pentose xylose suggesting that these biocatalysts utilize an alternate pathway, the pentose phosphate pathway, for xylose fermentation. In order to confirm that the pentose-phosphate pathway is used by the second generation biocatalysts for xylose metabolism, we determined the distribution pattern of C1-carbon of xylose into fermentation products since glyceraldehyde-3-phosphate directly yields pyruvate and products derived from pyruvate, lactate, acetate and ethanol. During the cleavage of xylulose-5-phosphate by phosphoketolase, carbon at 1-position of xylose is the C-2 carbon of acetate and ethanol. The lactic acid carbon skeleton is derived from the carbons 3–5 of xylose and in an organism with phosphoketolase pathway 13C1-label in xylose will not be found in lactate. If the pentose-phosphate pathway is the main pathway by which the pentose is metabolized, ⅖ of the C3-carbon of glyceraldehyde-3-phosphate will be derived from C1-carbon of xylose while ⅕ of the C1-carbon of glyceraldehyde-3-phosphate will originate from C1-carbon of xylose. The presence of 13C-label in lactate will confirm the metabolism of xylose through the pentose-phosphate pathway.
For these experiments, we used 13C1-xylose and followed the products produced by strains 36D1 and P4-102B by 13C-NMR. A typical 13C-NMR spectrum obtained with the 13C1-xylose fermentation products of strain 36D1 is presented in
The presence and operation of pentose phosphate pathway in these biocatalysts is significant since all the xylose carbon will be routed through pyruvate. This supports complete recovery of xylose carbon as ethanol by decarboxylation of pyruvate to acetaldehyde and further reduction to ethanol in engineered organisms. Xylose metabolism through phosphoketolase, on the other hand, would be expected to yield one glyceraldehyde-3-phosphate and one acetyl phosphate leading to production of one ethanol from pyruvate with at least 40% of xylose carbon lost as acetate.
Simultaneous Saccharification and Fermentation of Crystalline Cellulose (SSF)
The optimal conditions reported for commercially used fungal cellulases are pH 5.0 and 50° C. The biocatalysts we have isolated and characterized grew and fermented both hexoses and pentoses at 50° C. and pH 5.0. All four selected biocatalysts were found to be competent in SSF of crystalline cellulose (Solka Floc). Since strain 36D1 fermented both glucose and xylose effectively in minimal salts medium with corn steep liquor, this strain was used to evaluate the SSF characteristics of these second generation biocatalysts.
In the first set of experiments, SSF of Solka Floc (2%; 117 mM glucose equivalent with a 5% moisture content) was carried out in minimal salts medium with 1% corn steep liquor with 15 FPU/g glucan of fungal cellulases (Spezyme CE; generously provided by Genencor) at 50° C. and pH 5.0 (
At 15 FPU/g glucan cellulase level, lactate production started after a lag of about an hour and was linear for about 18 hours. Small amount of acetate and ethanol were also produced between 6 and 12 hours of fermentation. After about 36 hours, lactate production reached a slow phase and continued at this low rate past 96 hours. Volumetric productivity of lactate was 6.2 mmol L−1 h−1, the same as that of free glucose fermentation in minimal salts medium (Table 13). The product yield from cellulose at 96 hours of 180 mM is 77% of the expected maximum. Lactic acid accounted for about 78% of the products.
In order to determine the minimum amount of cellulase required for optimal SSF, fermentations were carried out at different cellulase concentrations (
The optimal pH for the SSF of Solka Floc using strain 36D1 was between 5.0 and 5.5 (
At a cellulase concentration of 15 FPU/g glucan and at pH 5.0, the rate of SSF of cellulose by strain 36D1 was highest at 55° C. Although the product yield did not significantly change between 43° C. and 55° C., the volumetric productivity of lactate was about 2-times higher at 55° C. than the 4.3 mmol L−1 h−1 at 43° C. (
Fermentation of Sugar Cane Bagasse Hemicellulose Hydrolysate
The sugar cane bagasse hemicellulose acid hydrolysate was generously provided by BC International. This hydrolysate had a total sugar concentration of 81.6 g/L with xylose accounting for 86.5% of the total. Small amount of glucose (11.5 g/L) and arabinose (1.2 g/L) were also present in the hydrolysate. The hydrolysate was adjusted to pH 5.0 with calcium hydroxide. The resulting calcium sulfate was removed by centrifugation and the supernatant was used in fermentations. Isolates 17C5 and 36D1 fermented hemicellulose hydrolysate at a concentration of 25% in mineral salts medium with 0.5% corn steep liquor. Increasing the hydrolysate concentration to 50% led to inhibition of fermentation. To minimize inhibition, the hemicellulose hydrolysate was over-limed with calcium hydroxide and the final pH was adjusted to 5.0.
Fermentations were conducted using three levels of total sugar: 256 mM (
Lactate yields were calculated based on sugar utilized and ranged from 0.9 g lactate per g sugar for the lower two sugar concentrations to 0.86 g lactate per g sugar for the highest sugar concentration (Table 14). Maximal volumetric rate of sugar metabolism was determined to be 5.5 mmol xylose L−1 h−1 (approximately 0.8 g sugar L−1 h−1).
Simultaneous Saccharification and Co-fermentation
In the next set of experiments strains 17C5 and 36D1 were evaluated for their ability to ferment sugar cane bagasse hemicellulose hydrolysate (over-limed) and Solka Floc (cellulose) simultaneously. Results of these experiments are presented in
Bacillus sp. isolate 17C5 was isolated from Old Faithful Geyser of California (Calistoga, Calif.) and grown on L-broth (tryptone, 1%; yeast extract; 0.5%, NaCl, 0.5%). Sugar cane bagasse hemicellulose hydrolysate was prepared using dilute sulfuric acid under proprietary conditions and was kindly provided by BC International, Dedham, Mass. This hydrolysate was treated with lime as described previously (Martinez A, Rodriguez M E, Wells M L, York S W, Preston J F, Ingram L O (2001) Detoxification of dilute acid hydrolysates of lignocellulose with lime. Biotechnol. Prog. 17: 287–93). Total sugar content after lime treatment was 81.3 g/l (xylose, 68.6 g/l; glucose, 11.5 g/l; arabinose, 1.2 g/l). Media used in fermentation experiments contained per liter: 50% to 90% v/v lime-treated hydrolysate; 6.25 g Na2HPO4, 0.75 g KH2PO4, 2.0 g NaCl, 0.2 g MgSO4.7 H20, 1.0 g (NH4)2SO4, 10 mg FeSO4.7H20, 10 mg Na2MoO4.2H2O, 1 ml trace mineral solution (Allen M B, Arnon D I (1955) Studies on nitrogen-fixing blue-green algae: I. Growth and nitrogen fixation by Anabaena cylindrica Lemm. Plant Physiol. 30: 366–372), and 5 ml corn steep liquor (50% dry solids; Grain Processing Corp., Muscatine, Iowa). Sterile concentrated solutions of salts and corn steep liquor were added to the lime-treated hemicellulose hydrolysate prior to pH adjustment to 5.0 and inoculation.
Optical purity of lactic acid was determined by HPLC using Chiralpak M A(+) column (Chiral Technologies Inc., Exton, Pa.) with 2 mM CuSO4 as the mobile phase at 0.4 ml per min (32° C.). Corn steep liquor used in the fermentations contained a racemic mixture of D(−)- and L(+)-lactic acids and 0.5% initial concentration used in these experiments introduced 2.6 mM D(−)-lactic acid and 3.4 mM L(+)-lactic acid into the fermentations.
Batch fermentations were carried out as previously described (Beall D S, Ohta K, Ingram L O (1991) Parametric studies of ethanol production from xylose and other sugars by recombinant Escherichia coli. Biotechnol. Bioeng. 38: 296–303) except at 50° C. and pH of 5.0. Broth pH was controlled by automatic addition of 2 M KOH. Fresh overnight cultures from L-agar were inoculated into L-broth (pH 5.0) with glucose (1%). After incubation for 2.5 h at 50° C. with shaking (200 rpm), this mid-exponential phase culture was used to provide a 1% v/v inoculum for pH-controlled fermenters. Sugar and fermentation products were measured using HPLC (Underwood S A, Zhou S, Causey T B, Yomano L P, Shanmugam K T, Ingram L O (2002) Genetic changes to optimize carbon partitioning between ethanol and biosynthesis in ethanologenic Escherichia coli. Appl. Environ. Microbiol. 68: 6263–6272).
Fermentations were conducted at an initial sugar concentration of 256 mM (
Lactate yields were calculated based on sugar utilized and ranged from 0.9 g lactate per g sugar for the lower two sugar concentrations to 0.86 g lactate per g sugar for the highest sugar concentration (Table 14). Maximal volumetric rates of sugar metabolism were determined to be 5.5 mM xylose/l.h (approximately 0.8 g sugar/l.h).
An analysis of products at the end of fermentation provides a quantitative basis to evaluate potential metabolic pathways for xylose metabolism in strain 17C5. Each mole of glucose can be converted into 2 moles lactate by all major glycolytic pathways for hexoses. Two primary pathways are known for pentose metabolism: the transaldolase/transketolase pathway and the phosphoketolase pathway. The transaldolase/transketolase pathway quantitatively converts the pentose sugars (xylose and arabinose) into the three carbon intermediate, pyruvate, providing the potential to produce 1.67 moles lactate per mole pentose. In contrast, the phosphoketolase pathway common to most lactic acid bacteria (Garde A, Jonsson G, Schmidt A S, Ahring B K (2002) Lactic acid production from wheat straw hemicellulose hydrolysate by Lactobacillus pentosus and Lactobacillus brevis. Bioresoure Technol. 81: 217–23) (Tanaka K, Komiyama A, Sonomoto K, Ishizaki A, Hall S J, Stanbury P E (2002) Two different pathways for D-xylose metabolism and the effect of xylose concentration on the yield coefficient of L-lactate in mixed-acid fermentation by the lactic acid bacterium Lactococcus lactis IO-1. Appl. Microbiol. Biotechnol. 60: 160–167), cleaves a five-carbon intermediate into glyceraldehyde 3-phosphate and acetyl-phosphate. The maximum yield from the phosphoketolase pathway is 1 mole lactate per mole pentose accompanied by equimolar acetate. Since lactate yields from strain 17C5 averaged over 100-fold that of acetate, strain 17C5 can be presumed to utilize the transaldolase/transketolase pathway for pentose metabolism. Observed lactate yields were about 90% of the theoretical yield calculated with this assumption. Small amounts of succinate, formate and ethanol were also produced during fermentation. With the transaldolase/transketolase pathway, the maximum theoretical yield for lactate is the same for both pentose and hexose sugars on weight basis (1 g lactate per g sugar).
Eucalyptus
Isolates starting with a “P” represent enrichment at pH 4.0 before isolation. For this enrichment, soil samples from various sources were mixed and used as a source of inoculum.
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. smithii
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. smithii
B. coagulans
B.
coagulans
B.
coagulans
B.
coagulans
B.
coagulans
B.
coagulans
B.
coagulans
B.
coagulans
B.
coagulans
B.
coagulans
B.
coagulans
B.
coagulans
B.
coagulans
B.
coagulans
B.
coagulans
B. coagulans (W)
B. coagulans (W)
B. coagulans (W)
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. smithii
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. coagulans
B. smithii
B. coagulans
B. coagulans
B. coagulans
B. coagulans 7050
B. coagulans 7050
B. coagulans
B. coagulans
Glucose concentration was 3% in both media. Lactic acid isomer was determined by HPLC using a chiral column.
13C-enrichment ratios for fermentation products
E. coli
Second generation biocatalyst, strain 36D1 or P4-102B, was grown in LB+Xylose to mid-exponential phase in a pH-stat at pH 5.0 at 50° C. For the experiment with non-growing cells, 40 ml of culture was centrifuged and the cells were washed with 5.0 ml of LB. The cells were resuspended in 4.75 ml of LB-xylose (1%). Enough 13C1-xylose was added to the culture to bring the xylose concentration to 1.2% and the 13C-enrichment to 20.8%. For the experiment with growing cells, cells from 0.5 ml of the mid-exponential phase culture were removed from the pH-stat, washed with equal volume of LB, and resuspended in 4.75 ml of LB-Xylose medium. Both fermentations were carried out at 50° C. with manual addition of 1.0 N KOH to maintain the pH between 6.0 and 7.0. When acid production stopped, cells were removed by centrifugation and the supernatant was subjected to HPLC for product analysis and also to 13C-NMR for identification of the 13C-enrichment. 13C1 propionate (50 mM) served as a reference.
For E. coli W3110, 20 ml of cells were grown under anaerobic conditions in LB+Xylose until late-exponential phase at 37° C. Cells were collected by centrifugation, washed once with LB and resuspended in 5.0 ml of LB-Xylose with 13C-enrichment. Fermentation was carried out at 37° C. with manual pH control between 6.0 and 7.0.
All enrichment ratios were based on the natural abundance of 13C at the indicated positions with C-2 of lactate and C-1of acetate and ethanol as reference. *represents that the C1-carbon of acetic acid and ethanol was not labeled or the amount of label at the C1-position was below the detection limit. The presented value was computed based on the sensitivity of the instrument for 13C.
Batch fermentation was carried out for 96 hrs.
aFermentations at three concentrations of total sugar (50° C. and pH 5.0). Averages with standard deviations are based on three independent fermentations. A single fermentation was conducted with the highest sugar concentration, 483 mM.
bSugar concentration at the beginning of fermentation.
cLime-treated sugar cane bagasse hemicellulose hydrolysate contained 66 mM acetate. Corn steep liquor at 0.5% final concentration in the fermentations contained 5.5 mM lactate, 0.2 mM acetate and 0.025 mM succinate. Appropriate amounts of these compounds were subtracted to obtain the net production by the biocatalyst. Carbon recovery as products (excluding cells) averaged 90%.
dProduct yield was calculated as a percentage of the maximum theoretical yield assuming 2 lactates per glucose and 1.67 lactates per pentose.
This invention was made with government support under NREL Sub-contract # XXL-9-29034-01 and DOE Grant # DE-FC36-01GO11073. The government may have certain rights in this invention.
| Number | Name | Date | Kind |
|---|---|---|---|
| 5079164 | Kirkovits et al. | Jan 1992 | A |
| 5801025 | Ohara et al. | Sep 1998 | A |
| 20040203122 | Otto | Oct 2004 | A1 |
| Number | Date | Country | |
|---|---|---|---|
| 20050250192 A1 | Nov 2005 | US |
