WO2002024865A2 - Modulation of secondary metabolite production by zinc binuclear cluster proteins - Google Patents
Modulation of secondary metabolite production by zinc binuclear cluster proteins Download PDFInfo
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- WO2002024865A2 WO2002024865A2 PCT/US2001/029288 US0129288W WO0224865A2 WO 2002024865 A2 WO2002024865 A2 WO 2002024865A2 US 0129288 W US0129288 W US 0129288W WO 0224865 A2 WO0224865 A2 WO 0224865A2
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- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P35/00—Preparation of compounds having a 5-thia-1-azabicyclo [4.2.0] octane ring system, e.g. cephalosporin
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- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P1/00—Preparation of compounds or compositions, not provided for in groups C12P3/00 - C12P39/00, by using microorganisms or enzymes
- C12P1/02—Preparation of compounds or compositions, not provided for in groups C12P3/00 - C12P39/00, by using microorganisms or enzymes by using fungi
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
- C12P17/02—Oxygen as only ring hetero atoms
- C12P17/06—Oxygen as only ring hetero atoms containing a six-membered hetero ring, e.g. fluorescein
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P37/00—Preparation of compounds having a 4-thia-1-azabicyclo [3.2.0] heptane ring system, e.g. penicillin
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/40—Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids
- C12P7/42—Hydroxy-carboxylic acids
Definitions
- the invention relates to secondary metabolite production by fungi. More particularly, the invention relates to modulation of secondary metabolite production by fungi through genetic manipulation of such fungi.
- Cyclosporin A a member of a class of cyclic undecapeptides, is produced by Tolypocladium.
- strains have been improved by manipulation of the genes encoding the biosynthetic enzymes that catalyze the reactions required for production of secondary metabolites.
- Penalva et al. (1998), Trends Biotechnol. 16: 483-489 discloses that production strains of P. chrysogenum have increased copy number of the penicillin synthesis structural genes.
- Other studies have modulated expression of other biosynthetic enzyme-encoding genes, thereby affecting overall metabolism in the fungus.
- Mingo et al. (1999), /. Biol. Chem. 21: 14545-14550 demonstrate that disruption of phacA, an enzyme in A.
- genetic manipulation holds promise for improving production of secondary metabolites.
- Genetic manipulation to increase the activity of biosynthetic enzymes for secondary metabolite production or to decrease the activity of competing biosynthetic pathways has proven effective for improving production.
- Maximum benefit can be achieved by combining several strategies of manipulation. For example, modulating the expression of genes that regulate the biosynthetic enzyme- encoding genes can improve production.
- genetic manipulation can be used to impact upon the challenges that are encountered in the fermentor run or downstream processing (e.g., energy cost, specific production of desired metabolite, maximal recovery of metabolite, cost of processing waste from fermentations).
- Gal4p a ZBC protein
- PLT(proline utilization) genes in a Saccharomyces cerevisiae strain lacking the normal gene for regulation of this pathway, PUT3.
- PCT Publication WO 00/20596 discloses that prtT, a ZBC protein, activates extracellular proteases in Aspergillus niger.
- Chem. 214: 19017-19024 discloses that nine distinct missense mutations in LEU3 affect the masking of the activation domain of that ZBC protein.
- Dickson et al. (1990), Nucleic Acids Res. 18: 5213-5217 discloses that single amino acid changes in the C terminal region of Gal4p and Lac9p, two ZBC proteins, lead to constitutive expression of target genes.
- Marczak and Brandriss (1991), Mol. Cell. Biol. 11: 2609- 2619 teaches that single point mutations in PUT3, a ZBC gene from Saccharomyces cerevisiae, lead to either constitutive or uninducible expression of proline utilization genes. Carvajal et al. (1997), Mol. Gen. Genet.
- the invention relates to secondary metabolite production by fungi. More particularly, the invention relates to modulation of secondary metabolite production by fungi through genetic manipulation of such fungi.
- the invention provides new commercial processes using ZBC proteins, or variants thereof, to significantly improve the production of useful secondary metabolites.
- the methods according to the invention comprise expressing in a fungus a ZBC protein or a variant thereof.
- the invention provides methods for improving production of a secondary metabolite by a fungus by increasing the yield of the secondary metabolite produced by the fungus.
- the methods according to this aspect of the invention comprise modulating the expression of a ZBC gene or gene variant in a manner that improves the yield of the secondary metabolite.
- the invention provides methods for improving production of a secondary metabolite by a fungus by increasing productivity of the secondary metabolite in the fungus, the methods comprising modulating the expression of a ZBC gene or gene variant in a manner that improves the productivity of the secondary metabolite.
- the invention provides methods for improving production of a secondary metabolite in a fungus by increasing efflux or excretion of the secondary metabolite, the method comprising modulating the expression of a ZBC gene or gene variant in a manner that increases efflux or excretion of the secondary metabolite.
- the invention provides methods for improving production of a secondary metabolite in a fungus by decreasing production of side products or non- desired secondary metabolites, the method comprising modulating the expression of a ZBC gene or gene variant in a manner that decreases production of side products or non-desired secondary metabolites.
- the invention provides methods for improving production of a secondary metabolite in a fungus by altering the characteristics of the fungus in a manner that is beneficial to the production of the secondary metabolite, the method comprising modulating the expression of a ZBC gene or gene variant in a manner that alters the characteristics of the fungus.
- the invention provides methods for improving production of a secondary metabolite in a fungus by causing conditional lysis of the fungus, the method comprising modulating the expression of a ZBC gene or gene variant in a manner that causes conditional lysis.
- the invention provides methods for improving production of a secondary metabolite in a fungus by increasing the resistance of the fungus to the deleterious effects of exposure to a secondary metabolite made by the same organism, the method comprising modulating the expression of a ZBC gene or gene variant in a manner that increases resistance to the deleterious effects of exposure to a secondary metabolite.
- the invention provides methods for improving production of a secondary metabolite in a fungus by modulating the expression of one or more genes, the method comprising modulating the expression of a ZBC gene or gene variant that does not normally modulate the expression of such gene or genes.
- the invention provides genetically modified fungi, wherein the genetically modified fungi have an ability to produce secondary metabolites and the ability of the genetically modified fungus to produce secondary metabolites has been improved by any of the methods according to the invention.
- the invention provides a method for making a secondary metabolite, the method comprising culturing a genetically modified fungus according to the invention under conditions suitable for the production of secondary metabolites.
- the invention relates to secondary metabolite production by fungi. More particularly, the invention relates to modulation of secondary metabolite production by fungi through genetic manipulation of such fungi.
- the invention provides new commercial processes using ZBC proteins, or variants thereof, to significantly increase useful secondary metabolite production.
- the methods according to the invention comprise expressing in a fungus a ZBC protein or a variant thereof. All aspects of the invention contemplate the modulation of one or more ZBC genes in a fungal cell of interest.
- the invention provides methods for improving production of a secondary metabolite by a fungus by increasing the yield of the secondary metabolite produced by the fungus.
- the methods according to this aspect of the invention comprise modulating the expression of a ZBC gene or gene variant in a manner that improves the yield of the secondary metabolite.
- the term "improving production of a secondary metabolite” means positively impacting one or more of the variables that affect the process of production of secondary metabolites in a fungal fermentation. These variables include, without limitation, the amount of secondary metabolite being produced, the volume required for production of sufficient quantities, the cost of raw materials and energy, the time of fermentor run, the amount of waste that must be processed after a fermentor run, the specific production of the desired metabolite, the percent of produced secondary metabolite that can be recovered from the fermentation broth, and the resistance of an organism producing a secondary metabolite to possible deleterious effects of contact with the secondary metabolite.
- secondary metabolite means a compound, derived from primary metabolites, that is produced by an organism, is not a primary metabolite, is not ethanol or a fusel alcohol, and is not required for growth under standard conditions. Secondary metabolites are derived from intermediates of many pathways of primary metabolism. These pathways include, without limitation, pathways for biosynthesis of amino acids, the shikimic acid pathway for biosynthesis of aromatic amino acids, the polyketide biosynthetic pathway from acetyl coenzyme A (CoA), the mevalonic acid pathway from acetyl CoA, and pathways for biosynthesis of polysaccharides and peptidopolysaccharides.
- CoA acetyl coenzyme A
- mevalonic acid pathway from acetyl CoA
- Secondary metabolism involves all primary pathways of carbon metabolism (Fungal Physiology, Chapter 9, pp 246-274, Griffin (ed.), John Wiley & Sons, Inc., New York, (1994)).
- Secondary metabolites also include intermediate compounds in the biosynthetic pathway for a secondary metabolite that are dedicated to the pathway for synthesis of the secondary metabolite.
- "Dedicated to the pathway for synthesis of the secondary metabolite” means that once the intermediate is synthesized by the cell, the cell will not convert the intermediate to a primary metabolite.
- Intermediate compounds also include secondary metabolite intermediate compounds which can be converted to useful compounds by subsequent chemical conversion or subsequent biotransformation.
- the yeast Saccharomyces cerevisiae is not known to produce secondary metabolites.
- the term "primary metabolite” means a natural product that has an obvious role in the functioning of the relevant organism. Primary metabolites include, without limitation, compounds involved in the biosynthesis of lipids, carbohydrates, proteins, and nucleic acids.
- the term “increasing the yield of the secondary metabolite” means increasing the quantity of the secondary metabolite present in the fermentation broth per unit volume of fermentation broth.
- ZBC gene means any gene encoding a protein having as part of its structure Cys-(Xaa) 2 -Cys-(Xaa) 6 -Cys-(Xaa) 5 - 16 -Cys-(Xaa) 2 -Cys-(Xaa) 6 - 8 -Cys (see e.g., Todd and Andrianopoulos (1997), Fungal Genetics and Biology 21: 388-405), wherein Xaa is any amino acid, each of which can be the same or different.
- Preferred ZBC genes according to this aspect of the invention include, without limitation, those genes identified in Table 1, below, and any fungal homologs thereof.
- AFLR_An 433 1299 Aspergillus nidulans 27 aflR_Ao 384 1152 Aspergillus oryzae 29 aflR_Ap 444 1332 Aspergillus parasiticus 31 alcR_An 821 2463 Aspergillus nidulans 33
- MAL63_YEAST 470 1410 Saccharomyces 167 cerevisiae
- MAL6_Scarlsber 473 1419 Saccharomyces 169 g carlsbergensis
- NJT4_Nc 1090 3270 Neurospora crassa 175 ntfl/thil_Sp 775 2325 Schizosaccharomyces 177 pombe
- YRR1_YEAST 810 2430 Saccharomyces 285 cerevisiae
- YHL6_YEAST 883 2649 Saccharomyces 295 cerevisiae
- a “fungal homolog" of a reference gene is a fungal gene encoding a product that is capable of performing at least a portion of the function of the product encoded by the reference gene, which is substantially identical to the reference gene, and/or which encodes a product which is substantially identical to the product encoded by the reference gene.
- “Substantially identical” means a polypeptide or nucleic acid exhibiting at least 25%, preferably 50%, more preferably 80%, and most preferably 90%, or even 95% identity to a reference amino acid sequence or nucleic acid sequence.
- the length of comparison sequences is generally at least 16 amino acids, preferably at least 20 amino acids, more preferably at least 25 amino acids, and most preferably 35 amino acids or greater.
- the length of comparison sequences is generally at least 50 nucleotides, preferably at least 60 nucleotides, more preferably at least 75 nucleotides, and most preferably 110 nucleotides or greater.
- Sequence identity is typically measured using sequence analysis software (for example, the Sequence Analysis Software Package of the Genetics Computer Group, University of Wisconsin Biotechnology Center, 1710 University Avenue, Madison WI 53705; or the BLAST, BEAUTY, or PILEUP/PRETTYBOX programs). For determining percentages of identity, a gap existence penalty of 11 and a gap extension penalty of 1 may be employed in such programs. For determining sequence similarity, such software assigns degrees of homology to various substitutions, deletions, and/or other modifications.
- Conservative substitutions typically include substitutions within the following groups: glycine, alanine, valine, isoleucine, leucine; aspartic acid, glutamic acid; asparagine, glutamine; serine, threonine; lysine, arginine; and phenylalanine, tyrosine.
- the ZBC gene when the secondary metabolite is aflatoxin or sterigmatocystin, the ZBC gene is not the aflR gene from Aspergillus spp.; and when the secondary metabolite is lovastatin, the ZBC gene is not the Aspergillus terreus lovE gene.
- ZBC gene or gene variant means any ZBC gene, or any useful mutant form of such gene.
- Many useful mutations of ZBC genes and/or proteins are contemplated by the present invention, including various dominant mutations.
- a "dominant mutation” is an allele of a gene that encodes a protein capable of changing the phenotype of an organism more than a non-mutated form of the gene.
- Preferred dominant mutations include dominant negative mutations, dominant positive mutations, and dominant neomorphic mutations.
- a “dominant negative mutation” is a dominant mutation that achieves its phenotypic effect by interfering with some function of the gene or gene product from which it was derived, or from a homolog thereof.
- a “dominant positive mutation” is a dominant mutation that achieves its phenotypic effect by activating some function of the gene or gene product from which it was derived, or from a homolog thereof.
- a “dominant neomorphic mutation” is a dominant mutation that achieves the phenotypic effect of providing a novel function to the gene or gene product from which it was derived, or from a homolog thereof.
- Preferred dominant mutations according to this aspect of the invention include: (1) Mutations that result in increased or decreased stability of the transcript of a gene. (2) Mutations that result in increased or decreased stability of the product of translation: For example, specific sequences near the amino terminus of a protein have been shown to cause increased or decreased protein stability. Similarly, sequences elsewhere in the protein, such as those required for ubiquitin-dependent degradation, can be mutated to increase the stability of a protein.
- Proteolytic cleavage is another post-translational mechanism for regulating the activity of a protein. Mutations that result in truncation of a protein can mimic activation by proteolysis. Mutations that change amino acids required for proteolysis can activate proteins that are negatively regulated by proteolysis.
- nucleotides are co-factors for many enzymes, and the nucleotide-binding domains of such proteins are highly conserved. Lysine to arginine substitutions in the nucleotide binding domain frequently result in the inhibition of enzymatic activity. Enzymatically inactive proteins can be dominant inactive molecules, acting by sequestering substrates from functional enzymes.
- Mutations in portions of genes that encode regulatory domains of proteins For example, many proteins, including kinases, contain regulatory domains that function as mechanisms to control the timing of activation. Mutations in these domains might result in constitutive activation. Regulatory domains include linker regions and C terminal regions in the case of some ZBC proteins.
- Mutations that create a new protein function For example, a mutation in a ZBC protein could result in altered DNA recognition specificity, such that the mutated ZBC protein can modulate the activity of pathways that it does not usually regulate.
- TAD Transcriptional activation domains
- the term "modulating the expression of a gene” means affecting the function of a gene's product, preferably by increasing or decreasing protein activity or creating a new protein activity through mutation; increasing or decreasing transcription; increasing or decreasing translation; increasing, decreasing or changing post-translational modification; altering intracellular localization; increasing or decreasing translocation; increasing or decreasing protein activity by fusion or by interaction of the protein with another molecule; and/or creating a new protein activity by interaction of the protein with another molecule.
- modulation is achieved by allowing or causing the expression of an exogenously supplied nucleic acid or gene, e.g., by transformation.
- other exogenously supplied molecules can mediate the modulation.
- the ZBC gene is from an organism in which it is not present within a biosynthetic cluster, or the ZBC gene is not present in the biosynthetic cluster of the desired secondary metabolite to be regulated.
- the ZBC gene is from an organism other than the production fungus, preferably from a different species or genus.
- the ZBC gene in its native locus regulates a different secondary metabolite than the desired secondary metabolite produced by the production fungus.
- the ZBC gene in its native locus does not regulate secondary metabolism.
- “Native locus” means the chromosomal locus in the original organism from which the gene was cloned.
- mutation means an alteration in DNA sequence, either by site-directed or random mutagenesis. Mutation encompasses point mutations as well as insertions, deletions, or rearrangements.
- mutant means an organism containing one or more mutations.
- the modulation is over-expression of the gene.
- “Over-expression of the gene” means transcription and/or translation and/or gene product maturation at a rate that exceeds by at least two-fold, preferably at least five-fold, and more preferably at least ten-fold, the level of such expression that would be present under similar growth conditions in the absence of the modulation of expression of the gene.
- Similar growth conditions means similar sources of nutrients such as carbon, nitrogen, and phosphate, as well as similar pH, partial oxygen pressure, temperature, concentration of drugs or other small molecules, and a similar substrate for growth, whether solid, semi-solid, or liquid.
- the modulation is expression of a dominant mutation of the gene.
- the term "dominant mutation” is as used before.
- Preferred dominant mutations according to this aspect of the invention are as used before.
- the modulation is conditional expression of the gene.
- "Conditional expression” of a gene means expression under certain growth conditions, but not under others. Such growth conditions that may be varied include, without limitation, carbon source, nitrogen source, phosphate source, pH, temperature, partial oxygen pressure, the presence or absence of small molecules such as drags, and the presence or absence of a solid substrate.
- the secondary metabolite is an anti-bacterial.
- An "anti-bacterial” is a molecule that has cytocidal or cytostatic activity against some or all bacteria.
- Preferred anti-bacterials include, without limitation, ⁇ -lactams.
- Preferred ⁇ -lactams include, without limitation, penicillins and cephalosporins.
- Preferred penicillins and biosynthetic intermediates include, without limitation, isopenicillin N, 6- aminopenicillanic acid (6-APA), penicillin G, penicillin N, and penicillin V.
- cephalosporins and biosynthetic intermediates include, without limitation, deacetoxycephalosporin V (DAOC V), deacetoxycephalosporin C (DAOC), deacetylcephalosporin C (DAC), 7-aminodeacetoxy-cephalosporanic acid (7-ADCA), cephalosporin C, 7- ⁇ -(5-carboxy-5-oxopentanamido)-cephalosporanic acid (keto- AD-7ACA), 7- ⁇ -(4-carboxybutanamido)-cephalosporanic acid (GL-7ACA), and 7- aminocephalosporanic acid (7 AC A).
- DAOC V deacetoxycephalosporin V
- DAOC deacetoxycephalosporin C
- DAC deacetylcephalosporin C
- 7-ADCA 7-aminodeacetoxy-cephalosporanic acid
- keto- AD-7ACA keto-
- the secondary metabolite is an anti-hypercholesterolemic.
- An "anti- hypercholesterolemic” is a drug administered to a patient diagnosed with elevated cholesterol levels, for the purpose of lowering the cholesterol levels.
- Preferred anti- hypercholesterolemics include, without limitation, lovastatin, mevastatin, simvastatin, and pravastatin.
- the secondary metabolite is an immunosuppressant.
- An "immunosuppressant” is a molecule that reduces or eliminates an immune response in a host when the host is challenged with an immunogenic molecule, including immunogenic molecules present on transplanted organs, tissues or cells.
- Preferred immunosuppressants include, without limitation, members of the cyclosporin family and beauverolide L.
- Preferred cyclosporins include, without limitation, cyclosporin A and cyclosporin C.
- the secondary metabolite is an ergot alkaloid.
- An "ergot alkaloid” is a member of a large family of alkaloid compounds that are most often produced in the sclerotia of fungi of the genus Claviceps.
- An "alkaloid” is a small molecule that contains nitrogen and has basic pH characteristics.
- the classes of ergot alkaloids include clavine alkaloids, lysergic acids, lysergic acid amides, and ergot peptide alkaloids.
- Preferred ergot alkaloids include, without limitation, ergotamine, ergosine, ergocristine, ergocryptine, ergocornine, ergotaminine, ergosinine, ergocristinine, ergocryptinine, ergocorninine, ergonovine, ergometrinine, and ergoclavine.
- the secondary metabolite is an inhibitor of angiogenesis.
- angiogenesis inhibitor is a molecule that decreases or prevents the formation of new blood vessels.
- Angiogenesis inhibitors have proven effective in the treatment of several human diseases including, without limitation, cancer, rheumatoid arthritis, and diabetic retinopathy.
- Preferred inhibitors of angiogenesis include, without limitation, fumagillin and ovalicin.
- the secondary metabolite is a glucan synthase inhibitor.
- a "glucan synthase inhibitor” is a molecule that decreases or inhibits the production of 1,3- ⁇ -D-glucan, a structural polymer of fungal cell walls.
- Glucan synthase inhibitors are a class of antifungal agents.
- Preferred glucan synthase inhibitors include, without limitation, echinocandin B, pneumocandin B, aculeacin A, and papulacandin.
- the secondary metabolite is a member of the gliotoxin family of compounds.
- the "gliotoxin family of compounds” are related molecules of the epipolythiodioxopiperazine class. Gliotoxins display diverse biological activities, including, without limitation, antimicrobial, antifungal, antiviral, and immunomodulating activities. Preferred members of the "gliotoxin family of compounds” include, without limitation, gliotoxin and aspirochlorine.
- the secondary metabolite is a fungal toxin.
- a "fungal toxin” is a compound that causes a pathological condition in a host, either plant or animal. Fungal toxins could be mycotoxins present in food products, toxins produced by phytopathogens, toxins from poisonous mushrooms, or toxins produced by zoopathogens.
- Preferred fungal toxins include, without limitation, aflatoxins, patulin, zearalenone, cytochalasin, griseofulvin, ergochrome, cercosporin, marticin, xanthocillin, coumarins, tricothecenes, fusidanes, sesterpenes, amatoxins, malformin A, phallotoxins, pentoxin, HC toxin, psilocybin, bufotenine, lysergic acid, sporodesmin, pulcheriminic acid, sordarins, fumonisins, ochratoxin A, and fusaric acid.
- the secondary metabolite is a modulator of cell surface receptor signaling.
- the term "cell surface receptor” means a molecule that resides at or in the plasma membrane, binds an extracellular signaling molecule, and transduces this signal to propagate a cellular response.
- Modulators of cell surface receptor signaling might function by one of several mechanisms including, without limitation, acting as agonists or antagonists; sequestering a molecule that interacts with a receptor, such as a ligand; or stabilizing the interaction of a receptor and a molecule with which it interacts.
- Preferred modulators of cell surface signaling include, without limitation, the insulin receptor agonist L-783,281 and the cholecystokinin receptor antagonist asperlicin.
- the secondary metabolite is a plant growth regulator.
- a "plant growth regulator” is a molecule that controls growth and development of a plant by affecting processes that include, without limitation, division, elongation, and differentiation of cells.
- Preferred plant growth regulators include, without limitation, cytokinin, auxin, gibberellin, abscisic acid, and ethylene.
- the secondary metabolite is a pigment.
- a "pigment” is a substance that imparts a characteristic color.
- Prefereed pigments include, without limitation, melanins and carotenoids.
- the secondary metabolite is an insecticide.
- An "insecticide” is a molecule that is toxic to at least some insects.
- a preferred insecticide is nodulisporic acid.
- the secondary metabolite is an anti-neoplastic compound.
- An "anti- neoplastic” compound is a molecule that prevents or reduces tumor formation.
- Preferred anti-neoplastic compounds include, without limitation, taxol (paclitaxel) and related taxoids.
- the methods further comprise purifying the secondary metabolite from a culture of the fungus.
- Purifying means obtaining the secondary metabolite in substantially pure form.
- substantially pure means comprising at least 90%, more preferably at least 95%, and most preferably at least 99%, of the purified composition on a dry- weight basis.
- the invention provides methods for improving production of a secondary metabolite by a fungus by increasing productivity of the secondary metabolite in the fungus, the methods comprising modulating the expression of a ZBC gene or gene variant in a manner that improves the productivity of the secondary metabolite.
- Significant advantages that might result from increasing productivity include, without limitation, a decrease in fermentor run-time, a decrease in the size of the , fermentor required for production of equivalent amounts of secondary metabolite, or a decrease in the biomass required for production, which translates into decreased waste that must be handled in downstream processing.
- a decrease in fermentor run-time a decrease in the size of the , fermentor required for production of equivalent amounts of secondary metabolite, or a decrease in the biomass required for production, which translates into decreased waste that must be handled in downstream processing.
- such increased productivity is by at least ten percent, more preferably at least 50 percent, and most preferably at least two-fold.
- Modulating the expression of a ZBC gene is as used before.
- the modulation is over-expression of the ZBC gene.
- “Over-expression of the gene” is as used before.
- the modulation is expression of a dominant mutation of the gene.
- the term "dominant mutation” is as used before.
- Preferred dominant mutations according to this aspect of the invention are as used before.
- the modulation is conditional expression of the gene.
- conditional expression of a gene is as used before.
- the term "secondary metabolite” is as used previously and preferred secondary metabolites include, without limitation, those discussed previously.
- the methods further comprise purifying the secondary metabolite from a culture of the fungus.
- purifying is as used before.
- the invention provides methods for improving production of a secondary metabolite in a fungus by increasing efflux or excretion of the secondary metabolite, the method comprising modulating the expression of a ZBC gene or gene variant in a manner that increases efflux or excretion of the secondary metabolite.
- Increasing efflux or excretion of the secondary metabolite means that, without lysing a fungal cell, a greater quantity of the secondary metabolite passes from the inside of the fungal cell to the outside of the fungal cell per unit time.
- Outside of the fungal cell is defined as being no longer contained wholly within the lipid bilayer of the cell and/or extractable from the cell with methods which do not release a majority of intracellular contents.
- Modulating the expression of a ZBC gene is as used before, except that the ZBC gene can be the Aspergillus spp. aflR gene when the secondary metabolite is aflatoxin or sterigmatocystin, and the ZBC gene can be lovE when the secondary metabolite is lovastatin.
- the modulation is over-expression of the gene.
- “Over- expression of the gene” is as used before.
- the modulation is expression of a dominant mutation of the gene.
- the term "dominant mutation” is as used before.
- Preferred dominant mutations according to this aspect of the invention are as used before.
- the modulation is conditional expression of the gene.
- conditional expression of a gene is as used before.
- secondary metabolite is as used previously and preferred secondary metabolites include, without limitation, those discussed previously, hi certain embodiments of the methods according to this aspect of the invention, the methods further comprise purifying the secondary metabolite from a culture of the fungus.
- purifying is as used before.
- the invention provides methods for improving production of a secondary metabolite in a fungus by decreasing production of side products or non- desired secondary metabolites, the method comprising modulating the expression of a ZBC gene or gene variant in a manner that decreases production of side products or non-desired secondary metabolites.
- “Decreasing production of side products or non-desired secondary metabolites” means reducing the amount of such side products or non-desired secondary metabolites that are synthesized or which are retained within the cells or the media surrounding the cells. Preferably, such reduction is at least by 25%, more preferably by at least 50%, even more preferably by at least 2-fold, and most preferably by at least 5-fold.
- Modulating the expression of a ZBC gene is as used for the third aspect of the invention.
- the modulation is over-expression of the gene.
- “Over-expression of the gene” is as used before.
- the modulation is expression of a dominant mutation of the gene.
- the term “dominant mutation” is as used before.
- Preferred dominant mutations according to this aspect of the invention are as used before.
- the modulation is conditional expression of the gene.
- conditional expression of a gene is as used before.
- the term "secondary metabolite" is as used previously and preferred secondary metabolites include, without limitation, those discussed previously.
- the methods further comprise purifying the secondary metabolite from a culture of the fungus.
- purifying is as used before.
- the invention provides methods for improving production of a secondary metabolite in a fungus by altering the characteristics of the fungus in a manner that is beneficial to the production of the secondary metabolite, the method comprising modulating the expression of a ZBC gene or gene variant in a manner that alters the characteristics of the fungus.
- alterations means changing the morphology or growth traits of the fungus.
- Preferred alterations include, without limitation, alterations that result in transition of the fungus from the hyphal to the yeast form; alterations that result in transition of the fungus from the yeast to the hyphal form; alterations that lead to more or less hyphal branching; alterations that increase or decrease flocculence, adherence, cell buoyancy, surface area of the fungus, cell wall integrity and/or stability, pellet size, vacuole formation, and/or ability to grow at higher or lower temperatures; and alterations that increase the saturating growth density of a culture or rate of pellet formation.
- Modulating the expression of a ZBC gene is as used for the third aspect of the invention.
- the modulation is over-expression of the gene.
- “Over-expression of the gene” is as used before.
- the modulation is expression of a dominant mutation of the gene.
- the term “dominant mutation” is as used before.
- Preferred dominant mutations according to this aspect of the invention are as used before.
- the modulation is conditional expression of the gene.
- conditional expression of a gene is as used before.
- the term "secondary metabolite” is as used previously and preferred secondary metabolites include, without limitation, those discussed previously.
- the methods further comprise purifying the secondary metabolite from a culture of the fungus.
- purifying is as used before.
- the invention provides methods for improving production of a secondary metabolite in a fungus by causing conditional lysis of the fungus, the method comprising modulating the expression of a ZBC gene or gene variant in a manner that causes conditional lysis.
- “Causing conditional lysis” means causing the fungus to grow without lysis under a first set of growth conditions and to lyse under a second and different set of conditions, which are not lytic to the unmodified fungus.
- the conditions that can be altered between the first and second growth conditions include, without limitation, the source or amount of nutrients such as carbon, nitrogen, and phosphate; the source or amount of specific enzymes; the source or amount of specific components found in cell walls; the amount of salts or osmolytes; the pH of the medium; the partial oxygen pressure; temperature; and the amount of specific small molecules.
- Modulating the expression of a ZBC gene is as used for the third aspect of the invention.
- the modulation is over-expression of the gene.
- “Over-expression of the gene” is as used before.
- the modulation is expression of a dominant mutation of the gene.
- the term “dominant mutation” is as used before.
- Preferred dominant mutations according to this aspect of the invention are as used before.
- the modulation is conditional expression of the gene.
- conditional expression of a gene is as used before.
- the term "secondary metabolite” is as used previously and preferred secondary metabolites include, without limitation, those discussed previously.
- the methods further comprise purifying the secondary metabolite from a culture of the fungus.
- purifying is as used before.
- the invention provides methods for improving production of a secondary metabolite in a fungus by increasing the resistance of the fungus to the deleterious effects of exposure to a secondary metabolite made by the same organism, the method comprising modulating the expression of a ZBC gene or gene variant in a manner that increases resistance to the deleterious effects of exposure to a secondary metabolite.
- the phrase "increasing the resistance of the fungus to the deleterious effects of exposure to a secondary metabolite” means to allow the fungus to survive, grow, or produce the secondary metabolite in conditions that otherwise would be toxic to the fungus or prevent the production of the secondary metabolite.
- the growth of a fungus that produces a secondary metabolite can be limited, in part, by the toxic effects of the secondary metabolite itself.
- decreased yields of the metabolite can be observed.
- Alexander et al. (1999), Mol. Gen. Genet. 261: 977-84 have shown that the trichothecene efflux pump of Fusarium sporotrichiodes, encoded by the gene TRI12, is required both for high level production of, and resistance to the toxic effects of, trichothecenes produced by this fungus.
- modifications that increase the resistance of a fungus to a toxic secondary metabolite that it produces can increase the saturation density and extend the metabolically active lifetime of the producing fungus.
- such attributes will have the beneficial effect of increasing the yield and productivity of a metabolite.
- Regulators of secondary metabolite production whose expression can be modulated to increase resistance of a fungus to toxic metabolites can include, without limitation, transporters that promote efflux of the metabolite from cells, enzymes that alter the chemical structure of the metabolite within cells to render it non-toxic, target(s) of the metabolite that mediate its toxicity, and gene products that alter cellular processes to counteract the toxic effects of a metabolite.
- Additional benefits of increasing efflux of secondary metabolites include increasing the amount of metabolite available for purification from the fermentation broth and mitigation of feedback inhibition of secondary metabolism that may be mediated by the metabolite itself.
- feedback inhibition of a biosynthetic pathway by a product of that pathway is well documented in many microorganisms, and this inhibition can act at the transcriptional, translational, and post-translational levels.
- yeast Several well- documented examples in yeast include the transcriptional repression of lysine biosynthetic genes by lysine (Feller et al. (1999), Eur. J. Biochem.
- Transcription factors that regulate the expression of efflux pumps could also be used to increase efflux of a drug from a fungal cell to increase the yields of a metabolite and decrease the toxicity of the secondary metabolite in a fermentation.
- Such transcription factors include, but are not limited to, ZBC genes such as PDR1, and PDR3 from S. cerevisiae and their homologs. Over-expression of each of these genes has been shown to up-regulate expression of transporters and cause increased resistance of S. cerevisiae to toxic compounds (for examples, see Reid et al. (1997), J. Biol. Chem. 272: 12091-9; Katzmann et al. (1994), Mol Cell. Biol. 14: 4653-61; Wendler et al. (1997), /. Biol. Chem. 272: 27091-8).
- RNA polymerase II RNA polymerase II
- alpha-amanitin RNA polymerase II
- HMG CoA reductase the target enzyme for the secondary metabolite lovastatin
- HMG CoA Reductase can also cause resistance to lovastatin (Ravid et al. (1999), /. Biol Chem. 274: 29341-51; Lum et al. (1996), Yeast 12: 1107-24).
- Taxol paclitaxel
- Dominant mutations affecting ⁇ -tubulin that confer resistance to taxol have been characterized (for example, see Gonzalez et al. (1999), J. Biol. Chem. 274: 23875-82) and could prove to be useful to confer resistance to this toxic metabolite in production strains.
- the pneumocandin and echinocandin families of metabolites are fungal secondary metabolites that inhibit the enzyme 1,3- ⁇ -D-glucan synthase.
- Dominant mutations in the C. albicans glucan synthase gene, FKSl have been shown to confer resistance to candins (Douglas et al. (1997), Antimicrob. Agents Chemother. 41: 2471-9).
- Glucan synthase mutations such as these could be used to generate fungal production strains with increased resistance to the candin class of antifungals.
- S. cerevisiae mutants resistant to the growth-inhibitory effects of the fungal secondary metabolite cyclosporin A have also been described (Cardenas et al.
- Modulating the expression of a ZBC gene is as used for the third aspect of the invention.
- the modulation is over-expression of the gene.
- “Over-expression of the gene” is as used before.
- the modulation is expression of a dominant mutation of the gene.
- the term “dominant mutation” is as used before.
- Preferred dominant mutations according to this aspect of the invention are as used before.
- the modulation is conditional expression of the gene.
- conditional expression of a gene is as used before.
- the term "secondary metabolite” is as used previously and preferred secondary metabolites include, without limitation, those discussed previously.
- the methods further comprise purifying the secondary metabolite from a culture of the fungus.
- purifying is as used before.
- the invention provides methods for improving production of a secondary metabolite in a fungus by modulating the expression of one or more genes, the method comprising modulating the expression of a ZBC gene or gene variant that does not normally modulate the expression of such gene or genes.
- the invention provides genetically modified fungi, wherein the genetically modified fungi have an ability to produce secondary metabolites and the ability of the genetically modified fungus to produce secondary metabolites has been improved by any of the methods according to the invention.
- the invention provides a method for making a secondary metabolite, the method comprising culturing a genetically modified fungus according to the invention under conditions suitable for the production of secondary metabolites.
- Atl8 gene from A. terreus was tested for effects on lovastatin production.
- At 18 SEQ ID NO 51
- MO1715 SEQ JD NO 1
- MO 1716 SEQ ID NO 2
- PCR polymerase chain reaction
- a GATEWAY Cloning Technology (Invitrogen Corp., Carlsbad, CA) entry vector was produced from the resultant PCR product and the GATEWAY pDONR206 entry plasmid according to manufacturer's instructions.
- the resultant vector, MB 1754 was then reacted in a with plasmid MB 1419 to form an expression vector according to manufacturer's instructions.
- MB1419 is derived from pLXZ161, a vector derived from pBC-phleo (Silar (1995), Fungal Genetics Newsletter 42: 73) that carries a phleomycin resistance cassette for selection of transformants in A. terreus, as well as a polylinker located between the A. nidulans PGK promoter and the A.
- nidulans trpC terminator pLXZ161 is constructed as follows: First, the A. nidulans trpC terminator is amplified from genomic DNA by the PCR using Turbo Pfu Polymerase as described by the manufacturer (Stratagene, La Jolla, CA). Primers used in this reaction are TRPC-1 (SEQ ID NO 3) and TRPC-2 (SEQ ID NO 4). The resultant product is digested with the restriction enzymes SacII and Notl, purified by agarose gel electrophoresis, and cloned into SacD/Notl-digested pBC-phleo DNA, to generate pLXZl 16. Second, the A.
- nidulans PGK promoter is amplified from A. nidulans genomic DNA by PCR using primers PGK1-1 (SEQ ID NO 5) and PGK1-2 (SEQ ID NO 6), Turbo Pfu Polymerase, and the reaction conditions as described above.
- the resultant product is digested with Apal and Clal and cloned into Apal/Clal-digested pLXZl 16, to generate pLXZ161.
- the ccdB (death gene) cassette from pEZC7201 (Invitrogen Corp., Carlsbad, CA) was amplified by PCR using oligos MO511 (SEQ JD NO 7) and MO512 (SEQ ID NO 8), digested with Clal and Notl, and cloned into Notl/Clal-digested pLXZl ⁇ l.
- the reactions using this vector allow configuration of any gene in an entry clone to be expressed under the control of the A.
- nidulans PGK promoter see GATEWAY Cloning Technology manual, Invitrogen Corp., Carlsbad, CA.
- the fungal selectable marker contained on this plasmid is He, which confers resistance to phleomycin.
- Reaction of MB 1754 with MB 1419 yielded a clone (MB 1970) which is configured to express At 18 under control of the A. nidulans PGK promoter, with the terminator region from the A. nidulans trpC gene acting as a transcriptional terminator.
- spores were first generated by culture of strain ATCC#20542 on petri plates containing potato dextrose agar (PDA, Becton Dickinson & Co., Sparks, MO) at 30°C for 3-6 days. Spores were removed from PDA either by resuspension in sterile water or Tween-80 (0.1%) or by scraping directly from the plate using a sterile spatula.
- PDA potato dextrose agar
- Yeast extract sucrose (YES ) medium (2% yeast extract, 6% sucrose) was inoculated to a density of 1-5 x 10 6 spores per ml and incubated with shaking in an Erlenmeyer flask at 26-30° C for 12-16 hr (250 rpm). Mycelia were harvested by centrifugation at 3200 rpm for 10 minutes, and washed in sterile water twice. Mycelia were resuspended in a filter-sterilized solution of Novozyme 234 (Sigma, St. Louis, MO) at 2-5 mg/ml in 1 M MgSO 4 and digested at room temperature with shaking (80 rpm) for 1-2 hr.
- Novozyme 234 Sigma, St. Louis, MO
- Undigested material was removed from the digest by filtration through a rayon-polyester cloth with acrylic binder and 22-25 ⁇ m pores (MIRACLOTH, Calbiochem, San Diego, CA). After adding 1-2 volumes of STC (0.8 M sorbitol, 25 mm Tris, pH 7.5, and 25 mM CaCl 2 ), the protoplasts were pelleted by centrifugation at 2500 rpm. Protoplasts were washed twice in STC by centrifugation.
- Resulting protoplasts were resuspended to a density of 5 x 10 7 per ml in a solution of STC, SPTC (40% polyethylene glycol in STC) and DMSO in a ratio of 9: 1 :0.1 and frozen at -80°C.
- Two aliquots (100 ⁇ l each) of protoplasts were mixed with 1-5 ⁇ g of either pBCphleo or MB 1970 DNA and incubated on ice for 30 min.
- An aliquot of SPTC (15 ⁇ l) was added to each tube and the reaction was incubated at room temperature for 15 minutes.
- An additional aliquot 500 ⁇ l was added with gentle mixing, and the reaction was incubated for an additional 15 minutes at room temperature.
- the reaction was next resuspended in 25 ml of molten regeneration medium (PDA from Sigma, St Louis, MO) with 0.8 M sucrose, maintained at 50°C), and poured onto a 150 mm petri plate containing 25 ml of solidified regeneration medium plus phleomycin (60-200 ⁇ g/ml). Transformants were typically visible after 2-5 days of incubation at 26-30°C.
- PDA molten regeneration medium
- phleomycin 60-200 ⁇ g/ml
- A. terreus transformants were grown on modified RPM medium (WO 00/37629) containing 4% glucose, 0.3% corn steep liquor (Sigma, St. Louis, MO), 0.2%KNO 3 , 0.3%KH 2 PO 4 , 0.05%MgSO 4 -7H 2 O, 0.05% NaCl, 0.05% polyglycol (Dow Chemical Co., Midland, MI), 0.1 % trace elements (14.3 g/1 ZnSO 4 -7H 2 O, 2.5 g/1 CuSO 4 -5H 2 O, 0.5 g/1 NiCl 2 -6H 2 0, 13.8 g/1 FeSO 4 7H 2 O, 8.5 g/1 MnSO 4 -H 2 O, 3 g/1 citric acid-H 2 O (add first), 1 g/1 H 3 BO 3 , 1 g/1 Na 2 MoO 4 , 2.5 g/1 CoCl 2 6H 2 O).
- Lovastatin is known to inhibit the enzyme HMG-CoA reductase (HMGR) which converts hydroxymethylglutaryl coenzyme A (HMGCoA) and NADPH to mevalonate and NADP. This reaction can be quantified by measuring the change in absorbance of NADPH.
- HMGR HMG-CoA reductase
- HMGCoA hydroxymethylglutaryl coenzyme A
- NADP mevalonate and NADP.
- This reaction can be quantified by measuring the change in absorbance of NADPH.
- 6-histidine tagged HMGR ((His) 6 HMGR) was first expressed in S. cerevisiae and purified with a nickel column. A. terreus samples were fermented as described above and 0.5 mL samples were taken at day 5-6, put in a 1 mL 96-well plate and centrifuged to remove mycelia before assaying. Samples were transferred to another 1 mL 96-well plate and frozen at
- the amounts of lovastatin produced by six Atl8 transformants and six pBC-phleo (vector) transformants were determined.
- the median value of lovastatin production by the vector transformants was approximately 100 micrograms/mL broth whereas that of the At 18 transformants was approximately 210 micrograms/ml broth.
- lovU (previously designated as orfl3 in A. terreus, Genbank ID 4959954) function in P. chrysogenum
- lovU was amplified by PCR under standard conditions well known to those in the art, using A. terreus first strand cDNA as template.
- A. terrer ⁇ (MF22; ATCC#20542) was grown for 45 hours in Production Media (Cerelose, 4.5% (w/v), Peptonized Milk, 2.5% (w/v), Autolyzed yeast, 0.25% (w/v), Polyglycol P2000, 0.25% (w/v), pH to 7.0) at 25°C.
- Mycelia were harvested in a 50 cc syringe plugged with sterile cotton wool using a vacuum apparatus, washed once with sterile H 2 O, and snap frozen in liquid nitrogen. Mycelia were then ground to a powder under liquid nitrogen with a mortar and pestle, and homogenized in RLC buffer (RNeasy Kit; Qiagen, Inc., Valencia, CA) using a GLH rotor-stator homogenizer (Omni International, Warrenton, VA.) Total RNA was purified using an RNeasy Maxi column according to the instructions of the manufacturer.
- the polyA+ fraction of the A. terreus total RNA was isolated using Oligotex beads (Qiagen, Inc., Valencia, CA). Purified polyA+ RNA (5 ⁇ g) was used to generate complementary DNA (cDNA) using SUPERSCRIPT reverse transcriptase (Gibco BRL, Rockville, MD) according to the manufacturer's instructions. First strand cDNA was used to amplify cDNA predicted to encode lovU using PCR. Oligos used to amplify the lovU cDNA were MO843 (SEQ ID NO 9) and MO844 (SEQ JD NO 10).
- the resultant lovU PCR product was cloned using GATEWAY Cloning Technology (Invitrogen Corp., Carlsbad, CA) to generate the entry clone MB1201. This vector was then used to generate the expression vector MB 1317 which encodes lovU under control of the A. nidulans PGK promoter.
- the dominant selectable marker for transformation on this vector is the ble gene under control of the A. nidulans GPD promoter, which confers resistance to the antimicrobial agent phleomycin.
- MB 1325 (a control plasmid expressing the ble marker gene which causes phleomycin resistance) and MB 1317 were transformed into P. chrysogenum strains MF1 (NRRL1951) and MF20 (ATCC 11702). Transformation was accomplished in the same manner as described above for A. terreus, except transformants were selected on 30 ⁇ g/mL phleomycin. To test levels of penicillin produced in P. chrysogenum transformants, a plug containing spores and mycelia was used as the inoculum. The medium used was the published P2 production medium (Lein (1986), in Overproduction of Microbial Metabolites, pp.
- Standard samples contained 0, 25, 50, 100, 200, 300, 400, and 500 ⁇ g/mL phenoxymethylpenicillin (sodium salt) dissolved in 10 mM potassium phosphate (pH 7.0), and assays were conducted as described below.
- Fermentation broth was clarified by centrifugation for 10 min at 4000 g, and 40 ⁇ L of clarified fermentation broth and penicillin standard solutions was pipetted into individual wells of a 96-well UV collection plate.
- 200 ⁇ L of imidazole reagent was pipetted into a 96-well filter plate (0.45 micron).
- the derivatization reaction of penicillin was initiated by vacuum filtration of imidazole reagent into a collection plate containing the aliquoted samples and standards. The collection plate was placed into a 96-well plate reader at 45 degrees while absorbance at 325 nm was monitored over 20 minutes.
- a Molecular Dynamics (Sunnyvale, CA) 96-well UV/Vis plate reader was used for all spectrophotometric detection.
- a 1.2 M aqueous imidazole solution containing mercuric chloride at a concentration of 1 mM, pH 6.8 was prepared as follows: 8.25 g of imidazole was dissolved in 60 mL of water, 10 mL of 5 M HC1 was added, and then 10 mL of a solution of mercuric chloride (0.27 g dissolved in 100 mL of water) was added.
- Ati ⁇ S construct according to Example 1 is used to transform A. terreus according to Example 2.
- Lovastatin concentration is determined according to Example 3, except that it is measured as the amount of lovastatin per unit volume of broth per gram of dry cell weight at each 24 hour time point of the fermentation and expressed as concentration as a function of fermentation time. Transformants with increased productivity, relative to vector controls, have a higher concentration of lovastatin at earlier time points.
- the At 18 construct according to Example 1 is used to transform A. terreus according to Example 2. Transformants are grown in production media and sampled at six and twelve days. The concentration of the undesired polyketide metabolite sulochrin is measured in samples of the whole fermentation broth (broth plus cell mass) at various time points for every sample. For each whole broth sample, the pH is adjusted to 1.1 and an equal volume of methanol is added. These whole broth/methanol extracts are assessed for the concentration of sulochrin at each time point using HPLC analysis. Conditions for determining sulochrin concentrations by HPLC are standard (see, e.g., Vinci et al. (1991), /. Ind. Microbiol.
- EXAMPLE 9 Construction of an Expression Vector for the LYS14 Gene from S. cerevisiae.
- LYS14 was amplified by PCR under standard conditions from S. cerevisiae genomic library DNA using primers MO931 (SEQ ID NO 11) and MO932 (SEQ ID NO 12).
- MO931 SEQ ID NO 11
- MO932 SEQ ID NO 12
- the resultant 2.4 kb PCR product was cloned using GATEWAY Cloning Technology (Invitrogen Corp., Carlsbad, CA) to generate entry clone MB 1567.
- MB 1567 was used to generate filamentous fungal expression plasmids MB1669, MB3130, and MB3139 which encode LYS14 under the control of, respectively, the A. nidulans PGK (MB1669 and MB3130) and A. nidulans GPD (MB3139) promoters.
- the dominant selectable marker for transformation on MB 1669 is the ble gene under control of the A. nidulans GPD promoter, which confers resistance to the antimicrobial agent phleomycin.
- MB3130 and MB3139 contain the ble gene under control of the A. nidulans trpC promoter.
- Corresponding vector-only controls for the LYS14 expression plasmids are MB2143 (GPD-b/e) and MB2941 (trpC-b/e).
- Example 8 The LYS14 constructs according to Example 8 was used to transform A. terreus according to the method of Example 2. Lovastatin concentration was determined according to the methods of Example 9.
- A. terreus strain MF22 was transformed with MB2143 (GPD-b/e vector control), MB 1669 (PGK-LYS14, GPD-b/e), MB2941 (trpC-b/e vector control), MB3130 (PGK-LYS14, trpC-b/e) and MB3139 (GPO-LYS14, trpC-b/e).
- Lovastatin concentration from the corresponding vector-only was used as a control.
- MB2143 was the vector control for MB 1669.
- the median value and highest data point for lovastatin production of the LYS14 expression plasmids MB 1669 and MB3139 was greater than that of the corresponding vector only controls.
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AU2001291114A AU2001291114A1 (en) | 2000-09-19 | 2001-09-19 | Modulation of secondary metabolite production by zinc binuclear cluster proteins |
US10/149,310 US7229784B2 (en) | 2000-09-19 | 2001-09-19 | Modulation of secondary metabolite production by zinc binuclear cluster proteins |
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-
2001
- 2001-09-19 EP EP01971200A patent/EP1409530A2/en not_active Withdrawn
- 2001-09-19 AU AU2001291114A patent/AU2001291114A1/en not_active Abandoned
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Also Published As
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US20040077039A1 (en) | 2004-04-22 |
US7229784B2 (en) | 2007-06-12 |
WO2002024865A3 (en) | 2004-02-26 |
EP1409530A2 (en) | 2004-04-21 |
CA2422730A1 (en) | 2002-03-28 |
AU2001291114A1 (en) | 2002-04-02 |
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