| 产品名称： | Beauveria bassiana (Balsamo) Vuillemin |
|---|---|
| 商品货号： | TS205494 |
| Deposited As： | Sporotrichum sulfurescens van Beyma |
| Strain Designations： | CBS 209.27 DSM 1344 |
| Application： | Hydrolyzes 1,2-dihydronaphthalene
Hydrolyzes 1,2-epoxyindene
Hydrolyzes styrene oxide
Hydroxylates polycyclic enones
Metabolizes phencyclidine
Oxidizes arteether
Oxidizes dialkylbenzen Hydroxylates e
Produces 2-deuterio-cycloalkanones
Produces 3-deuterio-cycloalkanones
Produces carbomycin derivatives magnamycin derivatives
Produces hydroxymethylpyridines (isomeric)
Produces leucomycin derivatives
Produces niddamycin derivatives
Hydroxylation of 7-azabrendane and 6-azatwistane derivatives
Hydroxylation of synthetic polycyclic enones
Reduction of alpha, beta-unsaturated ketones
Converts isosorbide dinitrate to isosorbide 5-mononitrate
Transformation of pergolide to pergolide sulfoxide
Glycosylation of 2,2,5,7,8-pentamethyl-6-hydroxychroman |
| Biosafety Level： | 1
Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country. |
| Product Format： | freeze-dried |
| Storage Conditions： | Frozen: -80°C or colder Freeze-Dried: 2°C to 8°C Live Culture: See Propagation Section |
| Type Strain： | yes (type strain of Sporotrichum sulfurescens) |
| Preceptrol®： | no |
| Medium： | ATCC® Medium 200: YM agar or YM broth ATCC® Medium 324: Malt extract agar ATCC® Medium 336: Potato dextrose agar (PDA) |
| Growth Conditions： | Temperature: 24°C to 26°C Atmosphere: Typical aerobic |
| Sequenced Data： |
18S ribosomal RNA gene, partial sequence; internal transcribed spacer 1, 5.8S ribosomal RNA gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, partial sequence GGTCTCCGTTGGTGAACCAGCGGAGGGATCATTACCGAGTTTTCAACTCCCTAACCCTTCTGTGAACCTACCTATCGTTGCTTCGGCGGACTCGCCCCAGCCCGGACGCGGACTGGACCAGCGGCCCGCCGGGGACCTCAAACTCTTGTATTCCAGCATCTTCTGAATACGCCGCAAGGCAAAACAAATGAATCAAAACTTTCAACAACGGATCTCTTGGCTCTGGCATCGATGAAGAACGCAGCGAAACGCGATAAGTAATGTGAATTGCAGAATCCAGTGAATCATCGAATCTTTGAACGCACATTGCGCCCGCCAGCATTCTGGCGGGCATGCCTGTTCGAGCGTCATTTCAACCCTCGACCTCCCCTTGGGGAGGTCGGCGTTGGGGACCGGCAGCACACCGCCGGCCCTGAAATGGAGTGGCGGCCCGTCCGCGGCGACCTCTGCGCAGTAATACAGCTCGCACCGGAACCCCGACGCGGCCACGCCGTAAAACACCCAACTTCTGAACGTTGACCTCGAATCAGGTAGGACTACCCGCTGAACTTAAGCATATCAATAA D1D2 region of the 28S ribosomal RNA gene ATATCAATAAGCGGAGGAAAAGAAACCAACAGGGATTGCCCCAGTAACGGCGAGTGAAGCGGCAACAGCTCAAATTTGAAATCTGGCTCTCAGGGCCCGAGTTGTAATTTGTAGAGGATGCTTTTGGCGAGGTGCCTTCCGAGTTCCCTGGAACGGGACGCCACAGAGGGTGAGAGCCCCGTATGGTCGGACACCGAGCCTCTGTAAAGCTCCTTCGACGAGTCGAGTAGTTTGGGAATGCTGCTCAAAATGGGAGGTATATGTCTTCTAAAGCTAAATATTGGCCAGAGACCGATAGCGCACAAGTAGAGTGATCGAAAGATGAAAAGCACTTTGAAAAGAGGGTTAAAAAGTACGTGAAATTGTTGAAAGGGAAGCGCCTATGACCAGACTTGCGCCCGGTGAATCACCCAGCGTTCTCGCTGGTGCACTTTGCCGGGCACAGGCCAGCATCAGTTCAGCGCGGGGGAGAAAGGCTTCGGGAATGTGGCTCCCTCGGGAGTGTTATAGCCCGCTGCGTAATGCCCTGCGCCGGACTGAGGTACGCGCATTGCAAGGATGCTGGCGTAATGGTCATCAGCGAC RNA polymerase II largest subunit gene (RPB1) CCATATAGAGCTGGCGAAACCTGTCTATCACCCTGGTTTCATCAAGAAAGTGAAAAAGGTTTTGGAGATTGTCTGCCACAACTGCAGCAAAGTGTTGGCCGATGAAGTTGGTCTTCCCTTTACTCCATGAAGCTCTGGAGCTTGCTGGATGCTAACGTGCATTATCAGAGCGATCCCGAATTCGTCACAGCTATTCATACTCGCGATCCGAAACTCCGATTCAAGCGCGTTTGGGCCGTATGCAAGAAGAAGCGCAAATGCGAGAATGAGGAGCGGCAAGACAAGAATAAAGACGAAGAGTTCGCTCCAGGTGTCAAGAACGTCGTTCTCGAAGGACATGGCGGATGTGGCAATATGCAGCCGCAGGTGAGACAGGCCGCGCTGCAACTCAAAGCTGCCTTCGAGGTTACTTCGGAAGAGGGTCCCAAGAGGAAAGAGACGGTTAATATCAGCGCCGAGATGGCGCATGGTATCCTTCGCCGCATCTCTGAGCGCGATCTGCACAATATTGGTCTTAACTCAGACTATGCTCGTCCCGAGTGGATGATCATCACTGTCCTGCCTGTACCCCCTCCTCCCGTGCGTCCTAGTATTTCCATGGATGGTACTGGTACTGGCACGAGAAACGAGGATGATCTGACCTACAAGCTTGGTGACATTATCCGCGCCAACGGAAATGTCAAGCAGGCCATTCGTGAAGGATCACCGCAACACATCGCGCGTGATTTTGAGGAGCTGCTGCAGTACCATGTTGCCACC |
| Name of Depositor： | CBS |
| Chain of Custody： | ATCC <-- CBS <-- F.H. van Beyma |
| Isolation： | Laboratory contaminant |
| References： | Ropenga JS, et al. Isosorbide dinitrate bioconversion by Beauveria strains: implication of glutathione transferase levels. Appl. Microbiol. Biotechnol. 31: 176-178, 1989. Pedragosa-Moreau S, et al. Microbiological transformations. 28. Enantiocomplementary epoxide hydrolyses as a preparative access to both enantiomers of styrene oxide. J. Org. Chem. 58: 5533-5536, 1993. Theriault RJ. Mycarosyl macrolide antibiotics. US Patent 3,784,447 dated Jan 8 1974 Taylor JJ. Further clarification of Sporotrichum species. Mycologia 62: 823, 1970. Johnson RA, et al. Microbial oxygenation of dialkylbenzenes. Bioorg Chem 2: 99-110, 1973. Kergomard A, et al. Microbiological reduction of alpha,beta-unsaturated ketones by Beauveria sulfurescens. J. Org. Chem. 47: 792-798, 1982. Hu Y, et al. Microbial oxidataion of the antimalarial drug arteether. Bioorg. Chem. 20: 148-154, 1992. Hufford CD, et al. Metabolism of phencyclidine by microorganisms. J. Pharm. Sci. 70: 155-158, 1981. PubMed: 7205218 Furstoss R, et al. Microbiological transformations 2. Hydroxylations of non activated carbons in globular type amides. Tetrahedron Lett 22: 445-448, 1981. Dauphin G, et al. Microbiological synthesis and circular dichroism of optically active 2-deuterio-cycloalkanones. Tetrahedron Lett 21: 4275-4278, 1980. Pedragosa-Moreau S, et al. Microbiological transformations. 31: Synthesis of enantiopure epoxides and vicinal diols using fungal epoxide hydrolase mediated hydrolysis. Tetrahedron Lett. 37: 3319-3322, 1996. Dauphin G, et al. Microbial glycosylation of 2, 2, 5, 7, 8-pentamethyl- 6-hydroxychroman. Agric Biol Chem 53: 1433-1435, 1989. Dauphin G, et al. Microbiological synthesis of optically active 3-deuterio-cycloalkanones. J. Chem. Soc. Chem. Commun. 1980: 318-319, 1980. Smith RV, et al. Microbial transformations of pergolide to pergolide sulfoxide and pergolide sulfone. J. Pharm. Sci. 72: 733-736, 1983. PubMed: 6684155 Modyanova LV, et al. Microbial transformation of nitrogen-containing heterocyclic compounds. I. Hydroxylation of isomeric monomethylpyridines and dimethylpyridines by microscopic fungi. Biotekhnologiya 3: 24-27, 1990. Hammoumi A, et al. Microbial hydroxylation and functionalization of synthetic polycyclic enones. Tetrahedron Asymmetry 4: 1295-1306, 1993. Xu Y, et al. Biosynthesis of the cyclooligomer depsipeptide bassianolide, an insecticidal virulence factor of Beauveria bassiana. Fungal Genet. Biol. 46: 353-364, 2009. PubMed: 19285149 Xu Y, et al. Biosynthesis of the cyclooligomer depsipeptide beauvericin, a virulence factor of the entomopathogenic fungus Beauveria bassiana. Chem. Biol. 15: 898-907, 2008. PubMed: 18804027 type strain of Sporotrichum sulfurescens |
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| 产品名称： | Beauveria bassiana (Balsamo) Vuillemin |
|---|---|
| 商品货号： | TS205494 |
| Deposited As： | Sporotrichum sulfurescens van Beyma |
| Strain Designations： | CBS 209.27 DSM 1344 |
| Application： | Hydrolyzes 1,2-dihydronaphthalene
Hydrolyzes 1,2-epoxyindene
Hydrolyzes styrene oxide
Hydroxylates polycyclic enones
Metabolizes phencyclidine
Oxidizes arteether
Oxidizes dialkylbenzen Hydroxylates e
Produces 2-deuterio-cycloalkanones
Produces 3-deuterio-cycloalkanones
Produces carbomycin derivatives magnamycin derivatives
Produces hydroxymethylpyridines (isomeric)
Produces leucomycin derivatives
Produces niddamycin derivatives
Hydroxylation of 7-azabrendane and 6-azatwistane derivatives
Hydroxylation of synthetic polycyclic enones
Reduction of alpha, beta-unsaturated ketones
Converts isosorbide dinitrate to isosorbide 5-mononitrate
Transformation of pergolide to pergolide sulfoxide
Glycosylation of 2,2,5,7,8-pentamethyl-6-hydroxychroman |
| Biosafety Level： | 1
Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country. |
| Product Format： | freeze-dried |
| Storage Conditions： | Frozen: -80°C or colder Freeze-Dried: 2°C to 8°C Live Culture: See Propagation Section |
| Type Strain： | yes (type strain of Sporotrichum sulfurescens) |
| Preceptrol®： | no |
| Medium： | ATCC® Medium 200: YM agar or YM broth ATCC® Medium 324: Malt extract agar ATCC® Medium 336: Potato dextrose agar (PDA) |
| Growth Conditions： | Temperature: 24°C to 26°C Atmosphere: Typical aerobic |
| Sequenced Data： |
18S ribosomal RNA gene, partial sequence; internal transcribed spacer 1, 5.8S ribosomal RNA gene, and internal transcribed spacer 2, complete sequence; and 28S ribosomal RNA gene, partial sequence GGTCTCCGTTGGTGAACCAGCGGAGGGATCATTACCGAGTTTTCAACTCCCTAACCCTTCTGTGAACCTACCTATCGTTGCTTCGGCGGACTCGCCCCAGCCCGGACGCGGACTGGACCAGCGGCCCGCCGGGGACCTCAAACTCTTGTATTCCAGCATCTTCTGAATACGCCGCAAGGCAAAACAAATGAATCAAAACTTTCAACAACGGATCTCTTGGCTCTGGCATCGATGAAGAACGCAGCGAAACGCGATAAGTAATGTGAATTGCAGAATCCAGTGAATCATCGAATCTTTGAACGCACATTGCGCCCGCCAGCATTCTGGCGGGCATGCCTGTTCGAGCGTCATTTCAACCCTCGACCTCCCCTTGGGGAGGTCGGCGTTGGGGACCGGCAGCACACCGCCGGCCCTGAAATGGAGTGGCGGCCCGTCCGCGGCGACCTCTGCGCAGTAATACAGCTCGCACCGGAACCCCGACGCGGCCACGCCGTAAAACACCCAACTTCTGAACGTTGACCTCGAATCAGGTAGGACTACCCGCTGAACTTAAGCATATCAATAA D1D2 region of the 28S ribosomal RNA gene ATATCAATAAGCGGAGGAAAAGAAACCAACAGGGATTGCCCCAGTAACGGCGAGTGAAGCGGCAACAGCTCAAATTTGAAATCTGGCTCTCAGGGCCCGAGTTGTAATTTGTAGAGGATGCTTTTGGCGAGGTGCCTTCCGAGTTCCCTGGAACGGGACGCCACAGAGGGTGAGAGCCCCGTATGGTCGGACACCGAGCCTCTGTAAAGCTCCTTCGACGAGTCGAGTAGTTTGGGAATGCTGCTCAAAATGGGAGGTATATGTCTTCTAAAGCTAAATATTGGCCAGAGACCGATAGCGCACAAGTAGAGTGATCGAAAGATGAAAAGCACTTTGAAAAGAGGGTTAAAAAGTACGTGAAATTGTTGAAAGGGAAGCGCCTATGACCAGACTTGCGCCCGGTGAATCACCCAGCGTTCTCGCTGGTGCACTTTGCCGGGCACAGGCCAGCATCAGTTCAGCGCGGGGGAGAAAGGCTTCGGGAATGTGGCTCCCTCGGGAGTGTTATAGCCCGCTGCGTAATGCCCTGCGCCGGACTGAGGTACGCGCATTGCAAGGATGCTGGCGTAATGGTCATCAGCGAC RNA polymerase II largest subunit gene (RPB1) CCATATAGAGCTGGCGAAACCTGTCTATCACCCTGGTTTCATCAAGAAAGTGAAAAAGGTTTTGGAGATTGTCTGCCACAACTGCAGCAAAGTGTTGGCCGATGAAGTTGGTCTTCCCTTTACTCCATGAAGCTCTGGAGCTTGCTGGATGCTAACGTGCATTATCAGAGCGATCCCGAATTCGTCACAGCTATTCATACTCGCGATCCGAAACTCCGATTCAAGCGCGTTTGGGCCGTATGCAAGAAGAAGCGCAAATGCGAGAATGAGGAGCGGCAAGACAAGAATAAAGACGAAGAGTTCGCTCCAGGTGTCAAGAACGTCGTTCTCGAAGGACATGGCGGATGTGGCAATATGCAGCCGCAGGTGAGACAGGCCGCGCTGCAACTCAAAGCTGCCTTCGAGGTTACTTCGGAAGAGGGTCCCAAGAGGAAAGAGACGGTTAATATCAGCGCCGAGATGGCGCATGGTATCCTTCGCCGCATCTCTGAGCGCGATCTGCACAATATTGGTCTTAACTCAGACTATGCTCGTCCCGAGTGGATGATCATCACTGTCCTGCCTGTACCCCCTCCTCCCGTGCGTCCTAGTATTTCCATGGATGGTACTGGTACTGGCACGAGAAACGAGGATGATCTGACCTACAAGCTTGGTGACATTATCCGCGCCAACGGAAATGTCAAGCAGGCCATTCGTGAAGGATCACCGCAACACATCGCGCGTGATTTTGAGGAGCTGCTGCAGTACCATGTTGCCACC |
| Name of Depositor： | CBS |
| Chain of Custody： | ATCC <-- CBS <-- F.H. van Beyma |
| Isolation： | Laboratory contaminant |
| References： | Ropenga JS, et al. Isosorbide dinitrate bioconversion by Beauveria strains: implication of glutathione transferase levels. Appl. Microbiol. Biotechnol. 31: 176-178, 1989. Pedragosa-Moreau S, et al. Microbiological transformations. 28. Enantiocomplementary epoxide hydrolyses as a preparative access to both enantiomers of styrene oxide. J. Org. Chem. 58: 5533-5536, 1993. Theriault RJ. Mycarosyl macrolide antibiotics. US Patent 3,784,447 dated Jan 8 1974 Taylor JJ. Further clarification of Sporotrichum species. Mycologia 62: 823, 1970. Johnson RA, et al. Microbial oxygenation of dialkylbenzenes. Bioorg Chem 2: 99-110, 1973. Kergomard A, et al. Microbiological reduction of alpha,beta-unsaturated ketones by Beauveria sulfurescens. J. Org. Chem. 47: 792-798, 1982. Hu Y, et al. Microbial oxidataion of the antimalarial drug arteether. Bioorg. Chem. 20: 148-154, 1992. Hufford CD, et al. Metabolism of phencyclidine by microorganisms. J. Pharm. Sci. 70: 155-158, 1981. PubMed: 7205218 Furstoss R, et al. Microbiological transformations 2. Hydroxylations of non activated carbons in globular type amides. Tetrahedron Lett 22: 445-448, 1981. Dauphin G, et al. Microbiological synthesis and circular dichroism of optically active 2-deuterio-cycloalkanones. Tetrahedron Lett 21: 4275-4278, 1980. Pedragosa-Moreau S, et al. Microbiological transformations. 31: Synthesis of enantiopure epoxides and vicinal diols using fungal epoxide hydrolase mediated hydrolysis. Tetrahedron Lett. 37: 3319-3322, 1996. Dauphin G, et al. Microbial glycosylation of 2, 2, 5, 7, 8-pentamethyl- 6-hydroxychroman. Agric Biol Chem 53: 1433-1435, 1989. Dauphin G, et al. Microbiological synthesis of optically active 3-deuterio-cycloalkanones. J. Chem. Soc. Chem. Commun. 1980: 318-319, 1980. Smith RV, et al. Microbial transformations of pergolide to pergolide sulfoxide and pergolide sulfone. J. Pharm. Sci. 72: 733-736, 1983. PubMed: 6684155 Modyanova LV, et al. Microbial transformation of nitrogen-containing heterocyclic compounds. I. Hydroxylation of isomeric monomethylpyridines and dimethylpyridines by microscopic fungi. Biotekhnologiya 3: 24-27, 1990. Hammoumi A, et al. Microbial hydroxylation and functionalization of synthetic polycyclic enones. Tetrahedron Asymmetry 4: 1295-1306, 1993. Xu Y, et al. Biosynthesis of the cyclooligomer depsipeptide bassianolide, an insecticidal virulence factor of Beauveria bassiana. Fungal Genet. Biol. 46: 353-364, 2009. PubMed: 19285149 Xu Y, et al. Biosynthesis of the cyclooligomer depsipeptide beauvericin, a virulence factor of the entomopathogenic fungus Beauveria bassiana. Chem. Biol. 15: 898-907, 2008. PubMed: 18804027 type strain of Sporotrichum sulfurescens |
