Beauveria bassiana (Balsamo) Vuillemin, anamorph (ATCC® 7159)

Strain Designations: CBS 209.27 [DSM 1344]  /  Product Format: freeze-dried

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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 dialkylbenzene
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
Product Format freeze-dried
Type Strain yes (type strain of Sporotrichum sulfurescens)
Preceptrol® no
Medium Medium 336: Potato dextrose agar (PDA)
Growth Conditions
Temperature: 24.0°C
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.

. . 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

. . Tetrahedron Lett. 22: 445-448, 1981.

. . 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.

. . 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.

type strain of Sporotrichum sulfurescens

type strain of Sporotrichum sulfurescens

Notice: Necessary PermitsPermits

These permits may be required for shipping this product:

  • Customers located in the state of Hawaii will need to contact the Hawaii Department of Agriculture to determine if an Import Permit is required. A copy of the permit or documentation that a permit is not required must be sent to ATCC in advance of shipment.
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