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  • 產(chǎn)品名稱(chēng)：ATCC9245雅致小克銀漢霉Cunninghamella elegans標(biāo)準(zhǔn)菌株菌種

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  • 產(chǎn)品廠商：ATCC
  • 產(chǎn)品文檔：
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簡(jiǎn)單介紹：
ATCC9245雅致小克銀漢霉Cunninghamella elegans標(biāo)準(zhǔn)菌株菌種
詳情介紹：
出品公司:ATCC
_菌_種名稱(chēng):ATCC9245, ATCC 9245
_菌_種又名:296 [CBS 167.53, DSM 1908, DSM 835, IMI 314507, NRRL 2310]
_菌_株類(lèi)型:雅致小克銀漢霉;綺麗小克銀漢霉;小克銀漢霉_菌_Cunninghamella elegans
存儲(chǔ)人:VM Cutter
分離來(lái)源:亞麻籽，加拿大馬尼托巴州溫克勒市亞麻籽
產(chǎn)品目錄號(hào):9245
其他保藏庫(kù)編號(hào):BCRC31841，ATCC 9245 ;CBS 167.53 ;DSM 1908 ;DSM 835 ;NRRL 2310;IMI 314507;VKM F-995
培養(yǎng)基:ATCC® Medium 200: YM agar or YM brothATCC® Medium 323: Malt agar mediumATCC® Medium 336: Potato dextrose agar (PDA)
生長(zhǎng)條件:24-26℃,  有氧
生物安_全等級(jí):1
模式_菌_株:否
應(yīng)用:科研，生產(chǎn)，主要用于水解sclareol，生產(chǎn)9,10-二甲基-1,2-苯并蒽7,12-二甲基苯并[a]蒽，產(chǎn)生肌鈣蛋白，生產(chǎn)卡霉素衍生物馬格霉素衍生物，產(chǎn)生亮霉素衍生物，生產(chǎn)尼達(dá)霉素衍生物，產(chǎn)生類(lèi)固醇，轉(zhuǎn)化阿莫沙平，轉(zhuǎn)換阿扎他定，轉(zhuǎn)化溴苯那敏，轉(zhuǎn)化撲爾敏，轉(zhuǎn)化氯丙嗪，轉(zhuǎn)化甲基二嗪，轉(zhuǎn)換苯那敏，轉(zhuǎn)化茄堿，阿莫沙平轉(zhuǎn)化為7-羥基阿莫沙平，倍半萜內(nèi)酯-科斯圖內(nèi)酯的轉(zhuǎn)化，藤架改為藤架亞砜
_菌_株特點(diǎn):
ATCC 9245是雅致小克銀漢霉,Cunninghamella elegans 。Nucleotide (GenBank) : M36310 Cunninghamella elegans 5S ribosomal RNA.
 
參考文獻(xiàn): Bloom BM, Shull GM. Epoxidation of unsaturated steroids by microorganisms. J. Am. Chem. Soc. 87: 5767-5768, 1965. Wong LK, et al. Metabolism of 7,12-dimethylbenz[a]anthracene by Cunninghamella elegans. Appl. Environ. Microbiol. 46: 1239-1242, 1983. PubMed: 6418073 Theriault RJ. Mycarosyl macrolide antibiotics. US Patent 3,784,447 dated Jan 8 1974 Wolf-Rainer A. Microbial hydroxylation of sclareol. Phytochemistry 36: 1421-1424, 1994. Zhang D, et al. Biotransformation of chlorpromazine and methdilazine by Cunninghamella elegans. Appl. Environ. Microbiol. 62: 798-803, 1996. PubMed: 8975609 Hansen EB Jr., et al. Fungal transformations of antihistamines: metabolism of brompheniramine, chlorpheniramine, and pheniramine to N-oxide and N- demethylated metabolites by the fungus Cunninghamella elegans. Xenobiotica 25: 1081-1092, 1995. PubMed: 8578764 Zhang D, et al. Fungal biotransformation of the antihistamine azatadine by Cunninghamella elegans. Appl. Environ. Microbiol. 62: 3477-3479, 1996. PubMed: 8795241 Moody JD, et al. Transformation of amoxapine by Cunninghamella elegans. Appl. Environ. Microbiol. 66: 3646-3649, 2000. PubMed: 10919836 Betts RE, et al. Microbial transformations of antitumor compounds. I. Conversion of acronycine to 9-hydroxyacronycine by Cunninghamella echinulata. J. Med. Chem. 17: 599-602, 1974. PubMed: 4829940 Clark AM, Hufford CD. Microbial transformations of the sesquiterpene lactone costunolide. J. Chem. Soc. Perkin Trans. 1979: 3022-3028, 1979. Smith RV, et al. Microbial transformations of pergolide to pergolide sulfoxide and pergolide sulfone. J. Pharm. Sci. 72: 733-736, 1983. PubMed: 6684155 Patel AV. Transformations of solasodine and derivatives of hecogenin by Cunninghamella elegans. Phytochemistry 35: 125-133, 1994. Walther G, et al. DNA barcoding in Mucorales: an inventory of biodiversity. Persoonia 30: 11-47, 2013. PubMed: 24027345 Vitale RG, et al. Antifungal susceptibility and phylogeny of opportunistic members of the order Mucorales. J Clin Microbiol 50: 66-75, 2012. PubMed: 22075600

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