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引用本文:李于善,贺艳.白首乌C21甾苷元C11α-羟化的两种微生物同步转化[J].中国现代应用药学,2009,(9):716-719.
LI Yushan, HE Yan.C11 α-hydroxylation of C21 Steroidal Aglycones in Cynanchum Auriculatum by Microbial Simultaneously Transformation[J].Chin J Mod Appl Pharm(中国现代应用药学),2009,(9):716-719.
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白首乌C21甾苷元C11α-羟化的两种微生物同步转化
李于善,贺艳
作者单位
李于善,贺艳  
摘要:
目的对白首乌C21甾苷元告达庭甾苷元和开德甾苷元(Ⅱ) 实现C11α-羟基化,要求副产物少,收率高。方法采用黑根霉(Rhizopus nigricans) 和犁头霉(Absidia sp.)两种微生物在水-正丁醇双相体系中同步转化的方法,羟化反应中控制值pH在5.0~6.0,于30 ℃温度下振荡培养70 h。结果产物经IR、MS、NMR分析确认是C11α-羟基化了的告达庭甾苷元(Ⅲ)和开德甾苷元(Ⅲ) ,副产物少,收率达70.1%。结论用黑根霉(Rhizopusnigricans) 和犁头霉(Absidia sp.)两种微生物在水-正丁醇双相体系中同步转化的方法是实现C11α-羟基化的有效方法。
关键词:  黑根霉  犁头霉  C11α-羟基化  同步转化
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C11 α-hydroxylation of C21 Steroidal Aglycones in Cynanchum Auriculatum by Microbial Simultaneously Transformation
LI Yushan, HE Yan
Abstract:
OBJECTIVE Two species of C21 steroidal aglycones of Caudatin steroidal aglycones and Kaider steroidal aglycones, which were extracted from Cynanchum auriculatum, could be C11 α-hydroxylated with low by-product content and high-yield objectives. METHODS Rhizopus nigricans and Absidia sp. Were used to synchronized transformation and by shaking cultivation for 70 hours at 30 ℃ in water/butanol two-phase system with pH=5.0-6.0. RESULTS The products were confirmed to be C11 α-hydroxylated Caudatin steroidal aglycones and Kaider steroidal aglycones by IR, MS, and NMR. The results also indicated that by-product content was low and the yield of objectives was up to 70.1%. CONCLUSIONS The method was high effective for C11 α-hydroxylation of C21 steroidal aglycones in water/butanol two-phase system by Rhizopus nigricans and Absidia sp
Key words:  Rhizopus nigricans  Absidia sp  C11 α-hydroxylation  synchronous
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