首页> 外文期刊>Journal of molecular catalysis, B. Enzymatic >Microbial oxidation and glucosidation of echinocystic acid by Nocardia corallina
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Microbial oxidation and glucosidation of echinocystic acid by Nocardia corallina

机译:诺卡氏菌对棘皮囊藻酸的微生物氧化和糖化作用

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摘要

Echinocystic acid (3β,16α-dihydroxy-olean-12-en-28-oic acid 1) is a complex compound with many bioactivities. Microbial transformation of echinocystic acid (1) by Nocardia corallina CGMCC4.1037 has been studied. Incubation of echinocystic acid with N. corallina CGMCC4.1037 afforded three metabolites: 3-oxo-l 6α-hydroxy-olean-12-en-28-oic acid (2), 3β,16α-dihydroxy-olean-12-en-28-oic acid 28-O-β-D-glucopyranoside (3), and 3-oxo-16α-hydroxy-olean-12-en-28-oic acid 28-O-β-D-glucopyranoside (4). Product (4) was a new product. Their structure elucidation was mainly based on the HRMS and NMR data. The possible mechanism of the regio-selective oxidation of the 3-OH and a probable sequence of these transformations were also discussed. This is the first report on the microbial transformation of echinocystic acid (1). This method may open a new route to the future modification of echinocystic acid(1).
机译:胆囊酸(3β,16α-二羟基-油酸-12-en-28-油酸1)是一种具有多种生物活性的复杂化合物。研究了诺卡氏菌CGMCC4.1037对棘皮囊藻酸(1)的微生物转化。棘孢囊藻酸与N.corallina CGMCC4.1037的温育提供了三种代谢物:3-氧代-16α-羟基-olean-12-en-28-oic酸(2),3β,16α-二羟基-olean-12-en- 28-酸28-O-β-D-吡喃葡萄糖苷(3)和3-氧代16α-羟基-油烷基-12-en-28-酸28-O-β-D-吡喃葡萄糖苷(4)。产品(4)是新产品。它们的结构阐明主要基于HRMS和NMR数据。还讨论了3-OH的区域选择性氧化的可能机理以及这些转化的可能序列。这是棘皮囊藻酸微生物转化的第一篇报道(1)。该方法可能为以后修饰棘皮囊酸开辟一条新途径(1)。

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