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Biotransformation of Cholesterol and 16α,17α-Epoxypregnenolone and Isolation of Hydroxylase in Burkholderia cepacia SE-1

机译:洋葱伯克霍尔德菌SE-1中胆固醇和16α,17α-环氧孕烯醇酮的生物转化和羟化酶的分离

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摘要

The metabolism of cholesterol is critical in eukaryotes as a precursor for vitamins, steroid hormones, and bile acids. Some steroid compounds can be transformed into precursors of steroid medicine by some microorganisms. In this study, the biotransformation products of cholesterol and 16α,17α-epoxypregnenolone produced by Burkholderia cepacia SE-1 were investigated, and a correlative enzyme, hydroxylase, was also studied. The biotransformation products, 7β-hydroxycholesterol, 7-oxocholesterol, and 20-droxyl-16α,17α-epoxypregn-1,4-dien-3-one, were purified by silica gel and Sephadex LH-20 column chromatography and identified by nuclear magnetic resonance and mass spectroscopy. The hydroxylase was isolated from the bacterium and the partial sequences of the hydroxylase, which belong to the catalases/peroxidase family, were analyzed using MS/MS analyses. The enzyme showed activity toward cholesterol and had a specific activity of 37.2 U/mg of protein at 30°C and pH 7.0.
机译:胆固醇的代谢在真核生物中作为维生素,类固醇激素和胆汁酸的前体至关重要。一些类固醇化合物可以被某些微生物转化为类固醇药物的前体。在这项研究中,研究了洋葱伯克霍尔德氏菌SE-1产生的胆固醇和16α,17α-环氧孕烯醇酮的生物转化产物,并研究了相关酶羟化酶。通过硅胶和Sephadex LH-20柱色谱法纯化生物转化产物7β-羟基胆固醇,7-氧胆固醇和20-droxyl-16α,17α-epoxypregn-1,4-dien-3-one,并通过核磁法鉴定共振和质谱。从细菌中分离羟化酶,并使用MS / MS分析法分析属于过氧化氢酶/过氧化物酶家族的羟化酶的部分序列。该酶对胆固醇表现出活性,在30°C和pH 7.0下的比活为37.2 U / mg蛋白质。

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