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胆固醇被戈尔道夫氏胆固醇单胞菌降解。

Cholesterol degradation by Gordonia cholesterolivorans.

机构信息

Departamento de Bioquímica y Biología Molecular I, Universidad Complutense de Madrid, 28040 Madrid, Spain.

出版信息

Appl Environ Microbiol. 2011 Jul;77(14):4802-10. doi: 10.1128/AEM.05149-11. Epub 2011 May 27.

DOI:10.1128/AEM.05149-11
PMID:21622796
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3147395/
Abstract

This paper reports physiological and genetic data about the type strain Gordonia cholesterolivorans, a strain that is able to degrade steroid compounds containing a long carbon side chain such as cholesterol (C(27)), cholestenone (C(27)), ergosterol (C(28)), and stigmasterol (C(29)). The length of the carbon side chain appears to be of great importance for this bacterium, as the strain is unable to grow using steroids with a shorter or nonaliphatic carbon side chain such as cholic acid (C(24)), progesterone (C(21)), testosterone, androsterone, 4-androstene-3,17-dione (all C(19)), and further steroids. This study also demonstrates that the degradation of cholesterol is a quite common feature of the genus Gordonia by comparing Gordonia cholesterolivorans with some other species of this genus (e.g., G. sihwensis, G. hydrophobica, G. australis, and G. neofelifaecis). Pyrosequencing of the genome of G. cholesterolivorans led to the identification of two conventional cholesterol oxidase genes on an 8-kb and a 12.8-kb genomic fragment with genetic organizations that are quite unique as compared to the genomes of other cholesterol-degrading bacteria sequenced so far. The identified two putative cholesterol oxidases of G. cholesterolivorans are both intracellularly acting enzymes of the class I type. Whereas one of these two cholesterol oxidases (ChoOx-1) shows high identity with an oxidoreductase of the opportunistic pathogen G. bronchialis and is not transcribed during growth with cholesterol, the other one (ChoOx-2) appears phylogenetically closer to cholesterol oxidases from members of the genus Rhodococcus and is transcribed constitutively. By using targeted gene disruption, a G. cholesterolivorans ChoOx-2 gene mutant strain that was unable to grow with steroids was obtained.

摘要

本文报告了胆固醇氧化菌 Gordonia cholesterolivorans 的生理和遗传数据,该菌株能够降解含有长侧链的甾体化合物,如胆固醇(C(27))、胆甾酮(C(27))、麦角固醇(C(28))和豆甾醇(C(29))。对于这种细菌来说,碳侧链的长度似乎非常重要,因为该菌株无法使用具有较短或非脂族碳侧链的甾体化合物生长,如胆酸(C(24))、孕酮(C(21))、睾酮、雄酮、4-雄烯-3,17-二酮(均为 C(19))和其他甾体化合物。本研究还通过将胆固醇氧化菌 Gordonia cholesterolivorans 与该属的其他一些物种(如 G. sihwensis、G. hydrophobica、G. australis 和 G. neofelifaecis)进行比较,证明了胆固醇的降解是 Gordonia 属的一个相当普遍的特征。对 G. cholesterolivorans 基因组的焦磷酸测序导致在 8kb 和 12.8kb 基因组片段上鉴定出两个常规胆固醇氧化酶基因,其遗传组织与迄今为止测序的其他胆固醇降解细菌的基因组相比非常独特。鉴定出的 G. cholesterolivorans 的两种推定胆固醇氧化酶都是 I 型的细胞内作用酶。虽然这两种胆固醇氧化酶之一(ChoOx-1)与机会性病原体 G. bronchialis 的氧化还原酶具有高度同一性,并且在生长过程中不转录胆固醇,但另一种(ChoOx-2)在系统发育上似乎更接近来自 Rhodococcus 属成员的胆固醇氧化酶,并且是组成型转录的。通过使用靶向基因敲除,获得了一种无法用类固醇生长的 G. cholesterolivorans ChoOx-2 基因缺失突变株。

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本文引用的文献

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ChoG is the main inducible extracellular cholesterol oxidase of Rhodococcus sp. strain CECT3014.ChoG 是 Rhodococcus sp. 菌株 CECT3014 的主要诱导型细胞外胆固醇氧化酶。
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The Structure of Mycobacterium tuberculosis CYP125: molecular basis for cholesterol binding in a P450 needed for host infection.结核分枝杆菌 CYP125 的结构:宿主感染所需 P450 中胆固醇结合的分子基础。
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Mycobacterial cytochrome p450 125 (cyp125) catalyzes the terminal hydroxylation of c27 steroids.分枝杆菌细胞色素 p450125(cyp125)催化 c27 甾体的末端羟化。
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Cytochrome P450 125 (CYP125) catalyses C26-hydroxylation to initiate sterol side-chain degradation in Rhodococcus jostii RHA1.细胞色素 P450 125(CYP125)催化 C26-羟化作用,从而启动红球菌 RHA1 中的甾醇侧链降解。
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Cholesterol oxidase: biochemistry and structural features.胆固醇氧化酶:生物化学与结构特征。
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Morphological, physiological, and molecular characterization of a newly isolated steroid-degrading actinomycete, identified as rhodococcus ruber strain Chol-4.新分离出的一株被鉴定为红球菌Chol-4的甾体降解放线菌的形态学、生理学及分子特征
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