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分枝杆菌 VKM Ac-1817D 生产 9-羟基雄烯二酮菌株的植物甾醇全基因组反应。

Genome-wide response on phytosterol in 9-hydroxyandrostenedione-producing strain of Mycobacterium sp. VKM Ac-1817D.

机构信息

Institute of Biochemistry and Physiology of Microorganisms, Federal Research Center "Pushchino Center for Biological Research of the Russian Academy of Sciences", Nauki, 5, Pushchino, Russian Federation, 142290.

Pharmins Ltd., Institutskaya, 4, Pushchino, Russian Federation, 142290.

出版信息

BMC Biotechnol. 2019 Jun 25;19(1):39. doi: 10.1186/s12896-019-0533-7.

Abstract

BACKGROUND

Aerobic side chain degradation of phytosterols by actinobacteria is the basis for the industrial production of androstane steroids which are the starting materials for the synthesis of steroid hormones. A native strain of Mycobacterium sp. VKM Ac-1817D effectively produces 9α-hydroxyandrost-4-ene-3,17-dione (9-OH-AD) from phytosterol, but also is capable of slow steroid core degradation. However, the set of the genes with products that are involved in phytosterol oxidation, their organisation and regulation remain poorly understood.

RESULTS

High-throughput sequencing of the global transcriptomes of the Mycobacterium sp. VKM Ac-1817D cultures grown with or without phytosterol was carried out. In the presence of phytosterol, the expression of 260 genes including those related to steroid catabolism pathways significantly increased. Two of the five genes encoding the oxygenase unit of 3-ketosteroid-9α-hydroxylase (kshA) were highly up-regulated in response to phytosterol (55- and 25-fold, respectively) as well as one of the two genes encoding its reductase subunit (kshB) (40-fold). Only one of the five putative genes encoding 3-ketosteroid-∆-dehydrogenase (KstD_1) was up-regulated in the presence of phytosterol (61-fold), but several substitutions in the conservative positions of its product were revealed. Among the genes over-expressed in the presence of phytosterol, several dozen genes did not possess binding sites for the known regulatory factors of steroid catabolism. In the promoter regions of these genes, a regularly occurring palindromic motif was revealed. The orthologue of TetR-family transcription regulator gene Rv0767c of M. tuberculosis was identified in Mycobacterium sp. VKM Ac-1817D as G155_05115.

CONCLUSIONS

High expression levels of the genes related to the sterol side chain degradation and steroid 9α-hydroxylation in combination with possible defects in KstD_1 may contribute to effective 9α-hydroxyandrost-4-ene-3,17-dione accumulation from phytosterol provided by this biotechnologically relevant strain. The TetR-family transcription regulator gene G155_05115 presumably associated with the regulation of steroid catabolism. The results are of significance for the improvement of biocatalytic features of the microbial strains for the steroid industry.

摘要

背景

放线菌对植物甾醇的需氧侧链降解是工业生产雄烷甾体的基础,而雄烷甾体又是合成甾体激素的起始原料。一种土生土长的分枝杆菌菌株 Mycobacterium sp. VKM Ac-1817D 可以有效地从植物甾醇中生产 9α-羟基雄甾-4-烯-3,17-二酮(9-OH-AD),但也能够缓慢地降解甾体核心。然而,参与植物甾醇氧化、其组织和调控的基因仍知之甚少。

结果

对 Mycobacterium sp. VKM Ac-1817D 培养物的全球转录组进行了高通量测序,这些培养物在有无植物甾醇的情况下生长。在植物甾醇存在的情况下,260 个基因(包括与类固醇分解代谢途径相关的基因)的表达显著增加。编码 3-酮类固醇-9α-羟化酶(kshA)氧合酶单位的五个基因中的两个,以及编码其还原酶亚基的两个基因中的一个(kshB)(分别为 55 倍和 25 倍),对植物甾醇的响应高度上调。在植物甾醇存在的情况下,五个假定的 3-酮类固醇-∆-脱氢酶(KstD_1)基因之一被上调(61 倍),但发现其产物在保守位置发生了几个取代。在植物甾醇存在下表达上调的基因中,有几十个基因不具有类固醇分解代谢已知调控因子的结合位点。在这些基因的启动子区域,发现了一个经常出现的回文基序。结核分枝杆菌 TetR 家族转录调节因子基因 Rv0767c 的同源物在分枝杆菌菌株 Mycobacterium sp. VKM Ac-1817D 中被鉴定为 G155_05115。

结论

与甾醇侧链降解和类固醇 9α-羟化相关的基因的高表达水平,加上 KstD_1 可能存在的缺陷,可能有助于这种具有生物技术相关性的菌株有效地从植物甾醇中积累 9α-羟基雄甾-4-烯-3,17-二酮。TetR 家族转录调节因子基因 G155_05115 可能与类固醇分解代谢的调控有关。这些结果对于改善微生物菌株在甾体工业中的生物催化特性具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94e6/6593523/81eda3066c8d/12896_2019_533_Fig1_HTML.jpg

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