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Overexpression of groESL in Clostridium acetobutylicum results in increased solvent production and tolerance, prolonged metabolism, and changes in the cell's transcriptional program.丙酮丁醇梭菌中groESL的过表达导致溶剂产量增加、耐受性增强、代谢延长以及细胞转录程序的改变。
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DNA array-based transcriptional analysis of asporogenous, nonsolventogenic Clostridium acetobutylicum strains SKO1 and M5.基于DNA阵列的不产芽孢、不产溶剂丙酮丁醇梭菌菌株SKO1和M5的转录分析。
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10
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丙酮丁醇梭菌中spo0A过表达的转录分析及其对细胞丁醇胁迫响应的影响。

Transcriptional analysis of spo0A overexpression in Clostridium acetobutylicum and its effect on the cell's response to butanol stress.

作者信息

Alsaker Keith V, Spitzer Thomas R, Papoutsakis Eleftherios T

机构信息

Department of Chemical Engineering, Northwestern University, Evanston, Illinois 60208, USA.

出版信息

J Bacteriol. 2004 Apr;186(7):1959-71. doi: 10.1128/JB.186.7.1959-1971.2004.

DOI:10.1128/JB.186.7.1959-1971.2004
PMID:15028679
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC374416/
Abstract

Spo0A is the regulator of stationary-phase events and is required for transcription of solvent formation genes in Clostridium acetobutylicum. In order to elucidate the role of spo0A in differentiation, we performed transcriptional analysis of 824(pMSPOA) (a spo0A-overexpressing C. acetobutylicum strain with enhanced sporulation) against a plasmid control strain. DNA microarray data were contrasted to data from a spo0A knockout strain (SKO1) that neither sporulates nor produces solvents. Transcripts of fatty acid metabolism genes, motility and chemotaxis genes, heat shock protein genes, and genes encoding the Fts family of cell division proteins were differentially expressed in the two strains, suggesting that these genes play roles in sporulation and the solvent stress response. 824(pMSPOA) alone showed significant downregulation of many glycolytic genes in stationary phase, which is consistent with metabolic flux analysis data. Surprisingly, spo0A overexpression resulted in only nominal transcriptional changes of regulatory genes (abrB and sigF) whose expression was significantly altered in SKO1. Overexpression of spo0A imparted increased tolerance and prolonged metabolism in response to butanol stress. While most of the differentially expressed genes appear to be part of a general stress response (similar to patterns in two plasmid control strains and a groESL-overexpressing strain), several genes were expressed at higher levels at early time points after butanol challenge only in 824(pMSPOA). Most of these genes were related to butyryl coenzyme A and butyrate formation and/or assimilation, but they also included the cell division gene ftsX, the gyrase subunit-encoding genes gyrB and gyrA, DNA synthesis and repair genes, and fatty acid synthesis genes, all of which might play a role in the immediate butanol stress response, and thus in enhanced butanol tolerance.

摘要

Spo0A是稳定期事件的调节因子,也是丙酮丁醇梭菌中溶剂形成基因转录所必需的。为了阐明spo0A在分化中的作用,我们对824(pMSPOA)(一种具有增强孢子形成能力的spo0A过表达丙酮丁醇梭菌菌株)与质粒对照菌株进行了转录分析。将DNA微阵列数据与来自spo0A敲除菌株(SKO1)的数据进行对比,SKO1既不形成孢子也不产生溶剂。脂肪酸代谢基因、运动和趋化性基因、热休克蛋白基因以及编码细胞分裂蛋白Fts家族的基因在这两种菌株中的表达存在差异,表明这些基因在孢子形成和溶剂应激反应中发挥作用。单独的824(pMSPOA)在稳定期显示出许多糖酵解基因的显著下调,这与代谢通量分析数据一致。令人惊讶的是,spo0A过表达仅导致调节基因(abrB和sigF)的转录变化很小,而这些调节基因在SKO1中的表达有显著改变。spo0A的过表达赋予了对丁醇胁迫更强的耐受性和更长的代谢时间。虽然大多数差异表达基因似乎是一般应激反应的一部分(类似于两个质粒对照菌株和一个groESL过表达菌株中的模式),但只有824(pMSPOA)中的几个基因在丁醇刺激后的早期时间点表达水平更高。这些基因中的大多数与丁酰辅酶A和丁酸的形成和/或同化有关,但它们还包括细胞分裂基因ftsX、编码gyrase亚基的基因gyrB和gyrA、DNA合成和修复基因以及脂肪酸合成基因,所有这些基因可能在即时丁醇应激反应中发挥作用,从而增强对丁醇的耐受性。