首页> 外文OA文献 >Effect of cell growth rate on expression of the anaerobic respiratory pathway operons frdABCD, dmsABC, and narGHJI of Escherichia coli.
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Effect of cell growth rate on expression of the anaerobic respiratory pathway operons frdABCD, dmsABC, and narGHJI of Escherichia coli.

机译:细胞生长速率对大肠杆菌厌氧呼吸途径操纵子frdABCD,dmsABC和narGHJI表达的影响。

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摘要

The fumarate reductase (frdABCD), dimethyl sulfoxide (DMSO)-trimethylamine-N-oxide (TMAO) reductase (dmsABC), and nitrate reductase (narGHJI) operons in Escherichia coli encode enzymes involved in anaerobic respiration to the electron acceptors fumarate, DMSO or TMAO, and nitrate, respectively. They are regulated in response to anaerobiosis and nitrate availability. To determine how each operon is regulated in response to changes in cell growth rate and in oxygen availability, expression of frdA-lacZ, dmsA-lacZ, and narG-lacZ fusion genes was examined during continuous culture. After a change in the cell growth rate, each anaerobic electron transport pathway operon fusion responded somewhat differently. Whereas frdA-lacZ expression increased by fivefold as the growth rate decreased from 0.60 to 0.12/hour during aerobic growth, little change was seen under anaerobic conditions. In contrast, growth rate-dependent expression of narG-lacZ expression occurred under anaerobic conditions but not under aerobic conditions. Finally, dmsA-lacZ expression did not vary greatly for any of the growth rates tested. When cells were shifted from aerobic to anaerobic growth conditions, expression of each fusion increased at a moderate rate and peaked or "overshot" before reaching a new equilibrium value. This "overshoot" phenomenon was independent of the fnr gene product, which functions as a transcriptional activator of each respiratory operon during anaerobic conditions. In contrast to the moderate rate of anaerobic induction seen for narG-lacZ expression, the addition of nitrate caused a rapid induction response. The cell appears to have many ways to adjust cell respiration in response to changes in cell growth conditions.
机译:大肠杆菌中的富马酸酯还原酶(frdABCD),二甲基亚砜(DMSO)-三甲胺-N-氧化物(TMAO)还原酶(dmsABC)和硝酸盐还原酶(narGHJI)操纵子编码参与厌氧呼吸至富马酸酯电子受体,DMSO或DMSO的酶TMAO和硝酸盐。它们被调节以响应厌氧菌和硝酸盐的供应。为了确定如何响应细胞生长速率和氧气利用率的变化调节每个操纵子,在连续培养过程中检查了frdA-lacZ,dmsA-lacZ和narG-lacZ融合基因的表达。细胞生长速度发生变化后,每个厌氧电子转运途径操纵子融合的反应都有些不同。在好氧生长过程中,frdA-lacZ表达随生长速率从0.60下降至0.12 /小时而增加了五倍,而在厌氧条件下几乎没有变化。相反,narG-lacZ表达的依赖生长的表达发生在厌氧条件下,而不发生在有氧条件下。最后,对于任何测试的生长速率,dmsA-lacZ表达都没有太大变化。当细胞从有氧生长条件变为无氧生长条件时,每种融合蛋白的表达均以中等速率增加,并在达到新的平衡值之前达到峰值或“超量”。这种“过冲”现象与fnr基因产物无关,后者在厌氧条件下充当每个呼吸操纵子的转录激活子。与narG-lacZ表达所见的中等厌氧诱导率相反,硝酸盐的添加引起了快速的诱导反应。该细胞似乎具有响应细胞生长条件变化而调节细胞呼吸的许多方法。

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