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大肠杆菌中环丙烷脂肪酸的生长阶段依赖性合成是一个依赖RpoS(KatF)的启动子加上酶不稳定性的结果。

The growth phase-dependent synthesis of cyclopropane fatty acids in Escherichia coli is the result of an RpoS(KatF)-dependent promoter plus enzyme instability.

作者信息

Wang A Y, Cronan J E

机构信息

Department of Microbiology, University of Illinois, Urbana 61801.

出版信息

Mol Microbiol. 1994 Mar;11(6):1009-17. doi: 10.1111/j.1365-2958.1994.tb00379.x.

Abstract

The formation of cyclopropane fatty acids (CFAs) in Escherichia coli is a post-synthetic modification of the phospholipid bilayer that occurs predominantly as cultures enter the stationary phase of growth. The mechanism of this growth phase-dependent regulation of CFA synthesis was unclear, since log-phase and stationary-phase cultures had been reported to contain similar levels of the enzyme catalysing the reaction (CFA synthase). We report that the timing of CFA synthesis can be explained by two unusual features. Fist, the gene encoding CFA synthase (cfa) was found to be transcribed from two promoters and the 5' ends of both transcripts were mapped by primer extension. One of the promoters was active only during the log-to-stationary phase transition and depended on the putative sigma factor encoded by the rpoS(katF) gene whereas the other promoter had a standard sigma 70 promoter consensus sequence and was expressed throughout the growth curve. Second, CFA synthase activity was shown to be unstable in vivo and a Cfa fusion protein was found to have a half life of < 5 min. The combination of these factors meant that, although CFA synthase was synthesized throughout the growth curve, a large increase in activity occurred during the log-to-stationary phase transition. As stationary phase progressed, the increased CFA synthase activity rapidly declined to the basal level. This transient increase in CFA synthase activity coupled with the cessation of net phospholipid synthesis in stationary phase provides an explanation for the unusual time course of CFA synthesis.

摘要

大肠杆菌中环丙烷脂肪酸(CFAs)的形成是磷脂双层的一种合成后修饰,主要在培养物进入生长稳定期时发生。此前尚不清楚这种依赖生长阶段的CFA合成调控机制,因为有报道称对数期和稳定期培养物中催化该反应的酶(CFA合酶)水平相似。我们的研究表明,CFA合成的时间可以通过两个不同寻常的特征来解释。其一,编码CFA合酶的基因(cfa)发现由两个启动子转录,两个转录本的5'端通过引物延伸法进行了定位。其中一个启动子仅在对数期向稳定期转变时活跃,依赖于rpoS(katF)基因编码的假定sigma因子,而另一个启动子具有标准的sigma 70启动子共有序列,在整个生长曲线中均有表达。其二,CFA合酶活性在体内显示不稳定,并且发现一个Cfa融合蛋白的半衰期小于5分钟。这些因素共同作用意味着,尽管CFA合酶在整个生长曲线中都有合成,但在对数期向稳定期转变期间活性大幅增加。随着稳定期的推进,增加的CFA合酶活性迅速下降至基础水平。CFA合酶活性的这种短暂增加,再加上稳定期净磷脂合成的停止,为CFA合成不同寻常的时间进程提供了解释。

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