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大肠杆菌磷限制期间合成蛋白质的全局分析。

Global analysis of proteins synthesized during phosphorus restriction in Escherichia coli.

作者信息

VanBogelen R A, Olson E R, Wanner B L, Neidhardt F C

机构信息

Department of Biotechnology, Parke-Davis Pharmaceutical Research, Division of Warner-Lambert, Ann Arbor, Michigan 48105, USA.

出版信息

J Bacteriol. 1996 Aug;178(15):4344-66. doi: 10.1128/jb.178.15.4344-4366.1996.

Abstract

The pattern of proteins synthesized in Escherichia coli during steady-state growth in media with ample inorganic phosphate (Pi), upon limitation for Pi (without an alternative phosphorous compound), and during steady-state growth in media containing phosphonate (PHN) as the sole P source was examined by two-dimensional gel electrophoresis. Of 816 proteins monitored in these experiments, all those with differential synthesis rates greater than 2.0 or less than 0.5 upon phosphate limitation (P limitation) or during growth on PHN compared with their rates in the cultures with Pi were classified as belonging to the PL or PHN stimulon, respectively. The PL stimulon included 413 proteins, 208 showing induced synthesis and 205 showing repressed synthesis. The PHN stimulon was smaller: it included 257 proteins; 227 showed induced synthesis and 30 showed repressed synthesis. The overlap of the two stimulons included 137 proteins: most (118) were ones showing induced synthesis. The promoter regions of genes for several of the proteins with induced or repressed synthesis contained sequences which resembled the consensus sequence for PhoB binding. The aggregate mass of proteins responding to P limitation or growth on PHN was 30 to 40% of the cells' total mass. By comparing the proteins responding to P limitation with those responding to growth on PHN, one can speculate which proteins are likely involved in adapting cells to new P sources or in preparing cells to survive stationary phase.

摘要

通过二维凝胶电泳,研究了大肠杆菌在含有充足无机磷酸盐(Pi)的培养基中稳态生长时、Pi受限(无替代磷化合物)时以及在以膦酸盐(PHN)作为唯一磷源的培养基中稳态生长时合成蛋白质的模式。在这些实验中监测的816种蛋白质中,所有在磷酸盐限制(P限制)或在PHN上生长时与在含Pi培养基中的合成速率相比,合成速率差异大于2.0或小于0.5的蛋白质,分别归类为属于PL或PHN刺激子。PL刺激子包括413种蛋白质,其中208种显示合成诱导,205种显示合成抑制。PHN刺激子较小:它包括257种蛋白质;227种显示合成诱导,30种显示合成抑制。两个刺激子的重叠部分包括137种蛋白质:大多数(118种)是显示合成诱导的蛋白质。几种合成诱导或抑制的蛋白质的基因启动子区域包含类似于PhoB结合共有序列的序列。响应P限制或在PHN上生长的蛋白质的总质量占细胞总质量的30%至40%。通过比较响应P限制的蛋白质与响应在PHN上生长的蛋白质,可以推测哪些蛋白质可能参与使细胞适应新的磷源或使细胞为在稳定期存活做准备。

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