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对分解代谢物阻遏不敏感的大肠杆菌鞭毛突变体的表征

Characterization of Escherichia coli flagellar mutants that are insensitive to catabolite repression.

作者信息

Silverman M, Simon M

出版信息

J Bacteriol. 1974 Dec;120(3):1196-203. doi: 10.1128/jb.120.3.1196-1203.1974.

DOI:10.1128/jb.120.3.1196-1203.1974
PMID:4373438
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC245899/
Abstract

In Escherichia coli, the synthesis of the flagellar organelle is sensitive to catabolite repression. Synthesis requires the presence of the cyclic adenosine monophosphate receptor protein (Crp) and 3',5'-cyclic adenosine monophosphate (cAMP); i.e., mutants that lack Crp or adenylcyclase (Cya) synthesize no flagella. We isolated and characterized a series of mutants (cfs) that restored flagella-forming ability in a Crp strain of E. coli. The mutations in these strains were transferred onto episomes and they were then introduced into a variety of other strains. The presence of the mutation resulted in flagella synthesis in Cya and Crp strains as well as in the wild type grown under conditions of catabolite repression. Deletion analysis and other genetic studies indicated that: (i) the cfs mutations had a dominant effect when they were in the transconfiguration in merodiploids: (ii) they occurred in or very close to the flaI gene: and (iii) their expression required the presence of an intact flaI gene adjacent to the cfs mutation. Biochemical studies showed that the synthesis of at least two flagellar polypeptides, the hook subunit and an amber fragment of flagellin, were absent in strains that carried a cya mutation. Their synthesis was depressed in strains grown under conditions of catabolite repression. The presence of the cfs mutation restored the specific synthesis of these two polypeptides. We suggest that the formation of the flaI gene product is the step in flagellar synthesis that is catabolite sensitive and requires cAMP. We propose a regulatory function for the product of the flaI gene.

摘要

在大肠杆菌中,鞭毛细胞器的合成对分解代谢物阻遏敏感。合成需要环磷酸腺苷受体蛋白(Crp)和3',5'-环磷酸腺苷(cAMP)的存在;即,缺乏Crp或腺苷酸环化酶(Cya)的突变体不合成鞭毛。我们分离并鉴定了一系列突变体(cfs),它们恢复了大肠杆菌Crp菌株的鞭毛形成能力。这些菌株中的突变被转移到附加体上,然后被引入到各种其他菌株中。该突变的存在导致Cya和Crp菌株以及在分解代谢物阻遏条件下生长的野生型中合成鞭毛。缺失分析和其他遗传学研究表明:(i)当cfs突变处于部分二倍体的反式构型时具有显性效应;(ii)它们发生在flaI基因内或非常靠近flaI基因的位置;(iii)它们的表达需要与cfs突变相邻的完整flaI基因的存在。生化研究表明,携带cya突变的菌株中不存在至少两种鞭毛多肽的合成,即钩形亚基和鞭毛蛋白的琥珀片段。在分解代谢物阻遏条件下生长的菌株中它们的合成受到抑制。cfs突变的存在恢复了这两种多肽的特异性合成。我们认为flaI基因产物的形成是鞭毛合成中对分解代谢物敏感且需要cAMP的步骤。我们提出flaI基因产物具有调节功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/787a/245899/d79d199ebe8d/jbacter00336-0216-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/787a/245899/d79d199ebe8d/jbacter00336-0216-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/787a/245899/d79d199ebe8d/jbacter00336-0216-a.jpg

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