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乙酰磷酸和渗透压调节因子OmpR对大肠杆菌鞭毛表达的调控

Modulation of flagellar expression in Escherichia coli by acetyl phosphate and the osmoregulator OmpR.

作者信息

Shin S, Park C

机构信息

Department of Biological Sciences, Korea Advanced Institute of Science and Technology, Yusong-Ku, Taejon.

出版信息

J Bacteriol. 1995 Aug;177(16):4696-702. doi: 10.1128/jb.177.16.4696-4702.1995.

Abstract

During the search for unknown factors involved in motility, we have found that expression of the flagellar master operon flhDC is affected by mutations of the pta and ackA genes, encoding phosphotransacetylase and acetate kinase, respectively (S. Shin, J. Sheen, and C. Park, Korean J. Microbiol. 31:504-511, 1993). Here we describe results showing that this effect is modulated by externally added acetate, except when both pta and ackA are mutated, suggesting the role of acetyl phosphate, an intermediate of acetate metabolism, as a regulatory effector. Furthermore, the following evidence indicates that the phosphorylation of OmpR, a trans factor for osmoregulation, regulates flagellar expression. First, in a strain lacking ompR, the expression of flhDC is no longer responsive to a change in the level of acetyl phosphate. Second, an increase in medium osmolarity does not decrease flhDC expression in an ompR mutant. It is known that such an increase normally enhances OmpR phosphorylation. Third, OmpR protein binds to the DNA fragment containing the flhDC promoter, and its affinity is increased with phosphorylation by acetyl phosphate. DNase I footprinting revealed the regions of the flhDC promoter protected by OmpR in the presence or absence of phosphorylation. Therefore, we propose that the phosphorylated OmpR, generated by either osmolarity change or the internal level of acetyl phosphate, negatively regulates the expression of flagella.

摘要

在寻找与运动性相关的未知因素的过程中,我们发现鞭毛主操纵子flhDC的表达受到pta和ackA基因(分别编码磷酸转乙酰酶和乙酸激酶)突变的影响(S. Shin、J. Sheen和C. Park,《韩国微生物学杂志》31:504 - 511,1993年)。在此我们描述的结果表明,除了pta和ackA都发生突变的情况外,这种影响会受到外部添加乙酸盐的调节,这表明乙酸代谢中间体乙酰磷酸作为一种调节效应物发挥作用。此外,以下证据表明渗透压调节的反式作用因子OmpR的磷酸化调节鞭毛表达。首先,在缺乏ompR的菌株中,flhDC的表达不再对乙酰磷酸水平的变化作出反应。其次,培养基渗透压的增加在ompR突变体中不会降低flhDC的表达。已知这种增加通常会增强OmpR的磷酸化。第三,OmpR蛋白与含有flhDC启动子的DNA片段结合,并且其亲和力会随着乙酰磷酸的磷酸化而增加。DNase I足迹法揭示了在存在或不存在磷酸化的情况下由OmpR保护的flhDC启动子区域。因此,我们提出由渗透压变化或乙酰磷酸的内部水平产生的磷酸化OmpR对鞭毛的表达起负调节作用。

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