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通过腺苷酸环化酶、环磷酸腺苷受体蛋白和phoM操纵子对大肠杆菌K-12 phoR突变体中细菌碱性磷酸酶合成及变异的控制

Control of bacterial alkaline phosphatase synthesis and variation in an Escherichia coli K-12 phoR mutant by adenyl cyclase, the cyclic AMP receptor protein, and the phoM operon.

作者信息

Wanner B L, Wilmes M R, Young D C

机构信息

Department of Biological Sciences, Purdue University, West Lafayette, Indiana 47907.

出版信息

J Bacteriol. 1988 Mar;170(3):1092-102. doi: 10.1128/jb.170.3.1092-1102.1988.

Abstract

Mutant phoR cells show a clonal variation phenotype with respect to bacterial alkaline phosphatase (BAP) synthesis. BAP clonal variation is characterized by an alternation between a Bap+ and Bap- phenotype. The switching is regulated by the phoM operon and the presence of glucose; the pho-510 mutant form of the phoM operon abolishes both BAP clonal variation and the effect of glucose (B.L. Wanner, J. Bacteriol. 169:900-903, 1987). In this paper we show that a mutation of the adenyl cyclase (cya) and the cyclic AMP receptor protein (crp) gene also abolish BAP clonal variation; either simultaneously reduces the amount of BAP made in phoR mutants. Also, the pho-510 mutation is epistatic; it increases BAP synthesis in delta cya phoR and delta crp phoR mutants. These data are consistent with the wild-type phoM operon having a negative, as well as a positive, regulatory role in gene expression. Furthermore, the data suggest that adenyl cyclase and Crp indirectly regulate BAP synthesis in a phoR mutant via an interaction with the phoM operon or its gene products. However, phoM operon expression was unaffected when tested with phoM operon lacZ transcriptional fusions. In addition, the switching Bap phenotype was not associated with an alternation in phoM operon expression.

摘要

突变型phoR细胞在细菌碱性磷酸酶(BAP)合成方面表现出克隆变异表型。BAP克隆变异的特征是Bap+和Bap-表型之间的交替。这种转换受phoM操纵子和葡萄糖的存在调控;phoM操纵子的pho - 510突变形式消除了BAP克隆变异和葡萄糖的影响(B.L. 万纳,《细菌学杂志》169:900 - 903,1987)。在本文中,我们表明腺苷酸环化酶(cya)和环腺苷酸受体蛋白(crp)基因的突变也消除了BAP克隆变异;二者同时降低了phoR突变体中BAP的合成量。此外,pho - 510突变是上位性的;它增加了δcya phoR和δcrp phoR突变体中BAP的合成。这些数据与野生型phoM操纵子在基因表达中具有负调控以及正调控作用一致。此外,数据表明腺苷酸环化酶和Crp通过与phoM操纵子或其基因产物的相互作用间接调节phoR突变体中BAP的合成。然而,用phoM操纵子lacZ转录融合体检测时,phoM操纵子的表达未受影响。此外,Bap表型的转换与phoM操纵子表达的交替无关。

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