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专性细胞内细菌普氏立克次体中σ73与核心聚合酶的摩尔比。

The molar ratio of sigma 73 to core polymerase in the obligate intracellular bacterium, Rickettsia prowazekii.

作者信息

Ding H F, Winkler H H

机构信息

Department of Microbiology and Immunology, University of South Alabama College of Medicine, Mobile 36688.

出版信息

Mol Microbiol. 1994 Mar;11(5):869-73. doi: 10.1111/j.1365-2958.1994.tb00365.x.

Abstract

In the obligate intracellular parasitic bacterium, Rickettsia prowazekii, the molar ratio of sigma 73 to core RNA polymerase, that is, the degree of saturation of the core polymerase by the catalytically active sigma factor, was very low. This ratio was determined from the radioactivity in rickettsial RNA polymerase immunoprecipitated from crude extracts of infected L929 cells in which the parasite was exponentially growing. If we assume that, as is true for the sigma subunit, in R. prowazekii and Escherichia coli the beta', and beta subunits of the RNA polymerase have similar methionine and cysteine contents (the radiolabelled amino acids), the molar ratio of sigma 73 to core polymerase in R. prowazekii would be 0.1. This is in striking contrast to E. coli where the ratio is typically 0.4. It remains to be established whether this low sigma saturation results in a limitation of active RNA polymerase in R. prowazekii and contributes to its slow growth.

摘要

在专性细胞内寄生细菌普氏立克次体中,σ73与核心RNA聚合酶的摩尔比,即核心聚合酶被具有催化活性的σ因子饱和的程度非常低。该比例是通过对感染处于指数生长期寄生虫的L929细胞粗提物中免疫沉淀的立克次体RNA聚合酶的放射性进行测定得出的。如果我们假设,正如σ亚基的情况一样,在普氏立克次体和大肠杆菌中,RNA聚合酶的β'和β亚基具有相似的甲硫氨酸和半胱氨酸含量(放射性标记氨基酸),那么普氏立克次体中σ73与核心聚合酶的摩尔比将为0.1。这与大肠杆菌形成了鲜明对比,在大肠杆菌中该比例通常为0.4。这种低σ饱和度是否导致普氏立克次体中活性RNA聚合酶受到限制并导致其生长缓慢,仍有待确定。

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