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普氏立克次体中tlc和gltA mRNA的鉴定及原位RNA半衰期的测定。

Identification of tlc and gltA mRNAs and determination of in situ RNA half-life in Rickettsia prowazekii.

作者信息

Cai J, 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

J Bacteriol. 1993 Sep;175(17):5725-7. doi: 10.1128/jb.175.17.5725-5727.1993.

Abstract

RNAs of Rickettsia prowazekii, an obligate intracytoplasmic bacterium, have been identified and analyzed by an RNase protection assay. Total RNA, a mixture of host cell RNA and rickettsial RNA, was isolated from rickettsia-infected mouse L929 cells by the hot-phenol method. After hybridization with specific antisense RNA probes and digestion with RNase, the protected products were analyzed by electrophoresis and autoradiography. The results show that there is only one mRNA species for the ATP/ADP translocase gene (tlc) but two mRNA species for the citrate synthase gene (gltA). RNA half-lives were determined by measuring the RNA remaining after addition of rifampin. The half-lives of tlc mRNA, gltA mRNA I, and gltA mRNA II in R. prowazekii are 8.4 +/- 0.6, 12.3 +/- 1.3, and 20.5 +/- 1.8 min, respectively. However, the half-lives of tlc mRNA and gltA mRNA I in recombinant Escherichia coli strains are 2.9 +/- 0.1 and 1.4 +/- 0.1 min, respectively. The 16S rRNA in R. prowazekii was also examined and shown to be stable.

摘要

通过核糖核酸酶保护试验对专性胞内细菌普氏立克次体的RNA进行了鉴定和分析。采用热酚法从感染立克次体的小鼠L929细胞中分离出总RNA,它是宿主细胞RNA和立克次体RNA的混合物。与特异性反义RNA探针杂交并用核糖核酸酶消化后,通过电泳和放射自显影对受保护产物进行分析。结果表明,ATP/ADP转位酶基因(tlc)只有一种mRNA,而柠檬酸合酶基因(gltA)有两种mRNA。通过测量加入利福平后剩余的RNA来确定RNA半衰期。普氏立克次体中tlc mRNA、gltA mRNA I和gltA mRNA II的半衰期分别为8.4±0.6、12.3±1.3和20.5±1.8分钟。然而,重组大肠杆菌菌株中tlc mRNA和gltA mRNA I的半衰期分别为2.9±0.1和1.4±0.1分钟。还对普氏立克次体中的16S rRNA进行了检测,结果显示其是稳定的。

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