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编码参与金黄色葡萄球菌蛋白质分泌的多蛋白复合物的基因在大肠杆菌中的克隆与表达。

Cloning and expression in Escherichia coli of genes encoding a multiprotein complex involved in secretion of proteins from Staphylococcus aureus.

作者信息

Adler L A, Arvidson S

机构信息

Department of Bacteriology, Karolinska Institutet, Stockholm, Sweden.

出版信息

J Bacteriol. 1988 Nov;170(11):5337-43. doi: 10.1128/jb.170.11.5337-5343.1988.

Abstract

The genes encoding the multiprotein membrane-bound ribosomal protein (MBRP) complex (mrp genes), associated with membrane-bound ribosomes in Staphylococcus aureus, were cloned in Escherichia coli. All four components (molecular sizes 71, 60, 46, and 41 kilodaltons) of the MBRP complex were expressed from an 8.5-kilobase DNA fragment as judged by Western blot (immunoblot) analysis. The order of the individual genes within the cloned DNA fragment was determined by deletion mutagenesis and subcloning of various restriction fragments. Three RNAs, transcribed from the same DNA strand, were identified within the MBRP-coding region: one large RNA of approximately 5.9 kilobases, presumably coding for all four MBRP components, and two minor RNAs, coding for MBRP-71 and MBRP-60. The two minor RNAs seemed to be transcribed from promoters within the large transcription unit. Attempts to make insertional inactivations of the mrp genes with an internal 600-base-pair DNA fragment of the MBRP-coding region as a target were unsuccessful, presumably because such insertions are lethal.

摘要

编码与金黄色葡萄球菌中膜结合核糖体相关的多蛋白膜结合核糖体蛋白(MBRP)复合体的基因(mrp基因)在大肠杆菌中被克隆。通过蛋白质免疫印迹(免疫印迹)分析判断,MBRP复合体的所有四个组分(分子大小分别为71、60、46和41千道尔顿)均由一个8.5千碱基的DNA片段表达。通过缺失诱变和各种限制酶片段的亚克隆确定了克隆DNA片段内各个基因的顺序。在MBRP编码区内鉴定出从同一条DNA链转录的三种RNA:一种约5.9千碱基的大RNA,可能编码所有四个MBRP组分,以及两种小RNA,分别编码MBRP - 71和MBRP - 60。这两种小RNA似乎是从大转录单元内的启动子转录而来。以MBRP编码区的一个600碱基对内部DNA片段为靶点对mrp基因进行插入失活的尝试未成功,推测是因为此类插入是致死性的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/15e3/211610/6003a00badc0/jbacter00189-0347-a.jpg

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