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

机译:编码多蛋白复合物的基因在大肠杆菌中的克隆和表达,该复合物与金黄色葡萄球菌蛋白质的分泌有关。

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摘要

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.
机译:编码多蛋白膜结合核糖体蛋白(MBRP)复合物的基因(mrp基因)与金黄色葡萄球菌中膜结合核糖体相关,被克隆到大肠杆菌中。通过蛋白质印迹(免疫印迹)分析判断,MBRP复合物的所有四个组分(分子大小分别为71、60、46和41道尔顿)均来自8.5碱基对的DNA片段。通过缺失诱变和各种限制性片段的亚克隆来确定克隆的DNA片段中各个基因的顺序。在MBRP编码区域内鉴定了从同一DNA链转录的三个RNA:一个大约5.9千碱基的大RNA,大概编码所有四个MBRP组分,两个次要RNA,编码MBRP-71和MBRP-60。这两个小RNA似乎是从大转录单位内的启动子转录而来的。尝试以MBRP编码区的内部600个碱基对的DNA片段为靶标使mrp基因的插入失活是失败的,大概是因为这种插入是致命的。

著录项

  • 作者

    Adler, L A; Arvidson, S;

  • 作者单位
  • 年度 1988
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  • 原文格式 PDF
  • 正文语种 en
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