[Investigation of Protein Translocation Sec-System with Heterologous Gene Expression in Shewanella oneidensis MR-1 Bacterium Cells].

N N Mordkovich, N A Okorokova, V P Veiko
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Abstract

A comparison of the primary structures of the protein translocation Sec-system proteins in the Shewanella oneidensis MR-1 and Escherichia coli bacteria was carried out. The process of translocation of recombinant pro-enteroxins (SEB and SEH) from Staphylococcus aureus and pro-streptavidin (SAV) from Streptomyces avidinii in the S. oneidensis MR-1 and E. coli cell periplasm was studied. It was demonstrated that these marker proteins are transferred into the periplasmic space of the S. oneidensis MR-1 transformant strain cells. The identity of N-terminal amino acid sequences of mature recombinant SEB, SEH, and SAV proteins (generated during post-translation proteolysis of leader peptide by the Sec-system both in E. coli and S. oneidensis MR-1) was established.

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单根希瓦氏菌MR-1细菌细胞中异源基因表达蛋白易位系统的研究
比较了希瓦氏菌MR-1和大肠杆菌中蛋白质易位sec系统蛋白的初级结构。研究了金黄色葡萄球菌重组原肠毒素(SEB和SEH)和亲和链霉菌重组原链亲和素(SAV)在同一株葡萄球菌MR-1和大肠杆菌细胞周质中的易位过程。结果表明,这些标记蛋白被转移到S. oneidensis MR-1转化株细胞的质周间隙中。建立了成熟的重组SEB、SEH和SAV蛋白n端氨基酸序列的同一性。这些蛋白是在大肠杆菌和s.o oneidensis MR-1中由sec系统对先导肽进行翻译后蛋白水解产生的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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