Meens J, Klose M, Freudl R
Institut für Biotechnologie 1, Forschungszentrum Jülich GmbH, FRG.
FEMS Microbiol Lett. 1994 Mar 15;117(1):113-9. doi: 10.1111/j.1574-6968.1994.tb06751.x.
A DNA fragment containing the genes secE, nusG and rplK of Staphylococcus carnsosus was cloned using the Escherichia coli rplK gene as a probe. The S. carnosus secE homologue encodes a protein of 65 amino acid residues which is homologous to the carboxyl-terminal region of the E. coli SecE protein. The S. carnosus SecE polypeptide which, in contrast to the E. coli SecE protein, contains only one putative transmembrane segment, could fully replace the E. coli SecE protein in two different secE mutants. These results strongly suggest that the identified secE gene encodes an important component of the S. carnosus protein export apparatus.
使用大肠杆菌rplK基因作为探针,克隆了一个含有肉葡萄球菌secE、nusG和rplK基因的DNA片段。肉葡萄球菌secE同源物编码一个由65个氨基酸残基组成的蛋白质,该蛋白质与大肠杆菌SecE蛋白的羧基末端区域同源。与大肠杆菌SecE蛋白不同,肉葡萄球菌SecE多肽仅包含一个推定的跨膜区段,它可以在两种不同的secE突变体中完全替代大肠杆菌SecE蛋白。这些结果强烈表明,所鉴定的secE基因编码肉葡萄球菌蛋白质输出装置的一个重要组分。