Kontinen V P, Sarvas M
Department of Molecular Bacteriology, National Public Health Institute, Helsinki, Finland.
Mol Microbiol. 1993 May;8(4):727-37. doi: 10.1111/j.1365-2958.1993.tb01616.x.
Mutations of the prsA gene of Bacillus subtilis have indicated that the gene is involved in protein secretion and it encodes a novel component of the cellular secretion machinery. We now demonstrate that the gene product is a membrane-associated lipoprotein, presumably bound to the outer face of the cytoplasmic membrane. Experiments to inactivate the prsA gene with insertions indicated that it is indispensable for viability. The cellular level of PrsA protein was shown to be decreased in prsA mutants with decreased level of exoproteins, consistent with an essential function in protein secretion. An increased amount of cellular PrsA protein was introduced by increasing the copy number of prsA in B. subtilis. This enhanced, from six- to twofold, the secretion of alpha-amylases and a protease in strains, which expressed high levels of these exoenzymes. This suggests that PrsA protein is the rate-limiting component of the secretion machinery, a finding that is of considerable biotechnological interest.
枯草芽孢杆菌prsA基因的突变表明,该基因参与蛋白质分泌,并且编码细胞分泌机制的一种新组分。我们现在证明,该基因产物是一种膜相关脂蛋白,可能结合在细胞质膜的外表面。用插入失活prsA基因的实验表明,它对于生存力是必不可少的。在胞外蛋白水平降低的prsA突变体中,PrsA蛋白的细胞水平显示降低,这与在蛋白质分泌中的基本功能一致。通过增加枯草芽孢杆菌中prsA的拷贝数,引入了增加量的细胞PrsA蛋白。这将表达高水平这些胞外酶的菌株中α-淀粉酶和一种蛋白酶的分泌提高了6至2倍。这表明PrsA蛋白是分泌机制的限速组分,这一发现具有相当大的生物技术意义。