Rajapandi T, Dolan K M, Oliver D B
Department of Microbiology, State University of New York, Stony Brook 11794-8626.
J Bacteriol. 1991 Nov;173(22):7092-7. doi: 10.1128/jb.173.22.7092-7097.1991.
TnphoA insertions in the first gene of the Escherichia coli secA operon, gene X, were isolated and analyzed. Studies of the Gene X-PhoA fusion proteins showed that gene X encodes a secretory protein, since the fusion proteins possessed normal alkaline phosphatase activity and a substantial portion of this activity was found in the periplasm. In addition, the Gene X-PhoA fusion proteins were initially synthesized with a cleavable signal peptide. A gene X::TnphoA insertion was used to construct a strain containing a disrupted chromosomal copy of gene X. Analysis of this strain indicated that gene X is nonessential for cell growth and viability and does not appear to play an essential role in the process of protein export.
分离并分析了大肠杆菌secA操纵子第一个基因(基因X)中的TnphoA插入突变。对基因X-PhoA融合蛋白的研究表明,基因X编码一种分泌蛋白,因为融合蛋白具有正常的碱性磷酸酶活性,并且在周质中发现了大部分这种活性。此外,基因X-PhoA融合蛋白最初是由可裂解的信号肽合成的。利用基因X::TnphoA插入突变构建了一个含有基因X染色体拷贝被破坏的菌株。对该菌株的分析表明,基因X对细胞生长和活力并非必需,并且似乎在蛋白质输出过程中不发挥重要作用。