Doi M, Wachi M, Ishino F, Tomioka S, Ito M, Sakagami Y, Suzuki A, Matsuhashi M
Institute of Applied Microbiology, University of Tokyo, Japan.
J Bacteriol. 1988 Oct;170(10):4619-24. doi: 10.1128/jb.170.10.4619-4624.1988.
The 6.5-kilobase mre region at 71 min in the Escherichia coli chromosome map, where genes involved in formation of a rod-shaped cell form a gene cluster, was analyzed by in vivo protein synthesis in a maxicell system and by base sequencing of DNA. An open reading frame that may code for a protein with an Mr of about 37,000 on sodium dodecyl sulfate-polyacrylamide gels was found and was correlated with the mreB gene. N-terminal amino acid sequencing of the hybrid mreB-lacZ protein confirmed the production by mreB of a protein of 347 amino acid residues with a molecular weight of 36,958. The amino acid sequence of this protein deduced from the DNA sequence showed close similarity with that of a protein of the ftsA gene which is involved in cell division of E. coli. Three other contiguous genes that formed three proteins with Mrs of about 40,000, 22,000, and 51,000, respectively, were detected downstream of the mreB gene by in vivo protein synthesis. The mreB protein and some of these three proteins may function together in determination of cell shape.
在大肠杆菌染色体图谱中71分钟处的6.5千碱基对的mre区域,参与杆状细胞形成的基因形成一个基因簇,我们通过在大细胞系统中的体内蛋白质合成以及DNA的碱基测序对其进行了分析。我们发现了一个开放阅读框,它可能编码一种在十二烷基硫酸钠-聚丙烯酰胺凝胶上Mr约为37,000的蛋白质,并且该开放阅读框与mreB基因相关。对杂交的mreB - lacZ蛋白进行N端氨基酸测序,证实mreB产生了一种由347个氨基酸残基组成、分子量为36,958的蛋白质。从DNA序列推导的该蛋白质的氨基酸序列与参与大肠杆菌细胞分裂的ftsA基因的一种蛋白质的氨基酸序列显示出密切相似性。通过体内蛋白质合成在mreB基因下游检测到另外三个相邻基因,它们分别形成了Mr约为40,000、22,000和51,000的三种蛋白质。mreB蛋白和这三种蛋白质中的一些可能在细胞形状的确定中共同发挥作用。