Andrésson O S, Davies J E
Mol Gen Genet. 1980;179(1):217-22. doi: 10.1007/BF00268466.
The assay for the ksgA-encoded S-adenosylmethionine--6-N',N'-adenosyl (rRNA) dimethyltransferase has been improved; the gel-filtration molecular weight of partially purified enzyme under two different sets of conditions was found to be 55,000 or 26,000 daltons. We have determined methyltransferase activities in strains where ksgA was brought under the control of the mitomycin C-inducible promoter of the colicin E1 gene. Our studies show that ksgA is transcribed counterclockwise on the Escherichia coli chromosome.
对由ksgA编码的S-腺苷甲硫氨酸-6-N',N'-腺苷基(rRNA)二甲基转移酶的测定方法进行了改进;在两组不同条件下,部分纯化酶的凝胶过滤分子量分别为55,000或26,000道尔顿。我们测定了将ksgA置于大肠杆菌素E1基因的丝裂霉素C诱导型启动子控制下的菌株中的甲基转移酶活性。我们的研究表明,ksgA在大肠杆菌染色体上逆时针转录。