Malo M S, Loughlin R E
Department of Biochemistry, University of Sydney, N.S.W., Australia.
Gene. 1990 Mar 1;87(1):127-31. doi: 10.1016/0378-1119(90)90504-k.
The cysD gene, involved in cysteine biosynthesis in Escherichia coli and Salmonella typhimurium, is positively regulated by the CysB regulatory protein. The cysD promoter of E. coli K-12 in a 492-bp PstI-Eco RI fragment was sequenced. The in vivo transcription start point (tsp) for the cysD gene was determined by the methods of T4 DNA polymerase mapping and mung-bean nuclease mapping. The -10 region of the cysD promoter (TATAGT) is closely homologous to the -10 consensus sequence (TATAAT) for E. coli promoters. The -35 region of this promoter (TTCATT) is less closely related to the -35 consensus sequence (TTGACA). Several mutants were obtained by using a chain-termination method for generating unidirectional deletions. Evidence is presented for a possible CysB protein binding site around -89, thought to be involved in regulation of expression of the cysD gene.
参与大肠杆菌和鼠伤寒沙门氏菌中半胱氨酸生物合成的cysD基因受CysB调节蛋白的正向调节。对大肠杆菌K-12中位于492 bp PstI-Eco RI片段的cysD启动子进行了测序。通过T4 DNA聚合酶图谱法和绿豆核酸酶图谱法确定了cysD基因的体内转录起始点(tsp)。cysD启动子的-10区(TATAGT)与大肠杆菌启动子的-10共有序列(TATAAT)高度同源。该启动子的-35区(TTCATT)与-35共有序列(TTGACA)的相关性较弱。通过使用链终止法产生单向缺失获得了几个突变体。有证据表明在-89左右可能存在一个CysB蛋白结合位点,认为其参与cysD基因表达的调节。