Gibert I, Llagostera M, Barbé J
Department of Genetics and Microbiology, Autonomous University of Barcelona, Bellaterra, Spain.
J Bacteriol. 1988 Mar;170(3):1346-9. doi: 10.1128/jb.170.3.1346-1349.1988.
To study the regulation of the expression in Escherichia coli of the ubiG gene, which codes for the last enzyme in the pathway of ubiquinone biosynthesis, a fusion between the ubiG and lacZ genes was constructed in vitro. The results showed that (i) the expression of the ubiG gene was higher under aerobic conditions than under anaerobic growth conditions, (ii) the presence of glucose in the culture medium decreased the transcription of the ubiG gene, and (iii) cya and crp mutants exhibited lower levels of ubiG gene expression than the wild-type strain. The addition of cyclic AMP increased the expression of the ubiG gene in both cya and wild-type strains but not in a crp mutant. This fact suggests that the cyclic AMP receptor protein-cyclic AMP complex positively modulates ubiG gene transcription. It was also determined that the transcription of the ubiG gene was in the counterclockwise direction on the E. coli map.
为了研究泛醌生物合成途径中最后一种酶的编码基因——大肠杆菌ubiG基因表达的调控机制,在体外构建了ubiG基因与lacZ基因的融合体。结果表明:(i)ubiG基因在有氧条件下的表达高于厌氧生长条件下的表达;(ii)培养基中葡萄糖的存在会降低ubiG基因的转录水平;(iii)cya和crp突变体中ubiG基因的表达水平低于野生型菌株。添加环腺苷酸可增加cya和野生型菌株中ubiG基因的表达,但在crp突变体中则无此作用。这一事实表明,环腺苷酸受体蛋白 - 环腺苷酸复合物对ubiG基因转录具有正向调节作用。还确定了ubiG基因在大肠杆菌染色体图谱上的转录方向是逆时针的。