Yang K, Han L, Vining L C
Department of Biology, Dallhousie University, Halifax, Nova Scotia, Canada.
J Bacteriol. 1995 Nov;177(21):6111-7. doi: 10.1128/jb.177.21.6111-6117.1995.
The nucleotide sequence of a region upstream of the type II polyketide synthase genes in the cluster for biosynthesis of the polyketide antibiotic jadomycin B in Streptomyces venezuelae contained an open reading frame encoding a sequence of 196 amino acids that resembeled sequences deduced for a group of repressor proteins. The strongest similarity was to EnvR of Escherichia coli, but the sequence also resembled MtrR, AcrR, TetC, and TcmR, all of which are involved in regulating resistance to antibiotics or toxic hydrophobic substances in the environment. Disruption of the nucleotide sequence of this putative S. venezuelae repressor gene (jadR2), by insertion of an apramycin resistance gene at an internal MluI site, and replacement of the chromosomal gene generated mutants that produced jadomycin B without the stress treatments (exposure to heat shock or to toxic concentrations of ethanol) required for jadomycin B production by the wild type. When cultures of the disruption mutants were ethanol stressed, they overproduced the antibiotic. From these results it was concluded that expression of the jadomycin B biosynthesis genes are negatively regulated by jadR2.
委内瑞拉链霉菌中聚酮类抗生素杰多霉素B生物合成基因簇内II型聚酮合酶基因上游区域的核苷酸序列包含一个开放阅读框,其编码一段由196个氨基酸组成的序列,该序列类似于一组阻遏蛋白推导得到的序列。与大肠杆菌的EnvR相似度最高,但该序列也类似于MtrR、AcrR、TetC和TcmR,它们均参与调节对环境中抗生素或有毒疏水性物质的抗性。通过在内部MluI位点插入安普霉素抗性基因破坏该推定的委内瑞拉链霉菌阻遏基因(jadR2)的核苷酸序列,并替换染色体基因,产生了无需野生型生产杰多霉素B所需的应激处理(热休克或乙醇毒性浓度处理)就能产生杰多霉素B的突变体。当破坏突变体的培养物受到乙醇胁迫时,它们会过量产生抗生素。从这些结果可以得出结论,杰多霉素B生物合成基因的表达受到jadR2的负调控。