Group Métabolisme Energétique des Streptomyces, Institut de Génétique et Microbiologie, UMR CNRS 8621, Université Paris Sud 11, 91405 Orsay Cedex, France.
Appl Environ Microbiol. 2010 Dec;76(23):7741-53. doi: 10.1128/AEM.00819-10. Epub 2010 Oct 8.
The overexpression of a regulatory gene of the TetR family (SCO3201) originating either from Streptomyces lividans or from Streptomyces coelicolor was shown to strongly repress antibiotic production (calcium-dependent antibiotic [CDA], undecylprodigiosin [RED], and actinorhodin [ACT]) of S. coelicolor and of the ppk mutant strain of S. lividans. Curiously, the overexpression of this gene also had a strong inhibitory effect on the sporulation process of S. coelicolor but not on that of S. lividans. SCO3201 was shown to negatively regulate its own transcription, and its DNA binding motif was found to overlap its -35 promoter sequence. The interruption of this gene in S. lividans or S. coelicolor did not lead to any obvious phenotypes, indicating that when overexpressed SCO3201 likely controls the expression of target genes of other TetR regulators involved in the regulation of the metabolic and morphological differentiation process in S. coelicolor. The direct and functional interaction of SCO3201 with the promoter region of scbA, a gene under the positive control of the TetR-like regulator, ScbR, was indeed demonstrated by in vitro as well as in vivo approaches.
来自链霉菌属浅青紫链霉菌或变铅青链霉菌的 TetR 家族调控基因 SCO3201 的过表达,强烈抑制了变铅青链霉菌及其 ppk 突变株的抗生素产生(钙依赖性抗生素 [CDA]、十一烷基灵菌红素 [RED]和放线紫红素 [ACT])。奇怪的是,该基因的过表达对变铅青链霉菌的孢子形成过程也有很强的抑制作用,但对浅青紫链霉菌的孢子形成过程没有影响。SCO3201 被证明可以负调控自身的转录,并且发现其 DNA 结合基序与 -35 启动子序列重叠。在变铅青链霉菌或浅青紫链霉菌中中断该基因不会导致任何明显的表型,表明当过表达时,SCO3201 可能控制了其他 TetR 调控因子的靶基因的表达,这些基因参与了变铅青链霉菌代谢和形态分化过程的调控。通过体外和体内方法,确实证明了 SCO3201 与 scbA 启动子区域的直接和功能相互作用,scbA 是 TetR 样调控因子 ScbR 正向调控的基因。