Ou Xijun, Zhang Bo, Zhang Lin, Zhao Guoping, Ding Xiaoming
State Key Laboratory of Genetic Engineering, Department of Microbiology and Microbial Engineering, School of Life Sciences, Fudan University, Shanghai 200433, China.
Appl Environ Microbiol. 2009 Apr;75(7):2158-65. doi: 10.1128/AEM.02209-08. Epub 2009 Feb 5.
Streptomyces not only exhibits complex morphological differentiation but also produces a plethora of secondary metabolites, particularly antibiotics. To improve our general understanding of the complex network of undecylprodigiosin (Red) biosynthesis regulation, we used an in vivo transposition system to identify novel regulators that influence Red production in Streptomyces coelicolor M145. Using this screening system, we obtained 25 Red-deficient mutants. Twenty-four of these mutants had a transposon inserted in the previously described Red biosynthetic gene cluster and produced different amounts of another secondary metabolite, actinorhodin (Act). One mutant was shown to have an insertion in a different region of the chromosome upstream of the previously uncharacterized gene rrdA (regulator of redD, sco1104), which encodes a putative TetR family transcription factor. Compared with wild-type strain M145, the rrdA null mutant exhibited increased Red production and decreased Act production. A high level of rrdA expression resulted in a severe reduction in Red production and Act overproduction. Reverse transcription-PCR analysis showed that RrdA negatively regulated Red production by controlling redD mRNA abundance, while no change was observed at the transcript level of the Act-specific activator gene, actII-orf4. The effects on Act biosynthesis might arise from competition for precursors that are common to both pathways.
链霉菌不仅表现出复杂的形态分化,还能产生大量的次级代谢产物,尤其是抗生素。为了增进我们对十一烷基灵菌红素(Red)生物合成调控复杂网络的总体理解,我们使用了一种体内转座系统来鉴定影响天蓝色链霉菌M145中Red产生的新型调控因子。利用这个筛选系统,我们获得了25个Red缺陷型突变体。其中24个突变体的转座子插入到了先前描述的Red生物合成基因簇中,并产生了不同量的另一种次级代谢产物放线紫红素(Act)。有一个突变体被证明在先前未表征的基因rrdA(redD的调控因子,sco1104)上游的染色体不同区域有插入,该基因编码一个假定的TetR家族转录因子。与野生型菌株M145相比,rrdA缺失突变体表现出Red产量增加和Act产量降低。高水平的rrdA表达导致Red产量严重降低和Act过量产生。逆转录PCR分析表明,RrdA通过控制redD mRNA丰度对Red产生负调控,而在Act特异性激活基因actII-orf4的转录水平上未观察到变化。对Act生物合成的影响可能源于对两条途径共有的前体的竞争。