Rico Sergio, Santamaría Ramón I, Yepes Ana, Rodríguez Héctor, Laing Emma, Bucca Giselda, Smith Colin P, Díaz Margarita
Instituto de Biología Funcional y Genómica (IBFG)/Departamento de Microbiología y Genética, Consejo Superior de Investigaciones Científicas (CSIC)/Universidad de Salamanca, Salamanca, Spain.
Appl Environ Microbiol. 2014 Apr;80(8):2417-28. doi: 10.1128/AEM.03378-13. Epub 2014 Feb 7.
The atypical two-component system (TCS) AbrC1/C2/C3 (encoded by SCO4598, SCO4597, and SCO4596), comprising two histidine kinases (HKs) and a response regulator (RR), is crucial for antibiotic production in Streptomyces coelicolor and for morphological differentiation under certain nutritional conditions. In this study, we demonstrate that deletion of the RR-encoding gene, abrC3 (SCO4596), results in a dramatic decrease in actinorhodin (ACT) and undecylprodiginine (RED) production and delays morphological development. In contrast, the overexpression of abrC3 in the parent strain leads to a 33% increase in ACT production in liquid medium. Transcriptomic analysis and chromatin immunoprecipitation with microarray technology (ChIP-chip) analysis of the ΔabrC3 mutant and the parent strain revealed that AbrC3 directly controls ACT production by binding to the actII-ORF4 promoter region; this was independently verified by in vitro DNA-binding assays. This binding is dependent on the sequence 5'-GAASGSGRMS-3'. In contrast, the regulation of RED production is not due to direct binding of AbrC3 to either the redZ or redD promoter region. This study also revealed other members of the AbrC3 regulon: AbrC3 is a positive autoregulator which also binds to the promoter regions of SCO0736, bdtA (SCO3328), absR1 (SCO6992), and SCO6809. The direct targets share the 10-base consensus binding sequence and may be responsible for some of the phenotypes of the ΔabrC3 mutant. The identification of the AbrC3 regulon as part of the complex regulatory network governing antibiotic production widens our knowledge regarding TCS involvement in control of antibiotic synthesis and may contribute to the rational design of new hyperproducer host strains through genetic manipulation of such systems.
非典型双组分系统(TCS)AbrC1/C2/C3(由SCO4598、SCO4597和SCO4596编码),由两个组氨酸激酶(HKs)和一个应答调节子(RR)组成,对天蓝色链霉菌中的抗生素生产以及在某些营养条件下的形态分化至关重要。在本研究中,我们证明缺失RR编码基因abrC3(SCO4596)会导致放线紫红素(ACT)和十一烷基灵菌红素(RED)产量大幅下降,并延迟形态发育。相反,在亲本菌株中过表达abrC3会使液体培养基中ACT产量增加33%。对ΔabrC3突变体和亲本菌株进行转录组分析以及利用微阵列技术的染色质免疫沉淀(ChIP-chip)分析表明,AbrC3通过与actII-ORF4启动子区域结合直接控制ACT的产生;这通过体外DNA结合试验得到了独立验证。这种结合依赖于5'-GAASGSGRMS-3'序列。相比之下,RED产量的调节并非由于AbrC3直接与redZ或redD启动子区域结合。本研究还揭示了AbrC3调控子的其他成员:AbrC3是一种正向自调节因子,它还与SCO0736、bdtA(SCO3328)、absR1(SCO6992)和SCO6809的启动子区域结合。直接靶点共享10个碱基的共有结合序列,可能是ΔabrC3突变体表型的部分原因。将AbrC3调控子鉴定为控制抗生素生产的复杂调控网络的一部分,拓宽了我们对双组分系统参与抗生素合成控制的认识,并可能通过对此类系统的基因操作,为合理设计新的高产宿主菌株做出贡献。