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Deciphering the Regulon of Streptomyces coelicolor AbrC3 a Positive Response Regulator of Antibiotic Production

机译:解密链霉菌天蓝色链霉菌AbrC3的调控抗生素生产的积极响应调节剂。

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摘要

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.
机译:非典型两组分系统(TCS)AbrC1 / C2 / C3(由SCO4598,SCO4597和SCO4596编码),包含两个组氨酸激酶(HK)和一个响应调节剂(RR),对于在链霉菌中生产抗生素和在某些营养条件下的形态分化。在这项研究中,我们证明删除RR编码基因abrC3(SCO4596),会导致放线菌丝蛋白(ACT)和十一烷基谷丙素(RED)产量急剧下降,并延迟了形态发育。相反,亲本菌株中abrC3的过表达导致液体培养基中ACT的产生增加33%。用微阵列技术(ChIP-chip)对ΔabrC3突变体和亲本菌株进行转录组学分析和染色质免疫沉淀,结果表明AbrC3通过与actII-ORF4启动子区结合直接控制ACT的产生。这已通过体外DNA结合测定独立验证。该结合取决于序列5'-GAASGSGRMS-3'。相反,RED产生的调节不是由于AbrC3与redZ或redD启动子区域的直接结合。这项研究还揭示了AbrC3调节子的其他成员:AbrC3是一种正向自调节子,还与SCO0736,bdtA(SCO3328),absR1( SCO6992 )和 SCO6809 的启动子区域结合。 em>。直接靶标共有10个碱基的共有结合序列,可能与Δ abrC3 突变体的某些表型有关。作为控制抗生素生产的复杂调控网络的一部分,对AbrC3调节子的鉴定扩大了我们有关TCS参与抗生素合成控制的知识,并可能通过此类系统的基因操作而有助于合理设计新的高产宿主菌株。

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