Mao Xu-Ming, Luo Shuai, Zhou Ri-Cheng, Wang Feng, Yu Pin, Sun Ning, Chen Xiao-Xia, Tang Yi, Li Yong-Quan
From the College of Life Sciences, Zhejiang University, Hangzhou 310058, China, Department of Chemical and Biomolecular Engineering, UCLA, Los, Angeles, California 90095, the Key Laboratory of Microbial Biochemistry and Metabolism Engineering of Zhejiang Province, Hangzhou 310058, China, and
From the College of Life Sciences, Zhejiang University, Hangzhou 310058, China, the Key Laboratory of Microbial Biochemistry and Metabolism Engineering of Zhejiang Province, Hangzhou 310058, China, and.
J Biol Chem. 2015 Mar 20;290(12):7992-8001. doi: 10.1074/jbc.M114.608273. Epub 2015 Feb 3.
Daptomycin is a cyclic lipopeptide antibiotic produced by Streptomyces roseosporus. To reveal the transcriptional regulatory mechanism of daptomycin biosynthesis, we used the biotinylated dptE promoter (dptEp) as a probe to affinity isolate the dptEp-interactive protein AtrA, a TetR family transcriptional regulator, from the proteome of mycelia. AtrA bound directly to dptEp to positively regulate gene cluster expression and daptomycin production. Meanwhile, both ΔatrA and ΔadpA mutants showed bald phenotype and null production of daptomycin. AdpA positively regulated atrA expression by direct interaction with atrA promoter (atrAp), and removal of ArpA in S. roseosporus, a homolog of the A-factor receptor, resulted in accelerated morphological development and increased daptomycin production, suggesting that atrA was the target of AdpA to mediate the A-factor signaling pathway. Furthermore, AtrA was positively autoregulated by binding to its own promoter atrAp. Thus, for the first time at the transcriptional level, we have identified an autoregulator, AtrA, that directly mediates the A-factor signaling pathway to regulate the proper production of daptomycin.
达托霉素是由玫瑰孢链霉菌产生的一种环状脂肽抗生素。为揭示达托霉素生物合成的转录调控机制,我们使用生物素化的dptE启动子(dptEp)作为探针,从菌丝体蛋白质组中亲和分离出与dptEp相互作用的蛋白AtrA,一种TetR家族转录调节因子。AtrA直接与dptEp结合,以正向调节基因簇表达和达托霉素的产生。同时,ΔatrA和ΔadpA突变体均表现出光秃表型且达托霉素产量为零。AdpA通过与atrA启动子(atrAp)直接相互作用正向调节atrA表达,并且在玫瑰孢链霉菌中去除A因子受体的同源物ArpA,导致形态发育加速和达托霉素产量增加,这表明atrA是AdpA介导A因子信号通路的靶点。此外,AtrA通过与其自身启动子atrAp结合而进行正向自我调节。因此,我们首次在转录水平上鉴定出一种自我调节因子AtrA,它直接介导A因子信号通路来调节达托霉素的正常产生。