Wang Juan, Xu Jie, Luo Shuai, Ma Zheng, Bechthold Andreas, Yu Xiaoping
Zhejiang Provincial Key Laboratory of Biometrology and Inspection & Quarantine, College of Life Sciences, China Jiliang University, Xueyuan Street, Xiasha Higher Education District, Hangzhou, 310018, Zhejiang, People's Republic of China.
Institute for Pharmaceutical Sciences, Pharmaceutical Biology and Biotechnology, University of Freiburg, 79104, Freiburg, Germany.
Curr Microbiol. 2018 Oct;75(10):1345-1351. doi: 10.1007/s00284-018-1529-6. Epub 2018 Jun 19.
AdpA is studied and considered as a pleiotropic regulator which is involved in morphological development and secondary metabolism in many Streptomyces. In this study, AdpA which was cloned from toyocamycin (TM)-producing strain Streptomyces diastatochromogenes 1628, was identified as an ortholog of AdpA and belongs to a large subfamily of the AraC/XylS family. In order to elucidate the correlation of AdpA with TM biosynthesis and morphological differentiation, adpA was placed under the control of the ermE* promoter in plasmid pIB139. By intergeneric conjugation, the resulting plasmid pIB139-adpA was introduced into mutant S. diastatochromogenes 1628-T62 that is defective in sporulation and had limited TM production as well as transcriptional level of gene adpA, yielding the recombinant strain S. diastatochromogenes 1628-T62A. As expected, due to over-expression of adpA, the S. diastatochromogenes 1628-T62A restored spore formation to a certain extent compared with control strain S. diastatochromogenes 1628-T62. Moreover, compared with control strain 1628-T62, the TM production of recombinant 1628-T62A was increased by 120.1% on 5 l fermenter. In addition, by using semi-quantitative reverse transcription-PCR analysis, we discovered that the transcriptional levels of gene adpA and the all toy genes involved in TM biosynthesis were elevated in recombinant 1628-T62A compared with S. diastatochromogenes 1628-T62. These results confirm that cloned adpA plays a positive role in TM biosynthesis and morphological differentiation.
AdpA被研究并认为是一种多效调节因子,它参与了许多链霉菌的形态发育和次级代谢。在本研究中,从产丰加霉素(TM)的菌株龟裂链霉菌1628中克隆的AdpA被鉴定为AdpA的直系同源物,属于AraC/XylS家族的一个大亚家族。为了阐明AdpA与TM生物合成和形态分化的相关性,将adpA置于质粒pIB139中ermE*启动子的控制下。通过属间接合,将所得质粒pIB139-adpA导入在孢子形成方面有缺陷且TM产量和基因adpA转录水平有限的龟裂链霉菌1628-T62突变体中,产生重组菌株龟裂链霉菌1628-T62A。正如预期的那样,由于adpA的过表达,与对照菌株龟裂链霉菌1628-T62相比,龟裂链霉菌1628-T62A在一定程度上恢复了孢子形成。此外,与对照菌株1628-T62相比,重组菌株1628-T62A在5升发酵罐中的TM产量提高了120.1%。此外,通过半定量逆转录PCR分析,我们发现与龟裂链霉菌1628-T62相比,重组菌株1628-T62A中基因adpA和所有参与TM生物合成的toy基因的转录水平均有所升高。这些结果证实,克隆的adpA在TM生物合成和形态分化中发挥了积极作用。