共 11 条
Transcriptional regulation of a leucine-responsive regulatory protein for directly controlling lincomycin biosynthesis in Streptomyces lincolnensis
被引:0
作者:
Yurong Xu
Yaqian Tang
Nian Wang
Jing Liu
Xinlu Cai
Hongyi Cai
Jie Li
Guoqing Tan
Ruihua Liu
Linquan Bai
Lixin Zhang
Hang Wu
Buchang Zhang
机构:
[1] Anhui University,School of Life Sciences, Institute of Physical Science and Information Technology
[2] Hefei Normal University,Department of Chemical and Chemical Engineering
[3] Xinyu Pharmaceutical Co. Ltd,State Key Laboratory of Bioreactor Engineering
[4] East China University of Science and Technology,State Key Laboratory of Microbial Metabolism
[5] Shanghai Jiao Tong University,undefined
来源:
Applied Microbiology and Biotechnology
|
2020年
/
104卷
关键词:
Leucine-responsive regulatory protein;
Metabolic regulation;
Lincomycin;
Transcriptional activator;
D O I:
暂无
中图分类号:
学科分类号:
摘要:
Leucine-responsive regulatory proteins (Lrps) are a family of transcription factors involved in diverse biological processes in bacteria. So far, molecular mechanism of Lrps for regulating antibiotics biosynthesis in actinomycetes remains largely unexplored. This study, for the first time in Streptomyces lincolnensis, identified an Lrp (named as SLCG_Lrp) associated with lincomycin production. SLCG_Lrp was validated to be a positive regulator for lincomycin biosynthesis by directly stimulating transcription of two structural genes (lmbA and lmbV), three resistance genes (lmrA, lmrB and lmrC), and a regulatory gene (lmbU) within the lincomycin biosynthetic gene (lin) cluster. SLCG_Lrp was transcriptionally self-inhibited and triggered the expression of its adjacent gene SLCG_3127 encoding a LysE superfamily protein. Further, the binding site of SLCG_Lrp in the intergenic region of SLCG_3127 and SLCG_Lrp was precisely identified. Inactivation of SLCG_3127 in S. lincolnensis resulted in yield improvement of lincomycin, which was caused by intracellular accumulation of proline and cysteine. Arginine and phenylalanine were identified as specific regulatory ligands, respectively, to reduce and promote DNA-binding affinity of SLCG_Lrp. We further found that SLCG_Lrp was directly repressed by SLCG_2919, the first identified transcription factor outside lin cluster for lincomycin production. Therefore, our findings revealed SLCG_Lrp-mediated transcriptional regulation of lincomycin biosynthesis. This study extends the understanding of molecular mechanisms underlying lincomycin biosynthetic regulation.
引用
收藏
页码:2575 / 2587
页数:12
相关论文