首页 | 本学科首页   官方微博 | 高级检索  
     

卡伍尔氏链霉菌NA4的Ⅱ型聚酮基因簇的靶向激活及其产物鉴定
引用本文:刘晶莹,白岩,潘华奇,胡江春. 卡伍尔氏链霉菌NA4的Ⅱ型聚酮基因簇的靶向激活及其产物鉴定[J]. 微生物学报, 2023, 63(10): 3891-3904
作者姓名:刘晶莹  白岩  潘华奇  胡江春
作者单位:沈阳药科大学制药工程学院, 辽宁 沈阳 110016;中国科学院沈阳应用生态研究所, 辽宁 沈阳 110016
基金项目:国家自然科学基金(41776178);辽宁省应用基础研究计划(2022JH2/101300185);中国科学院青年创新促进会优秀会员项目(Y2022063)
摘    要:【目的】以基因组信息为导向,定向激活海洋来源卡伍尔氏链霉菌(Streptomyces cavourensis) NA4中沉默的Ⅱ型聚酮类次级代谢产物生物合成基因簇,鉴定新产生的次级代谢产物的结构和抑菌活性。【方法】通过添加启动子和敲除负调控基因的方法激活实验室培养条件下沉默或低表达的生物合成基因簇,并完成目标化合物的分离与纯化,通过电喷雾质谱(electrospray ionization-mass spectrometry,ESI-MS)和核磁共振(nuclear magnetic resonance,NMR)数据分析鉴定目标化合物结构,对目标化合物进行抑菌活性鉴定,基于生物信息学信息推导化合物的生物合成途径。【结果】根据基因组生物信息学分析,从海洋来源链霉菌Streptomyces cavourensis NA4中选取一个编码PKSⅡ型次级代谢产物的生物合成基因簇开展研究,成功激活目标基因簇,从中分离到1个PKSⅡ型化合物,推导了其生物合成途径并进行了抑菌活性鉴定。【结论】基因组导向下的天然产物挖掘,可以目标明确地分离产物,充分挖掘链霉菌编码次级代谢产物的潜力。

关 键 词:链霉菌  基因组挖掘  次级代谢产物  生物合成
收稿时间:2023-03-01
修稿时间:2023-05-08

Targeted activation and product identification of the type II polyketone gene cluster of Streptomyces cavourensis NA4
LIU Jingying,BAI Yan,PAN Huaqi,HU Jiangchun. Targeted activation and product identification of the type II polyketone gene cluster of Streptomyces cavourensis NA4[J]. Acta microbiologica Sinica, 2023, 63(10): 3891-3904
Authors:LIU Jingying  BAI Yan  PAN Huaqi  HU Jiangchun
Affiliation:School of Pharmaceutical Engineering, Shenyang Pharmaceutical University, Shenyang 110016, Liaoning, China;Institute of Applied Ecology, Chinese Academy of Sciences, Shenyang 110016, Liaoning, China
Abstract:[Objective] To activate the silenced gene cluster for the biosynthesis of type II polyketides in Streptomyces cavourensis NA4 isolated from a marine environment, and identify the structure and antibacterial activity of the newly produced secondary metabolite. [Methods] The silenced or low-expressed biosynthetic gene cluster under laboratory culture conditions was activated by the addition of promoters and the knockout of negative regulator genes. The target compound was separated. The structure of the target compound was identified by electrospray ionization-mass spectrometry (ESI-MS) and nuclear magnetic resonance (NMR). Furthermore, the antibacterial activity of the target compound was determined, and the biosynthetic pathway of the compound was deduced based on bioinformatics information. [Results] A biosynthetic gene cluster encoding type II polyketides was mined from the genome of S. cavourensis NA4 and successfully activated. A type II polyketide was separated from the expression products. The biosynthetic pathway of this compound was deduced and the antibacterial activity was determined. [Conclusion] Genome-oriented natural product mining can facilitate the separation of target products and fully tap the potential of Streptomyces in the production of secondary metabolites.
Keywords:Streptomyces  genome mining  secondary metabolites  biosynthesis
点击此处可从《微生物学报》浏览原始摘要信息
点击此处可从《微生物学报》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号