Collaborative Innovation Center for Genetics and Development, State Key Laboratory of Genetic Engineering, Department of Microbiology, School of Life Sciences, Fudan University, Shanghai, 200438, People's Republic of China.
Institute of Quality and Standard for Agro-products, Zhejiang Academy of Agricultural Sciences, Hangzhou, People's Republic of China.
Appl Microbiol Biotechnol. 2018 Mar;102(6):2621-2633. doi: 10.1007/s00253-018-8748-4. Epub 2018 Feb 8.
The genus Streptomyces have been highly regarded for their important source of natural products. Combined with the technology of genome sequencing and mining, we could identify the active ingredients from fermentation broth quickly. Here, we report on Streptomyces sp. strain fd1-xmd, which was isolated from a soil sample collected in Shanghai. Interestingly, the fermentation broth derived from this strain demonstrated broad-spectrum antimicrobial activity against gram-positive bacteria, gram-negative bacteria, and eukaryotes. To identify the antimicrobial substances and their biosynthetic gene clusters, we sequenced the fd1-xmd strain and obtained a genome 7,929,999 bp in length. The average GC content of the chromosome was 72.5 mol%. Knockout experiments demonstrated that out of eight biosynthetic gene clusters we could identify, two are responsible for the biosynthesis of the antibiotics streptothricin (ST) and tunicamycin (TM). The ST biosynthetic gene cluster from fd1-xmd was verified via successful heterologous expression in Streptomyces coelicolor M1146. ST production had a yield of up to 0.5 g/L after the optimization of culture conditions. This study describes a novel producer of ST and TM and outlines the complete process undertaken for Streptomyces sp. strain fd1-xmd genome mining.
链霉菌属因其天然产物的重要来源而备受关注。结合基因组测序和挖掘技术,我们可以快速从发酵液中鉴定出活性成分。在这里,我们报告了一株从上海土壤样本中分离到的链霉菌属菌株 fd1-xmd。有趣的是,该菌株发酵液对革兰氏阳性菌、革兰氏阴性菌和真核生物具有广谱抗菌活性。为了鉴定抗菌物质及其生物合成基因簇,我们对 fd1-xmd 菌株进行了测序,获得了一个长 7929999bp 的基因组。染色体的平均 GC 含量为 72.5mol%。敲除实验表明,在我们能够鉴定的八个生物合成基因簇中,有两个负责抗生素链丝菌素(ST)和衣霉素(TM)的生物合成。通过在变铅青链霉菌 M1146 中的成功异源表达,验证了来自 fd1-xmd 的 ST 生物合成基因簇。在优化培养条件后,ST 的产量最高可达 0.5g/L。本研究描述了一株新型 ST 和 TM 的产生菌,并概述了链霉菌属菌株 fd1-xmd 基因组挖掘所采用的完整过程。