The complete genome sequence of Streptomyces sp. FIM 95-F1, a marine actinomycete that produces the antifungal antibiotic scopafungin

被引：0

作者：

Peng, Fei ^{[1
]}

Lin, Yangjun ^{[1
]}

Zhuang, Yuee ^{[1
]}

Lin, Ping ^{[1
]}

Liu, Chengzhi ^{[1
]}

Chen, Linlin ^{[1
]}

Jiang, Hong ^{[2
]}

Lian, Yunyang ^{[2
]}

Zhang, Wenzhou ^{[1
]}

Huang, Youxia ^{[1
]}

机构：

[1] Quanzhou Med Coll, Quanzhou 362000, Peoples R China

[2] Fujian Inst Microbiol, Fujian key Lab Screening Novel Microbial Prod, Fuzhou 350007, Peoples R China

来源：

MARINE GENOMICS | 2024年 / 78卷

关键词：

Streptomyces; Secondary metabolite; Scopafungin; Biosynthetic potential; Sequencing; Data analysis; HETEROLOGOUS EXPRESSION; DISCOVERY; GENES;

D O I：

10.1016/j.margen.2024.101146

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

Streptomyces FIM95-F1, an actinomycete originating from mangroves of Quanzhou bay, exhibits the capability to produce the antifungal antibiotic scopafungin. Here, the complete genome of Streptomyces sp. FIM95-F1 is presented with a GC content of 71.04 %, comprising a 9,718,239-bp linear chromosome, 8236 protein-coding genes, 18 rRNA genes, 64 tRNA genes, 2 prophages, and 58 CRISPR regions. In silico analysis revealed the presence of 42 biosynthetic gene clusters (BGCs), the majority of which demonstrated similarity to both known and novel BGCs responsible for the biosynthesis of previously known and novel bioactive agents of microbial origin. A comprehensive comparison between the scopafungin BGC and niphimycin BGC has indicated a potential shared pathway for the biosynthesis of scopafungin. One of the intriguing findings of this study was the discovery of at least two novel BGCs (namely Cluster 26 and Cluster 32) present within biosynthetic gene clusters. Our findings suggest that Streptomyces sp. FIM95-F1 possesses significant potential in producing a diverse array of both known and novel bioactive compounds, which could be valuable in the field of drug discovery.

引用

页数：5

共 29 条

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