Complete genome sequence of Streptomyces sp. HNA39, a new cyclizidine producer isolated from a South China Sea sediment

被引:2
作者
Li, Suzhen [1 ]
Jiang, Yong-Jun [1 ,2 ]
Ma, Zhongjun [1 ,3 ]
Wang, Nan [1 ,3 ]
机构
[1] Zhejiang Univ, Ocean Coll, Zhoushan 316021, Peoples R China
[2] Zhejiang Ocean Univ, Sch Food & Pharm, Zhoushan 316022, Peoples R China
[3] Zhejiang Univ, Hainan Inst, Sanya 572025, Peoples R China
基金
中国国家自然科学基金;
关键词
Genome mining; Cyclizidine; Biosynthesis; Biosynthetic gene cluster; Sediment; Bafilomycin; CLUSTER;
D O I
10.1016/j.margen.2023.101033
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Streptomyces sp. HNA39 is a promising candidate for the production of antineoplastic metabolites screened from a collection of 448 actinomycetes derived from coastal sediments. The complete genome sequence of HNA39 comprises a 7,351,753-bp linear chromosome with a GC content of 71.94%. Whole genome analysis reveals the presence of 29 putative biosynthetic gene clusters (BGCs) encoding secondary metabolites. Among them, a type I PKS BGC shows an 82% similarity with the cyclizidine (CLD) BGC identified from Streptomyces NCIB 11649. LCMS profiles further supported the production of new CLD congeners. Bafilomycins were also found produced in abundance, corresponding to another type I PKS BGC highly homologous to that of bafilomycin B1 from S. lohii. CLDs are indolizidine alkaloids consisting a fused five- and six-membered ring system with an intriguing cyclopropane terminal linked by a trans-dienic chain. The cyclization mechanism of the cylopropyl ring, one of its pharmacophores, is still unknown. Genome sequencing of the new CLD producer and subsequent comparative analysis of their gene clusters would further our understanding of the chemistry behind cyclopropane formation.
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