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.
引用
收藏
页数:4
相关论文
共 19 条
  • [11] Canu: scalable and accurate long-read assembly via adaptive k-mer weighting and repeat separation
    Koren, Sergey
    Walenz, Brian P.
    Berlin, Konstantin
    Miller, Jason R.
    Bergman, Nicholas H.
    Phillippy, Adam M.
    [J]. GENOME RESEARCH, 2017, 27 (05) : 722 - 736
  • [12] tRNAscan-SE On-line: integrating search and context for analysis of transfer RNA genes
    Lowe, Todd M.
    Chan, Patricia P.
    [J]. NUCLEIC ACIDS RESEARCH, 2016, 44 (W1) : W54 - W57
  • [13] Mungan M D., 2020, Nucleic Acids Res, V48, pW546, DOI DOI 10.1093/NAR/GKAA374
  • [14] Genomics-Driven Natural Product Discovery in Actinomycetes
    Niu, Guoqing
    [J]. TRENDS IN BIOTECHNOLOGY, 2018, 36 (03) : 238 - 241
  • [15] Deciphering Piperidine Formation in Polyketide-Derived Indolizidines Reveals a Thioester Reduction, Transamination, and Unusual Imine Reduction Process
    Peng, Haidong
    Wei, Erman
    Wang, Jiali
    Zhang, Yanan
    Cheng, Lin
    Ma, Hongmin
    Deng, Zixin
    Qu, Xudong
    [J]. ACS CHEMICAL BIOLOGY, 2016, 11 (12) : 3278 - 3283
  • [16] Visualizing and comparing circular genomes using the CGView family of tools
    Stothard, Paul
    Grant, Jason R.
    Van Domselaar, Gary
    [J]. BRIEFINGS IN BIOINFORMATICS, 2019, 20 (04) : 1576 - 1582
  • [17] Terlouw B.R., NUCL ACIDS RES
  • [18] Pilon: An Integrated Tool for Comprehensive Microbial Variant Detection and Genome Assembly Improvement
    Walker, Bruce J.
    Abeel, Thomas
    Shea, Terrance
    Priest, Margaret
    Abouelliel, Amr
    Sakthikumar, Sharadha
    Cuomo, Christina A.
    Zeng, Qiandong
    Wortman, Jennifer
    Young, Sarah K.
    Earl, Ashlee M.
    [J]. PLOS ONE, 2014, 9 (11):
  • [19] Characterization of the Bafilomycin Biosynthetic Gene Cluster from Streptomyces lohii
    Zhang, Wei
    Fortman, Jeffrey L.
    Carlson, Jacob C.
    Yan, Jinyong
    Liu, Yi
    Bai, Fali
    Guan, Wenna
    Jia, Junyong
    Matainaho, Teatulohi
    Sherman, David H.
    Li, Shengying
    [J]. CHEMBIOCHEM, 2013, 14 (03) : 301 - 306