Analysis of a draft genome sequence of Kitasatospora cheerisanensis KCTC 2395 producing bafilomycin antibiotics
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  • 作者:Jae Yoon Hwang (1)
    Soo Hee Kim (1)
    Hye Ryeung Oh (1)
    Eunju Kwon (2)
    Doo Hyun Nam (1)

    1. College of Pharmacy
    ; Yeungnam University ; Gyongsan ; 712-749 ; Republic of Korea
    2. Institute for Drug Development
    ; Yeungnam University ; Gyongsan ; 712-749 ; Republic of Korea
  • 关键词:draft genome ; Kitasatospora ; MurE ; polyketide synthase ; bafilomycin
  • 刊名:Journal of Microbiology
  • 出版年:2015
  • 出版时间:January 2015
  • 年:2015
  • 卷:53
  • 期:1
  • 页码:84-89
  • 全文大小:614 KB
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  • 刊物主题:Microbiology;
  • 出版者:Springer Netherlands
  • ISSN:1976-3794
文摘
Kitasatospora cheerisanensis KCTC 2395, producing bafilomycin antibiotics belonging to plecomacrolide group, was isolated from a soil sample at Mt. Jiri, Korea. The draft genome sequence contains 8.04 Mb with 73.6% G+C content and 7,810 open reading frames. All the genes for aerial mycelium and spore formations were confirmed in this draft genome. In phylogenetic analysis of MurE proteins (UDP-N-acetylmuramyl-L-alanyl-D-glutamate:DAP ligase) in a conserved dcw (division of cell wall) locus, MurE proteins of Kitasatospora species were placed in a separate clade between MurEs of Streptomyces species incorporating LL-diaminopimelic acid (DAP) and MurEs of Saccharopolyspora erythraea as well as Mycobacterium tuberculosis ligating meso-DAP. From this finding, it was assumed that Kitasatospora MurEs exhibit the substrate specificity for both LL-DAP and meso-DAP. The bafilomycin biosynthetic gene cluster was located in the left subtelomeric region. In 71.3 kb-long gene cluster, 17 genes probably involved in the biosynthesis of bafilomycin derivatives were deduced, including 5 polyketide synthase (PKS) genes comprised of 12 PKS modules.

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