Assembly of a novel biosynthetic pathway for gentamicin B production in Micromonospora echinospora
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  • 作者:Xianpu Ni ; Zhenpeng Sun ; Yawen Gu ; Hao Cui ; Huanzhang Xia
  • 关键词:Micromonospora echinospora ; Gentamicin B ; Metabolic engineering ; Artificial biosynthetic pathway
  • 刊名:Microbial Cell Factories
  • 出版年:2016
  • 出版时间:December 2016
  • 年:2016
  • 卷:15
  • 期:1
  • 全文大小:1,709 KB
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  • 作者单位:Xianpu Ni (1)
    Zhenpeng Sun (1)
    Yawen Gu (1)
    Hao Cui (1)
    Huanzhang Xia (1)

    1. School of Life Science and Biopharmaceutics, Shenyang Pharmaceutical University, No.103 Wenhua Road, Shenyang, Liaoning, China
  • 刊物类别:Chemistry and Materials Science
  • 刊物主题:Biotechnology
    Applied Microbiology
    Environmental Engineering/Biotechnology
  • 出版者:BioMed Central
  • ISSN:1475-2859
文摘
Background Isepamicin is a weakly toxic but highly active aminoglycoside antibiotic derivative of gentamicin B. Gentamicin B is a naturally occurring minor component isolated from Micromonospora echinospora. 2ʹ-NH2-containing gentamicin C complex is a dominant compound produced by wild-type M. echinospora; by contrast, 2ʹ-OH-containing gentamicin B is produced as a minor component. However, the biosynthetic pathway of gentamicin B remains unclear. Considering that gentamicin B shares a unique C hydroxyl group with kanamycin A, we aimed to design a new biosynthetic pathway of gentamicin B by combining twelve steps of gentamicin biosynthesis and two steps of kanamycin biosynthesis.

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