Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/30899
English  |  正體中文  |  简体中文  |  Items with full text/Total items : 18295/20522 (89%)
Visitors : 36524113      Online Users : 30553
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version


    jsp.display-item.identifier=請使用永久網址來引用或連結此文件: https://ir.cnu.edu.tw/handle/310902800/30899


    题名: Resistance Gene-Guided Genome Mining: Serial Promoter Exchanges in Aspergillus nidulans Reveal the Biosynthetic Pathway for Fellutamide B, a Proteasome Inhibitor
    作者: Yeh, Hsu-Hua
    Ahuja, Manmeet
    Chiang, Yi-Ming
    Oakley, C. Elizabeth
    Moore, Shauna
    Yoon, Olivia
    Hajoysky, Heather
    Bok, Jin-Woo
    Keller, Nancy P.
    Wang, Clay C. C.
    Oakley, Berl R.
    贡献者: Univ Southern Calif, Sch Pharm, Dept Pharmacol & Pharmaceut Sci, Los Angeles
    Univ Kansas, Dept Mol Biosci
    Chia Nan Univ Pharm & Sci, Dept Pharm
    Univ Wisconsin, Dept Bacteriol
    Univ Wisconsin, Dept Med Microbiol & Immunol
    Univ Southern Calif, Dept Chem, Dornsife Coll Letters Arts & Sci
    Chia Nan Univ Pharm & Sci, Drug Discovery & Dev Ctr
    Reliance Ind Ltd, Ind Biotechnol Div, Reliance Technol Grp
    关键词: polyketide
    clusters
    fungus
    metabolites
    sequence
    system
    日期: 2016-08
    上传时间: 2018-01-18 11:37:31 (UTC+8)
    出版者: Amer Chemical Soc
    摘要: Fungal genome projects are revealing thousands of cryptic secondary metabolism (SM) biosynthetic gene clusters that encode pathways that potentially produce valuable compounds. Heterologous expression systems should allow these clusters to be expressed and their products obtained, but approaches are needed to identify the most valuable target clusters. The inp cluster of Aspergillus nidulans contains a gene, inpE, that encodes a proteasome subunit, leading us to hypothesize that the inp cluster produces a proteasome inhibitor and inpE confers resistance to this compound. Previous efforts to express this cluster have failed, but by sequentially replacing the promoters of the genes of the cluster with a regulatable promotor, we have expressed them successfully. Expression reveals that the product of the inp cluster is the proteasome inhibitor fellutamide B, and our data allow us to propose a biosynthetic pathway for the compound. By deleting inpE and activating expression of the inp cluster, we demonstrate that inpE is required for resistance to internally produced fellutamide B. These data provide experimental validation for the hypothesis that some fungal SM clusters contain genes that encode resistant forms of the enzymes targeted by the compound produced by the cluster.
    關聯: Acs Chemical Biology, v.11 n.8, pp.2275-2284
    显示于类别:[Dept. of Pharmacy] Periodical Articles

    文件中的档案:

    档案 描述 大小格式浏览次数
    index.html0KbHTML1847检视/开启


    在CNU IR中所有的数据项都受到原著作权保护.

    TAIR相关文章

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback