English  |  正體中文  |  简体中文  |  Items with full text/Total items : 17482/19768 (88%)
Visitors : 6300156      Online Users : 206
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
    Please use this identifier to cite or link to this item: http://ir.cnu.edu.tw/handle/310902800/30899

    標題: 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.
    貢獻者: 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
    關鍵字: polyketide
    日期: 2016-08
    上傳時間: 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
    Appears in Collections:[藥學系(所)] 期刊論文

    Files in This Item:

    File Description SizeFormat

    All items in CNU IR are protected by copyright, with all rights reserved.

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