Suppr超能文献

afsQ1的一个工程化等位基因有助于隐秘天然产物的发现与研究。

An Engineered Allele of afsQ1 Facilitates the Discovery and Investigation of Cryptic Natural Products.

作者信息

Daniel-Ivad Martin, Hameed Nabeela, Tan Stephanie, Dhanjal Rachna, Socko Daniel, Pak Patricia, Gverzdys Tomas, Elliot Marie A, Nodwell Justin R

机构信息

Department of Biochemistry, University of Toronto , MaRS Centre - West Tower, 661 University Avenue, Toronto, Ontario M5G 1M1, Canada.

Department of Biology, McMaster University , 1280 Main Street W, Hamilton, Ontario L8S 4K1, Canada.

出版信息

ACS Chem Biol. 2017 Mar 17;12(3):628-634. doi: 10.1021/acschembio.6b01002. Epub 2017 Jan 19.

Abstract

New approaches to antimicrobial discovery are needed to address the growing threat of antibiotic resistance. The Streptomyces genus, a proven source of antibiotics, is recognized as having a large reservoir of untapped secondary metabolic genes, many of which are likely to produce uncharacterized compounds. However, most of these compounds are currently inaccessible, as they are not expressed under standard laboratory conditions. Here, we present a novel methodology for activating these "cryptic" metabolites by heterologously expressing a constitutively active pleiotropic regulator. By screening wild Streptomyces isolates, we identified the antibiotic siamycin-I, a lasso peptide that we show is active against multidrug pathogens. We further revealed that siamycin-I interferes with cell wall integrity via lipid II. This new technology has the potential to be broadly applied for use in the discovery of additional "cryptic" metabolites.

摘要

需要新的抗菌药物发现方法来应对日益增长的抗生素耐药性威胁。链霉菌属是一种已被证实的抗生素来源,被认为拥有大量未开发的次生代谢基因库,其中许多基因可能产生未被表征的化合物。然而,目前这些化合物大多无法获取,因为它们在标准实验室条件下不表达。在此,我们提出了一种新方法,通过异源表达一种组成型活性多效调节剂来激活这些“隐性”代谢产物。通过筛选野生链霉菌分离株,我们鉴定出了抗生素西amycin-I,一种套索肽,我们发现它对多重耐药病原体具有活性。我们进一步揭示,西amycin-I通过脂质II干扰细胞壁完整性。这项新技术有潜力被广泛应用于发现更多的“隐性”代谢产物。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验