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本文引用的文献

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Chem Rev. 2017 Oct 11;117(19):12415-12474. doi: 10.1021/acs.chemrev.7b00283. Epub 2017 Sep 27.
3
Phylogeny-guided (meta)genome mining approach for the targeted discovery of new microbial natural products.用于靶向发现新型微生物天然产物的系统发育引导(元)基因组挖掘方法。
J Ind Microbiol Biotechnol. 2017 Feb;44(2):285-293. doi: 10.1007/s10295-016-1874-z. Epub 2016 Nov 24.
4
Discovery of microbial natural products by activation of silent biosynthetic gene clusters.微生物天然产物的发现:沉默生物合成基因簇的激活。
Nat Rev Microbiol. 2015 Aug;13(8):509-23. doi: 10.1038/nrmicro3496. Epub 2015 Jun 29.
5
Complestatin exerts antibacterial activity by the inhibition of fatty acid synthesis.补体抑制素通过抑制脂肪酸合成发挥抗菌活性。
Biol Pharm Bull. 2015;38(5):715-21. doi: 10.1248/bpb.b14-00824.
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antiSMASH: rapid identification, annotation and analysis of secondary metabolite biosynthesis gene clusters in bacterial and fungal genome sequences.antiSMASH:快速识别、注释和分析细菌和真菌基因组序列中次生代谢产物生物合成基因簇。
Nucleic Acids Res. 2011 Jul;39(Web Server issue):W339-46. doi: 10.1093/nar/gkr466. Epub 2011 Jun 14.
7
Origins and evolution of antibiotic resistance.抗生素耐药性的起源与演变。
Microbiol Mol Biol Rev. 2010 Sep;74(3):417-33. doi: 10.1128/MMBR.00016-10.
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Antibacterial resistance worldwide: causes, challenges and responses.全球抗菌药物耐药性:原因、挑战及应对措施
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Autolysins of Bacillus subtilis: multiple enzymes with multiple functions.枯草芽孢杆菌的自溶素:具有多种功能的多种酶
Microbiology (Reading). 2000 Feb;146 ( Pt 2):249-262. doi: 10.1099/00221287-146-2-249.
10
Chemistry, Biology, and Medicine of the Glycopeptide Antibiotics.糖肽类抗生素的化学、生物学与医学
Angew Chem Int Ed Engl. 1999 Aug;38(15):2096-2152. doi: 10.1002/(sici)1521-3773(19990802)38:15<2096::aid-anie2096>3.0.co;2-f.

基于系统发育的方法得到具有独特作用的糖肽。

Phylogeny-Guided Approach Yields Glycopeptides with Unique Action.

机构信息

Department of Chemistry, Emory University, 1515 Dickey Dr., Atlanta, GA 30322, USA.

Department of Chemistry, Emory University, 1515 Dickey Dr., Atlanta, GA 30322, USA.

出版信息

Trends Pharmacol Sci. 2020 May;41(5):297-299. doi: 10.1016/j.tips.2020.03.002. Epub 2020 Apr 1.

DOI:10.1016/j.tips.2020.03.002
PMID:32247549
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7259425/
Abstract

Bacteria are extremely adept at overcoming the effects of antibiotics through a variety of mechanisms. As a result, researchers are constantly searching for antibiotics with new mechanisms of action. Culp and coworkers recently utilized a phylogeny-guided approach to mine the genomes of Actinomycetes species for glycopeptides with novel targets. Their efforts yielded the identification of complestatin and corbomycin as antibiotics with a different target than other glycopeptides.

摘要

细菌非常擅长通过多种机制来克服抗生素的作用。因此,研究人员一直在寻找具有新作用机制的抗生素。Culp 及其同事最近利用系统发育指导的方法从放线菌属物种的基因组中挖掘具有新型靶标的糖肽。他们的努力确定了 complestatin 和 corbomycin 是具有不同于其他糖肽的靶标的抗生素。