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泰国伯克霍尔德菌中隐秘生物合成基因簇的全球觉醒

Global Awakening of Cryptic Biosynthetic Gene Clusters in Burkholderia thailandensis.

作者信息

Gupta Ashish, Bedre Renesh, Thapa Sudarshan Singh, Sabrin Afsana, Wang Guannan, Dassanayake Maheshi, Grove Anne

机构信息

Department of Biological Sciences, ‡School of Plant, Environmental and Soil Sciences, Louisiana State University , Baton Rouge, Louisiana 70803, United States.

出版信息

ACS Chem Biol. 2017 Dec 15;12(12):3012-3021. doi: 10.1021/acschembio.7b00681. Epub 2017 Nov 8.

DOI:10.1021/acschembio.7b00681
PMID:29087175
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5732026/
Abstract

Many bacteria encode biosynthetic proteins that produce a vast array of natural products. These compounds are often synthesized during host invasion as they function as virulence factors. In addition, such secondary metabolites have yielded numerous molecular scaffolds with pharmaceutical and clinical importance. The gene clusters that encode proteins responsible for synthesis of these compounds are typically silenced or "cryptic" under laboratory growth conditions, hampering discovery of novel lead compounds. We report here that MftR is a global repressor of secondary metabolite synthesis in Burkholderia thailandensis and that urate functions as a physiologically relevant inducer of gene expression. Biosynthetic gene clusters under MftR control include those associated with production of the antimicrobial bactobolins, the iron siderophore malleobactin, and the virulence factor malleilactone. MftR also controls additional genes associated with survival in a host environment, such as genes encoding components of the type III secretion system (T3SS) and proteins linked to anaerobic respiration. This observation not only has implications for understanding activation of gene regulatory networks during host invasion, but it also paves the way for isolation of novel therapeutic leads.

摘要

许多细菌编码能产生大量天然产物的生物合成蛋白。这些化合物在宿主入侵期间常作为毒力因子发挥作用,因此通常在宿主入侵期间合成。此外,这类次生代谢产物产生了众多具有药学和临床重要性的分子骨架。在实验室生长条件下,编码负责合成这些化合物的蛋白质的基因簇通常处于沉默或“隐蔽”状态,这阻碍了新型先导化合物的发现。我们在此报告,MftR是泰国伯克霍尔德菌次生代谢产物合成的全局阻遏物,尿酸作为基因表达的生理相关诱导物发挥作用。受MftR调控的生物合成基因簇包括与抗菌杆菌肽、铁载体马勒伯克菌素以及毒力因子马勒内酯产生相关的基因簇。MftR还控制与在宿主环境中生存相关的其他基因,例如编码III型分泌系统(T3SS)组分的基因以及与无氧呼吸相关的蛋白质。这一发现不仅对理解宿主入侵期间基因调控网络的激活具有启示意义,还为新型治疗先导物的分离铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24ab/5732026/09971f986d55/nihms919529f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24ab/5732026/3ac099843b0a/nihms919529f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24ab/5732026/377a50d3305d/nihms919529f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24ab/5732026/d6aa60bca2d3/nihms919529f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24ab/5732026/bb1e6e8eea1a/nihms919529f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24ab/5732026/09971f986d55/nihms919529f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24ab/5732026/3ac099843b0a/nihms919529f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24ab/5732026/377a50d3305d/nihms919529f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24ab/5732026/d6aa60bca2d3/nihms919529f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24ab/5732026/bb1e6e8eea1a/nihms919529f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24ab/5732026/09971f986d55/nihms919529f5.jpg

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