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利用 CRISPR 干扰和激活系统在链霉菌中激活天然产物合成。

Activating natural product synthesis using CRISPR interference and activation systems in Streptomyces.

机构信息

Department of BioSciences, Rice University, 6100 Main Street, MS 140, Houston, TX 77005, USA.

Department of Bioengineering, Rice University, 6100 Main Street, MS 142, Houston, TX 77005, USA.

出版信息

Nucleic Acids Res. 2022 Jul 22;50(13):7751-7760. doi: 10.1093/nar/gkac556.

Abstract

The rise of antibiotic-resistant bacteria represents a major threat to global health, creating an urgent need to discover new antibiotics. Natural products derived from the genus Streptomyces represent a rich and diverse repertoire of chemical molecules from which new antibiotics are likely to be found. However, a major challenge is that the biosynthetic gene clusters (BGCs) responsible for natural product synthesis are often poorly expressed under laboratory culturing conditions, thus preventing the isolation and screening of novel chemicals. To address this, we describe a novel approach to activate silent BGCs through rewiring endogenous regulation using synthetic gene regulators based upon CRISPR-Cas. First, we refine CRISPR interference (CRISPRi) and create CRISPR activation (CRISPRa) systems that allow for highly programmable and effective gene repression and activation in Streptomyces. We then harness these tools to activate a silent BGC by perturbing its endogenous regulatory network. Together, this work advances the synthetic regulatory toolbox for Streptomyces and facilitates the programmable activation of silent BGCs for novel chemical discovery.

摘要

抗生素耐药菌的兴起对全球健康构成了重大威胁,因此迫切需要发现新的抗生素。来源于链霉菌属的天然产物代表了丰富多样的化学分子库,很可能从中发现新的抗生素。然而,主要的挑战是,负责天然产物合成的生物合成基因簇(BGCs)在实验室培养条件下往往表达不佳,从而阻止了新型化学物质的分离和筛选。为了解决这个问题,我们描述了一种通过使用基于 CRISPR-Cas 的合成基因调节剂重新布线内源性调控来激活沉默 BGC 的新方法。首先,我们改进了 CRISPR 干扰(CRISPRi)并创建了 CRISPR 激活(CRISPRa)系统,这些系统允许在链霉菌中进行高度可编程和有效的基因抑制和激活。然后,我们利用这些工具通过干扰其内源性调控网络来激活沉默 BGC。总之,这项工作推进了链霉菌的合成调控工具箱,并促进了沉默 BGC 的可编程激活,以用于新型化学物质的发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b875/9303295/d5c478616e0b/gkac556fig1.jpg

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