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光遗传学操作可预防工程化铜绿假单胞菌在表面形成生物膜。

Optogenetics Manipulation Enables Prevention of Biofilm Formation of Engineered Pseudomonas aeruginosa on Surfaces.

作者信息

Pu Lu, Yang Shuai, Xia Aiguo, Jin Fan

机构信息

Hefei National Laboratory for Physical Sciences at the Microscale, University of Science and Technology of China , Hefei 230026, PR China.

Department of Polymer Science and Engineering, University of Science and Technology of China , Hefei 230026, PR China.

出版信息

ACS Synth Biol. 2018 Jan 19;7(1):200-208. doi: 10.1021/acssynbio.7b00273. Epub 2017 Oct 31.

DOI:10.1021/acssynbio.7b00273
PMID:29053252
Abstract

Synthetic biologists have attempted to solve real-world problems, such as those of bacterial biofilms, that are involved in the pathogenesis of many clinical infections and difficult to eliminate. To address this, we employed a blue light responding system and integrated it into the chromosomes of Pseudomonas aeruginosa. With making rational adaptions and improvements of the light-activated system, we provided a robust and convenient means to spatiotemporally control gene expression and manipulate biological processes with minimal perturbation in P. aeruginosa. It increased the light-induced gene expression up to 20-fold. Moreover, we deliberately introduced a functional protein gene PA2133 containing an EAL domain to degrade c-di-GMP into the modified system, and showed that the optimally engineered optogenetic tool inhibited the formation of P. aeruginosa biofilms through the induction of blue light, resulting in much sparser and thinner biofilms. Our approach establishes a methodology for leveraging the tools of synthetic biology to guide biofilm formation and engineer biofilm patterns with unprecedented spatiotemporal resolution. Furthermore, the findings suggest that the synthetic optogenetic system may provide a promising strategy that could be applied to control and fight biofilms.

摘要

合成生物学家试图解决现实世界中的问题,比如那些涉及许多临床感染发病机制且难以消除的细菌生物膜问题。为了解决这一问题,我们采用了一种蓝光响应系统,并将其整合到铜绿假单胞菌的染色体中。通过对光激活系统进行合理的调整和改进,我们提供了一种强大且便捷的方法,能够在铜绿假单胞菌中以最小的干扰对基因表达进行时空控制并操纵生物过程。它将光诱导的基因表达提高了20倍。此外,我们特意将一个含有EAL结构域的功能性蛋白基因PA2133引入到改良系统中以降解环二鸟苷酸,并表明经过优化设计的光遗传学工具通过蓝光诱导抑制了铜绿假单胞菌生物膜的形成,从而使生物膜变得更加稀疏和薄。我们的方法建立了一种利用合成生物学工具来引导生物膜形成并以前所未有的时空分辨率设计生物膜模式的方法。此外,这些发现表明合成光遗传学系统可能提供一种有前景的策略,可应用于控制和对抗生物膜。

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