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在枯草芽孢杆菌中开发一种用于检测靶向细菌细胞包膜的抗生素的全细胞生物传感器。

Development of a whole-cell biosensor for detection of antibiotics targeting bacterial cell envelope in Bacillus subtilis.

机构信息

College of Biotechnology and Bioengineering, Zhejiang University of Technology, Hangzhou, 310014, Zhejiang, China.

出版信息

Appl Microbiol Biotechnol. 2022 Jan;106(2):789-798. doi: 10.1007/s00253-022-11762-z. Epub 2022 Jan 11.

DOI:10.1007/s00253-022-11762-z
PMID:35015142
Abstract

It is an urgent need to develop novel antibiotics to treat infections caused by multi-drug-resistant bacteria. One promising strategy could be the use of whole-cell biosensors, which have been extensively studied to monitor environmental pollutants and intracellular metabolites. Here, we used the σ-mediated regulatory system of Bacillus subtilis to construct a whole-cell biosensor for the detection of cell envelope-acting antibiotics. Using polymyxin B as the inducer for bacterial cell envelope stress and enhanced green fluorescent protein (EGFP) as the reporter, we found that the promoter of ypuA (P) had the lowest background noise and the most significant changes in the fluorescence output. The whole-cell biosensor displayed dose-dependent and time-dependent responses in fluorescence signals. The detection range of this biosensor for polymyxin B was between 0.125 and 12 μg/mL. The response of the biosensor is specific to antibiotics that target the cell envelope. Besides determination in liquid cultures, the output signal of the biosensor can be easily determined on agar surfaces. Using this biosensor, we successfully detected polymyxins secreted by its producing strain and bacteria that produce cell envelope-acting antibiotics. KEY POINTS: • A whole-cell biosensor was constructed based on the σ-mediated regulatory system. • The response of the biosensor is specific to cell envelope-acting antibiotics. • The biosensor can be used to screen novel cell envelope-acting antibiotics.

摘要

开发新型抗生素来治疗多药耐药菌引起的感染是当务之急。一种有前途的策略可能是使用全细胞生物传感器,它已被广泛研究用于监测环境污染物和细胞内代谢物。在这里,我们使用枯草芽孢杆菌的 σ 介导调控系统来构建用于检测细胞包膜作用抗生素的全细胞生物传感器。我们使用多粘菌素 B 作为细菌细胞包膜应激的诱导剂和增强型绿色荧光蛋白 (EGFP) 作为报告蛋白,发现 ypuA 的启动子(P)具有最低的背景噪声和荧光输出的最显著变化。全细胞生物传感器在荧光信号中表现出剂量依赖性和时间依赖性反应。该生物传感器对多粘菌素 B 的检测范围在 0.125 至 12μg/mL 之间。生物传感器的响应特异性针对作用于细胞壁的抗生素。除了在液体培养物中的测定外,生物传感器的输出信号也可以很容易地在琼脂表面上确定。使用该生物传感器,我们成功地检测到其产生菌株分泌的多粘菌素和产生细胞壁作用抗生素的细菌。关键点:

  • 基于 σ 介导的调控系统构建了全细胞生物传感器。

  • 生物传感器的响应特异性针对细胞壁作用抗生素。

  • 该生物传感器可用于筛选新型细胞壁作用抗生素。

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