Department of Fundamental Microbiology, University of Lausanne, Lausanne, Switzerland.
Institute for Environmental Engineering, ETH Zürich, Zürich, Switzerland.
Appl Environ Microbiol. 2018 Aug 31;84(18). doi: 10.1128/AEM.01362-18. Print 2018 Sep 15.
, commonly used in chemotaxis studies, is attracted mostly by amino acids, sugars, and peptides. We envisioned modifying the chemotaxis specificity of by expressing heterologous chemoreceptors from enabling attraction either to toluene or benzoate. The gene encoding the type 40-helical bundle (40H) methyl-accepting chemoreceptor for toluene from MT53 and the gene for the type 40H receptor for benzoate and related molecules from F1 were expressed from the promoter on a plasmid in motile wild-type MG1655. cells expressing McpT accumulated in chemoattraction assays to sources with 60 to 200 μM toluene, although less strongly than the response to 100 μM serine, but statistically significantly stronger than that to sources without any added attractant. An McpT-mCherry fusion protein was detectably expressed in and yielded weak but distinguishable membranes and polar foci in 1% of cells. cells expressing PcaY showed weak attraction to 0.1 to 1 mM benzoate, but 50 to 70% of cells localized the PcaY-mCherry fusion to their membrane. We conclude that implementing heterologous receptors in the chemotaxis network is possible and, upon improvement of the compatibility of the type 40H chemoreceptors, may bear interest for biosensing. Bacterial chemotaxis might be harnessed for the development of rapid biosensors, in which chemical availability is deduced from cell accumulation to chemoattractants over time. Chemotaxis of has been well studied, but the bacterium is not attracted to chemicals of environmental concern, such as aromatic solvents. We show here that heterologous chemoreceptors for aromatic compounds from at least partly functionally complement the chemotaxis network, yielding cells attracted to toluene or benzoate. Complementation was still inferior to native chemoattractants, like serine, but our study demonstrates the potential for obtaining selective sensing for aromatic compounds in .
, 常用于趋化性研究,主要被氨基酸、糖和肽吸引。我们设想通过表达来自 的异源化学感受器来修饰 的趋化性特异性,从而使 对甲苯或苯甲酸产生吸引力。来自 MT53 的用于甲苯的 40 螺旋束 (40H) 甲基受体的 基因和来自 F1 的用于苯甲酸和相关分子的 40H 受体的 基因,从运动型野生型 的 启动子在一个质粒上表达。表达 McpT 的 细胞在趋化吸引测定中积累到含有 60 至 200 μM 甲苯的源中,尽管不如对 100 μM 丝氨酸的反应强烈,但与没有添加任何吸引剂的源相比,统计学上显著更强。McpT-mCherry 融合蛋白在 中可检测到表达,并在 1%的细胞中产生微弱但可区分的膜和极性焦点。表达 PcaY 的 细胞对 0.1 至 1 mM 苯甲酸表现出微弱的吸引力,但 50%至 70%的细胞将 PcaY-mCherry 融合蛋白定位到它们的膜上。我们得出结论,在 趋化作用网络中实施异源受体是可能的,并且在改进 40H 化学感受器的兼容性后,可能对生物传感具有兴趣。细菌趋化性可用于开发快速生物传感器,其中通过随时间推移细胞积累到趋化剂来推断化学物质的可用性。 已被很好地研究,但该细菌不会被环境关注的化学物质(如芳香溶剂)吸引。我们在这里表明,来自 的芳香族化合物的异源化学感受器至少部分地功能互补 趋化作用网络,产生对甲苯或苯甲酸有吸引力的细胞。互补性仍然不如天然趋化剂,如丝氨酸,但我们的研究证明了在 中获得对芳香族化合物的选择性传感的潜力。