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首页> 外文期刊>Frontiers in Bioengineering and Biotechnology >Sensitive and Rapid Phenotyping of Microbes With Soluble Methane Monooxygenase Using a Droplet-Based Assay
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Sensitive and Rapid Phenotyping of Microbes With Soluble Methane Monooxygenase Using a Droplet-Based Assay

机译:使用液滴的测定法与可溶性甲烷单氧化酶的微生物敏感和快速表型

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Methanotrophs with soluble methane monooxygenase (sMMO) show high potential for various ecological and biotechnological applications. Here, we developed a high throughput method to identify sMMO-producing microbes by integrating droplet microfluidics and a genetic circuit-based biosensor system. sMMO-producers and sensor cells were encapsulated in monodispersed droplets with benzene as the substrate and incubated for 5 h. The sensor cells were analyzed as the reporter for phenol-sensitive transcription activation of fluorescence. Various combinations of methanotrophs and biosensor cells were investigated to optimize the performance of our droplet-integrated transcriptional factor biosensor system. As a result, the conditions to ensure sMMO activity to convert the starting material, benzene, into phenol, were determined. The biosensor signals were sensitive and quantitative under optimal conditions, showing that phenol is metabolically stable within both cell species and accumulates in picoliter-sized droplets, and the biosensor cells are healthy enough to respond quantitatively to the phenol produced. These results show that our system would be useful for rapid evaluation of phenotypes of methanotrophs showing sMMO activity, while minimizing the necessity of time-consuming cultivation and enzyme preparation, which are required for conventional analysis of sMMO activity.
机译:具有可溶性甲烷单氧化酶(SMMO)的甲胰蛋白表现出各种生态和生物技术应用的高潜力。在这里,我们开发了一种高通量方法来识别通过整合液滴微流体和基于遗传电路的生物传感器系统来识别SMMO的微生物。将SMMO-生产者和传感器电池用苯作为基材的单分散液滴中封装在苯乙烯中并孵育5小时。分析传感器电池作为荧光的酚类敏感转录激活的报道。研究了各种甲蛋白酶和生物传感器细胞的组合,优化了我们液滴整合转录因子生物传感器系统的性能。结果,确定了确保SMMO活性将原料,苯,苯酚转化为苯酚的条件。在最佳条件下,生物传感器信号敏感和定量,表明苯酚在细胞物种中均可稳定,并在Picoliter尺寸的液滴中积聚,并且生物传感器细胞足够健康,以定量为生产的酚类以衡量。这些结果表明,我们的系统可用于快速评估显示SMMO活性的甲蛋白的表型,同时最小化常规分析SMMO活性的常规培养和酶制剂的必要性。

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