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使用基于液滴的检测方法,通过可溶性甲烷单加氧酶对微生物进行灵敏且快速的表型分析。

Sensitive and Rapid Phenotyping of Microbes With Soluble Methane Monooxygenase Using a Droplet-Based Assay.

作者信息

Lee Hyewon, Baek Ji In, Kim Su Jin, Kwon Kil Koang, Rha Eugene, Yeom Soo-Jin, Kim Haseong, Lee Dae-Hee, Kim Dong-Myung, Lee Seung-Goo

机构信息

Synthetic Biology and Bioengineering Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, South Korea.

Department of Chemical Engineering and Applied Chemistry, Chungnam National University, Daejeon, South Korea.

出版信息

Front Bioeng Biotechnol. 2020 Apr 24;8:358. doi: 10.3389/fbioe.2020.00358. eCollection 2020.

DOI:10.3389/fbioe.2020.00358
PMID:32391352
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7193049/
Abstract

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.

摘要

具有可溶性甲烷单加氧酶(sMMO)的甲烷营养菌在各种生态和生物技术应用中显示出巨大潜力。在此,我们开发了一种高通量方法,通过整合微滴微流控技术和基于遗传电路的生物传感器系统来鉴定产生sMMO的微生物。将产生sMMO的微生物和传感器细胞封装在以苯为底物的单分散微滴中,并孵育5小时。以传感器细胞作为荧光对苯酚敏感转录激活的报告物进行分析。研究了甲烷营养菌和生物传感器细胞的各种组合,以优化我们的微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活性将起始原料苯转化为苯酚的条件。在最佳条件下,生物传感器信号灵敏且具有定量性,表明苯酚在两种细胞类型中代谢稳定,并在皮升大小的微滴中积累,并且生物传感器细胞健康到足以对产生的苯酚进行定量响应。这些结果表明,我们的系统将有助于快速评估具有sMMO活性的甲烷营养菌的表型,同时最大限度地减少传统sMMO活性分析所需的耗时培养和酶制备的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/180b/7193049/b31616e6e6f9/fbioe-08-00358-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/180b/7193049/3fa2f1d645c5/fbioe-08-00358-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/180b/7193049/20ee6c87d156/fbioe-08-00358-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/180b/7193049/0df8aecd48c9/fbioe-08-00358-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/180b/7193049/1cb6914d3e89/fbioe-08-00358-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/180b/7193049/b31616e6e6f9/fbioe-08-00358-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/180b/7193049/3fa2f1d645c5/fbioe-08-00358-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/180b/7193049/20ee6c87d156/fbioe-08-00358-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/180b/7193049/0df8aecd48c9/fbioe-08-00358-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/180b/7193049/1cb6914d3e89/fbioe-08-00358-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/180b/7193049/b31616e6e6f9/fbioe-08-00358-g005.jpg

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