1.重庆工商大学环境与资源学院,重庆 400067
2.中国科学院天津工业生物技术研究所,中国科学院低碳合成工程生物学重点实验室,天津 300308
3.天津科技大学生物工程学院,天津 300457
[ "涂然(1979—),女,博士,正高级工程师,教授,硕士生导师。研究方向为合成生物学、高通量检测和筛选技术等。E-mail:tu_r@ctbu.edu.cn" ]
[ "王猛(1982—),男,博士,研究员,博士生导师。研究方向为合成生物学、高通量自动化技术等。E-mail:wangmeng@tib.cas.cn" ]
收稿:2021-12-05,
修回:2022-01-18,
纸质出版:2023-02-28
移动端阅览
涂然, 李世新, 李昊霓, 王猛. 液滴微流控技术在微生物工程菌株选育中的应用进展[J]. 合成生物学, 2023, 4(1): 165-184
TU Ran, LI Shixin, LI Haoni, WANG Meng. Advances and applications of droplet-based microfluidics in evolution and screening of engineered microbial strains[J]. Synthetic Biology Journal, 2023, 4(1): 165-184
涂然, 李世新, 李昊霓, 王猛. 液滴微流控技术在微生物工程菌株选育中的应用进展[J]. 合成生物学, 2023, 4(1): 165-184 DOI: 10.12211/2096-8280.2021-105.
TU Ran, LI Shixin, LI Haoni, WANG Meng. Advances and applications of droplet-based microfluidics in evolution and screening of engineered microbial strains[J]. Synthetic Biology Journal, 2023, 4(1): 165-184 DOI: 10.12211/2096-8280.2021-105.
微生物工程菌株是生物制造的重要基础,但大多数的工程菌株需要进化改造才能适用于生物制造。在菌种选育过程中,如何高效地筛选获得具有目标性状的微生物工程菌株是进行生物制造应用的关键影响因素之一。液滴微流控技术作为近年来发展起来的一种基于微芯片的高通量检测筛选技术,可以生成大小均一、相互独立的微体积液滴小室,并应用于单细胞的培养、检测和分离,在微生物菌株改造尤其是分泌型菌株的改造中得到广泛应用。本文首先概述液滴微流控技术的组成部分,对关键性的技术进行简要介绍;其次根据液滴检测信号的来源、液滴筛选流程的难易程度和液滴分选仪器的适用范围,对液滴微流控技术在工程菌株选育中的应用进行总结分析;最后对液滴微流控技术在应用中存在的问题和研究方向进行展望,为深化其在微生物合成生物学中的应用提供指导。
Microbial strains are perquisites for biomanufacting through microbial culture and fermentation. However
most strains usually need to be engineered to improve their performances for industrial applications. Therefore how to efficiently screen and isolate robust strains is a c
ritical step of strain engineering. As an advanced high-throughput screening technology
droplet-based microfluidics developed with micro-chips can generate highly independent and uniform micro- or nano-liter droplets
in which single cells can be encapsulated
inoculated
detected
and analyzed for strain engineering. It is especially useful in the evolution of microbial strains for producing extracellular products. In this review
we first introduce the basic components of the droplet-based microfluidic system and the main steps involved in the strain screening. We then summarize key factors for the application of the droplet-based microfluidic technology in strain engineering
such as the signal sources of droplet detection
the difficulties of handling droplet screening
and the scopes of droplet sorting instruments. Based on the instruments used for the droplet sorting
we group the application cases into two types either
via
fluorescence-activated droplet sorting (FADS) using microfluidic equipment or
via
fluorescence-activated cell sorting (FACS) using flow cytometry instrument. While FADS using single-layer water-in-oil droplet can be further classified into cellular signature
fluorescent reporter protein
and substrate-based reaction according to the signal sources
FACS can be divided into double-layers water-in-oil-in-water (W/O/W) droplet or microgel droplet according to the droplet property. Finally
we outline challenges and prospects for the droplet microfluidic technology
and provide some guidelines for its applications in synthetic biology. Compared with traditional screening methods such as shaking flask or microplate with a throughput of hundreds to thousands of samples per day in milli- or micro-liter volume
the droplet-based microfluidic technology can achieve millions of samples per day in pico- or nano-liter volume
resulting in an increase of thousand-folds in screening speed and cost-saving for million-folds. By integrating with an automated station
t
he droplet-based microfluidic technology can be further improved for its screening efficiencies and application potentials in microbial synthetic biology.
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