1.中国科学院大连化学物理研究所,中国科学院分离分析化学重点实验室,辽宁 大连 116023
2.大连理工大学化学学院,辽宁 大连 116024
3.中国科学院大学,北京 100049
[ "吴玉洁(1998—),女,博士研究生。研究方向为面向合成生物学的蛋白质组学分析方法。E-mail:yujiewu@dicp.ac.cn" ]
[ "杨开广(1981—),男,研究员,博士生导师。研究方向为蛋白质组学新技术新方法。E-mail:yangkaiguang@dicp.ac.cn" ]
[ "随志刚(1979—),男,副研究员,硕士生导师。研究方向为基于质谱的蛋白质及代谢物高通量分析方法开发。E-mail:zhigangsui@dicp.ac.cn" ]
收稿:2023-04-17,
修回:2023-06-26,
纸质出版:2023-10-31
移动端阅览
吴玉洁, 刘欣欣, 刘健慧, 杨开广, 随志刚, 张丽华, 张玉奎. 基于高通量液相色谱质谱技术的菌株筛选与关键分子定量分析研究进展[J]. 合成生物学, 2023, 4(5): 1000-1019
WU Yujie, LIU Xinxin, LIU Jianhui, Yang Kaiguang, SUI Zhigang, ZHANG Lihua, ZHANG Yukui. Research progress of strain screening and quantitative analysis of key molecules based on high-throughput liquid chromatography and mass spectrometry[J]. Synthetic Biology Journal, 2023, 4(5): 1000-1019
吴玉洁, 刘欣欣, 刘健慧, 杨开广, 随志刚, 张丽华, 张玉奎. 基于高通量液相色谱质谱技术的菌株筛选与关键分子定量分析研究进展[J]. 合成生物学, 2023, 4(5): 1000-1019 DOI: 10.12211/2096-8280.2023-031.
WU Yujie, LIU Xinxin, LIU Jianhui, Yang Kaiguang, SUI Zhigang, ZHANG Lihua, ZHANG Yukui. Research progress of strain screening and quantitative analysis of key molecules based on high-throughput liquid chromatography and mass spectrometry[J]. Synthetic Biology Journal, 2023, 4(5): 1000-1019 DOI: 10.12211/2096-8280.2023-031.
合成生物学是21世纪新兴的交叉学科,已经为医药、化工、能源、食品和农业等领域带来了显著的改变。微生物细胞工厂(microbial cell factory,MCF)的构建和应用是合成生物学的重要研究内容,正迅速向实用化、产业化的方向发展。得益于基因编辑技术的进步,MCF菌株文库构建的能力大幅提升,亦产生了数量庞大的待测样本,亟需发展高通量自动化的分析检测方法与之匹配。此外,针对关键代谢酶或代谢物的高通量检测技术,也对MCF改造乃至工业化生产有重要的指导意义。液相色谱质谱技术是生物分子检测分析的重要手段,在蛋白质、代谢物定量分析方面占据重要地位。因此本文总结回顾了近年来高通量液相色谱质谱技术在微生物菌株筛选及关键分子定量分析方面的研究进展,从样品制备、色谱分离、质谱分析及数据处理等层面展开阐述,并对这一领域与自动化平台结合的前景及如何深度融合的挑战进行简要概括,为推动基于合成生物学生物智造领域的快速发展提供指导。
Synthetic biology is an emerging interdisciplinary research area and has brought significant changes to fields such as medicine
chemical engineering
energy
food and agriculture. The construction and application of microbial cell factories (MCFs) is an important task of synthetic biology
which will lead the way to a sustainable industrial-scale manufacturing sector. With the progress of genome editing technology
the construction strategy of MCFs has evolved from random mutation to customized transformation at the whole genome level. Biologists can obtain 10
3
~10
7
strain mutant libraries in a short time
creating an urgent need for the development of high-throughput screening methods. In addition
the demand for precise quantitative analysis of key mole
cules in metabolic pathways
such as metabolic enzymes and metabolites
is increasingly prominent in the process of strain transformation
evolution
and fermentation monitoring. Liquid chromatography (LC) offers excellent separation capability
allowing efficient separation of target molecules
while mass spectrometry (MS) provides strong detection ability due to its high specificity and sensitivity. Therefore
LC and MS techniques have been widely applied in the field of life sciences
especially for the qualitative and quantitative analyses of proteins and metabolites. With the development of high-throughput LC and MS technologies
these methods have become powerful tools for screening strains and quantitative research of key molecules in synthetic biology. Therefore
this work reviews the research progresses of LC and/or MS based strain screening and quantification of key molecules
focusing on the following aspects: sample preparation
chromatographic separation
mass spectrometric analysis and data processing. Finally
we briefly summarize the future prospects and challenges in this field. It is expected that with the continuous progress of LC and MS
the deep integration with automatic devices and data processing platforms
the advantages of LC and MS in high-throughput screening of synthetic biology strains and quantitative analysis of key molecules will become increasingly prominent
which will certainly promote the rapid development of biological intelligence based on synthetic biology.
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