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Identification of Factors Regulating Escherichia coli 2,3-Butanediol Production by Continuous Culture and Metabolic Flux Analysis

Authors
Lu, MingshouLee, SoojinKim, BorimPark, ChanghunOh, MinkyuPark, KyungmoonLee, Sang YupLee, Jinwon
Issue Date
May-2012
Publisher
KOREAN SOC MICROBIOLOGY & BIOTECHNOLOGY
Keywords
2,3-Butanediol fermentation; continuous culture; pH influence; metabolic flux analysis; intracellular metabolic measurements
Citation
JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY, v.22, no.5, pp.659 - 667
Journal Title
JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY
Volume
22
Number
5
Start Page
659
End Page
667
URI
https://scholarworks.bwise.kr/hongik/handle/2020.sw.hongik/18963
DOI
10.4014/jmb.1112.12018
ISSN
1017-7825
Abstract
2,3-Butanediol (2,3-BDO) is an organic compound with a wide range of industrial applications. Although Escherichia call is often used for the production of organic compounds, the wild-type E. coli does not contain two essential genes in the 2,3-BDO biosynthesis pathway, and cannot ferment 2,3-BDO. Therefore, a 2,3-BDO biosynthesis mutant strain of Escherichia coli was constructed and cultured. To determine the optimum culture factors for 2,3-BDO production, experiments were conducted under different culture environments ranging from strongly acidic to neutral pH. The extracellular metabolite profiles were obtained using high-performance liquid chromatography (HPLC), and the intracellular metabolite profiles were analyzed by ultra-performance liquid chromatography and quadruple time-of-flight mass spectrometry (UPLC/Q-TOF-MS). Metabolic flux analysis (MFA) was used to integrate these profiles. The metabolite profiles showed that 2,3-BDO production favors an acidic environment (pH 5), whereas cell mass favors a neutral environment. Furthermore, when the pH of the culture fell below 5, both the cell growth and 2,3-BDO production were inhibited.
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