Effect of pH on the metabolic flux of Klebsiella oxytoca producing 2,3-butanediol in continuous cultures at different dilution rates
- Authors
- Park, Changhun; Lu, Mingshou; Yun, Seokhun; Park, Kyungmoon; Lee, Jinwon
- Issue Date
- Jun-2013
- Publisher
- SPRINGER
- Keywords
- Metabolic flux analysis; Klebsiella oxytoca; 2,3-Butanediol; Continuous cultures; pH
- Citation
- BIOPROCESS AND BIOSYSTEMS ENGINEERING, v.36, no.6, pp.845 - 855
- Journal Title
- BIOPROCESS AND BIOSYSTEMS ENGINEERING
- Volume
- 36
- Number
- 6
- Start Page
- 845
- End Page
- 855
- URI
- https://scholarworks.bwise.kr/hongik/handle/2020.sw.hongik/17121
- DOI
- 10.1007/s00449-013-0932-4
- ISSN
- 1615-7591
- Abstract
- The efficiency of the bioconversion process and the achievable end-product concentration decides the economic feasibility of microbial 2,3-butanediol (2,3-BDO) production. In 2,3-BDO production, optimization of culture condition is required for cell growth and metabolism. Also, the pH is an important factor that influences microbial performance. For different microorganisms and substrates, it has been shown that the distribution of the metabolites in 2,3-BDO fermentation is greatly affected by pH, and the optimum pH for 2,3-BDO production seems dependently linked to the particular strain and the substrate employed. Quantification analysis of intracellular metabolites and metabolic flux analysis (MFA) were used to investigate the effect of pH on the Klebsiella oxytoca producing 2,3-BDO and other organic acids. The main objectives of MFA are the estimation of intracellular metabolic fluxes and the identification of rate-limiting step and the key enzymes. This study was conducted under continuous aerobic conditions at different dilution rates (0.1, 0.2, and 0.3 h(-1)) and different pH values (pH 5.5 and 7.0) for the steady-state experimental data. In order to obtain the flux distribution, the extracellular specific rates were calculated from the experimental data using the metabolic network model of K. oxytoca. Intracellular metabolite concentration profiles were generated using ultra-performance liquid chromatography/quadrupole time-of-flight mass spectrometry.
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