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Study of the role of anaerobic metabolism in succinate production by Enterobacter aerogenes
Authors:Yoshinori Tajima  Kenichi Kaida  Atsushi Hayakawa  Keita Fukui  Yousuke Nishio  Kenichi Hashiguchi  Ryosuke Fudou  Kazuhiko Matsui  Yoshihiro Usuda  Koji Sode
Institution:1. Institute for Innovation, Ajinomoto Co., Inc., 1-1 Suzuki-cho, Kawasaki-ku, Kawasaki, 210-8681, Japan
2. Research Institute for Bioscience Product & Fine Chemicals, Ajinomoto Co., Inc., 1-1 Suzuki-cho, Kawasaki-ku, Kawasaki, 210-8681, Japan
3. Japan Bioindustry Association, 2-26-9 Hatchobori, Chuo-Ku, Tokyo, 104-0032, Japan
4. Business Strategy and Development Department, Ajinomoto Co., Inc., 15-1 Kyobashi, 1-Chome, Chuo-Ku, Tokyo, 104-8315, Japan
5. Department of Biotechnology, Graduate School of Engineering, Tokyo University of Agriculture and Technology, 2-24-16 Naka-cho, Koganei, Tokyo, 184-8588, Japan
Abstract:Succinate is a core biochemical building block; optimizing succinate production from biomass by microbial fermentation is a focus of basic and applied biotechnology research. Lowering pH in anaerobic succinate fermentation culture is a cost-effective and environmentally friendly approach to reducing the use of sub-raw materials such as alkali, which are needed for neutralization. To evaluate the potential of bacteria-based succinate fermentation under weak acidic (pH <6.2) and anaerobic conditions, we characterized the anaerobic metabolism of Enterobacter aerogenes AJ110637, which rapidly assimilates glucose at pH 5.0. Based on the profile of anaerobic products, we constructed single-gene knockout mutants to eliminate the main anaerobic metabolic pathways involved in NADH re-oxidation. These single-gene knockout studies showed that the ethanol synthesis pathway serves as the dominant NADH re-oxidation pathway in this organism. To generate a metabolically engineered strain for succinate production, we eliminated ethanol formation and introduced a heterogeneous carboxylation enzyme, yielding E. aerogenes strain ΔadhE/PCK. The strain produced succinate from glucose with a 60.5 % yield (grams of succinate produced per gram of glucose consumed) at pH <6.2 and anaerobic conditions. Thus, we showed the potential of bacteria-based succinate fermentation under weak acidic conditions.
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