Suppression of lactate production in fed-batch culture of some lactic acid bacteria with sucrose as the carbon source

被引:9
|
作者
Kawai, Mio [1 ]
Tsuchiya, Asami [2 ]
Ishida, Junya [2 ]
Yoda, Nobuo [2 ]
Yashiki-Yamasaki, Shino [3 ]
Katakura, Yoshio [3 ]
机构
[1] Kansai Univ, Grad Sch Sci & Engn, 3-3-35 Yamate, Suita, Osaka 5648680, Japan
[2] Meiji Co Ltd, Food Sci & Technol Res Labs, R&D Div, 1-29-1 Nanakuni, Tokyo 1920919, Japan
[3] Kansai Univ, Fac Chem Mat & Bioengn, Dept Life Sci & Biotechnol, 3-3-35 Yamate, Suita, Osaka 5648680, Japan
基金
日本学术振兴会;
关键词
Lactic acid bacteria; Fed-batch culture; Sucrose; Redox balance; Glucose repression; Flux analysis; SACCHAROMYCES-CEREVISIAE; LACTOBACILLUS-REUTERI; ARGININE CATABOLISM; LACTOCOCCUS-LACTIS; STREPTOCOCCUS-CREMORIS; CYTOPLASMIC PH; GROWTH-RATE; GLUCOSE; MANNITOL; EXCHANGE;
D O I
10.1016/j.jbiosc.2019.11.009
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
We report a method for suppression of lactate production by lactic acid bacteria (LAB) in culture. LAB produce lactate to regenerate NADD that is consumed during glycolysis. Glucose suppresses NADD regeneration pathways other than lactate dehydrogenase and non-glycolytic ATP production pathways. Therefore, the carbon source was changed to sucrose, and fed-batch culture was performed to limit the glycolytic flux and thus suppress lactate production. As a result, lactate productivity (i.e., the amount of lactate produced per amount of grown cell) in the sucrose/fed-batch culture was decreased compared to that in glucose/batch culture, in all five LAB strains examined. The productivity level decreased to 24% and 46% in Lactobacillus reuteri JCM 1112 and Lactococcus lactis JCM 7638, respectively. Metabolic flux analysis of Lactobacillus reuteri JCM 1112 revealed increased contributions of the mannitol production pathway to NADD regeneration and the arginine deiminase pathway to ATP production in the sucrose/fed-batch culture. (C) 2019, The Society for Biotechnology, Japan. All rights reserved.
引用
收藏
页码:535 / 540
页数:6
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