Literature DB >> 18600996

Acetic acid formation in Escherichia coli fermentation.

K Han1, H C Lim, J Hong.   

Abstract

Acetic acid formation in Escherichia coli fermentation has been studied in continuous cultures. Experimental results suggest that the limited capacity of the oxidative metabolism (perhaps the limited capacity of TCA cycle) may be responsible for acetic acid formation. At low growth rates, both anabolic and catabolic requirements may be satisfied by the oxidative metabolism. However, at high growth rates these two demands may exceed the capacity of the oxidative metabolism alone. It is proposed that under these circumstances, E. coli reorganizes the oxidative metabolism to first meet the anabolic requisition and then supply the necessary amount of energy using both the remaining capacity of the oxidative metabolism and acetic acid formation metabolism. Escherichia coli selects acetic acid synthesis as the aerobic energy source because it generates the second largest amount of ATP and NADH(2). According to our proposition, acetic acid formation could be reduced by decreasing the anabolic requirement, i.e., reducing glucose uptake, or by increasing the capacity of the oxidative metabolism. These two approaches were experimentally confirmed by observing reduced acetic acid formation by reducing the glucose uptake with a yeast extract addition and enhancing the capacity of oxidative metabolism with a methionine addition.

Entities:  

Year:  1992        PMID: 18600996     DOI: 10.1002/bit.260390611

Source DB:  PubMed          Journal:  Biotechnol Bioeng        ISSN: 0006-3592            Impact factor:   4.530


  40 in total

1.  Expression of an anaplerotic enzyme, pyruvate carboxylase, improves recombinant protein production in Escherichia coli.

Authors:  J C March; M A Eiteman; E Altman
Journal:  Appl Environ Microbiol       Date:  2002-11       Impact factor: 4.792

2.  Flux to acetate and lactate excretions in industrial fermentations: physiological and biochemical implications.

Authors:  Mansi El-Mansi
Journal:  J Ind Microbiol Biotechnol       Date:  2004-07-15       Impact factor: 3.346

Review 3.  The acetate switch.

Authors:  Alan J Wolfe
Journal:  Microbiol Mol Biol Rev       Date:  2005-03       Impact factor: 11.056

4.  Rational design and analysis of an Escherichia coli strain for high-efficiency tryptophan production.

Authors:  Yuanye Chen; Yongfei Liu; Dongqin Ding; Lina Cong; Dawei Zhang
Journal:  J Ind Microbiol Biotechnol       Date:  2018-02-20       Impact factor: 3.346

5.  Oxygen- and growth rate-dependent regulation of Escherichia coli fumarase (FumA, FumB, and FumC) activity.

Authors:  C P Tseng; C C Yu; H H Lin; C Y Chang; J T Kuo
Journal:  J Bacteriol       Date:  2001-01       Impact factor: 3.490

6.  Phosphoenolpyruvate:glucose phosphotransferase system modification increases the conversion rate during L-tryptophan production in Escherichia coli.

Authors:  Lina Liu; Sheng Chen; Jing Wu
Journal:  J Ind Microbiol Biotechnol       Date:  2017-07-19       Impact factor: 3.346

7.  Enhanced D-ribose biosynthesis in batch culture of a transketolase-deficient Bacillus subtilis strain by citrate.

Authors:  Lin Wu; Zhimin Li; Qin Ye
Journal:  J Ind Microbiol Biotechnol       Date:  2009-07-15       Impact factor: 3.346

8.  Kinetics of growth and leukotoxin production by Mannheimia haemolytica in continuous culture.

Authors:  James C du Preez; Eugéne van Rensburg; Stephanus G Kilian
Journal:  J Ind Microbiol Biotechnol       Date:  2008-02-19       Impact factor: 3.346

9.  Quantifying the effects of the division of labor in metabolic pathways.

Authors:  Emily Harvey; Jeffrey Heys; Tomáš Gedeon
Journal:  J Theor Biol       Date:  2014-07-17       Impact factor: 2.691

10.  Glucose and acetate influences on the behavior of the recombinant strain Escherichia coli HB 101 (GAPDH).

Authors:  A Gschaedler; N Thi Le; J Boudrant
Journal:  J Ind Microbiol       Date:  1994-07
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