Literature DB >> 7993084

Acetate metabolism by Escherichia coli in high-cell-density fermentation.

G L Kleman1, W R Strohl.   

Abstract

Little is known about the cellular physiology of Escherichia coli at high cell densities (e.g., greater than 50 g [dry cell weight] per liter), particularly in relation to the cellular response to different growth conditions. E. coli W3100 cultures were grown under identical physical and nutritional conditions, by using a computer-controlled fermentation system which maintains the glucose concentration at 0.5 g/liter, to high cell densities at pH values of 6.0, 6.5, 7.0, and 7.5. The data suggest a relationship between the pH of the environment and the amount of acetate excreted by the organism during growth. At pH values of 6.0 and 6.5, the acetate reached a concentration of 6 g/liter, whereas at pH 7.5, the acetate reached a concentration of 12 g/liter. Furthermore, at pH values of 6.0 to 7.0, the E. coli culture undergoes a dramatic metabolic switch in which oxygen and glucose consumption and CO2 evolution all temporarily decreased by 50 to 80%, with a concomitant initiation of acetate utilization. After a 30-min pause in which approximately 50% of the available acetate is consumed, the culture recovers and resumes consuming glucose and oxygen and producing acetate and CO2 at preswitch levels. During the switch period, the specific activity of isocitrate lyase typically increases approximately fourfold.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 7993084      PMCID: PMC201921          DOI: 10.1128/aem.60.11.3952-3958.1994

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  20 in total

1.  A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding.

Authors:  M M Bradford
Journal:  Anal Biochem       Date:  1976-05-07       Impact factor: 3.365

Review 2.  The central metabolic pathways of Escherichia coli: relationship between flux and control at a branch point, efficiency of conversion to biomass, and excretion of acetate.

Authors:  W H Holms
Journal:  Curr Top Cell Regul       Date:  1986

3.  Control of carbon flux to acetate excretion during growth of Escherichia coli in batch and continuous cultures.

Authors:  E M el-Mansi; W H Holms
Journal:  J Gen Microbiol       Date:  1989-11

4.  The enzymic interconversion of acetate and acetyl-coenzyme A in Escherichia coli.

Authors:  T D Brown; M C Jones-Mortimer; H L Kornberg
Journal:  J Gen Microbiol       Date:  1977-10

Review 5.  The role and control of the glyoxylate cycle in Escherichia coli.

Authors:  H L Kornberg
Journal:  Biochem J       Date:  1966-04       Impact factor: 3.857

Review 6.  Is acetyl phosphate a global signal in Escherichia coli?

Authors:  W R McCleary; J B Stock; A J Ninfa
Journal:  J Bacteriol       Date:  1993-05       Impact factor: 3.490

7.  Isolation and Characterization of acetate kinase and phosphotransacetylase mutants of Escherichia coli and Salmonella typhimurium.

Authors:  S M LeVine; F Ardeshir; G F Ames
Journal:  J Bacteriol       Date:  1980-08       Impact factor: 3.490

8.  Phosphate transfer between acetate kinase and enzyme I of the bacterial phosphotransferase system.

Authors:  D K Fox; N D Meadow; S Roseman
Journal:  J Biol Chem       Date:  1986-10-15       Impact factor: 5.157

9.  Comparison of growth, acetate production, and acetate inhibition of Escherichia coli strains in batch and fed-batch fermentations.

Authors:  G W Luli; W R Strohl
Journal:  Appl Environ Microbiol       Date:  1990-04       Impact factor: 4.792

10.  Regulation of the acetate operon in Escherichia coli: purification and functional characterization of the IclR repressor.

Authors:  J C Cortay; D Nègre; A Galinier; B Duclos; G Perrière; A J Cozzone
Journal:  EMBO J       Date:  1991-03       Impact factor: 11.598

View more
  39 in total

1.  Regulation of acetyl coenzyme A synthetase in Escherichia coli.

Authors:  S Kumari; C M Beatty; D F Browning; S J Busby; E J Simel; G Hovel-Miner; A J Wolfe
Journal:  J Bacteriol       Date:  2000-08       Impact factor: 3.490

2.  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

3.  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

4.  Distinct signatures for mutator sensitivity of lacZ reversions and for the spectrum of lacI/lacO forward mutations on the chromosome of nondividing Escherichia coli.

Authors:  Shanti M Bharatan; Manjula Reddy; J Gowrishankar
Journal:  Genetics       Date:  2004-02       Impact factor: 4.562

5.  Reduction of aerobic acetate production by Escherichia coli.

Authors:  W R Farmer; J C Liao
Journal:  Appl Environ Microbiol       Date:  1997-08       Impact factor: 4.792

Review 6.  The acetate switch.

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

7.  A complete computer monitoring and control system using commercially available, configurable software for laboratory and pilot plant Escherichia coli fermentations.

Authors:  R S Blackmore; J S Blome; J O Neway
Journal:  J Ind Microbiol       Date:  1996-06

8.  Strategy for pH control and pH feedback-controlled substrate feeding for high-level production of L-tryptophan by Escherichia coli.

Authors:  Li-Kun Cheng; Jian Wang; Qing-Yang Xu; Chun-Guang Zhao; Zhi-Qiang Shen; Xi-Xian Xie; Ning Chen
Journal:  World J Microbiol Biotechnol       Date:  2013-01-03       Impact factor: 3.312

9.  Multi-omics Quantification of Species Variation of Escherichia coli Links Molecular Features with Strain Phenotypes.

Authors:  Jonathan M Monk; Anna Koza; Miguel A Campodonico; Daniel Machado; Jose Miguel Seoane; Bernhard O Palsson; Markus J Herrgård; Adam M Feist
Journal:  Cell Syst       Date:  2016-09-22       Impact factor: 10.304

10.  Cloning, characterization, and functional expression of acs, the gene which encodes acetyl coenzyme A synthetase in Escherichia coli.

Authors:  S Kumari; R Tishel; M Eisenbach; A J Wolfe
Journal:  J Bacteriol       Date:  1995-05       Impact factor: 3.490

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.