Literature DB >> 8669901

The relationship between growth enhancement and pet expression in Escherichia coli.

H G Lawford1, J D Rousseau.   

Abstract

The pet operon consists of genes coding for enzymes responsible for ethanol production and consists of pyruvate dehydrogenase and alcohol dehydrogenase II from the high-performance ethanologen Zymomonas mobilis. This article describes the physiological influence of pet expression in Escherichia coli B (ATCC 11303) in terms of growth rate and overall concentrations of cell mass and catabolic end products achieved under well-defined cultivation conditions that included constant pH and carbon (energy) limitation. Glucose, mannose, and xylose were used as substrates, because they represent the principal fermentable components of lignocellulosic biomass and because fermentation of these sugars involves different metabolic pathways. Two different types of ethanologenic recombinants were used-a strain in which pet expression was via a multicopy plasmid (pLO1297) and a chromosomal integrant, strain KO11. Under the condition of sugar substrate limitation, there was no growth enhancement by pet expression with either glucose or mannose. Whereas the host strain produced exclusively lactic acid from glucose and mannose, both recombinants produced mostly ethanol. Both the plasmid-carrying strain and the pet integrant exhibited slower growth compared to the host culture with glucose or mannose as fermentation substrate. With mannose, the plasmid recombinant grew appreciably slower than either the host culture or the recombinant KO11. Use of a magnesium-deficient medium produced different results with glucose since substrate and turbidometric measurements proved to be unreliable in terms of estimating overall biomass levels. At pH 6.3, pet expression improved overall biomass yield; but at pH 7.0, the cell yields exhibited by the plasmid recombinant and the host strain were the same. E. coli B did not grow well on xylose as sole carbon source. With xylose, pet expression increased the growth rate, but had no effect on the overall biomass yield. In comparing our observations with the reports of others, it was concluded that the effect of pet expression on growth of E.coli is dependent on several different biochemical, physiological, genetic, and environmental factors, which largely precludes a statement of generality regarding this phenomenon.

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Year:  1996        PMID: 8669901     DOI: 10.1007/978-1-4612-0223-3_25

Source DB:  PubMed          Journal:  Appl Biochem Biotechnol        ISSN: 0273-2289            Impact factor:   2.926


  29 in total

1.  Fermentation of sweet whey by ethanologenic Escherichia coli.

Authors:  W V Guimaraes; G L Dudey; L O Ingram
Journal:  Biotechnol Bioeng       Date:  1992-06-05       Impact factor: 4.530

2.  Defined media optimization for growth of recombinant Escherichia coli X90.

Authors:  L Yee; H W Blanch
Journal:  Biotechnol Bioeng       Date:  1993-01-20       Impact factor: 4.530

3.  Efficient fermentation of Pinus sp. acid hydrolysates by an ethanologenic strain of Escherichia coli.

Authors:  M F Barbosa; M J Beck; J E Fein; D Potts; L O Ingram
Journal:  Appl Environ Microbiol       Date:  1992-04       Impact factor: 4.792

4.  Expression of Different Levels of Ethanologenic Enzymes from Zymomonas mobilis in Recombinant Strains of Escherichia coli.

Authors:  L O Ingram; T Conway
Journal:  Appl Environ Microbiol       Date:  1988-02       Impact factor: 4.792

5.  Organization and expression of the pyruvate dehydrogenase complex genes of Escherichia coli K12.

Authors:  J R Guest; S T Cole; K Jeyaseelan
Journal:  J Gen Microbiol       Date:  1981-11

6.  Factors contributing to the loss of ethanologenicity of Escherichia coli B recombinants pL0I297 and KO11.

Authors:  H G Lawford; J D Rousseau
Journal:  Appl Biochem Biotechnol       Date:  1996       Impact factor: 2.926

7.  Effects of pH and acetic acid on glucose and xylose metabolism by a genetically engineered ethanologenic Escherichia coli.

Authors:  H G Lawford; J D Rousseau
Journal:  Appl Biochem Biotechnol       Date:  1993       Impact factor: 2.926

8.  Effect of alteration of the acetic acid synthesis pathway on the fermentation pattern of escherichia coli.

Authors:  J C Diaz-Ricci; L Regan; J E Bailey
Journal:  Biotechnol Bioeng       Date:  1991-12-20       Impact factor: 4.530

9.  Influence of expression of the pet operon on intracellular metabolic fluxes of Escherichia coli.

Authors:  J C Diaz-Ricci; M Tsu; J E Bailey
Journal:  Biotechnol Bioeng       Date:  1992-01-05       Impact factor: 4.530

10.  Effect of oxygen on ethanol production by a recombinant ethanologenic E. coli.

Authors:  H G Lawford; J D Rousseau
Journal:  Appl Biochem Biotechnol       Date:  1994       Impact factor: 2.926

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  1 in total

1.  Stabilization of pet operon plasmids and ethanol production in Escherichia coli strains lacking lactate dehydrogenase and pyruvate formate-lyase activities.

Authors:  R B Hespell; H Wyckoff; B S Dien; R J Bothast
Journal:  Appl Environ Microbiol       Date:  1996-12       Impact factor: 4.792

  1 in total

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