Literature DB >> 15516572

Pyruvate formate lyase and acetate kinase are essential for anaerobic growth of Escherichia coli on xylose.

Adnan Hasona1, Youngnyun Kim, F G Healy, L O Ingram, K T Shanmugam.   

Abstract

During anaerobic growth of bacteria, organic intermediates of metabolism, such as pyruvate or its derivatives, serve as electron acceptors to maintain the overall redox balance. Under these conditions, the ATP needed for cell growth is derived from substrate-level phosphorylation. In Escherichia coli, conversion of glucose to pyruvate yields 2 net ATPs, while metabolism of a pentose, such as xylose, to pyruvate only yields 0.67 net ATP per xylose due to the need for one (each) ATP for xylose transport and xylulose phosphorylation. During fermentative growth, E. coli produces equimolar amounts of acetate and ethanol from two pyruvates, and these reactions generate one additional ATP from two pyruvates (one hexose equivalent) while still maintaining the overall redox balance. Conversion of xylose to acetate and ethanol increases the net ATP yield from 0.67 to 1.5 per xylose. An E. coli pfl mutant lacking pyruvate formate lyase cannot convert pyruvate to acetyl coenzyme A, the required precursor for acetate and ethanol production, and could not produce this additional ATP. E. coli pfl mutants failed to grow under anaerobic conditions in xylose minimal medium without any negative effect on their survival or aerobic growth. An ackA mutant, lacking the ability to generate ATP from acetyl phosphate, also failed to grow in xylose minimal medium under anaerobic conditions, confirming the need for the ATP produced by acetate kinase for anaerobic growth on xylose. Since arabinose transport by AraE, the low-affinity, high-capacity, arabinose/H+ symport, conserves the ATP expended in pentose transport by the ABC transporter, both pfl and ackA mutants grew anaerobically with arabinose. AraE-based xylose transport, achieved after constitutively expressing araE, also supported the growth of the pfl mutant in xylose minimal medium. These results suggest that a net ATP yield of 0.67 per pentose is only enough to provide for maintenance energy but not enough to support growth of E. coli in minimal medium. Thus, pyruvate formate lyase and acetate kinase are essential for anaerobic growth of E. coli on xylose due to energetic constraints.

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Year:  2004        PMID: 15516572      PMCID: PMC524897          DOI: 10.1128/JB.186.22.7593-7600.2004

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  33 in total

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3.  Organization and regulation of the D-xylose operons in Escherichia coli K-12: XylR acts as a transcriptional activator.

Authors:  S Song; C Park
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Authors:  M R de Graef; S Alexeeva; J L Snoep; M J Teixeira de Mattos
Journal:  J Bacteriol       Date:  1999-04       Impact factor: 3.490

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Authors:  W T Self; A Hasona; K T Shanmugam
Journal:  Microbiology       Date:  2001-11       Impact factor: 2.777

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Authors:  T B Causey; S Zhou; K T Shanmugam; L O Ingram
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Journal:  Appl Environ Microbiol       Date:  2003-01       Impact factor: 4.792

8.  Molybdate and regulation of mod (molybdate transport), fdhF, and hyc (formate hydrogenlyase) operons in Escherichia coli.

Authors:  J K Rosentel; F Healy; J A Maupin-Furlow; J H Lee; K T Shanmugam
Journal:  J Bacteriol       Date:  1995-09       Impact factor: 3.490

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Authors:  J H Lee; P Patel; P Sankar; K T Shanmugam
Journal:  J Bacteriol       Date:  1985-04       Impact factor: 3.490

Review 10.  Phosphoenolpyruvate:carbohydrate phosphotransferase systems of bacteria.

Authors:  P W Postma; J W Lengeler; G R Jacobson
Journal:  Microbiol Rev       Date:  1993-09
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  40 in total

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Authors:  Youngnyun Kim; L O Ingram; K T Shanmugam
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2.  Detection of Bacteria-Specific Metabolism Using Hyperpolarized [2-13C]Pyruvate.

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Journal:  ACS Infect Dis       Date:  2018-02-13       Impact factor: 5.084

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4.  Dispensability of Escherichia coli's latent pathways.

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5.  Complex physiology and compound stress responses during fermentation of alkali-pretreated corn stover hydrolysate by an Escherichia coli ethanologen.

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Journal:  Appl Environ Microbiol       Date:  2012-03-02       Impact factor: 4.792

6.  Accumulation of d-glucose from pentoses by metabolically engineered Escherichia coli.

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7.  A vector library for silencing central carbon metabolism genes with antisense RNAs in Escherichia coli.

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8.  Deletion of the pflA gene in Escherichia coli LS5218 and its effects on the production of polyhydroxyalkanoates using beechwood xylan as a feedstock.

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9.  Fermentative utilization of glycerol by Escherichia coli and its implications for the production of fuels and chemicals.

Authors:  Abhishek Murarka; Yandi Dharmadi; Syed Shams Yazdani; Ramon Gonzalez
Journal:  Appl Environ Microbiol       Date:  2007-12-21       Impact factor: 4.792

10.  Complete genome sequence and comparative metabolic profiling of the prototypical enteroaggregative Escherichia coli strain 042.

Authors:  Roy R Chaudhuri; Mohammed Sebaihia; Jon L Hobman; Mark A Webber; Denisse L Leyton; Martin D Goldberg; Adam F Cunningham; Anthony Scott-Tucker; Paul R Ferguson; Christopher M Thomas; Gad Frankel; Christoph M Tang; Edward G Dudley; Ian S Roberts; David A Rasko; Mark J Pallen; Julian Parkhill; James P Nataro; Nicholas R Thomson; Ian R Henderson
Journal:  PLoS One       Date:  2010-01-20       Impact factor: 3.240

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