Document Detail


Pyruvate oxidase contributes to the aerobic growth efficiency of Escherichia coli.
MedLine Citation:
PMID:  11390679     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The metabolic importance of pyruvate oxidase (PoxB), which converts pyruvate directly to acetate and CO(2), was assessed using an isogenic set of genetically engineered strains of Escherichia coli. In a strain lacking the pyruvate dehydrogenase complex (PDHC), PoxB supported acetate-independent aerobic growth when the poxB gene was expressed constitutively or from the IPTG-inducible tac promoter. Using aerobic glucose-limited chemostat cultures of PDH-null strains, it was found that steady-states could be maintained at a low dilution rate (0.05 h(-1)) when PoxB is expressed from its natural promoter, but not at higher dilution rates (up to at least 0.25 h(-1)) unless expressed constitutively or from the tac promoter. The poor complementation of PDH-deficient strains by poxB plasmids was attributed to several factors including the stationary-phase-dependent regulation of the natural poxB promoter and deleterious effects of the multicopy plasmids. As a consequence of replacing the PDH complex by PoxB, the growth rate (mu(max)), growth yield (Y(max)) and the carbon conversion efficiency (flux to biomass) were lowered by 33%, 9-25% and 29-39% (respectively), indicating that more carbon has to be oxidized to CO(2) for energy generation. Extra energy is needed to convert PoxB-derived acetate to acetyl-CoA for further metabolism and enzyme analysis indicated that acetyl-CoA synthetase is induced for this purpose. In similar experiments with a PoxB-null strain it was shown that PoxB normally makes a significant contribution to the aerobic growth efficiency of E. coli. In glucose minimal medium, the respective growth rates (mu(max)), growth yields (Y(max)) and carbon conversion efficiencies were 16%, 14% and 24% lower than the parental values, and correspondingly more carbon was fluxed to CO(2) for energy generation. It was concluded that PoxB is used preferentially at low growth rates and that E. coli benefits from being able to convert pyruvate to acetyl-CoA by a seemingly wasteful route via acetate.
Authors:
A M Abdel-Hamid; M M Attwood; J R Guest
Related Documents :
14755639 - Endogenous nadph-dependent aldose reductase activity influences product formation durin...
21131529 - Assessment of the diversity of dairy lactococcus lactis subsp. lactis isolates by an in...
12421079 - Persistence and functional impact of a microbial inoculant on native microbial communit...
20947339 - A uv-induced mutant of pichia stipitis with increased ethanol production from xylose an...
8987689 - A direct comparison of approaches for increasing carbon flow to aromatic biosynthesis i...
594089 - Dose-response effects of alcohol upon rat strains bred for differences in reactivity to...
14518969 - 2-dodecylcyclobutanone does not induce mutations in the escherichia coli tryptophan rev...
22191479 - First-line treatment with cephalosporins in spontaneous bacterial peritonitis provides ...
11327109 - A simple classification method for residual antibiotics using e. coli cells transformed...
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Microbiology (Reading, England)     Volume:  147     ISSN:  1350-0872     ISO Abbreviation:  Microbiology (Reading, Engl.)     Publication Date:  2001 Jun 
Date Detail:
Created Date:  2001-06-06     Completed Date:  2001-11-01     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  9430468     Medline TA:  Microbiology     Country:  England    
Other Details:
Languages:  eng     Pagination:  1483-98     Citation Subset:  IM    
Affiliation:
The Krebs Institute for Biomolecular Research, Department of Molecular Biology and Biotechnology, University of Sheffield, Western Bank, Sheffield S10 2TN, UK.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Aerobiosis
Biomass
Energy Metabolism
Escherichia coli / growth & development,  metabolism*
Genes, Bacterial*
Phenotype
Plasmids
Pyruvate Dehydrogenase Complex / genetics,  metabolism
Pyruvate Oxidase / genetics,  metabolism*
Up-Regulation
Chemical
Reg. No./Substance:
0/Pyruvate Dehydrogenase Complex; EC 1.2.3.3/Pyruvate Oxidase

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  An NMR and enzyme study of the carbon metabolism of Neisseria meningitidis.
Next Document:  A peptidorhamnomannan from the mycelium of Pseudallescheria boydii is a potential diagnostic antigen...