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PMID: 18757793 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S.

Highly conserved genes in Geobacter species with expression patterns indicative of acetate limitation.

Microbiology (Reading, England) ·Vol. 154 ·No. Pt 9 ·2008-09-00 ·Pages 2589-2599

Risso C, Methé BA, Elifantz H, Holmes DE, Lovley DR

Abstract

Analysis of the genome of Geobacter sulfurreducens revealed four genes encoding putative symporters with homology to ActP, an acetate transporter in Escherichia coli. Three of these genes, aplA, aplB and aplC, are highly similar (over 90 % identical) and fell within a tight phylogenetic cluster (Group I) consisting entirely of Geobacter homologues. Transcript levels for all three genes increased in response to acetate limitation. The fourth gene, aplD, is phylogenetically distinct (Group II) and its expression was not influenced by acetate availability. Deletion of any one of the three genes in Group I did not significantly affect acetate-dependent growth, suggesting functional redundancy. Attempts to recover mutants in which various combinations of two of these genes were deleted were unsuccessful, suggesting that at least two of these three transporter genes are required to support growth. Closely related Group I apl genes were found in the genomes of other Geobacter species whose genome sequences are available. Furthermore, related genes could be detected in genomic DNA extracted from a subsurface environment undergoing in situ uranium bioremediation. The transporter genes recovered from the subsurface were most closely related to Group I apl genes found in the genomes of cultured Geobacter species that were isolated from contaminated subsurface environments. The increased expression of these genes in response to acetate limitation, their high degree of conservation among Geobacter species and the ease with which they can be detected in environmental samples suggest that Group I apl genes of the Geobacteraceae may be suitable biomarkers for acetate limitation. Monitoring the expression of these genes could aid in the design of strategies for acetate-mediated in situ bioremediation of uranium-contaminated groundwater.

MeSH Terms
Acetates/metabolism Biodegradation, Environmental DNA, Bacterial/genetics Escherichia coli/genetics Escherichia coli Proteins/genetics Gene Deletion Gene Expression Genes, Bacterial Genome, Bacterial Geobacter/genetics,metabolism Membrane Transport Proteins/genetics Monocarboxylic Acid Transporters Phylogeny Uranium/metabolism
Chemicals
Acetates ActP protein, E coli DNA, Bacterial Escherichia coli Proteins Membrane Transport Proteins Monocarboxylic Acid Transporters Uranium
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Risso Carla
Department of Microbiology, 203N Morrill Science Center IVN, University of Massachusetts Amherst, Amherst, MA 01003, USA.
Methé Barbara A
J. Craig Venter Institute, 9712 Medical Center Drive, Rockville, MD 20850, USA.
Elifantz Hila
Department of Microbiology, 203N Morrill Science Center IVN, University of Massachusetts Amherst, Amherst, MA 01003, USA.
Holmes Dawn E
Department of Microbiology, 203N Morrill Science Center IVN, University of Massachusetts Amherst, Amherst, MA 01003, USA.
Lovley Derek R
Department of Microbiology, 203N Morrill Science Center IVN, University of Massachusetts Amherst, Amherst, MA 01003, USA.
Article Info
Journal
Microbiology (Reading, England)
Abbr.
Microbiology (Reading)
ISSN
1350-0872
Published
2008-09-00
Pages
2589-2599
Language
English
Region
England
NLM ID
9430468
Subset
IM
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