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Development of a biomarker for Geobacter activity and strain composition; Proteogenomic analysis of the citrate synthase protein during bioremediation of U(VI)

Monitoring the activity of target microorganisms during stimulated bioremediation is a key problem for the development of effective remediation strategies. At the US Department of Energy's Integrated Field Research Challenge (IFRC) site in Rifle, CO, the stimulation of Geobacter growth and acti...

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Autores principales: Wilkins, Michael J., Callister, Stephen J., Miletto, Marzia, Williams, Kenneth H., Nicora, Carrie D., Lovley, Derek R., Long, Philip E., Lipton, Mary S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815795/
https://www.ncbi.nlm.nih.gov/pubmed/21255372
http://dx.doi.org/10.1111/j.1751-7915.2010.00194.x
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author Wilkins, Michael J.
Callister, Stephen J.
Miletto, Marzia
Williams, Kenneth H.
Nicora, Carrie D.
Lovley, Derek R.
Long, Philip E.
Lipton, Mary S.
author_facet Wilkins, Michael J.
Callister, Stephen J.
Miletto, Marzia
Williams, Kenneth H.
Nicora, Carrie D.
Lovley, Derek R.
Long, Philip E.
Lipton, Mary S.
author_sort Wilkins, Michael J.
collection PubMed
description Monitoring the activity of target microorganisms during stimulated bioremediation is a key problem for the development of effective remediation strategies. At the US Department of Energy's Integrated Field Research Challenge (IFRC) site in Rifle, CO, the stimulation of Geobacter growth and activity via subsurface acetate addition leads to precipitation of U(VI) from groundwater as U(IV). Citrate synthase (gltA) is a key enzyme in Geobacter central metabolism that controls flux into the TCA cycle. Here, we utilize shotgun proteomic methods to demonstrate that the measurement of gltA peptides can be used to track Geobacter activity and strain evolution during in situ biostimulation. Abundances of conserved gltA peptides tracked Fe(III) reduction and changes in U(VI) concentrations during biostimulation, whereas changing patterns of unique peptide abundances between samples suggested sample‐specific strain shifts within the Geobacter population. Abundances of unique peptides indicated potential differences at the strain level between Fe(III)‐reducing populations stimulated during in situ biostimulation experiments conducted a year apart at the Rifle IFRC. These results offer a novel technique for the rapid screening of large numbers of proteomic samples for Geobacter species and will aid monitoring of subsurface bioremediation efforts that rely on metal reduction for desired outcomes.
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spelling pubmed-38157952014-02-12 Development of a biomarker for Geobacter activity and strain composition; Proteogenomic analysis of the citrate synthase protein during bioremediation of U(VI) Wilkins, Michael J. Callister, Stephen J. Miletto, Marzia Williams, Kenneth H. Nicora, Carrie D. Lovley, Derek R. Long, Philip E. Lipton, Mary S. Microb Biotechnol Research Articles Monitoring the activity of target microorganisms during stimulated bioremediation is a key problem for the development of effective remediation strategies. At the US Department of Energy's Integrated Field Research Challenge (IFRC) site in Rifle, CO, the stimulation of Geobacter growth and activity via subsurface acetate addition leads to precipitation of U(VI) from groundwater as U(IV). Citrate synthase (gltA) is a key enzyme in Geobacter central metabolism that controls flux into the TCA cycle. Here, we utilize shotgun proteomic methods to demonstrate that the measurement of gltA peptides can be used to track Geobacter activity and strain evolution during in situ biostimulation. Abundances of conserved gltA peptides tracked Fe(III) reduction and changes in U(VI) concentrations during biostimulation, whereas changing patterns of unique peptide abundances between samples suggested sample‐specific strain shifts within the Geobacter population. Abundances of unique peptides indicated potential differences at the strain level between Fe(III)‐reducing populations stimulated during in situ biostimulation experiments conducted a year apart at the Rifle IFRC. These results offer a novel technique for the rapid screening of large numbers of proteomic samples for Geobacter species and will aid monitoring of subsurface bioremediation efforts that rely on metal reduction for desired outcomes. Blackwell Publishing Ltd 2011-01 2010-12-23 /pmc/articles/PMC3815795/ /pubmed/21255372 http://dx.doi.org/10.1111/j.1751-7915.2010.00194.x Text en Copyright © 2010 Battelle Memorial Institute. Journal compilation © 2010 Society for Applied Microbiology and Blackwell Publishing Ltd
spellingShingle Research Articles
Wilkins, Michael J.
Callister, Stephen J.
Miletto, Marzia
Williams, Kenneth H.
Nicora, Carrie D.
Lovley, Derek R.
Long, Philip E.
Lipton, Mary S.
Development of a biomarker for Geobacter activity and strain composition; Proteogenomic analysis of the citrate synthase protein during bioremediation of U(VI)
title Development of a biomarker for Geobacter activity and strain composition; Proteogenomic analysis of the citrate synthase protein during bioremediation of U(VI)
title_full Development of a biomarker for Geobacter activity and strain composition; Proteogenomic analysis of the citrate synthase protein during bioremediation of U(VI)
title_fullStr Development of a biomarker for Geobacter activity and strain composition; Proteogenomic analysis of the citrate synthase protein during bioremediation of U(VI)
title_full_unstemmed Development of a biomarker for Geobacter activity and strain composition; Proteogenomic analysis of the citrate synthase protein during bioremediation of U(VI)
title_short Development of a biomarker for Geobacter activity and strain composition; Proteogenomic analysis of the citrate synthase protein during bioremediation of U(VI)
title_sort development of a biomarker for geobacter activity and strain composition; proteogenomic analysis of the citrate synthase protein during bioremediation of u(vi)
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815795/
https://www.ncbi.nlm.nih.gov/pubmed/21255372
http://dx.doi.org/10.1111/j.1751-7915.2010.00194.x
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