Coupling a genome‐scale metabolic model with a reactive transport model to describe in situ uranium bioremediation

The increasing availability of the genome sequences of microorganisms involved in important bioremediation processes makes it feasible to consider developing genome‐scale models that can aid in predicting the likely outcome of potential subsurface bioremediation strategies. Previous studies of the in situ bioremediation of uranium‐contaminated groundwater have demonstrated that Geobacter species are often the dominant members of the groundwater community during active bioremediation and the primary organisms catalysing U(VI) reduction. Therefore, a genome‐scale, constraint‐based model of the metabolism of Geobacter sulfurreducens was coupled with the reactive transport model HYDROGEOCHEM in an attempt to model in situ uranium bioremediation. In order to simplify the modelling, the influence of only three growth factors was considered: acetate, the electron donor added to stimulate U(VI) reduction; Fe(III), the electron acceptor primarily supporting growth of Geobacter; and ammonium, a key nutrient. The constraint‐based model predicted that growth yields of Geobacter varied significantly based on the availability of these three growth factors and that there are minimum thresholds of acetate and Fe(III) below which growth and activity are not possible. This contrasts with typical, empirical microbial models that assume fixed growth yields and the possibility for complete metabolism of the substrates. The coupled genome‐scale and reactive transport model predicted acetate concentrations and U(VI) reduction rates in a field trial of in situ uranium bioremediation that were comparable to the predictions of a calibrated conventional model, but without the need for empirical calibration, other than specifying the initial biomass of Geobacter. These results suggest that coupling genome‐scale metabolic models with reactive transport models may be a good approach to developing models that can be truly predictive, without empirical calibration, for evaluating the probable response of subsurface microorganisms to possible bioremediation approaches prior to implementation.

[1]  D. Schüler,et al.  N2-dependent growth and nitrogenase activity in the metal-metabolizing bacteria, Geobacter and Magnetospirillum species. , 2000, Environmental microbiology.

[2]  B. Palsson,et al.  Genome-scale models of microbial cells: evaluating the consequences of constraints , 2004, Nature Reviews Microbiology.

[3]  Wolfgang Kinzelbach,et al.  Simulation of reactive processes related to biodegradation in aquifers: 1. Structure of the three-dimensional reactive transport model , 1998 .

[4]  Nan Xiao,et al.  Integrating metabolic, transcriptional regulatory and signal transduction models in Escherichia coli , 2008, Bioinform..

[5]  Steven B. Yabusaki,et al.  A general simulator for reaction-based biogeochemical processes , 2006, Comput. Geosci..

[6]  E. Roden,et al.  Biogeochemical processes in ethanol stimulated uranium-contaminated subsurface sediments. , 2008, Environmental science & technology.

[7]  Derek R. Lovley,et al.  Kinetic Analysis of Competition Between Sulfate Reducers and Methanogens for Hydrogen in Sediments , 1982, Applied and environmental microbiology.

[8]  Regina A. O'Neil,et al.  Subsurface clade of Geobacteraceae that predominates in a diversity of Fe(III)-reducing subsurface environments , 2007, The ISME Journal.

[9]  Edward R. Landa,et al.  Microbial reduction of uranium , 1991, Nature.

[10]  Adam M. Feist,et al.  The growing scope of applications of genome-scale metabolic reconstructions using Escherichia coli , 2008, Nature Biotechnology.

[11]  D. Lovley,et al.  Reduction of uranium by Desulfovibrio desulfuricans , 1992, Applied and environmental microbiology.

[12]  Radhakrishnan Mahadevan,et al.  Computational and Experimental Analysis of Redundancy in the Central Metabolism of Geobacter sulfurreducens , 2008, PLoS Comput. Biol..

[13]  Mark D. White,et al.  Scalable Modeling of Carbon Tetrachloride Migration at the Hanford Site Using the STOMP Simulator , 2008 .

[14]  Radhakrishnan Mahadevan,et al.  Geobacter sulfurreducens strain engineered for increased rates of respiration. , 2008, Metabolic engineering.

[15]  Robert T. Anderson,et al.  Microbial incorporation of 13C-labeled acetate at the field scale: detection of microbes responsible for reduction of U(VI). , 2005, Environmental science & technology.

[16]  D. Stahl,et al.  Metabolic modeling of a mutualistic microbial community , 2007, Molecular systems biology.

[17]  Yilin Fang,et al.  Uranium removal from groundwater via in situ biostimulation: Field-scale modeling of transport and biological processes. , 2007, Journal of contaminant hydrology.

[18]  Abraham Esteve-Núñez,et al.  Growth of Geobacter sulfurreducens under nutrient-limiting conditions in continuous culture. , 2005, Environmental microbiology.

[19]  Jizhong Zhou,et al.  Microbial Communities in Contaminated Sediments, Associated with Bioremediation of Uranium to Submicromolar Levels , 2008, Applied and Environmental Microbiology.

[20]  Kelly P. Nevin,et al.  Potential for Bioremediation of Uranium-Contaminated Aquifers with Microbial U(VI) Reduction , 2002 .

[21]  C. Steefel,et al.  Reactive transport modeling: An essential tool and a new research approach for the Earth sciences , 2005 .

[22]  Stephen S Fong,et al.  Metabolic gene–deletion strains of Escherichia coli evolve to computationally predicted growth phenotypes , 2004, Nature Genetics.

[23]  Derek R. Lovley,et al.  Cleaning up with genomics: applying molecular biology to bioremediation , 2003, Nature Reviews Microbiology.

[24]  Crawford,et al.  Environmental biotechnology , 2009 .

[25]  L. Krumholz,et al.  Uranium reduction. , 2006, Annual review of microbiology.

[26]  D. Lovley,et al.  Quantifying expression of Geobacter spp. oxidative stress genes in pure culture and during in situ uranium bioremediation , 2009, The ISME Journal.

[27]  Kelly P. Nevin,et al.  Dissimilatory Fe(III) and Mn(IV) reduction. , 1991, Advances in microbial physiology.

[28]  B. Palsson,et al.  Characterization of Metabolism in the Fe(III)-Reducing Organism Geobacter sulfurreducens by Constraint-Based Modeling , 2006, Applied and Environmental Microbiology.

[29]  Donald R. Metzler,et al.  Stimulating the In Situ Activity of Geobacter Species To Remove Uranium from the Groundwater of a Uranium-Contaminated Aquifer , 2003, Applied and Environmental Microbiology.

[30]  Yinjie J. Tang,et al.  Flux Analysis of Central Metabolic Pathways in Geobacter metallireducens during Reduction of Soluble Fe(III)-Nitrilotriacetic Acid , 2007, Applied and Environmental Microbiology.

[31]  Timothy Scheibe,et al.  Supplemental material: Transport and biogeochemical reaction of metals in a physically and chemically heterogeneous aquifer , 2006, Geosphere.

[32]  P. Régnier,et al.  Incorporating geomicrobial processes in reactive transport models of subsurface environments , 2005 .

[33]  Derek R. Lovley,et al.  Minimum Threshold for Hydrogen Metabolism in Methanogenic Bacteria , 1985, Applied and environmental microbiology.

[34]  Kelly P. Nevin,et al.  DNA Microarray Analysis of Nitrogen Fixation and Fe(III) Reduction in Geobacter sulfurreducens , 2005, Applied and Environmental Microbiology.

[35]  B. Palsson,et al.  Escherichia coli K-12 undergoes adaptive evolution to achieve in silico predicted optimal growth , 2002, Nature.

[36]  William D. Burgos,et al.  A general paradigm to model reaction‐based biogeochemical processes in batch systems , 2003 .

[37]  Regina A. O'Neil,et al.  Potential for Quantifying Expression of the Geobacteraceae Citrate Synthase Gene To Assess the Activity of Geobacteraceae in the Subsurface and on Current-Harvesting Electrodes , 2005, Applied and Environmental Microbiology.

[38]  D. Lovley,et al.  Preferential Reduction of Fe(III) over Fumarate by Geobacter sulfurreducens , 2004, Journal of bacteriology.

[39]  Dawn E. Holmes,et al.  Enrichment of Members of the Family Geobacteraceae Associated with Stimulation of Dissimilatory Metal Reduction in Uranium-Contaminated Aquifer Sediments , 2002, Applied and Environmental Microbiology.

[40]  B. Palsson,et al.  Towards multidimensional genome annotation , 2006, Nature Reviews Genetics.

[41]  J. Lloyd,et al.  Microbial detoxification of metals and radionuclides. , 2001, Current opinion in biotechnology.

[42]  F. Doyle,et al.  Dynamic flux balance analysis of diauxic growth in Escherichia coli. , 2002, Biophysical journal.

[43]  M. McInerney,et al.  Anaerobic microbial metabolism can proceed close to thermodynamic limits , 2002, Nature.

[44]  U. Sauer,et al.  Systematic evaluation of objective functions for predicting intracellular fluxes in Escherichia coli , 2007, Molecular systems biology.

[45]  B. Palsson,et al.  Stoichiometric interpretation of Escherichia coli glucose catabolism under various oxygenation rates , 1993, Applied and environmental microbiology.

[46]  Philip E. Long,et al.  Microbiological and Geochemical Heterogeneity in an In Situ Uranium Bioremediation Field Site , 2005, Applied and Environmental Microbiology.

[47]  Regina A. O'Neil,et al.  Gene transcript analysis of assimilatory iron limitation in Geobacteraceae during groundwater bioremediation. , 2008, Environmental Microbiology.