Sunday, August 10, 2008
P49

Integrated microbiological study of chromium-tolerant bacteria from chromium-contaminated 100H site at Hanford

Romy Chakraborty1, Eoin L. Brodie1, Boris A Faybishenko1, Gary L. Andersen1, Carl Abulencia2, Martin Keller3, Joy Van Nostrand4, Jizhong Zhou4, and Terry C. Hazen5. (1) Microbial Ecology, Earth Sciences, Lawrence Berkeley National Lab, 1 Cyclotron Road, MS 70A-3317, Berkeley, CA 94720, (2) Verenium, Cambridge, MA 02142, (3) Oak Ridge National Laboratory, P.O. Box 2006 MS6035, Oak Ridge, TN 37831-6035, (4) University of Oklahoma, Norman, OK 73072, (5) Ecology Department, University of California, MS 70A-3317, One Cyclotron Rd., Berkeley, CA 94720

Hexavalent chromium is a widespread contaminant found in groundwater. In order to stimulate microbially mediated Cr(VI)-reduction, a poly-lactate compound was injected into Cr(VI)-contaminated aquifers at site 100H at Hanford. Investigation of bacterial community composition using high-density DNA microarray analysis of 16S rRNA gene products revealed a stimulation of Pseudomonas, Desulfovibrio and Geobacter species amongst others. Enrichment of these organisms coincided with continued Cr(VI) depletion. Functional gene-array analysis of DNA from monitoring well indicated high abundance of genes involved in nitrate-reduction, sulfate-reduction, iron-reduction, methanogenesis, chromium tolerance/reduction. Clone-library data revealed Psedomonas was the dominant genus in these samples. Based on above results, we conducted lab investigations to study the dominant anaerobic culturable microbial populations present at this site and their role in Cr(VI)-reduction. Enrichments using defined anaerobic media resulted in isolation of an iron-reducing, a sulfate-reducing and a nitrate-reducing isolate among several others. Preliminary 16S rDNA sequence analysis identified the isolates as Geobacter metallireducens, Pseudomonas stutzeri and Desulfovibrio vulgaris species respectively. The Pseudomonas isolate utilized acetate, lactate, glycerol and pyruvate as alternative carbon sources, and reduced Cr(VI). Anaerobic washed cell suspension of strain HLN reduced almost 95mM Cr(VI) within 4 hr. Further, with 100mM Cr(VI) as sole electron-acceptor, cells grew to 4.05 x 107 /ml over 24 h after an initial lag, demonstrating direct enzymatic Cr(VI) reduction coupled to growth. These results demonstrate that Cr(VI)-immobilization at Hanford 100H site could be mediated by direct microbial metabolism in addition to indirect chemical reduction of Cr(VI) by end-products of microbial  activity.