431-4 Evaluating Bacteria Binding Mechanisms to Soil Minerals with FTIR Spectroscopy.

See more from this Division: SSSA Division: Soil Chemistry
See more from this Session: Symposium--Organic Molecule Interactions with Mineral Surfaces As Key Regulators of Soil Processes: I
Wednesday, November 5, 2014: 8:55 AM
Long Beach Convention Center, Room 203C
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Sanjai J. Parikh1, Lizette Andrea Aguilera2, Fungai N.D. Mukome3 and Andrew John Margenot2, (1)One Shields Ave, University of California-Davis, Davis, CA
(2)University of California-Davis, Davis, CA
(3)Land, Air and Water Resources, University of California-Davis, Davis, CA

Reactions occurring at the bacteria-mineral interface play a critical role in a number of important soil processes involving nutrient cycling, contaminant biodegradation, redox transformations, and pathogen transport. Our research has utilized attenuated total reflectance (ATR) Fourier transform infrared (FTIR) spectroscopy to probe the molecular-level interactions of bacteria (Pseudomonas putida, P. aeruginosa, Escherichia coli) with pure mineral phases (hematite [α-Fe2O3], goethite [α-FeOOH])  and current efforts are underway to examine interactions with kaolinite and natural soils dominated by these mineral phases. In addition to bacteria, the interactions of mixed amino acids, polypeptide extracts, deoxyribonucleic acid (DNA), and a suite of model compounds have also been evaluate. These compounds represent carboxyl, catecholate, amide, and phosphate groups present in siderophores, amino acids, polysaccharides, phospholipids, and DNA IR peaks corresponding to outer-sphere or unbound (1400 cm-1) and inner-sphere (1310-1320 cm-1) coordinated carboxyl groups are noted following reaction of bacteria and biomolecules with α-Fe2O3 and α-FeOOH have been observed. However, the IR spectra also show that low-levels (i.e., 0.45-0.79%) of biomolecular phosphorous groups result in strong IR bands at ~1043 cm-1, corresponding to inner-sphere Fe-O-P bonds. This data highlights the importance of bacteria associated P-containing groups in biomolecule and cell adhesion. In addition, spectral comparisons show somewhat greater P-O-Fe contributions for bacteria (Pseudomonad, E. coli) deposited on α-FeOOH, as compared to α-Fe2O3. This data demonstrates that slight differences in bacterial adhesion to Fe oxides can be attributed to bacterial species and Fe-oxide minerals. However, of more importance, the strong binding affinity of phosphate in bacteria and model compounds to both Fe-oxides results in the formation of inner-sphere Fe-O-P bonds, underscoring the critical role of biomolecular P in the initiation of bacterial adhesion.  Similar analyses are underway for bacteria and model compound interactions with Fe-oxide and kaolinite dominated soils.

 

See more from this Division: SSSA Division: Soil Chemistry
See more from this Session: Symposium--Organic Molecule Interactions with Mineral Surfaces As Key Regulators of Soil Processes: I