Evolution of biofilms during the colonization process of pyrite by Acidithiobacillus thiooxidans
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We have applied epifluorescence principles, atomic force microscopy, and Raman studies to the analysis of the colonization process of pyrite (FeS 2) by sulfuroxidizing bacteria Acidithiobacillus thiooxidans after 1, 15, 24, and 72 h. For the stages examined, we present results comprising the evolution of biofilms, speciation of S n 2- /S 0 species, adhesion forces of attached cells, production and secretion of extracellular polymeric substances (EPS), and its biochemical composition. After 1 h, highly dispersed attached cells in the surface of the mineral were observed. The results suggest initial non-covalent, weak interactions (e.g., van der Waal%27s, hydrophobic interactions), mediating an irreversible binding mechanism to electrooxidized massive pyrite electrode (eMPE), wherein the initial production of EPS by individual cells is determinant. The mineral surface reached its maximum cell cover between 15 to 24 h. Longer biooxidation times resulted in the progressive biofilm reduction on the mineral surface. Quantification of attached cell adhesion forces indicated a strong initial mechanism (8.4 nN), whereas subsequent stages of mineral colonization indicated stability of biofilms and of the adhesion force to an average of 4.2 nN. A variable EPS (polysaccharides, lipids, and proteins) secretion at all stages was found; thus, different architectural conformation of the biofilms was observed during 120 h. The main EPS produced were lipopolysaccharides which may increase the hydrophobicity of A. thiooxidans biofilms. The highest amount of lipopolysaccharides occurred between 15-72 h. In contrast with abiotic surfaces, the progressive depletion of S n 2- /S 0 was observed on biotic eMPE surfaces, indicating consumption of surface sulfur species. All observations indicated a dynamic biooxidation mechanism of pyrite by A. thiooxidans, where the biofilms stability and composition seems to occur independently from surface sulfur species depletion. © 2011 Springer-Verlag.
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We have applied epifluorescence principles, atomic force microscopy, and Raman studies to the analysis of the colonization process of pyrite (FeS 2) by sulfuroxidizing bacteria Acidithiobacillus thiooxidans after 1, 15, 24, and 72 h. For the stages examined, we present results comprising the evolution of biofilms, speciation of S n 2- /S 0 species, adhesion forces of attached cells, production and secretion of extracellular polymeric substances (EPS), and its biochemical composition. After 1 h, highly dispersed attached cells in the surface of the mineral were observed. The results suggest initial non-covalent, weak interactions (e.g., van der Waal's, hydrophobic interactions), mediating an irreversible binding mechanism to electrooxidized massive pyrite electrode (eMPE), wherein the initial production of EPS by individual cells is determinant. The mineral surface reached its maximum cell cover between 15 to 24 h. Longer biooxidation times resulted in the progressive biofilm reduction on the mineral surface. Quantification of attached cell adhesion forces indicated a strong initial mechanism (8.4 nN), whereas subsequent stages of mineral colonization indicated stability of biofilms and of the adhesion force to an average of 4.2 nN. A variable EPS (polysaccharides, lipids, and proteins) secretion at all stages was found; thus, different architectural conformation of the biofilms was observed during 120 h. The main EPS produced were lipopolysaccharides which may increase the hydrophobicity of A. thiooxidans biofilms. The highest amount of lipopolysaccharides occurred between 15-72 h. In contrast with abiotic surfaces, the progressive depletion of S n 2- /S 0 was observed on biotic eMPE surfaces, indicating consumption of surface sulfur species. All observations indicated a dynamic biooxidation mechanism of pyrite by A. thiooxidans, where the biofilms stability and composition seems to occur independently from surface sulfur species depletion. © 2011 Springer-Verlag.
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Acidithiobacillus thiooxidans; Biofilms evolution; Electrooxidation; Interfacial analysis; Proteins quantification; Pyrite Abiotic surfaces; Acidithiobacillus thiooxidans; Adhesion forces; Bio-oxidation; Biochemical composition; Cell adhesion force; Colonization process; Epifluorescences; Extracellular polymeric substances; Hydrophobic interactions; Individual cells; Interfacial analysis; Irreversible binding; Lipopolysaccharides; Mineral surfaces; Raman studies; Sulfur oxidizing bacteria; Weak interactions; Adhesion; Atomic force microscopy; Cell adhesion; Cells; Electrooxidation; Hydrophobicity; Physiology; Polysaccharides; Pyrites; Silicate minerals; Sulfur; Biofilms; bacterial protein; polysaccharide; pyrite; sulfur; adhesion; atomic force microscopy; bacterium; biochemical composition; biofilm; biological production; chemical binding; colonization; cytology; electrochemistry; fluorescence; lipid; microbial activity; oxidation; polymer; polysaccharide; protein; pyrite; secretion; speciation (chemistry); Acidithiobacillus thiooxidans; article; atomic force microscopy; bacterial colonization; bacterial strain; bacterium adherence; binding kinetics; biochemical composition; biofilm; cell adhesion; epifluorescence microscopy; hydrophobicity; molecular evolution; molecular interaction; nonhuman; oxidation; protein conformation; protein depletion; protein secretion; protein stability; Raman spectrometry; roentgen spectroscopy; surface property; Acidithiobacillus thiooxidans; Bacterial Adhesion; Biofilms; Iron; Microscopy, Atomic Force; Microscopy, Fluorescence; Polysaccharides, Bacterial; Spectrum Analysis, Raman; Sulfides; Time Factors; Acidithiobacillus thiooxidans
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