Temperature effect on the sulfur isotope fractionation during sulfate reduction by two strains of the hyperthermophilic Archaeoglobus fulgidus

• Published in: Environmental microbiology Vol. 11; no. 12; pp. 2998 - 3006
• Main Authors: Mitchell, Kristen, Heyer, Anne, Canfield, Donald E, Hoek, Joost, Habicht, Kirsten S
• Format: Journal Article
• Language: English
• Published: Oxford, UK Oxford, UK : Blackwell Publishing Ltd 01-12-2009; Blackwell Publishing Ltd
• Subjects: Archaeoglobus fulgidus - growth & development; Archaeoglobus fulgidus - metabolism; Chemical Fractionation; Extreme Heat; Sulfates - metabolism; Sulfur Isotopes; Temperature
• ISSN: 1462-2912; 1462-2920
• DOI: 10.1111/j.1462-2920.2009.02002.x

Sulfur isotope fractionation during dissimilatory sulfate reduction by two strains of the thermophilic archaeon Archaeoglobus fulgidus (strains VC-16 and Z) was explored over the entire temperature range of growth. The optimal cell-specific sulfate reduction rate (14 fmol cell⁻¹ h⁻¹) was found at 82-84°C but growth was measured as low as 54°C. The fractionation ranged between 0.52[per thousand] and 27[per thousand], with largest fractionations were found at intermediate temperatures and the smallest fractionations at the lowest and highest temperatures. There was an inverse relationship between the cell-specific sulfate reduction rate and fractionation, and the cell-specific rate was a good indicator of the expected fractionations regardless of whether temperature or substrate concentrations controlled the rate. Comparison of the fractionation trend found in this study with similar measurements for seven other sulfate-reducers showed that sulfate-reducing organisms respond to temperature in three different ways and this correlated with their maximum fractionation value, but not with the cell-specific sulfate reduction rate. A sulfur isotope model was used to reproduce the observed variation of fractionation with temperature. This approach predicted the rate of internal sulfur transformations as having the major influence on the observed fractionations in the intermediate temperature range, whereas the exchange of sulfate across the cell membrane controls fractionation at low and high temperatures.