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Carbon isotopic fractionations associated with thermophilic bacteria Thermotoga maritima and Persephonella marina
Authors:Zhang Chuanlun L  Ye Qi  Reysenbach Anna-Louise  Götz Dorothee  Peacock Aaron  White David C  Horita Juske  Cole David R  Fong Jon  Pratt Lisa  Fang Jiasong  Huang Yongsong
Institution:;Department of Geological Sciences, University of Missouri, Columbia, MO 65211, USA. ;Department of Biology, Portland State University, Portland, OR 97201, USA. ;Institute for Applied Microbiology, The University of Tennessee, Knoxville, TN 37932–2575, USA. ;Chemical and Analytical Sciences Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831–6110, USA. ;Department of Geological Sciences, Indiana University, Bloomington, IN 47405, USA. ;Department of Civil and Environmental Engineering, University of Michigan, Ann Arbor, MI 48109–2099, USA. ;Department of Geological Sciences, Brown University, Providence, RI 02912, USA.
Abstract:Stable carbon isotopes can provide insight into carbon cycling pathways in natural environments. We examined carbon isotope fractionations associated with a hyperthermophilic fermentative bacterium, Thermotoga maritima, and a thermophilic chemolithoautotrophic bacterium Persephonella marina. In T. maritima, phospholipid fatty acids (PLFA) are slightly enriched in 13C relative to biomass (epsilon = 0.1-0.8 per thousand). However, PLFA and biomass are depleted in 13C relative to the substrate glucose by approximately 8 per thousand. In P. marina, PLFA are 1.8-14.5 per thousand enriched in 13C relative to biomass, which suggests that the reversed tricarboxylic acid (TCA) cycle or the 3-hydroxypropionate pathway may be used for CO2 fixation. This is supported by small fractionation between biomass and CO2 (epsilon = -3.8 per thousand to -5.0 per thousand), which is similar to fractionations reported for other organisms using similar CO2 fixation pathways. Identification of the exact pathway will require biochemical assay for specific enzymes associated with the reversed TCA cycle or the 3-hydroxypropionate pathway.
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