Zaarur Shikma, Wang David T, Ono Shuhei, Bosak Tanja
Department of Earth, Atmospheric and Planetary Sciences, Massachusetts Institute of TechnologyCambridge, MA, United States.
Front Microbiol. 2017 May 29;8:890. doi: 10.3389/fmicb.2017.00890. eCollection 2017.
We investigated the influence of organic substrates and phosphate concentration on the rates of dissimilatory microbial sulfate reduction and the S/S isotopic fractionation produced by several species. Our experiments corroborate the previously reported species-specific correlation between sulfur isotope fractionation and cell-specific sulfate reduction rates. We also identify cell size as a key factor that contributes to the species-effect of this correlation. Phosphate limitation results in larger cells and contributes to a small decrease in sulfur isotope fractionation concomitant with an apparent increase in cell-specific sulfate reduction rates. Sulfur isotope fractionation in phosphate-limited cultures asymptotically approaches a lower limit of approximately 5‰ as cell-specific sulfate reduction rates increase to >100 fmol cell day. These experimental results test models that link the reversibilities of enzymatic steps in dissimilatory sulfate reduction to sulfur isotope fractionation and show that these models can provide consistent predictions across large variations in physiological states experienced by sulfate reducing bacteria.
我们研究了有机底物和磷酸盐浓度对几种微生物异化硫酸盐还原速率以及硫同位素分馏的影响。我们的实验证实了先前报道的硫同位素分馏与细胞特异性硫酸盐还原速率之间的物种特异性相关性。我们还确定细胞大小是导致这种相关性产生物种效应的关键因素。磷酸盐限制会导致细胞变大,并伴随着细胞特异性硫酸盐还原速率的明显增加,使硫同位素分馏略有下降。随着细胞特异性硫酸盐还原速率增加到>100 fmol细胞·天,磷酸盐限制培养物中的硫同位素分馏渐近地接近约5‰的下限。这些实验结果检验了将异化硫酸盐还原中酶促步骤的可逆性与硫同位素分馏联系起来的模型,并表明这些模型能够在硫酸盐还原细菌所经历的生理状态的大范围内提供一致的预测。