Organic Geochemistry Group, MARUM-Center for Marine Environmental Sciences, University of Bremen, Leobener Strasse 8, 28359 Bremen, Germany.
Hydrothermal Geomicrobiology Group, MARUM-Center for Marine Environmental Sciences, University of Bremen, Leobener Strasse 13, 28359 Bremen, Germany.
FEMS Microbiol Ecol. 2019 Oct 1;95(10). doi: 10.1093/femsec/fiz131.
Polar lipid-derived fatty acids (PLFAs) and their stable carbon isotopes are frequently combined to characterize microbial populations involved in the degradation of organic matter, offering a link to biogeochemical processes and carbon sources used. However, PLFA patterns derive from multiple species and may be influenced by substrate types. Here, we investigated such dependencies by monitoring the transformation of position-specifically 13C-labeled amino acids (AAs) in coastal marine sediments dominated by heterotrophic bacteria. Alanine was assimilated into straight-chain FAs, while valine and leucine incorporation led to the characteristic production of even- and odd-numbered iso-series FAs. This suggests that identical microbial communities adjust lipid biosynthesis according to substrate availability. Transformation into precursor molecules for FA biosynthesis was manifested in increased 13C recoveries of the corresponding volatiles acetate, isobutyrate and isovalerate of up to 39.1%, much higher than for PLFAs (<0.9%). A significant fraction of 13C was found in dissolved inorganic carbon (up to 37.9%), while less was recovered in total organic carbon (up to 17.3%). We observed a clear discrimination against the carboxyl C, whereby C2 and C3 positions were preferentially incorporated into PLFAs. Therefore, position-specific labeling is an appropriate tool for reconstructing the metabolic fate of protein-derived AAs in marine environments.
极性脂衍生脂肪酸(PLFAs)及其稳定碳同位素经常被结合起来,用于表征参与有机物降解的微生物种群,为生物地球化学过程和所使用的碳源提供了联系。然而,PLFA 模式源自多种物种,并且可能受到基质类型的影响。在这里,我们通过监测受异养细菌主导的沿海海洋沉积物中位置特异性 13C 标记氨基酸(AA)的转化来研究这种依赖性。丙氨酸被同化到直链 FA 中,而缬氨酸和亮氨酸的掺入导致特征性的偶数和奇数同系列 FA 的产生。这表明相同的微生物群落根据基质的可用性来调整脂类生物合成。转化为 FA 生物合成的前体分子表现为相应挥发性乙酸盐、异丁酸盐和异戊酸盐的 13C 回收率增加了 39.1%,明显高于 PLFA(<0.9%)。在溶解无机碳(高达 37.9%)中发现了很大一部分 13C,而在总有机碳(高达 17.3%)中回收的则较少。我们观察到对羧基 C 的明显歧视,其中 C2 和 C3 位置优先被纳入 PLFA。因此,位置特异性标记是重建海洋环境中蛋白质衍生 AA 的代谢命运的合适工具。