State Key Laboratory of Marine Environmental Science, College of Ocean and Earth Sciences, Xiamen University, Xiamen 361102, People's Republic of China; Institute of Marine Microbes and Ecospheres, Fujian Key Laboratory of Marine Carbon Sequestration, Xiamen University, Xiamen 361102, People's Republic of China.
State Key Laboratory of Marine Environmental Science, College of Ocean and Earth Sciences, Xiamen University, Xiamen 361102, People's Republic of China; Institute of Marine Microbes and Ecospheres, Fujian Key Laboratory of Marine Carbon Sequestration, Xiamen University, Xiamen 361102, People's Republic of China.
Sci Total Environ. 2020 Sep 1;733:139216. doi: 10.1016/j.scitotenv.2020.139216. Epub 2020 May 11.
Dissolved organic matter (DOM) accounts for >95% of total marine organic matter, and >95% of marine DOM is refractory to biodegradation. The recalcitrancy of DOM determines its residence time and thus is of great concern regarding to carbon sequestration in the ocean. However, the recalcitrancy of DOM not only varies among different compounds but also within different conformations of a same molecule such as L-amino acids (L-AAs) and D-amino acids (D-AAs). While the former is labile, the latter is refractory and used as a proxy for estimation of bacterial refractory DOM in the ocean. However, some D-AAs are also reported to be bioavailable. To clarify the controversy, we examined the bioavailability of two types of D-AAs: canonical D-AAs, which mainly present as bacterial cell wall components, and non-canonical D-AAs (NCDAAs), which are secreted by various bacteria as signaling molecules in bacterial physiology. Bioassay experiments were conducted with nine marine bacterial strains and a natural microbial community. D-AAs were poorly utilized by the strains as sole carbon or nitrogen sources compared with L-AAs, in addition, NCDAAs were barely used compared with canonical D-AAs. In comparison, the microbial community consumed all three canonical D-AAs (D-alanine, D-aspartic acid and D-glutamic acid) as efficiently as their corresponding L-AAs when supplied separately; however, L-AAs were preferentially used over D-AAs when both forms were provided simultaneously. Remarkably, two NCDAAs, D-methionine and D-leucine, were poorly utilized regardless of the presence of the L-enantiomers. It was found for the first time that NCDAAs are relatively more refractory than canonical D-AAs to microbial utilization. This novel recognition of difference in recalcitrancy between NCDAAs and canonical D-AAs lays the foundation for a better understanding of carbon cycling and more accurate estimation of carbon storage in the ocean.
溶解有机质(DOM)占海洋有机物质总量的>95%,其中>95%的 DOM 难以生物降解。DOM 的抗降解性决定了其停留时间,因此对于海洋中的碳封存具有重要意义。然而,DOM 的抗降解性不仅在不同化合物之间存在差异,而且在同一分子的不同构象中也存在差异,如 L-氨基酸(L-AAs)和 D-氨基酸(D-AAs)。前者是不稳定的,而后者是抗降解的,常用于估算海洋中细菌抗降解 DOM。然而,也有报道称一些 D-AAs 是可利用的。为了澄清争议,我们研究了两种类型的 D-AAs 的生物可利用性:主要作为细菌细胞壁成分的典型 D-AAs 和各种细菌作为细菌生理信号分子分泌的非典型 D-AAs(NCDAAs)。通过 9 株海洋细菌和一个自然微生物群落进行了生物测定实验。与 L-AAs 相比,D-AAs 作为唯一的碳源或氮源,菌株利用效率较低,此外,与典型 D-AAs 相比,NCDAAs 几乎未被利用。相比之下,当分别供应时,微生物群落有效地消耗了所有三种典型 D-AAs(D-丙氨酸、D-天冬氨酸和 D-谷氨酸),就像它们的 L-对映体一样;然而,当同时提供两种形式时,L-AAs 优先于 D-AAs 被利用。值得注意的是,两种 NCDAAs,D-蛋氨酸和 D-亮氨酸,无论是否存在 L-对映体,都难以被利用。这是首次发现 NCDAAs 相对于微生物利用比典型 D-AAs 更难降解。这种对 NCDAAs 和典型 D-AAs 之间抗降解性差异的新认识为更好地理解碳循环和更准确地估计海洋中的碳储存奠定了基础。