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C-13 isotopic fractionation during biodegradation of agricultural wastes

机译:农业废弃物生物降解过程中的C-13同位素分级

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摘要

Significant differences in delta C-13 signatures occur within and between plant tissues and their constituent biochemical entities, and also within and between heterotrophic bacteria and fungi and their metabolic products. Furthermore, C-13 isotopic fractionation occurs during the biodegradation of organic molecules as seen in the substrate, respired CO2 and the microbial biomass, which could be related to substrate composition and/or microbial metabolism. The C-13 isotopic fractionation observed during the decomposition of a single defined C substrate appears to be due to the intra-molecular heterogeneity in C-13 in the substrate and to C-13 isotopic fractionation during microbial metabolism. Very limited data suggest that the latter may be quantitatively more important than the former. Studies with defined fungi in culture media have highlighted the complexities associated with the interpretation of the observed patterns of C-13 isotopic fractionation when a single defined C source is added to the culture medium which itself contains one or more C sources. Techniques involving C-13 enrichment or paired treatments involving an equivalent C-3- and C-4-derived substrate have been devised to overcome the problem of background C in the culture medium and C-13 isotopic fractionation during metabolism. Studies with complex substrates have shown an initial C-13 depletion phase in respired CO2 followed by a C-13 enrichment phase which may or may not be followed by another C-13 depletion phase. Basic studies involving an integrated approach are required to gain a new insight into C-13 isotopic fractionation during organic residue decomposition, by simultaneous measurements of delta C-13 in all C moieties. New analytical tools to measure real-time changes in delta(CO2)-C-13 and the intra-molecular delta C-13 distribution within plant biochemical entities offer new opportunities for unravelling the complex interactions between substrate and microbial metabolism with respect to C-13 isotopic fractionation during biodegradation.
机译:在植物组织及其组成的生化实体之间以及之间,以及在异养细菌和真菌及其代谢产物之间以及之间,δC-13标记存在显着差异。此外,如在底物,呼吸的CO2和微生物生物量中所见,在有机分子的生物降解过程中会发生C-13同位素分馏,这可能与底物组成和/或微生物代谢有关。在单一定义的C底物分解过程中观察到的C-13同位素分馏似乎是由于底物中C-13中的分子内异质性以及微生物代谢过程中的C-13同位素分馏所致。非常有限的数据表明,后者可能在数量上比前者更为重要。在培养基中添加限定真菌的研究突显了将单一定义的C源添加至本身包含一个或多个C源的培养基时,与所观察到的C-13同位素分馏模式的解释相关的复杂性。已经设计出涉及C-13富集的技术或涉及等效的C-3和C-4衍生底物的配对处理,以克服培养基中背景C和代谢期间C-13同位素分级分离的问题。对复杂基质的研究表明,在呼出的CO2中最初的C-13耗尽阶段紧随其后的是C-13富集阶段,之后可能会也可能不会是另一个C-13耗尽阶段。通过同时测量所有C部分中的C-13增量,需要涉及综合方法的基础研究来获得对有机残渣分解过程中C-13同位素分级的新认识。新的分析工具可实时测量植物生化实体中δ(CO2)-C-13和分子内δ-C-13分布的实时变化,为揭示底物与微生物代谢之间关于C-的复杂相互作用提供了新的机会生物降解过程中的13同位素分级分离。

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