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Patterns of intramolecular carbon isotopic heterogeneity within amino acids of autotrophs and heterotrophs

机译:自养生物和异养生物的氨基酸分子内碳同位素异质性模式

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A survey of the intramolecular C isotopic composition of a variety of organisms was conducted to investigate the potential of intramolecular isotopic measurements as a tracer of biological or geochemical processes. Based on a consideration of inorganic C sources and enzymatic fractionations, contrasting predictions were made for the relative 13C enrichments of the α-carboxyl carbons fixed by the anapleurotic (β)-carboxylation pathway during amino acid synthesis by photoautotrophs and heterotrophs. To test the model predictions, the stable C isotopic compositions of the acid hydrolyzable C fraction, the total amino acid α-carboxyl C fraction and the α-carboxyl C of glutamate from a variety of autotrophic and heterotrophic organisms were compared. The relative 13C enrichments of carboxyl carbons in the bulk amino acid fraction and in glutamate conformed qualitatively to model predictions. Macroalgal taxa possessed a significantly less enriched carboxyl C fraction than did either C3 or C4 vascular plants, indicating the presence of a different β-carboxylation pathway operating in these organisms. In most multicellular heterotrophs, the isotopic composition of the amino acid carboxyl carbons closely resembled that of their food sources. Amino acids are apparently assimilated into tissue proteins directly from their diets without significant metabolic modification. However, shifts in the isotopic composition of the carboxyl C fractions in some organisms were detected that were consistent with the occurrence of significant resynthesis of amino acids from non-amino acid precursors. Comparison of plant leaves and roots provided evidence of environmentally controlled assimilate partitioning. Intramolecular isotopic measurements of biological molecules provide unique insights into the origins and transformations of bio-molecules.
机译:进行了各种生物的分子内C同位素组成的调查,以调查分子内同位素测量作为生物或地球化学过程示踪剂的潜力。基于无机碳源和酶促分离的考虑,对比预测了光合自养生物和异养生物在氨基酸合成过程中由无磷(β)-羧化途径固定的α-羧基碳的相对13 C富集度。 。为了检验模型预测,比较了各种自养生物和异养生物的酸可水解C馏分,总氨基酸α-羧基C馏分和谷氨酸的α-羧基C的稳定C同位素组成。氨基酸大部分和谷氨酸中羧基碳的相对13 C富集在质量上与模型预测相符。相比于C3或C4维管植物,大型藻类的富集羧基C部分要少得多,这表明在这些生物中存在着不同的β-羧化途径。在大多数多细胞异养生物中,氨基酸羧基碳的同位素组成与它们的食物来源极为相似。显然,氨基酸可以直接从饮食中吸收到组织蛋白中,而没有明显的代谢改变。但是,检测到某些生物中羧基C馏分的同位素组成发生了变化,这与从非氨基酸前体大量重新合成氨基酸的发生是一致的。植物叶和根的比较提供了环境控制的同化物分配的证据。生物分子的分子内同位素测量提供了对生物分子的起源和转化的独特见解。

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