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Elucidation of metabolic pathways in glycogen-accumulating organisms with in vivo C-13 nuclear magnetic resonance

机译:阐明体内C-13核磁共振的糖原积累生物体内的代谢途径

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Glycogen-accumulating organisms (GAOs) are found in enhanced biological phosphorus removal systems where they compete with polyphosphate-accumulating organisms for external carbon substrates. C-13 nuclear magnetic resonance (C-13-NMR) was used to elucidate the metabolic pathways operating in an enriched GAO culture dominated by two known GAOs (81.2%). The experiments consisted of adding C-13-acetate (labelled on position 1 or 2) to the culture under anaerobic conditions, and operating the culture through a cycle consisting of an anaerobic, an aerobic and a further anaerobic phase. The carbon transformations over the cycle were monitored using in vivo(13)C-NMR. The two-carbon moieties in hydroxybutyrate and hydroxyvalerate were derived from acetate, while the propionyl precursor of hydroxyvalerate was primarily derived from glycogen, with only a small fraction originating from acetate. Comparison of the labelling patterns in hydroxyvalerate at the end of the first and the second anaerobic periods in pulse experiments with 2-C-13-acetate showed that the Entner-Doudoroff (ED) pathway was used for the breakdown of glycogen. This conclusion was further supported by the labelling pattern on glycogen observed in the pulse experiments with 1-C-13-acetate, which can only be explained by the operation of ED with recycling of pyruvate and glyceraldehyde 3-phosphate via gluconeogenesis. The activity of the ED pathway for glycogen degradation by GAOs is demonstrated here for the first time. In addition, the decarboxylating part of the tricarboxylic acid cycle was confirmed to operate also under anaerobic conditions.
机译:糖原累积生物(GAO)在增强型生物除磷系统中发现,它们与多磷酸盐累积生物竞争外部碳基质。 C-13核磁共振(C-13-NMR)用于阐明在以两种已知的GAO(81.2%)为主的富集GAO培养中的代谢途径。实验包括在厌氧条件下向培养物中添加C-13-乙酸盐(标记在位置1或2上),并通过包含厌氧,需氧和进一步厌氧相的循环操作培养物。使用体内(13)C-NMR监测循环中的碳转化率。羟基丁酸酯和羟基戊酸酯中的两个碳部分衍生自乙酸盐,而羟基戊酸酯的丙酰基前体主要源自糖原,只有一小部分源自乙酸酯。在2-C-13-乙酸酯脉冲实验中比较第一和第二个厌氧期末羟基戊酸酯的标记模式,结果表明Entner-Doudoroff(ED)途径用于糖原分解。用1-C-13-乙酸酯在脉冲实验中观察到的糖原上的标记模式进一步支持了这一结论,这只能用ED通过丙酮异生作用回收丙酮酸和3-磷酸甘油醛的操作来解释。首次展示了ED途径通过GAO降解糖原的活性。另外,证实了三羧酸循环的脱羧部分也可在厌氧条件下运行。

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