Nieto R, Cruz F, Tejedor J M, Barroso G, Cerdán S
Instituto de Investigaciones Biomédicas del CSIC, Madrid, Spain.
Biochimie. 1992 Sep-Oct;74(9-10):903-11. doi: 10.1016/0300-9084(92)90074-o.
The sources of ammonia used by isolated, intact rat liver mitochondria in the production of citrulline have been investigated in situ using a novel methodology based on the analysis of 13C-15N heteronuclear couplings observed by 13C NMR. Isolated mitochondria from rat liver were incubated with ornithine, 13CO3H- and 15NH4Cl, using unlabeled glutamate or glutamine as alternative, intramitochondrial nitrogen donors. The production of (7-13C, 8-15N) or (7-13C, 8-14N) citrulline was determined in situ by 13C NMR and the relative proportions of 15N- and 14N-citrullines confirmed by high resolution 13C NMR analysis of the C-7 citrulline resonance observed in perchloric acid extracts prepared at the end of the incubations. The 15N fractional enrichment of the intramitochondrial NH3 pool was manipulated either by modifying the 15N enrichment of added 15NH4Cl, or by altering the concentration of the unlabeled nitrogen donors in the incubation medium. Fractional 15N enrichments measured in the N-8 nitrogen of the resulting (7-13C) citrulline closely paralleled those of the external 15NH4Cl with minor dilutions derived from the unlabeled nitrogen contribution from the alternative substrates. In the presence of 10 mM 15NH4Cl, 10 mM glutamate contributed 4% of the citrulline N-8 nitrogen. Under similar conditions, the contribution of nitrogen from 10 mM glutamine to N-8 citrulline was 6%. These results indicate that the primary source of ammonia used for citrulline synthesis by isolated, intact rat liver mitochondria is extramitochondrial, providing also an illustration of the use of 13C-15N spin coupling patterns observed by 13C NMR, as a new tool in the study of ammonia metabolism.
利用一种基于对通过13C NMR观察到的13C-15N异核耦合进行分析的新方法,在原位研究了分离的完整大鼠肝线粒体在瓜氨酸生成过程中所使用的氨的来源。将大鼠肝脏分离的线粒体与鸟氨酸、13CO3H-和15NH4Cl一起孵育,使用未标记的谷氨酸或谷氨酰胺作为替代的线粒体内氮供体。通过13C NMR原位测定(7-13C, 8-15N)或(7-13C, 8-14N)瓜氨酸的生成,并通过对孵育结束时制备的高氯酸提取物中观察到的C-7瓜氨酸共振进行高分辨率13C NMR分析来确认15N-和14N-瓜氨酸的相对比例。通过改变添加的15NH4Cl的15N富集度,或通过改变孵育培养基中未标记氮供体的浓度,来控制线粒体内NH3池的15N分数富集。在所生成的(7-13C)瓜氨酸的N-8氮中测得的15N分数富集与外部15NH4Cl的15N分数富集密切平行,只是由于替代底物中未标记氮的贡献而有少量稀释。在存在10 mM 15NH4Cl的情况下,10 mM谷氨酸对瓜氨酸N-8氮的贡献为4%。在类似条件下,10 mM谷氨酰胺的氮对N-8瓜氨酸的贡献为6%。这些结果表明,分离的完整大鼠肝线粒体用于瓜氨酸合成的氨的主要来源是线粒体外的,这也说明了利用13C NMR观察到的13C-15N自旋耦合模式作为氨代谢研究中的一种新工具。