Department of Biology, Queen's University, Kingston, Ontario, Canada, K7L 3N6.
Plant Physiol. 1990 Sep;94(1):284-90. doi: 10.1104/pp.94.1.284.
The rate of NH(4) (+) assimilation by N-limited Selenastrum minutum (Naeg.) Collins cells in the dark was set as an independent variable and the relationship between NH(4) (+) assimilation rate and in vivo activity of phosphoenolpyruvate carboxylase (PEPC) was determined. In vivo activity of PEPC was measured by following the incorporation of H(14)CO(-) (3) into acid stable products. A linear relationship of 0.3 moles C fixed via PEPC per mole N assimilated was observed. This value agrees extremely well with the PEPC requirement for the synthesis of the amino acids found in total cellular protein. Determinations of metabolite levels in vivo at different rates of N assimilation indicated that the known metabolite effectors of S. minutum PEPC in vitro (KA Schuller, WC Plaxton, DH Turpin, [1990] Plant Physiol 93: 1303-1311) are important regulators of this enzyme during N assimilation. As PEPC activity increased in response to increasing rates of N assimilation, there was a corresponding decline in the level of PEPC inhibitors (2-oxoglutarate, malate), an increase in the level of PEPC activators (glutamine, dihydroxyacetone phosphate), and an increase in the Gln/Glu ratio. Treatment of N-limited cells with azaserine caused an increase in the Gln/Glu ratio resulting in increased PEPC activity in the absence of N assimilation. We suggest glutamate and glutamine play a key role in regulating the anaplerotic function of PEPC in this C(3) organism.
将 NH(4) (+) 的同化率作为一个独立变量,测定了 NH(4) (+) 同化率与体内磷酸烯醇丙酮酸羧化酶 (PEPC) 活性之间的关系。用 H(14)CO(-) (3) 追踪掺入到酸稳定产物中的方法来测定 PEPC 的体内活性。观察到 0.3 摩尔 C 通过 PEPC 固定与 1 摩尔 N 同化之间的线性关系。这个值与在总细胞蛋白中发现的氨基酸的合成所需的 PEPC 值非常吻合。在不同氮同化率下对体内代谢物水平的测定表明,沙蚕体内已知的 PEPC 代谢物效应物(KA Schuller、WC Plaxton、DH Turpin,[1990]植物生理学 93: 1303-1311)在氮同化过程中是该酶的重要调节因子。随着氮同化率的增加,PEPC 活性增加,PEPC 抑制剂(2-氧戊二酸、苹果酸)的水平相应下降,PEPC 激活剂(谷氨酰胺、二羟丙酮磷酸)的水平增加,Gln/Glu 比值增加。用偶氮丝氨酸处理氮限制细胞会导致 Gln/Glu 比值增加,从而在没有氮同化的情况下增加 PEPC 活性。我们认为谷氨酸和谷氨酰胺在调节该 C(3)生物中 PEPC 的氨甲酰化功能方面发挥着关键作用。