Bachmann M., McMichael R. W., Huber J. L., Kaiser W. M., Huber S. C.
United States Department of Agriculture, Agricultural Research Service, and Department of Crop Science, North Carolina State University, Raleigh, North Carolina 27695-7631 (M.B., R.W.M., S.C.H.).
Plant Physiol. 1995 Jul;108(3):1083-1091. doi: 10.1104/pp.108.3.1083.
Evidence is accumulating that the activity of spinach (Spinacia oleracea L.) leaf NADH:nitrate reductase (NR) is modulated both in vitro and in vivo by protein phosphorylation. From the present study we report the partial purification of the two protein factors needed for NR inactivation. We identified NR-protein kinase (NR-PK) as a calcium-dependent and metabolite-regulated protein kinase and have provided additional evidence that phosphorylation of NR is necessary but not sufficient to inactivate the enzyme. The inhibitor protein required for inactivation of phospho-NR was purified 625-fold by polyethylene glycol fractionation and sequential column chromatography. Using partially purified inhibitor protein and NR-PK, we characterized NR inactivation (increased sensitivity to Mg2+ inhibition) in a reconstituted in vitro system. NR-PK activity was inhibited by a variety of metabolic phosphate esters including di-hydroxyacetone phosphate, glucose-6-phosphate, and fructose-1,6-bisphosphate. Light-to-dark transition experiments with a starchless tobacco (Nicotiana sylvestris) mutant, which accumulates phosphate esters during the photoperiod, indicated that NR inactivation in vivo might, indeed, be down-regulated by metabolites. Additionally, we postulate that cytosolic free calcium could play an important role in the regulation of NR activity in vivo.
越来越多的证据表明,菠菜(Spinacia oleracea L.)叶片NADH:硝酸还原酶(NR)的活性在体外和体内均受蛋白质磷酸化的调节。从本研究中,我们报告了NR失活所需的两种蛋白质因子的部分纯化。我们将NR蛋白激酶(NR-PK)鉴定为一种钙依赖性和代谢物调节的蛋白激酶,并提供了额外的证据表明NR的磷酸化对于使该酶失活是必要的,但并不充分。通过聚乙二醇分级分离和连续柱色谱法,将磷酸化NR失活所需的抑制蛋白纯化了625倍。使用部分纯化的抑制蛋白和NR-PK,我们在重组的体外系统中对NR失活(对Mg2+抑制的敏感性增加)进行了表征。NR-PK活性受到多种代谢磷酸酯的抑制,包括磷酸二羟丙酮、6-磷酸葡萄糖和1,6-二磷酸果糖。对一种无淀粉烟草(Nicotiana sylvestris)突变体进行的光暗转换实验表明,该突变体在光周期中积累磷酸酯,体内NR失活可能确实受代谢物的下调。此外,我们推测胞质游离钙可能在体内NR活性的调节中起重要作用。