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菠菜叶蔗糖磷酸合酶和硝酸还原酶在体外被多种蛋白激酶磷酸化/失活。

Spinach Leaf Sucrose-Phosphate Synthase and Nitrate Reductase Are Phosphorylated/Inactivated by Multiple Protein Kinases in Vitro.

作者信息

McMichael R. W., Bachmann M., Huber S. C.

机构信息

United States Department of Agriculture, Agricultural Research Service, and Department of Crop Science, North Carolina State University, Raleigh, North Carolina 27695-7631.

出版信息

Plant Physiol. 1995 Jul;108(3):1077-1082. doi: 10.1104/pp.108.3.1077.

Abstract

The regulation of sucrose-phosphate synthase (SPS) and nitrate reductase (NR) activities from mature spinach (Spinacia oleracea L.) leaves share many similarities in vivo and in vitro. Both enzymes are light/dark modulated by processes that involve, at least in part, reversible protein phosphorylation. Experiments using desalted crude extracts show that the ATP-dependent inactivation of spinach SPS and NR is sensitive to inhibition by glucose-6-phosphate. Also, a synthetic peptide homolog of the spinach SPS phosphorylation site inhibits the ATP-dependent inactivation of both enzymes with a similar concentration dependence. We have addressed the possibility that SPS and NR are regulated by the same protein kinase by partially purifying the protein kinases involved. Three unique kinase activities can be separated by anion-exchange and size-exclusion chromatography. Each peak of activity has a different substrate specificity. By gel filtration, they have apparent molecular masses of approximately 45, 60, and 150 kD. Additionally, the activities of the two smaller kinases are dependent on micromolar concentrations of Ca2+, whereas the 150-kD kinase is not. Finally, the 150-kD kinase has a subunit molecular mass of about 65 kD as determined by renaturing the kinase activity in situ following sodium dodecyl sulfate-polyacrylamide gel electrophoresis.

摘要

成熟菠菜(Spinacia oleracea L.)叶片中蔗糖磷酸合酶(SPS)和硝酸还原酶(NR)活性的调节在体内和体外有许多相似之处。这两种酶都通过至少部分涉及可逆蛋白质磷酸化的过程受到光/暗调节。使用脱盐粗提物进行的实验表明,菠菜SPS和NR的ATP依赖性失活对6-磷酸葡萄糖的抑制敏感。此外,菠菜SPS磷酸化位点的合成肽同源物以相似的浓度依赖性抑制这两种酶的ATP依赖性失活。我们通过部分纯化所涉及的蛋白激酶来探讨SPS和NR是否由同一蛋白激酶调节的可能性。三种独特的激酶活性可以通过阴离子交换和尺寸排阻色谱法分离。每个活性峰具有不同的底物特异性。通过凝胶过滤,它们的表观分子量约为45、60和150 kD。此外,两种较小激酶的活性依赖于微摩尔浓度的Ca2+,而150-kD激酶则不依赖。最后,通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳后原位复性激酶活性测定,150-kD激酶的亚基分子量约为65 kD。

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