Institute of Plant Physiology, University of Bern, Altenbergrain 21, CH-3013 Bern, Switzerland.
Plant Physiol. 1992 Dec;100(4):2100-5. doi: 10.1104/pp.100.4.2100.
The catabolism of nuclear-encoded stromal proteins was investigated in intact chloroplasts isolated mechanically from pea (Pisum sativum) leaves. Glutamine synthetase, phosphoribulokinase, and nitrite reductase (quantified by immunoblotting) were more rapidly degraded in the light than in the dark. Furthermore, the degradation rates depended on exogenously supplied metabolites. For example, 2-oxoglutarate accelerated the catabolism of all three enzymes in chloroplasts incubated in the light, whereas oxaloacetate stabilized glutamine synthetase and at the same time destabilized the other two enzymes.
我们研究了从豌豆(Pisum sativum)叶片中机械分离的完整叶绿体中核编码基质蛋白的分解代谢。与黑暗相比,在光照下,谷氨酰胺合成酶、磷酸核糖激酶和亚硝酸盐还原酶(通过免疫印迹定量)更快降解。此外,降解速率取决于外源性代谢物。例如,在光照下孵育的叶绿体中,2-氧戊二酸加速了这三种酶的分解代谢,而草酰乙酸稳定了谷氨酰胺合成酶,同时使其他两种酶失稳。