Laboratoire de Physiologie Végétale Métabolique, ERA CNRS no 799, Bâtiment 430, Université de Paris Sud, Centre d'Orsay, F-91405, Orsay-Cedex, France.
Planta. 1982 Jun;155(1):17-23. doi: 10.1007/BF00402926.
During the greening of etiolated rice leaves, total glutamine synthetase activity increases about twofold, and after 48 h the level of activity usually observed in green leaves is obtained. A density-labeling experiment with deuterium demonstrates that the increase in enzyme activity is due to a synthesis of the enzyme. The enhanced activity obtained upon greening is the result of two different phenomena: there is a fivefold increase of chloroplastic glutamine synthetase content accompanied by a concommitant decrease (twofold) of the cytosolic glutamine synthetase. The increase of chloroplastic glutamine synthetase (GS2) is only inhibited by cycloheximide and not by lincomycin. This result indicates a cytosolic synthesis of GS2. The synthesis of GS2 was confirmed by a quantification of the protein by an immunochemical method. It was demonstrated that GS2 protein content in green leaves is fivefold higher than in etiolated leaves.
在黄化水稻叶片的复绿过程中,总谷氨酰胺合成酶的活性增加了约两倍,48 小时后,通常可以获得绿叶中的酶活性水平。氘标记实验表明,酶活性的增加是由于酶的合成。复绿时获得的增强活性是两种不同现象的结果:叶绿体谷氨酰胺合成酶的含量增加了五倍,同时细胞质谷氨酰胺合成酶的含量减少了(两倍)。叶绿体谷氨酰胺合成酶(GS2)的增加仅被环己酰亚胺抑制,而不受林可霉素抑制。这一结果表明 GS2 的细胞质合成。通过免疫化学方法对蛋白质进行定量,证实了 GS2 的合成。结果表明,绿叶中 GS2 蛋白的含量是黄化叶片的五倍。