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发育中和萌发中的豌豆种子子叶中精氨酸代谢酶的活性

Activity of enzymes of arginine metabolism in the cotyledons of developing and germinating pea seeds.

作者信息

de Ruiter H, Kollöffel C

机构信息

Botanical Laboratory, State University of Utrecht, Utrecht, The Netherlands.

出版信息

Plant Physiol. 1982 Jul;70(1):313-5. doi: 10.1104/pp.70.1.313.

Abstract

Ornithine carbamoyltransferase, argininosuccinate synthetase, argininosuccinate lyase, and arginase activity were measured in extracts from cotyledons of developing and germinating seeds of Pisum sativum L. The course of activity of these four urea cycle enzymes showed a similar pattern during seed development. The activity per cotyledon increased sharply initially and reached a maximum about 5 weeks after anthesis, when the relative water content of the seeds was about 60%. About 8 weeks after anthesis, the seeds were mature (air-dry) and had enzyme activities which were much lower. The activities of the enzymes differed considerably. Ornithine carbamoyltransferase showed the highest activity, followed in order of decreasing activity by arginase, argininosuccinate lyase, and finally argininosuccinate synthetase.The course of the activity of the four enzymes was different during germination. Arginase activity increased sharply 7 hours after the onset of germination and remained at a constant level during the following days. Argininosuccinate synthetase activity decreased; the other enzymes showed a small increase in activity and a subsequent decrease. Results are discussed in relation to the regulation of the arginine metabolism during pea seed development and germination.

摘要

在豌豆(Pisum sativum L.)发育中和萌发种子的子叶提取物中测定了鸟氨酸氨甲酰转移酶、精氨琥珀酸合成酶、精氨琥珀酸裂解酶和精氨酸酶的活性。这四种尿素循环酶的活性变化过程在种子发育期间呈现出相似的模式。每个子叶的活性最初急剧增加,并在开花后约5周达到最大值,此时种子的相对含水量约为60%。开花后约8周,种子成熟(风干),其酶活性低得多。这些酶的活性差异很大。鸟氨酸氨甲酰转移酶活性最高,其次是精氨酸酶、精氨琥珀酸裂解酶,活性依次降低,最后是精氨琥珀酸合成酶。这四种酶在萌发过程中的活性变化过程不同。萌发开始7小时后,精氨酸酶活性急剧增加,并在随后的几天内保持在恒定水平。精氨琥珀酸合成酶活性降低;其他酶的活性先略有增加,随后降低。结合豌豆种子发育和萌发过程中精氨酸代谢的调控对结果进行了讨论。

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Enzymes of arginine and urea synthesis.精氨酸和尿素合成的酶。
Adv Enzymol Relat Areas Mol Biol. 1973;39:1-90. doi: 10.1002/9780470122846.ch1.

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