期刊文献+

水稻叶片的蔗糖合成酶 被引量:20

Sucrose Synthetase in Rice Leaves
下载PDF
导出
摘要 糖型叶水稻、小麦、苜蓿叶片中SS的活力≥SPS。中间型叶高粱、菠菜叶片和淀粉型叶烟草、大豆叶片中SS的活力<SPS。糖型叶蚕豆叶片中SS的活力亦小于SPS,但SS活力是可观的. 水稻叶片SS催化的反应是可逆的,蔗糖合成反应的最适pH 8.0~9,5,蔗糖裂解反应的最适 pH6.5。蔗糖合成反应的速率随Mg^(2+)浓度增大而加强,逆反应的速率与Mg^(2+)浓度呈负相关。PPi与ATP对蔗糖合成反应无明显影响,对逆反应起抑制作用;UTP对正—逆反应都有抑制作用。ADP,GDP,CDP可取代UDP作为逆反应的底物之一,但效率较差。 The activities of sucrose synthetase andsucrose phosphate synthetase can be detectedin leaves. The activity of sucrose synthetase ishigher than or approximately equals to that ofsucrose phosphate synthetase in plants withsugar leaves, such as rice, wheat, and alfalfa.But in plants with starch leaves and with inter-mediate type of 1eaves, such as soybean, tobacco,spinach and sorghum, the activity of sucroseSynthetase is lower than that of sucrose phos-phate synthetase (Fig. 1). The reaction catalyzed by sucrose synthe-tase in rice leaves is reversible (Table 1). Thesucrose synthesis (forward) reaction catalyzedby this enzyme has a broad pH optimum bet-wee n 8.0~9.5 and the sucrose cleavage (back-ward) reaction has a sharp optimum at pH 6.5(Fig. 2). The rate of forward reaction increasedwhile the rate of backward rcaction decreasedwith the increase of the concentration of Mg^(2+)(Fig. 3). PP_i and ATP had no effect on the forwardreaction but inhibited the backward reaction(Fig.4) The reaction rate of sucrose cleavagedecreased when the PP_i concentration increased.The reactions in both directions were inhibitedby ADP and UTP. Sucrose synthetase can acceptADP, GDP and CDP instead of UDP as asubstrate for the backward reaction, but the rateof fructose formation is lower than UDP. Thesucrose synthesis and cleavage reactions cataly-zed by rice leaf sucrose synthetase are regulatedby pH, Mg^(2+), PPi and nucleotides.
出处 《植物生理学报(0257-4829)》 CSCD 1989年第3期239-243,共5页 Acta Phytophysiologica Sinica
关键词 水稻 蔗糖合成酶 核苷酸 叶片 leaves sucrose synthetase sucrose phosphate synthetase pH Mg^(2+) PPi nucleotides
  • 相关文献

参考文献3

  • 1苏丽英,植物生理学报,1989年,15卷,117页
  • 2夏淑芳,光合作用研究进展.3,1984年
  • 3夏淑芳,植物生理学报,1981年,7卷,135页

同被引文献218

引证文献20

二级引证文献413

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部