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蚕豆保卫细胞磷酸烯醇式丙酮酸羧化酶性质的组织化学方法。

Histochemical Approach to Properties of Vicia faba Guard Cell Phosphoenolpyruvate Carboxylase.

机构信息

Department of Biology (1137), Washington University, Saint Louis, Missouri 63130.

出版信息

Plant Physiol. 1979 Aug;64(2):269-72. doi: 10.1104/pp.64.2.269.

Abstract

Properties of phosphoenolpyruvate carboxylase in guard cells dissected from frozen-dried Vicia faba L. leaflets were studied using quantitative histochemical techniques. Control experiments with palisade cells and whole leaflet extract proved that the single cell approach was valid. Most characteristics of enzyme activity in guard cells were identical to those in the leaflet extract. The activities were highly dependent on temperature, with maximum activity at 25 to 35 C. Half-maximum activity (with 1 millimolar phosphoenolpyruvate [PEP]) was observed at 0.1 millimolar Mg(2+). Two-hundred millimolar NaCl inhibited the reaction by 50%. With frozen-dried leaflet extract, the apparent K(m(PEP)) was 0.15 millimolar at pH 7.7; with guard cells, the values were 1.49, 0.5 to 0.8, and 0.24 millimolar in three successive experiments. Additional experiments showed that apparent K(m(PEP)) of guard cell activity from plants within a single growth lot was reproducible and did not change during stomatal opening. Mixed extract experiments proved that soluble compounds were not responsible for the difference observed between leaflet and guard cell activities. The differences in apparent K(m(PEP)) of guard cell activity could not be unambiguously interpreted. The physiological implications of the properties of this enzyme in guard cells are discussed.

摘要

使用定量组织化学技术研究了从冷冻干燥的蚕豆小叶中分离出的保卫细胞中磷酸烯醇丙酮酸羧化酶的性质。用栅栏细胞和整片叶提取物进行的对照实验证明了单细胞方法是有效的。保卫细胞中酶活性的大多数特征与叶提取物中的特征相同。该活性对温度高度依赖,在 25 至 35°C 时达到最大活性。在 1 毫摩尔磷酸烯醇丙酮酸(PEP)下观察到半最大活性(Mg2+)为 0.1 毫摩尔。200 毫摩尔 NaCl 抑制反应 50%。用冷冻干燥的小叶提取物,在 pH 值为 7.7 时,表观 K(m(PEP))为 0.15 毫摩尔;在三个连续实验中,对于保卫细胞,值分别为 1.49、0.5 至 0.8 和 0.24 毫摩尔。进一步的实验表明,来自单个生长批次植物的保卫细胞活性的表观 K(m(PEP))是可重现的,并且在气孔开放期间不会改变。混合提取物实验证明,可溶性化合物不是导致叶和保卫细胞活性之间观察到的差异的原因。无法明确解释保卫细胞中该酶的表观 K(m(PEP))的差异。讨论了该酶在保卫细胞中的特性的生理意义。

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