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2
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Electrophoretic Assay for Ribulose 1,5-Bisphosphate Carboxylase/Oxygenase in Guard Cells and Other Leaf Cells of Vicia faba L.豌豆保卫细胞和其他叶片细胞中核酮糖 1,5-二磷酸羧化酶/加氧酶的电泳分析
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7
Photosynthetic Carbon Fixation in Guard Cell Protoplasts of Vicia faba L. : Evidence from Radiolabel Experiments.蚕豆保卫细胞原生质体的光合碳固定:放射性标记实验的证据。
Plant Physiol. 1988 Mar;86(3):700-5. doi: 10.1104/pp.86.3.700.
8
Red Light-Dependent CO(2) Uptake and Oxygen Evolution in Guard Cell Protoplasts of Vicia faba L.: Evidence for Photosynthetic CO(2) Fixation.蚕豆保卫细胞原生质体中依赖红光的二氧化碳吸收与氧气释放:光合二氧化碳固定的证据
Plant Physiol. 1987 May;84(1):7-9. doi: 10.1104/pp.84.1.7.
9
Light Activation of NADP-Malate Dehydrogenase in Guard Cell Protoplasts from Vicia faba L.蚕豆保卫细胞原生质体中 NADP-苹果酸脱氢酶的光激活
Plant Physiol. 1985 Nov;79(3):829-32. doi: 10.1104/pp.79.3.829.

本文引用的文献

1
Light Activation of NADP-Malate Dehydrogenase in Guard Cell Protoplasts from Vicia faba L.蚕豆保卫细胞原生质体中 NADP-苹果酸脱氢酶的光激活
Plant Physiol. 1985 Nov;79(3):829-32. doi: 10.1104/pp.79.3.829.
2
Light-Stimulated Changes in the Acidity of Suspensions of Oat Protoplasts: Dependence upon Photosynthesis.光照对燕麦原生质体悬浮液酸度的影响:依赖于光合作用。
Plant Physiol. 1983 Jun;72(2):351-5. doi: 10.1104/pp.72.2.351.
3
Effect of Fusicoccin on Dark CO(2) Fixation by Vicia faba Guard Cell Protoplasts.佛司可林对蚕豆保卫细胞原生质体暗 CO2 固定的影响。
Plant Physiol. 1982 Dec;70(6):1700-3. doi: 10.1104/pp.70.6.1700.
4
Carbon dioxide metabolism in leaf epidermal tissue.叶片表皮组织中的二氧化碳代谢。
Plant Physiol. 1973 Nov;52(5):448-52. doi: 10.1104/pp.52.5.448.
5
Reversible pH Changes in Cells of Chlamydomonas reinhardi Resulting from CO(2) Fixation in the Light and Its Evolution in the Dark.莱茵衣藻细胞中因光照下二氧化碳固定及黑暗中其释放而导致的可逆pH变化
Plant Physiol. 1971 May;47(5):700-4. doi: 10.1104/pp.47.5.700.
6
Photosynthetic carbon reduction pathway is absent in chloroplasts of Vicia faba guard cells.蚕豆保卫细胞的叶绿体中不存在光合碳还原途径。
Proc Natl Acad Sci U S A. 1979 Dec;76(12):6371-5. doi: 10.1073/pnas.76.12.6371.

蚕豆保卫细胞原生质体悬浮液的光诱导碱化作用

Light-Induced Alkalinization of the Suspending Medium of Guard Cell Protoplasts from Vicia faba L.

机构信息

Department of Pure and Applied Sciences, College of Arts and Sciences, University of Tokyo, Tokyo 153.

出版信息

Plant Physiol. 1985 Nov;79(3):825-8. doi: 10.1104/pp.79.3.825.

DOI:10.1104/pp.79.3.825
PMID:16664498
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1074977/
Abstract

The light-dependent pH changes in the suspending medium of guard cell protoplasts (GCP) from Vicia faba were studied. Upon illumination, the medium was initially slightly alkalinized and then acidified. The extent of alkalinization was lower in CO(2)-free air than in normal air. This initial alkalinization was inhibited by DCMU. Acidification in CO(2)-free air became observable in shorter duration of light exposure than that in normal air. The rate of acidification was higher in CO(2)-free air than in normal air. The CO(2) level of the medium decreased in the light, and increased in the dark. (14)CO(2) uptake was enhanced 2- to 3-fold by light, but not in the presence of DCMU. These results indicate that photosynthetic CO(2) fixation does take place in GCP and that the initial alkalinization is due to this photosynthetic CO(2) uptake. Diethylstilbestrol, a nonmitochondrial membrane-bound ATPase inhibitor, inhibited the acidification, suggesting that the acidification resulted from H(+) extrusion by GCP. The acidification in light was also prevented by KCN, and partly by DCMU. Possible mechanisms of alkalinization and acidification are discussed in relation to guard cell metabolism.

摘要

我们研究了蚕豆保卫细胞原生质体悬浮液在依赖光照时的 pH 值变化。照光后,介质最初略有碱化,然后酸化。在无 CO2 的空气中,碱化程度比在正常空气中低。这种初始的碱化作用被 DCMU 抑制。在无 CO2 的空气中,光暴露时间较短时即可观察到酸化,而在正常空气中则需要较长时间。无 CO2 的空气中的酸化速度比正常空气中快。光照下介质中的 CO2 水平下降,黑暗中上升。(14)CO2 摄取在光照下增强了 2-3 倍,但在 DCMU 存在下则没有。这些结果表明,光合作用 CO2 固定确实发生在 GCP 中,而初始碱化是由于这种光合作用 CO2 摄取。非线粒体膜结合型 ATP 酶抑制剂己烯雌酚抑制了酸化,表明酸化是由 GCP 排出 H+引起的。KCN 和部分 DCMU 也能阻止光照下的酸化。讨论了与保卫细胞代谢有关的碱化和酸化的可能机制。