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本文引用的文献

1
Improving the efficiency of photosynthesis.提高光合作用效率。
Science. 1975 May 9;188(4188):626-33. doi: 10.1126/science.188.4188.626.
2
Isolation of Functionally Intact Rhodoplasts from Griffithsia monilis (Ceramiaceae, Rhodophyta).从纤细海膜(仙菜科,红藻门)中分离功能完整的红藻质体
Plant Physiol. 1981 Jan;67(1):5-8. doi: 10.1104/pp.67.1.5.
3
Effect of CO(2), O(2), and Light on Photosynthesis and Photorespiration in Wheat.CO2、O2 和光对小麦光合作用和光呼吸的影响。
Plant Physiol. 1980 Dec;66(6):1032-6. doi: 10.1104/pp.66.6.1032.
4
Oxygen exchange in leaves in the light.叶片在光照下的氧气交换
Plant Physiol. 1980 Aug;66(2):302-7. doi: 10.1104/pp.66.2.302.
5
Light-driven Uptake of Oxygen, Carbon Dioxide, and Bicarbonate by the Green Alga Scenedesmus.光照驱动的绿藻小球藻对氧气、二氧化碳和碳酸氢盐的摄取。
Plant Physiol. 1980 Apr;65(4):723-9. doi: 10.1104/pp.65.4.723.
6
Photosynthetic oxygen reduction in isolated intact chloroplasts and cells in spinach.菠菜中分离出的完整叶绿体和细胞中的光合氧还原作用
Plant Physiol. 1979 Oct;64(4):656-9. doi: 10.1104/pp.64.4.656.
7
Fixation of O(2) during Photorespiration: Kinetic and Steady-State Studies of the Photorespiratory Carbon Oxidation Cycle with Intact Leaves and Isolated Chloroplasts of C(3) Plants.光呼吸过程中氧气的固定:对C₃植物完整叶片和分离叶绿体光呼吸碳氧化循环的动力学和稳态研究
Plant Physiol. 1978 Dec;62(6):954-67. doi: 10.1104/pp.62.6.954.
8
Kinetics and Apparent K(m) of Oxygen Cycle under Conditions of Limiting Carbon Dioxide Fixation.二氧化碳固定受限条件下氧循环的动力学及表观米氏常数(K(m))
Plant Physiol. 1978 Jun;61(6):915-7. doi: 10.1104/pp.61.6.915.
9
Oxygen Concentration in Isolated Chloroplasts during Photosynthesis.光合作用期间分离叶绿体中的氧浓度。
Plant Physiol. 1977 Dec;60(6):903-6. doi: 10.1104/pp.60.6.903.
10
Rapid isolation of mesophyll cells from leaves of soybean for photosynthetic studies.快速分离大豆叶片中叶肉细胞用于光合作用研究。
Plant Physiol. 1977 Apr;59(4):587-90. doi: 10.1104/pp.59.4.587.

大豆细胞分离物中的光合 O(2)交换动力学。

Photosynthetic o(2) exchange kinetics in isolated soybean cells.

机构信息

Department of Biological Sciences, University of Maryland Baltimore County (UMBC), Catonsville, Maryland 21228.

出版信息

Plant Physiol. 1982 Jul;70(1):179-85. doi: 10.1104/pp.70.1.179.

DOI:10.1104/pp.70.1.179
PMID:16662441
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1067108/
Abstract

Light-dependent O(2) exchange was measured in intact, isolated soybean (Glycine max. var. Williams) cells using isotopically labeled O(2) and a mass spectrometer. The dependence of O(2) exchange on O(2) and CO(2) was investigated at high light in coupled and uncoupled cells. With coupled cells at high O(2), O(2) evolution followed similar kinetics at high and low CO(2). Steady-state rates of O(2) uptake were insignificant at high CO(2), but progressively increased with decreasing CO(2). At low CO(2), steady-state rates of O(2) uptake were 50% to 70% of the maximum CO(2)-supported rates of O(2) evolution. These high rates of O(2) uptake exceeded the maximum rate of O(2) reduction determined in uncoupled cells, suggesting the occurrence of another light-induced O(2)-uptake process (i.e. photorespiration).Rates of O(2) exchange in uncoupled cells were half-saturated at 7% to 8% O(2). Initial rates (during induction) of O(2) exchange in uninhibited cells were also half-saturated at 7% to 8% O(2). In contrast, steady-state rates of O(2) evolution and O(2) uptake (at low CO(2)) were half-saturated at 18% to 20% O(2). O(2) uptake was significantly suppressed in the presence of nitrate, suggesting that nitrate and/or nitrite can compete with O(2) for photoreductant.These results suggest that two mechanisms (O(2) reduction and photorespiration) are responsible for the light-dependent O(2) uptake observed in uninhibited cells under CO(2)-limiting conditions. The relative contribution of each process to the rate of O(2) uptake appears to be dependent on the O(2) level. At high O(2) concentrations (>/=40%), photorespiration is the major O(2)-consuming process. At lower (ambient) O(2) concentrations (</=20%), O(2) reduction accounts for a significant portion of the total light-dependent O(2) uptake.

摘要

使用同位素标记的 O(2) 和质谱仪,在完整的、分离的大豆(Glycine max. var. Williams)细胞中测量了依赖于光的 O(2) 交换。在耦合和非耦合细胞中,在高光下研究了 O(2) 交换对 O(2) 和 CO(2) 的依赖性。在高 O(2) 下,耦合细胞的 O(2) 演化在高 CO(2) 和低 CO(2) 下遵循相似的动力学。高 CO(2) 下 O(2) 摄取的稳态速率微不足道,但随着 CO(2) 的降低而逐渐增加。在低 CO(2) 下,O(2) 摄取的稳态速率为最大 CO(2) 支持的 O(2) 演化速率的 50% 至 70%。这些高 O(2) 摄取速率超过了在非耦合细胞中确定的 O(2) 还原的最大速率,表明发生了另一种光诱导的 O(2)摄取过程(即光呼吸)。非耦合细胞中的 O(2) 交换速率在 7% 至 8% 的 O(2) 下半饱和。未受抑制的细胞中 O(2) 交换的初始速率(在诱导期间)也在 7% 至 8% 的 O(2) 下半饱和。相比之下,O(2) 演化和 O(2) 摄取的稳态速率(在低 CO(2) 下)在 18% 至 20% 的 O(2) 下半饱和。硝酸盐的存在显著抑制了 O(2) 的摄取,表明硝酸盐和/或亚硝酸盐可以与 O(2) 竞争光还原剂。这些结果表明,在 CO(2) 限制条件下,两种机制(O(2) 还原和光呼吸)负责观察到的未受抑制细胞中依赖于光的 O(2) 摄取。每个过程对 O(2) 摄取速率的贡献似乎取决于 O(2) 水平。在高 O(2) 浓度(>=40%)下,光呼吸是主要的 O(2) 消耗过程。在较低(环境)O(2) 浓度(<=20%)下,O(2) 还原占总依赖于光的 O(2) 摄取的重要部分。