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本文引用的文献

1
Oxygen sensitivity of photosynthesis and photorespiration in different photosynthetic types in the genus Flaveria.黄顶菊属不同光合类型中光合作用和光呼吸作用的氧敏感性
Planta. 1996 Apr;198(4):563-571. doi: 10.1007/BF00262643. Epub 2017 Mar 18.
2
On the relationship between the quantum yield of Photosystem II electron transport, as determined by chlorophyll fluorescence and the quantum yield of CO2-dependent O 2 evolution.关于由叶绿素荧光测定的光系统 II 电子传递量子产率与 CO2 依赖性 O2 释放量子产率之间的关系。
Photosynth Res. 1992 Jul;33(1):51-62. doi: 10.1007/BF00032982.
3
Light dependence of quantum yields of Photosystem II and CO2 fixation in C 3 and C 4 plants.光对 C3 和 C4 植物的光系统 II 和 CO2 固定量子产率的依赖性。
Photosynth Res. 1993 Mar;35(3):265-74. doi: 10.1007/BF00016557.
4
Estimation of diffusive resistance of bundle sheath cells to CO2 from modeling of C 4 photosynthesis.从 C4 光合作用模型估算维管束鞘细胞对 CO2 的扩散阻力。
Photosynth Res. 1996 Sep;49(3):195-208. doi: 10.1007/BF00034781.
5
The relationship between the redox state of Q A and photosynthesis in leaves at various carbon-dioxide, oxygen and light regimes.在不同二氧化碳、氧气和光照条件下,QA 的氧化还原状态与叶片光合作用之间的关系。
Planta. 1985 Oct;166(2):219-26. doi: 10.1007/BF00397352.
6
Partitioning of photosynthetic electron flow between CO2 and O 2 reduction in a C 3 leaf (Phaseolus vulgaris L.) at different CO 2 concentrations and during drought stress.在不同 CO2 浓度和干旱胁迫下,C3 叶(菜豆)中 CO2 和 O2 还原之间光合作用电子流的分配。
Planta. 1991 Jan;183(2):178-84. doi: 10.1007/BF00197786.
7
Mechanism of c(4) photosynthesis: a model describing the inorganic carbon pool in bundle sheath cells.C(4)光合作用的机制:描述束鞘细胞中无机碳库的模型。
Plant Physiol. 1989 Dec;91(4):1372-81. doi: 10.1104/pp.91.4.1372.
8
CO(2) Concentrating Mechanism of C(4) Photosynthesis: Permeability of Isolated Bundle Sheath Cells to Inorganic Carbon.C4 光合作用的 CO2 浓缩机制:分离束鞘细胞对无机碳的通透性。
Plant Physiol. 1989 Dec;91(4):1364-71. doi: 10.1104/pp.91.4.1364.
9
Photorespiratory rates in wheat and maize as determined by o-labeling.通过氧标记法测定的小麦和玉米的光呼吸速率。
Plant Physiol. 1989 Jun;90(2):500-11. doi: 10.1104/pp.90.2.500.
10
Partitioning of Nitrogen among Ribulose-1,5-bisphosphate Carboxylase/Oxygenase, Phosphoenolpyruvate Carboxylase, and Pyruvate Orthophosphate Dikinase as Related to Biomass Productivity in Maize Seedlings.在玉米幼苗中,与生物量生产力相关的核酮糖-1,5-二磷酸羧化酶/加氧酶、磷酸烯醇丙酮酸羧化酶和丙酮酸 orthophosphate dikinase 之间的氮分配。
Plant Physiol. 1984 Jul;75(3):665-9. doi: 10.1104/pp.75.3.665.

氧气需求与C4光合作用的抑制。对缺乏C3和C4循环的C4植物的分析 对缺乏C3和C4循环的C4植物的分析。

Oxygen Requirement and Inhibition of C4 Photosynthesis. An analysis of c4 plants deficient in the c3 and c4 cycles An Analysis of C4 Plants Deficient in the C3 and C4 Cycles.

作者信息

Maroco JP, Ku MSB, Lea PJ, Dever LV, Leegood RC, Furbank RT, Edwards GE

机构信息

Department of Botany, Washington State University, Pullman, Washington 99164 (J.P.M., M.S.B.K., G.E.E.)

出版信息

Plant Physiol. 1998 Feb 1;116(2):823-32. doi: 10.1104/pp.116.2.823.

DOI:10.1104/pp.116.2.823
PMID:9490774
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC35142/
Abstract

The basis for O2 sensitivity of C4 photosynthesis was evaluated using a C4-cycle-limited mutant of Amaranthus edulis (a phosphoenolpyruvate carboxylase-deficient mutant), and a C3-cycle-limited transformant of Flaveria bidentis (an antisense ribulose-1,5-bisphosphate carboxylase/oxygenase [Rubisco] small subunit transformant). Data obtained with the C4-cycle-limited mutant showed that atmospheric levels of O2 (20 kPa) caused increased inhibition of photosynthesis as a result of higher levels of photorespiration. The optimal O2 partial pressure for photosynthesis was reduced from approximately 5 kPa O2 to 1 to 2 kPa O2, becoming similar to that of C3 plants. Therefore, the higher O2 requirement for optimal C4 photosynthesis is specifically associated with the C4 function. With the Rubisco-limited F. bidentis, there was less inhibition of photosynthesis by supraoptimal levels of O2 than in the wild type. When CO2 fixation by Rubisco is limited, an increase in the CO2 concentration in bundle-sheath cells via the C4 cycle may further reduce the oxygenase activity of Rubisco and decrease the inhibition of photosynthesis by high partial pressures of O2 while increasing CO2 leakage and overcycling of the C4 pathway. These results indicate that in C4 plants the investment in the C3 and C4 cycles must be balanced for maximum efficiency.

摘要

利用苋菜(一种磷酸烯醇式丙酮酸羧化酶缺陷型突变体)的C4循环受限突变体以及黄顶菊(一种反义核酮糖-1,5-二磷酸羧化酶/加氧酶[Rubisco]小亚基转化体)的C3循环受限转化体,评估了C4光合作用对O2敏感性的基础。用C4循环受限突变体获得的数据表明,由于光呼吸水平较高,大气中的O2水平(20 kPa)导致光合作用受到更大抑制。光合作用的最佳O2分压从约5 kPa O2降至1至2 kPa O2,与C3植物的相似。因此,最佳C4光合作用对O2的较高需求与C4功能具体相关。对于Rubisco受限的黄顶菊,超最佳O2水平对光合作用的抑制作用比野生型小。当Rubisco固定CO2受到限制时,通过C4循环增加叶肉细胞中CO2的浓度可能会进一步降低Rubisco的加氧酶活性,并减少高O2分压对光合作用的抑制,同时增加CO2泄漏和C4途径的过度循环。这些结果表明,在C4植物中,C3和C4循环的投入必须平衡以实现最大效率。