Effect of CO2 content in air on functioning of Arabidopsis thaliana photosynthetic electron transport chain.

IF 2.6 4区 生物学 Q2 PLANT SCIENCES
Boris N Ivanov, Marina A Kozuleva, Natalia N Rudenko, Lyudmila K Ignatova, Elena M Nadeeva, Ilya A Naydov, Daria V Vetoshkina, Daria V Vilyanen, Maria M Borisova-Mubarakshina
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引用次数: 0

Abstract

The functioning of the photosynthetic electron transport chain and the proceeding of accompanying processes were studied in Arabidopsis thaliana plants acclimated during 2weeks to reduced (150ppm) or elevated (1000ppm) CO2 concentrations in air. Measured at ambient CO2 , the quantum yields of both photosystems were lower in plants acclimated to these CO2 concentrations as compared with control plants grown at ambient CO2 . The difference was more pronounced at the beginning of the illumination. It is discussed that this difference resulted from the difference in Rubisco content, which at both reduced and elevated CO2 in air was lower than in control plants. The quantum yield of regulated non-photochemical energy loss in photosystem II under both reduced and elevated CO2 was lower than in control plants. This correlated with reduced expression of the PsbS protein gene. H2 O2 content in the leaves increased during the first days of plant adaptation to 150ppm CO2 , but then decreased. The increase resulted from enhanced rates of both photorespiration and Mehler reaction, while the following decrease resulted from enhancing contents of ascorbate peroxidases in all cell compartments.

空气中CO2含量对拟南芥光合电子传递链功能的影响
研究了拟南芥(Arabidopsis thaliana)在空气中二氧化碳浓度降低(150ppm)或升高(1000ppm) 2周后的光合电子传递链功能及其相关过程。在环境CO2下测量,与在环境CO2下生长的对照植物相比,适应这些CO2浓度的植物的两个光系统的量子产率都较低。这种差别在开始照明时更为明显。讨论了这种差异是由于Rubisco含量的差异造成的,在空气中CO2降低和升高时,Rubisco含量都低于对照植物。在CO2浓度降低和升高的情况下,光系统II调控的非光化学能量损失量子产率均低于对照植物。这与PsbS蛋白基因的表达减少有关。在150ppm CO2处理下,叶片H2 O2含量在植物适应初期呈上升趋势,随后呈下降趋势。增加是由于光呼吸和梅勒反应的速率增加,而随后的减少是由于所有细胞区室中抗坏血酸过氧化物酶的含量增加。
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来源期刊
Functional Plant Biology
Functional Plant Biology 生物-植物科学
CiteScore
5.50
自引率
3.30%
发文量
156
审稿时长
1 months
期刊介绍: Functional Plant Biology (formerly known as Australian Journal of Plant Physiology) publishes papers of a broad interest that advance our knowledge on mechanisms by which plants operate and interact with environment. Of specific interest are mechanisms and signal transduction pathways by which plants adapt to extreme environmental conditions such as high and low temperatures, drought, flooding, salinity, pathogens, and other major abiotic and biotic stress factors. FPB also encourages papers on emerging concepts and new tools in plant biology, and studies on the following functional areas encompassing work from the molecular through whole plant to community scale. FPB does not publish merely phenomenological observations or findings of merely applied significance. Functional Plant Biology is published with the endorsement of the Commonwealth Scientific and Industrial Research Organisation (CSIRO) and the Australian Academy of Science. Functional Plant Biology is published in affiliation with the Federation of European Societies of Plant Biology and in Australia, is associated with the Australian Society of Plant Scientists and the New Zealand Society of Plant Biologists.
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