Changes in Organization of Activity of Photosystem II in Oat Leaves under Osmotic Stress

S. A. Churakova, E. M. Lisitsyn, G. A. Batalova
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Abstract

The parameters of chlorophyll α rapid fluorescence were assessed in husked oats (A. sativa subsp. sativa) and naked oats (A. sativa subsp. nudisativa). The goal of the study was to identify differences between two subspecies of oats with respect to the control of primary energy storage processes under the influence of osmotic stress for the subsequent selection of parameters and oat-breeding strategies to increase photosynthetic productivity in early drought conditions. Plants were grown on a complete Knop’s nutrient solution; osmotic stress was created by 10% polyethylene glycol (PEG‑400), and osmotic pressure was 0.709 mPa. Fluorescence parameters were determined using a Fluor Pen FP 110/S fluorometer (Photon Systems Instruments, Czech Republic). The data was processed by principal component analysis. In husked genotypes, the four main factors were responsible for 94.2% (control) and 91.4% (stress) variability of the assessed parameters. In naked oats, three principal factors were found (90.5% of variability) in the absence of stress and four factors (97.1% variability) under stress conditions. The flows of trapped energy (TR0/RC) and electronic transport (ET0/RC) were controlled in naked oat by one and the same factor under stress and by two different factors in the absence of stress, whereas those in husked genotypes were by one factor in the absence of stress and by two different factors under stress. Osmotic stress led to passing the control over adsorbed (ABS/RC) and trapped (TR0/RC) energy flows from one factor to two factors in husked oats but did not affect naked oats. The parameter of efficiency of electron transfer to the primary acceptors of photosystem I (δRE) was controlled by two different factors and enhanced their effect (factor loading from 0.564 to 0.74). Under stress, the δRE parameter weakened the effect of both factors in naked genotypes (factor loading –0.625 and ‒0.705) and reduced the effect of one factor and strengthened the second factor in husked genotypes (factor loading –0.552 and 0.687).

渗透胁迫下燕麦叶片光系统 II 活动组织的变化
摘要 评估了有壳燕麦(A. sativa subsp.该研究的目的是确定两个燕麦亚种在渗透胁迫影响下一次能量储存过程控制方面的差异,以便随后选择参数和燕麦育种策略,提高早期干旱条件下的光合生产力。植物生长在完整的克诺普氏营养液中;渗透胁迫由 10%的聚乙二醇(PEG-400)产生,渗透压为 0.709 mPa。荧光参数使用 Fluor Pen FP 110/S 荧光仪(捷克共和国,Photon Systems Instruments 公司)测定。数据经过主成分分析处理。在去壳基因型中,四个主要因子分别占评估参数变异性的 94.2%(对照)和 91.4%(胁迫)。在裸燕麦中,发现在无胁迫条件下有三个主因子(占变异性的 90.5%),而在胁迫条件下有四个因子(占变异性的 97.1%)。裸燕麦的截留能量流(TR0/RC)和电子传输流(ET0/RC)在胁迫条件下受一个相同因子的控制,在无胁迫条件下受两个不同因子的控制,而带壳基因型的截留能量流在无胁迫条件下受一个因子的控制,在胁迫条件下受两个不同因子的控制。在有壳燕麦中,渗透胁迫导致对吸附能量流(ABS/RC)和捕获能量流(TR0/RC)的控制从一个因子变为两个因子,但对裸燕麦没有影响。光系统 I 主受体的电子传递效率参数(δRE)受到两个不同因子的控制,并增强了其效果(因子负荷从 0.564 到 0.74)。在胁迫条件下,δRE 参数在裸露基因型中削弱了两个因子的作用(因子载荷-0.625 和-0.705),在有壳基因型中降低了一个因子的作用,加强了第二个因子的作用(因子载荷-0.552 和 0.687)。
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