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终产物反馈对光合作用电子传递的影响。

End product feedback effects on photosynthetic electron transport.

机构信息

Department of Biology, University of Natal, 4001, Durban, South Africa.

出版信息

Photosynth Res. 1993 Jan;35(1):5-14. doi: 10.1007/BF02185407.

Abstract

The inhibition of photosynthetic electron transport when starch and sucrose synthesis limit the overall rate of photosynthesis was studied inPhaseolus vulgaris L. andXanthium strumarium L. The starch and sucrose limitation was established by reducing photorespiration by manipulation of the partial pressure of O2 and CO2. Chlorophylla fluorescence quenching, the redox state of Photosystem I (estimated by the redox status of NADP-dependent malate dehydrogenase), and the intermediates of the xanthophyll cycle were investigated. Non-photochemical fluorescence quenching increased, NADP-dependent malate dehydrogenase remained at 100% activity, and the amount of violaxanthin decreased when starch and sucrose synthesis limited photosynthesis. In addition, O2-induced feedback caused a decrease in photochemical quenching. These results are consistent with a downward regulation of photosynthetic electron transport during end product feedback on photosynthesis. When leaves were held in high CO2 for 4 hours, the efficiency of Photosystem II was reduced when subsequently measured under low light. The results indicate that the quantum efficiency of open Photosystem II centers was reduced by the 4 hour treatment. We interpret the results to indicate that feedback from starch and sucrose synthesis on photosynthetic electron transport stimulates mechanisms for dissipating excess light energy but that these mechanisms do not completely protect leaves from long-term inhibition of photosynthetic electron transport capacity.

摘要

在菜豆(Phaseolus vulgaris L.)和豚草(Xanthium strumarium L.)中研究了当淀粉和蔗糖合成限制光合作用整体速率时对光合电子传递的抑制作用。通过操纵 O2 和 CO2 的分压来减少光呼吸,从而建立淀粉和蔗糖的限制。研究了叶绿素荧光猝灭、光系统 I 的氧化还原状态(通过 NADP 依赖性苹果酸脱氢酶的氧化还原状态估计)和叶黄素循环的中间体。当淀粉和蔗糖合成限制光合作用时,非光化学荧光猝灭增加,NADP 依赖性苹果酸脱氢酶保持 100%的活性,紫黄质的量减少。此外,O2 诱导的反馈导致光化学猝灭降低。这些结果与光合作用终产物反馈时对光合电子传递的下调一致。当叶子在高 CO2 下保持 4 小时时,随后在低光下测量时,PSII 的效率降低。结果表明,4 小时的处理降低了开放 PSII 中心的量子效率。我们解释这些结果表明,来自淀粉和蔗糖合成的对光合电子传递的反馈刺激了耗散多余光能的机制,但这些机制并不能完全保护叶片免受光合作用电子传递能力的长期抑制。

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