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关于碳酸氢盐不是光合放氧过程中底物的证据。

Evidence that bicarbonate is not the substrate in photosynthetic oxygen evolution.

作者信息

Clausen Juergen, Beckmann Katrin, Junge Wolfgang, Messinger Johannes

机构信息

Abteilung Biophysik, Universität Osnabrück, 49069 Osnabrueck, Germany.

出版信息

Plant Physiol. 2005 Nov;139(3):1444-50. doi: 10.1104/pp.105.068437. Epub 2005 Oct 21.

Abstract

It is widely accepted that the oxygen produced by photosystem II of cyanobacteria, algae, and plants is derived from water. Earlier proposals that bicarbonate may serve as substrate or catalytic intermediate are almost forgotten, though not rigorously disproved. These latter proposals imply that CO2 is an intermediate product of oxygen production in addition to O2. In this work, we investigated this possible role of exchangeable HCO3- in oxygen evolution in two independent ways. (1) We studied a possible product inhibition of the electron transfer into the catalytic Mn4Ca complex during the oxygen-evolving reaction by greatly increasing the pressure of CO2. This was monitored by absorption transients in the near UV. We found that a 3,000-fold increase of the CO2 pressure over ambient conditions did not affect the UV transient, whereas the S(3) --> S(4) --> S(0) transition was half-inhibited by raising the O2 pressure only 10-fold over ambient, as previously established. (2) The flash-induced O2 and CO2 production by photosystem II was followed simultaneously with membrane inlet mass spectrometry under approximately 15% H2(18)O enrichment. Light flashes that revealed the known oscillatory O2 release failed to produce any oscillatory CO2 signal. Both types of results exclude that exchangeable bicarbonate is the substrate for (and CO2 an intermediate product of) oxygen evolution by photosynthesis. The possibility that a tightly bound carbonate or bicarbonate is a cofactor of photosynthetic water oxidation has remained.

摘要

人们普遍认为,蓝细菌、藻类和植物的光系统II产生的氧气来自水。早期提出的碳酸氢盐可能作为底物或催化中间体的观点几乎被遗忘了,尽管没有被严格反驳。后一种观点意味着,除了氧气之外,二氧化碳也是氧气产生的中间产物。在这项工作中,我们通过两种独立的方式研究了可交换的HCO₃⁻在氧气释放中的这种可能作用。(1)我们通过大幅提高二氧化碳压力,研究了在放氧反应过程中电子转移到催化性Mn₄Ca复合物时可能的产物抑制作用。这通过近紫外吸收瞬变进行监测。我们发现,与环境条件相比,二氧化碳压力增加3000倍不会影响紫外瞬变,而如先前确定的那样,仅将氧气压力提高到比环境压力高10倍时,S(3)→S(4)→S(0)转变就被抑制了一半。(2)在大约15%的H₂¹⁸O富集条件下,用膜进样质谱法同时跟踪光系统II的闪光诱导的氧气和二氧化碳产生。揭示已知振荡性氧气释放的闪光未能产生任何振荡性二氧化碳信号。这两种结果都排除了可交换的碳酸氢盐是光合作用放氧的底物(以及二氧化碳是中间产物)的可能性。紧密结合的碳酸盐或碳酸氢盐是光合水氧化辅因子的可能性仍然存在。

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