A mechanism for water splitting and oxygen production in photosynthesis

被引:114
作者
Barber, James [1 ]
机构
[1] Imperial Coll London, Dept Life Sci, Sir Ernst Chain Bldg,South Kensington Campus, London SW7 2AZ, England
关键词
O BOND FORMATION; MONONUCLEAR RUTHENIUM COMPLEXES; PHOTOSYSTEM-II; EVOLVING COMPLEX; O-2-EVOLVING COMPLEX; CRYSTAL-STRUCTURE; S-2; STATE; OXIDATION; MODEL; EVOLUTION;
D O I
10.1038/nplants.2017.41
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Sunlight is absorbed and converted to chemical energy by photosynthetic organisms. At the heart of this process is the most fundamental reaction on Earth, the light-driven splitting of water into its elemental constituents. In this way molecular oxygen is released, maintaining an aerobic atmosphere and creating the ozone layer. The hydrogen that is released is used to convert carbon dioxide into the organic molecules that constitute life and were the origin of fossil fuels. Oxidation of these organic molecules, either by respiration or combustion, leads to the recombination of the stored hydrogen with oxygen, releasing energy and reforming water. This water splitting is achieved by the enzyme photosystem II (PSII). Its appearance at least 3 billion years ago, and linkage through an electron transfer chain to photosystem I, directly led to the emergence of eukaryotic and multicellular organisms. Before this, biological organisms had been dependent on hydrogen/electron donors, such as H2S, NH3, organic acids and Fe2+, that were in limited supply compared with the oceans of liquid water. However, it is likely that water was also used as a hydrogen source before the emergence of PSII, as found today in anaerobic prokaryotic organisms that use carbon monoxide as an energy source to split water. The enzyme that catalyses this reaction is carbon monoxide dehydrogenase (CODH). Similarities between PSII and the iron-and nickel-containing form of this enzyme (Fe-Ni CODH) suggest a possible mechanism for the photosynthetic O-O bond formation.
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页数:5
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