FP6Индивидуална стипендия2004–2006

O2FROMPSII · How plants can live on solar energy and water; biophysical investigations of O2 evolution in photosystem II, the key reaction in photosynthesis

6РП — Действия „Мария Кюри“

Период
2004-12-01 → 2006-11-30
Финансиране от ЕС
159 151 €
Участници
1
Схема
IIF

Линиите свързват координатора с партньорите.

Накратко на български

Процесът на разцепване на водата до кислород в протеина Фотосистема II се анализира чрез специална спектроскопия. Разбирането на този механизъм помага да се разбере как растенията превръщат слънчевата енергия и водата в кислород и храна.

Този кратък обзор е генериран от изкуствен интелект

Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.

Резултати накратко

Final Activity Report Summary - O2FROMPSII (How plants can live on solar energy and water. Biophysical investigations of O2 evolution in Photosystem II, the key reaction in photosynthesis)

Photosynthesis is the key to life on earth as we know it. Not only is it the energy source of plants, algae and certain bacteria, which form the ultimate basis of the food chain in the complex ecosystems of our planet, oxygenic photosynthesis from cyanobacteria and plants also produce the oxygen that we breathe. This is achieved by the splitting of water into oxygen and protons, an energetically extremely demanding process that these organisms are remarkably able to perform at mild physiological conditions. This is made possible by a protein called Photosystem II (PSII), and this is where the engine for water splitting, the oxygen evolving centre (OEC), is found. It consists of a metal cluster, CaMn4, and a nearby redox active tyrosine, YZ. It is the CaMn4 cluster that ultimately extracts electrons from water during water splitting. Despite many years of research, neither the mechanism by which this occurs, nor the structure of the cluster, are precisely known. Our research has focussed on studying the flow of proton and electrons within the OEC better understand this most important of reactions. During water splitting the CaMn4 is oxidised stepwise in the so-called 'S-cycle'. We have developed a technique using Electron paramagnetic resonance (EPR) spectroscopy at room temperature to monitor the changes in the cluster in real-time. Traditional techniques have relied on cryogenic temperatures to slow down or freeze in extremely rapid reactions that take place, but we have been able to exploit another important tyrosine in PSII, YD, to follow the formation and decay of the various steps of the S-cycle (the 'S-states'). We found that the relaxation properties of YD also changed in an S-state dependent manner, which allowed YD to used as a new probe for studying the mechanistic details of the S-cycle. Being at room temperature, this technique gives a dynamic picture of the reactions under physiological conditions. It is a new tool in the arsenal of spectroscopic techniques for discovering the structural and mechanistic details of the OEC. Cryogenic studies, however, are also important, trapping unstable states and species. We have extensively studied the so-called EPR 'split signals', believed to arise from the interaction of the CaMn4 cluster with the YZ* radical, generated and trapped by illumination at < 20 K. These signals are distinct for each S-state, reflecting changes in the magnetic properties of the cluster. We have demonstrated that these signals respond to changes in the environment, revealing important information about how electron and proton transfers take place, and how substrate molecules interact with the cluster. For instance, methanol, a molecule closely related to water, causes significant changes in these split signals. By combining experimental concentration dependence data with a theoretical framework for the signals' origins, we were able to deduce that the magnetic coupling between the Mn ions were changed by the binding of methanol to the same Mn ion of the cluster in all S-states for which split signals were known. Molecular modelling based on the best PSII structure currently available supported this conclusion, and identified which of the Mn ions is likely to be the binding site. This investigation revealed moreover channels within PSII which may act as conduits for the approach of methanol and water to the CaMn4 cluster, and critical regions in these channels were bordered by amino acid residues known to be of mechanistic importance. Complementary studies using advanced optical spectroscopic studies have also been performed in collaboration with a leading group in Australia. We have obtained kinetic data of various redox active species under split signal induction conditions, as well as PSII spectra under various conditions, including the first known S-state dependent optical spectra. We have also seen indications of S-state dependent shifts in spectral bands as a result of split signal inducing illuminations. Combined with EPR data, we are ever closer to discovering the minutiae of how plants can live on sunlight and water.

Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз

Цел на проекта

Research topic. The photosynthetic conversion of solar energy to chemical energy is by no comparison the most important energy process on earth. The biosphere is dominated by the oxygen evolving (or water oxidizing) organisms i.e. plants, algae and cyanobacteria. These use water as substrate: thereby they can live almost everywhere. The key reaction is the light-driven oxidation of water that provides the biosphere with an unlimited electron source. This fundamental reaction is carried out by Photosystem II, which oxidizes water to oxygen and protons. This seems to be a simple reaction, but in nature only PSII reaches potentials (>+lV) high enough to oxidize water. The difficulty is also clear from chemistry and there exists few, if any, man-made catalyst s able to carry out the reaction.The applicant will study the mechanism of the oxygen evolving machinery (water oxidizing complex) in Photosystem II (PSII). In particular we concentrate on proton currents between the Mn-cluster and the tyrosine in the intermediate redox states (S-states). We study these components by state-of-the-art EPR spectroscopy in synchronized PSII centres at different pH,by illumination at ultra-low temperature etc. The intention is to bring the applicant up-to-date in the use of EPR spectroscopy and other biophysical techniques, a topic at the forefront of today's biophysical research. The oxidative chemistry and the biochemistry in PSII offer a range of highly interesting and unique reactions. The applicant will focus on these reactions in his research.Training program. The applicant has chosen the group to learn and use sophisticated EPRspectroscopy. This will be accomplished by EPR courses specifically designed to fit the applicant's needs to carry out his research project. The training program also contains courses in photosynthesis, participation in outside courses in EPR and other relevant activities at outside institutions.

Оригинален текст от CORDIS (на английски).

Участници

  • UPPSALA UNIVERSITY · UPPSALAКоординаторШвеция

Връзки

Данни: CORDIS, © Европейски съюз