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"Time-nested acclimation to excitation pressure: the transcriptome, proteome and phosphoproteome"

"Time-nested acclimation to excitation pressure: the transcriptome, proteome and phosphoproteome"
“对激发压力的时间嵌套适应:转录组、蛋白质组和磷酸化蛋白质组”
批准号:
2246-2012
负责人:
Huner, Norman
金额:
$4.08万
依托单位国家:
加拿大
项目类别:
Discovery Grants Program - Individual
财政年份:
2013
资助国家:
加拿大
项目状态:
已结题
起止时间:
2013-01-01 至 2014-12-31

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中文摘要
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英文摘要
The ultimate source of the energy for almost all organisms on this planet is sunlight. The chloroplasts of plants and algae are crucial in linking all other living organisms to the sun through the ability to absorb, trap, and transform this light energy to reduce CO2 to complex carbohydrates. This requires the integration of extremely fast, temperature-insensitive photochemical reactions to trap the energy with much slower, temperature-dependent metabolic processes that consume this energy. As a consequence, photosynthetic organisms are predisposed to exhibit an imbalance in cellular energy budget which can be quantified in vivo as excitation pressure (EP). Exquisite solutions to the problem of cellular energy budget reflect part of the magic of photosynthesis and are the result of the dynamic capacity of plants and algae to remodel the structure and function of the photosynthetic apparatus to an ever-changing environment in order to maintain an energy balance by minimizing EP. The long-term objective of my research programme is to elucidate the molecular basis by which plants and algae sense and respond to short-term changes in EP due to alterations in environmental light and temperature conditions and integrate this information over time to remodel the photosynthetic apparatus and generate a phenotypic change during long-term, steady-state acclimation and adaptation to EP. The proposed research will identify the nature and number of potential molecular sensors of EP present within chloroplasts and the mechanism(s) by which these sensors alter not only the structure of the photosynthetic apparatus but also the phenotype of the model plant, Arabidopsis thaliana. This will be combined with research that exploits the unique photosynthetic apparatus of a novel, cold-adapted, non-model, Antarctic green alga, Chlamydomonas raudensis UWO241, to elucidate the dynamic mechanism by which it regulates photosynthetic electron flow to modulate EP. The proposed research will alter our conventional view of the structure and function of the photosynthetic apparatus, not only as a dynamic global cellular energy sensor but also as a dynamic energy transformer.
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