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Harvesting Light for Life: Green Proteins as the Interface between Sun Energy and Biosphere

Project description

A genetics analysis of light-harvesting complexes

Light-harvesting complex II (LHCII) catalyses the first stages of photosynthesis, and it is the most abundant membrane protein, binding most of chlorophyll on Earth. However, current methods lack the ability to conduct a complete genetic analysis of LHCII proteins. The ERC-funded GrInSun project will conduct an in-depth analysis of LHCII proteins in algae and plants by deploying new techniques that have been recently used in the study of light-harvesting complexes of green plants. Using reverse genetics, researchers will reveal the domains involved in the regulation of photon harvesting, photoprotection and growth. Forward genetics analysis will aid in identifying determinants of protein functions.

Objective

Life on earth feeds on photons. Photosynthesis in green algae and land plants has been the world’s most successful biological process and has conquered the most diverse environments. Photosynthetic reaction centres are extremely well conserved, an unlikely basis for the ability to adapt. Antenna systems are widely diversified and yet only the Light-Harvesting Complexes (LHCs) have been selected for growth in the land environment. The distinctive property of GreenCut organisms lies in their light-harvesting mechanisms, which ensure efficient photon harvesting and photoprotection. Despite being the most abundant membrane proteins on earth, binding most of chlorophyll that makes the planet green, the secrets of LHCs are still concealed because we lack experimental systems that make possible the reverse and forward genetic analysis of LHCII proteins. Indeed, the clustered-genes encoding LHCII has resisted targeting by classic genetics. I propose an in-depth analysis of LHCII proteins in algae and plants by deploying a new technology that we have developed with our experience in studying LHCs. Firstly, we deleted all genes-encoding LHCII in model species of both land plants and green algae by genome editing and complemented plant ΔLHCII lines with site-directed, mutated sequences, demonstrating that reverse genetics can reveal the domains involved in the regulation of photon harvesting, photoprotection and growth. Secondly, forward genetics, on the other hand, will enable the identification of protein determinants by selecting specific phenotypes on complementing mixotrophic algal ΔLHCII lines with randomly mutagenized sequences. This will lead to a map of structures and functions that identifies the specific biological role of each component of the antenna system in vivo and in vitro. The project’s outcome will be the ability to design in a rational way the light-harvesting systems of plants and algae in the context of sustainable agriculture and bio-industry.

Host institution

UNIVERSITA DEGLI STUDI DI VERONA
Net EU contribution
€ 2 418 313,00
Address
VIA DELL ARTIGLIERE 8
37129 Verona
Italy

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Region
Nord-Est Veneto Verona
Activity type
Higher or Secondary Education Establishments
Links
Total cost
€ 2 418 313,00

Beneficiaries (1)