“Life is bottled sunshine” – Wynwood Reade, Martyrdom of Man, 1924.
Every drop of energy humans consume originates from sunlight. The plants we eat capture the sun’s energy through photosynthesis, and the animals we eat are fed by plants.
But the thing that makes all that life possible is the same thing that can break plants’ ability to photosynthesize. Too much light can wreak havoc on a plant’s photosystem II, a molecular nanomachine that extracts electrons from water in photosynthesis. The damage to photosystem II affects photosynthetic efficiency and makes plants expend energy to repair the damage. Purdue’s Sujith Puthiyaveetil, an assistant professor of biochemistry, is interested in determining how plants repair their photosystems, and he recently received a $500,000 grant from the U.S. Department of Energy to find out.
“The water-splitting activity of photosystem II is a remarkable chemical feat. With it, however, comes an inherent risk for photodamage,” said Puthiyaveetil, who is a member of the Purdue Center for Plant Biology.
The light-induced damage to photosystem II occurs even in low light, but high-intensity light exacerbates it. An hour of bright sunlight on a summer day can breakdown all of photosystem II in a square meter leaf area in a plant.
Sujith Puthiyaveetil will use a U.S. Department of Energy grant to explore the mechanisms plants use to repair photosystems suffering light-induced damage. (Pudue Agricultural Communication photo/Tom Campbell) Understanding how the plant photosystem II is damaged and how it repairs itself could lead to plants designed to withstand more light or more easily fix their photosystems, freeing up energy and resources for plant growth and reproduction.
“Light-induced photosystem damage is the plant equivalent of sunburn,” Puthiyaveetil said. “The photosystem becomes defective. It repairs itself through a robust and ingenious mechanism, but we don’t fully understand the intricacies of it.”
Scientists know that in light, photosystem II undergoes phosphorylation in several places. The addition of these phosphate groups to photosystem II proteins likely aids in the disassembly of damaged photosystems and their eventual repair.
“Phosphorylation likely loosens the molecular glue that binds photosystem components together,” Puthiyaveetil said. “Our research aims to tease apart the complex relationship between damage, disassembly and phosphorylation.
“Photosystem II is a huge pigment-protein complex and if a plant had to replace the entire 30 or so of its protein subunits, it would be very costly,” Puthiyaveetil added. “Instead, it seems to replace the only one or two subunits that are damaged.”
He likened it to having a vehicle break down. Rather than buying an expensive new car, the owner might be able to replace one or two damaged parts and get back on the road.
Puthiyaveetil’s co-principal investigator, Amit Dhingra, a professor of genomics and biotechnology from Washington State University, will engineer tobacco plants that lack photosystem II phosphorylation sites or replace them with glutamate residues, which look as if the phosphorylation is always on. This forces the repair mechanisms to go to work, allowing Puthiyaveetil’s lab to study the precise role of phosphorylation in photosystem II repair.
“Photosystem II repair is a highly orchestrated molecular origami and elucidating its basic mechanisms informs about photosynthetic light energy conversion,” Puthiyaveetil said.
