Photosystem I light-harvesting proteins regulate photosynthetic electron transfer and hydrogen production

Linear electron flow (LEF) and cyclic electron flow (CEF) compete for light-driven electrons transferred from the acceptor side of photosystem I (PSI). Under anoxic conditions, such highly reducing electrons also could be used for hydrogen (H-2) production via electron transfer between ferredoxin and hydrogenase in the green alga Chlamydomonas reinhardtii. Partitioning between LEF and CEF is regulated through PROTON-GRADIENT REGULATION5 (PGR5). There is evidence that partitioning of electrons also could be mediated via PSI remodeling processes. This plasticity is linked to the dynamics of PSI-associated light-harvesting proteins (LHCAs) LHCA2 and LHCA9. These two unique light-harvesting proteins are distinct from all other LHCAs because they are loosely bound at the PSAL pole. Here, we investigated photosynthetic electron transfer and H-2 production in single, double, and triple mutants deficient in PGR5, LHCA2, and LHCA9. Our data indicate that lhca2 and lhca9 mutants are efficient in photosynthetic electron transfer, that LHCA2 impacts the pgr5 phenotype, and that pgr5/lhca2 is a potent H-2 photo-producer. In addition, pgr5/lhca2 and pgr5/lhca9 mutants displayed substantially different H-2 photo-production kinetics. This indicates that the absence of LHCA2 or LHCA9 impacts H-2 photo-production independently, despite both being attached at the PSAL pole, pointing to distinct regulatory capacities. Alteration of the light-harvesting composition of photosystem I impacts photosynthetic electron transfer and hydrogen production.

Automated summary

Linear electron flow (LEF) and cyclic electron flow (CEF) compete for light-driven electrons, which can also be used for hydrogen production in anoxic conditions. The partitioning of electrons is regulated by PROTON-GRADIENT REGULATION5 (PGR5) and PSI remodeling processes. The plasticity of photosystem I-associated light-harvesting proteins LHCA2 and LHCA9 affects photosynthetic electron transfer and hydrogen production.