Abstract In photosynthetic reaction centers from purple bacteria, bacteriochlorophyll a (the special pair PAPB and accessory bacteriochlorophyll BA) and bacteriopheophytin a (HA) form the active electron-transfer branch and uniquely contain a polar methyl-keto (3-acetyl) group. However, despite its importance in defining local polarity, even the highest-resolution structures currently available (∼2 Å) cannot unambiguously distinguish the methyl carbon from the keto oxygen, limiting insight into its functional role. Here, we investigate how the methyl-keto orientations of the PB and HA cofactors influence the energetics of charge-separated intermediates, using a quantum mechanical/molecular mechanical approach. We identify two kinetically isolated methyl-keto conformations of PB, Tyr-OH…BA and Tyr-OH…PB, each associated with a distinct charge-separation pathway: the canonical PAPB* → PAPB•+BA•– and alternative BA* → BA•+HA•– pathways, respectively. For HA, methyl-keto reorientation stabilizes HA•– when forward transfer to the primary quinone (QA) is inhibited. These results show that distinct methyl-keto conformations tune charge-separation routes while also contributing to the oxidative robustness of bacteriochlorin macrocycles.
Noji et al. (Thu,) studied this question.