Time-resolved FTIR difference spectroscopy for the study of photosystem I with high potential naphthoquinones incorporated into the A1 binding site 2: Identification of neutral state quinone bands

Abstract

Time-resolved step-scan FTIR difference spectroscopy at 77 K has been used to study cyanobacterial photosystem I (PSI) from Synechocystis sp. PCC 6803 with four high-potential, 1,4-naphthoquinones (NQs) incorporated into the A 1 binding site. The incorporated quinones are 2-chloro-NQ (2ClNQ), 2bromo-NQ (2BrNQ), 2,3-dichloro-NQ (Cl 2 NQ), and 2,3-dibromo-NQ (Br 2 NQ). For completeness 2methyl-NQ (2MNQ) was also incorporated and studied. Here we focus on spectra in the previously unexplored 1400 − 1200 cm − 1 spectral region. In this region several bands are identi ed and assigned to the neutral state of the incorporated quinones. This is important as identi cation of neutral state quinone bands in the regular 1700 − 1600 cm − 1 region has proven di cult in the past.For neutral PhQ in PSI a broad, intense band appears at 1300 cm − 1 . For the symmetric di-substituted NQs (Cl 2 NQ/Br 2 NQ) a single intense neutral state band is found at ~ 1280/1269 cm − 1 , respectively. For both mono-substituted NQs, 2ClNQ and 2BrNQ, however, two neutral state bands are observed near 1280 and 1250 cm − 1 , respectively. These observations from time-resolved spectra agree well with conclusions drawn from absorption spectra of the NQs in THF, which are also presented here. Density functional theory (DFT) based vibrational frequency calculations are also undertaken allowing an identi cation of the normal modes associated with the neutral state quinone bands.Multiple types of double difference spectra are compared and it is shown that this comparison is a potent approach for band identi cation in highly convoluted spectra.