D1-Asp170 is structurally coupled to the oxygen evolving complex in photosystem II as revealed by light-induced Fourier transform infrared differencespectroscopy

Citation
Ha. Chu et al., D1-Asp170 is structurally coupled to the oxygen evolving complex in photosystem II as revealed by light-induced Fourier transform infrared differencespectroscopy, BIOCHEM, 40(7), 2001, pp. 2312-2316
Citations number
43
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOCHEMISTRY
ISSN journal
00062960 → ACNP
Volume
40
Issue
7
Year of publication
2001
Pages
2312 - 2316
Database
ISI
SICI code
0006-2960(20010220)40:7<2312:DISCTT>2.0.ZU;2-H
Abstract
We report both mid-frequency (1800-1200 cm(-1)) and low-frequency (670-350 cm(-1)) S-2/S-1 FTIR difference spectra of photosystem II (PSII) particles isolated from wild-type* and D1-D170H mutant cells of the cyanobacterium Sy nechocystis sp. PCC 6803. Both mid- and low-frequency S-2/S-1 spectra of th e Synechocystis wild-type* PSII particles closely resemble those from spina ch PSII samples, which confirms an earlier result by Noguchi and co-workers [Noguchi, T., Inoue, Y., and Tang, X.-S. (1997) Biochemistry 36, 14705-147 11] and indicates that the coordination environment of the oxygen evolving complex (OEC) in Synechocystis is very similar to that in spinach. We also found that there is no appreciable difference between the mid-frequency S-2 /S-1 spectra of wild-type* and of D1-D170H mutant PSII particles, from whic h we conclude that D1-Asp170 does not undergo a significant structural chan ge during the S-1 to S-2 transition. This result also suggests that, if D1- Asp170 ligates Mn, it does not ligate the Mn ion that is oxidized during th e S-1 to S-2 State transition. Finally, we found that a mode at 606 cm(-1) in the low-frequency wild-type* S-2/S-1 spectrum shifts to 612 cm(-1) in th e D1-D170H mutant spectrum. Because this 606 cm(-1) mode has been previousl y assigned to an Mn-O-Mn cluster mode of the OEC [Chu, H.-A., Sackett, H., and Babcock, G. T. (2000) Biochemistry 39, 14371-14376], we conclude that D 1-Asp170 is structurally coupled to the Mn-O-Mn cluster structure that give s rise to this band. Our results suggest that D1-Asp170 either directly Lig ates Mn or Ca2+ or participates in a hydrogen bond to the Mn4Ca2+ cluster. Our results demonstrate that combining FTIR difference spectroscopy with si te-directed mutagenesis has the potential to provide insights into structur al changes in Mn and Ca2+ coordination environments in the different S stat es of the OEC.