Evidence from Biosynthetically Incorporated Strontium and FTIR Difference Spectroscopy that the C-Terminus of the D1 Polypeptide of Photosystem II Does Not Ligate Calcium
- 27 May 2005
- journal article
- Published by American Chemical Society (ACS) in Biochemistry
- Vol. 44 (24) , 8571-8577
- https://doi.org/10.1021/bi050653y
Abstract
Recent FTIR studies have provided evidence that the C-terminal alpha-COO(-) group of the D1 polypeptide at D1-Ala344 is a unidentate ligand of a Mn ion in photosystem II [Chu, H.-A., Hiller, W., and Debus, R. J. (2004) Biochemistry 43, 3152-3166; Kimura, Y., Mizusawa, N., Yamanari, T., Ishii, A., and Ono, T.-A. (2005) J. Biol. Chem. 280, 2078-2083]. However, the FTIR data could not exclude Ca ligation. Furthermore, the recent approximately 3.5 A X-ray crystallographic structural model positions the alpha-COO(-) group of D1-Ala344 near a Ca ion [Ferreira, K. N., Iverson, T. M., Maghlaoui, K., Barber, J., and Iwata, S. (2004) Science 303, 1831-1838]. Therefore, to conclusively establish whether the alpha-COO(-) group of D1-Ala344 ligates Mn or Ca, the symmetric carboxylate stretching mode of the alpha-COO(-) group of D1-Ala344 was identified in the S(2)-minus-S(1) FTIR difference spectrum of PSII particles having Sr substituted for Ca. Cells of the cyanobacterium Synechocystis sp. PCC 6803 were propagated in media having Sr substituted for Ca and containing either l-[1-(13)C]alanine or unlabeled ((12)C) alanine. The S(2)-minus-S(1) FTIR difference spectra of the purified PSII particles show that substituting Sr for Ca alters several carboxylate stretching modes, including some that may correspond to one or more metal ligands, but importantly does not alter the symmetric carboxylate stretching mode of the alpha-COO(-) group of D1-Ala344. In unlabeled PSII particles, this mode appears at approximately 1356 cm(-)(1) in the S(1) state and at either approximately 1337 or approximately 1320 cm(-)(1) in the S(2) state, irrespective of whether the PSII particles contain Ca or Sr. These data are inconsistent with Ca ligation and show, therefore, that the C-terminal alpha-COO(-) group of the D1 polypeptide ligates a Mn ion. These data also show that substituting Ca with the larger Sr ion perturbs other unidentified carboxylate groups, at least one of which may ligate the Mn(4) cluster.Keywords
This publication has 10 references indexed in Scilit:
- Mid- to Low-Frequency Fourier Transform Infrared Spectra of S-State Cycle for Photosynthetic Water Oxidation inSynechocystissp. PCC 6803Biochemistry, 2004
- Biosynthetic Ca2+/Sr2+ Exchange in the Photosystem II Oxygen-evolving Enzyme of Thermosynechococcus elongatusJournal of Biological Chemistry, 2004
- Functional and structural study on chelator-induced suppression of S2/S1 FTIR spectrum in photosynthetic oxygen-evolving complexJournal of Inorganic Biochemistry, 2003
- Photosystem II and photosynthetic oxidation of water: an overviewPhilosophical Transactions Of The Royal Society B-Biological Sciences, 2002
- Characteristic Changes of the S2/S1 Difference FTIR Spectrum Induced by Ca2+ Depletion and Metal Cation Substitution in the Photosynthetic Oxygen-Evolving ComplexBiochemistry, 2002
- Chelator-Induced Disappearance of Carboxylate Stretching Vibrational Modes in S2/S1 FTIR Spectrum in Oxygen-Evolving Complex of Photosystem IIBiochemistry, 2001
- An FTIR study on the structure of the oxygen-evolving Mn-cluster of Photosystem II in different spin forms of the S2 statePhotosynthesis Research, 2000
- Inhomogeneity of the EPR multiline signal from the S2-state of the photosystem II oxygen-evolving enzymeJBIC Journal of Biological Inorganic Chemistry, 1997
- A carboxylate ligand interacting with water in the oxygen-evolving center of photosystem II as revealed by Fourier transform infrared spectroscopyBiochimica et Biophysica Acta (BBA) - Bioenergetics, 1995
- Calcium reconstitutes high rates of oxygen evolution in polypeptide depleted Photosystem II preparationsFEBS Letters, 1984