4.5 Article

Crystallization and electron paramagnetic resonance characterization of the complex of photosystem I with its natural electron acceptor ferredoxin

Journal

BIOPHYSICAL JOURNAL
Volume 83, Issue 4, Pages 1760-1773

Publisher

BIOPHYSICAL SOCIETY
DOI: 10.1016/S0006-3495(02)73942-8

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The formation of a transient complex between photosystem I and ferredoxin is involved in the process of ferredoxin photoreduction in oxygenic photosynthetic organisms. Reduced ferredoxin is an essential redox intermediate involved in many assimilatory processes and is necessary for the reduction of NADP(+) to NADPH. Single crystals from a complex of photosystem I with ferredoxin were grown using PEG 400 and CaCl2 as precipitation agents. The crystals diffract x-rays to a resolution of 7-8 Angstrom. The space group was determined to be orthorhombic with the unit cell dimensions a = 194 Angstrom, b = 208 Angstrom, and c = 354 Angstrom. The crystals contain photosystem I and ferredoxin in a 1:1 ratio. Electron paramagnetic resonance (EPR) measurements on these crystals are reported, where EPR signals of the three [4Fe-4S] clusters F-A, F-B, F-X, and the [2Fe-2S] cluster of ferredoxin were detected. From the EPR spectra observed at three particular orientations of the crystal in the magnetic field, the full orientation pattern of the F-A(-) g-tensor was simulated. This simulation is consistent with the presence of 12 magnetically inequivalent F-A(-) clusters per unit cell with the C-3 axis of the PSI trimers oriented at (23degrees, 72degrees, 77degrees) to the unit cell axes.

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