Abstract
Only quinones with a 2-methoxy group can act simultaneously as the primary (QA) and secondary (QB) electron acceptors in photosynthetic reaction centers from Rhodobacter sphaeroides. (13)C hyperfine sublevel correlation measurements of the 2-methoxy in the semiquinone states, SQA and SQB, were compared with quantum mechanics calculations of the (13)C couplings as a function of the dihedral angle. X-ray structures support dihedral angle assignments corresponding to a redox potential gap (ΔEm) between QA and QB of ~180 mV. This is consistent with the failure of a ubiquinone analogue lacking the 2-methoxy to function as QB in mutant reaction centers with a ΔEm of ≈160-195 mV.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, Non-P.H.S.
MeSH terms
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Bacterial Proteins / chemistry
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Bacterial Proteins / genetics
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Bacterial Proteins / metabolism
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Binding Sites
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Coenzymes / chemistry*
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Coenzymes / metabolism
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Electron Transport
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Kinetics
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Models, Molecular
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Oxidation-Reduction
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Photosynthetic Reaction Center Complex Proteins / chemistry
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Photosynthetic Reaction Center Complex Proteins / genetics
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Photosynthetic Reaction Center Complex Proteins / metabolism
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Quinones / chemistry*
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Quinones / metabolism
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Rhodobacter sphaeroides / chemistry
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Rhodobacter sphaeroides / enzymology*
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Rhodobacter sphaeroides / genetics
Substances
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Bacterial Proteins
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Coenzymes
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Photosynthetic Reaction Center Complex Proteins
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Quinones