Tuning cofactor redox potentials: the 2-methoxy dihedral angle generates a redox potential difference of >160 mV between the primary (Q(A)) and secondary (Q(B)) quinones of the bacterial photosynthetic reaction center

Biochemistry. 2013 Oct 15;52(41):7164-6. doi: 10.1021/bi4011896. Epub 2013 Oct 2.

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

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Bacterial Proteins / chemistry
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Binding Sites
  • Coenzymes / chemistry*
  • Coenzymes / metabolism
  • Electron Transport
  • Kinetics
  • Models, Molecular
  • Oxidation-Reduction
  • Photosynthetic Reaction Center Complex Proteins / chemistry
  • Photosynthetic Reaction Center Complex Proteins / genetics
  • Photosynthetic Reaction Center Complex Proteins / metabolism
  • Quinones / chemistry*
  • Quinones / metabolism
  • Rhodobacter sphaeroides / chemistry
  • Rhodobacter sphaeroides / enzymology*
  • Rhodobacter sphaeroides / genetics

Substances

  • Bacterial Proteins
  • Coenzymes
  • Photosynthetic Reaction Center Complex Proteins
  • Quinones