» Articles » PMID: 1731944

Proton and Electron Transfer in the Acceptor Quinone Complex of Rhodobacter Sphaeroides Reaction Centers: Characterization of Site-directed Mutants of the Two Ionizable Residues, GluL212 and AspL213, in the QB Binding Site

Overview
Journal Biochemistry
Specialty Biochemistry
Date 1992 Jan 28
PMID 1731944
Citations 39
Authors
Affiliations
Soon will be listed here.
Abstract

Proton and electron transfer events in reaction centers (RCs) from Rhodobacter sphaeroides were investigated by site-directed mutagenesis of glutamic acid at position 212 and aspartic acid at 213 in the secondary quinone (QB) binding domain of the L subunit. These residues were mutated singly to the corresponding amides (mutants L212EQ and L213DN) and together to give the double mutant (L212EQ/L213DN). In the double mutant RCs, the rate of electron transfer from the primary (QA) to the secondary (QB) acceptor quinones is fast (tau approximately 300 microseconds) and is pH independent from pH 5 to 11. The rate of recombination between the oxidized primary donor, P+, and QB- is also pH independent and much slower (tau approximately 10 s) than in the wild type (Wt), indicating a significant stabilization of the QB- semiquinone. In the double mutant, and in L213DN mutant RCs at low pH, the P+QB- decay is suggested to occur significantly via a direct recombination rather than by repopulating the P+QA- state, as in the Wt. Comparison of the behavior of Wt and the three mutant RC types leads to the following conclusions: the pK of AspL213 in the Wt is approximately 4 for the QAQB state (pKQB) and approximately 5 for the QAQB-state (pKQB-); for GluL212, pKQB approximately 9.5 and pKQB- approximately 11. In L213DN mutant RCs, pKQB of GluL212 is less than or equal to 7, indicating that the high pK values of GluL212 in the Wt are due largely to electrostatic interaction with the ionized AspL213 which contributes a shift of at least 2.5 pH units. Transfer of the second electron and all associated proton uptake to form QBH2 is drastically inhibited in double mutant and L213DN mutant RCs. At pH greater than or equal to 8, the rates are at least 10(4)-fold slower than in Wt RCs. In L212EQ mutant RCs the second electron transfer and proton uptake are biphasic. The fast phase of the electron transfer is similar to that of the Wt, but the extent of rapid transfer is pH dependent, revealing the pH dependence of the equilibrium QA(-)QB- in equilibrium with QAQBH-. The estimated limits on the pK values--pKQA-QB-less than or equal to 7.3, pKQAQB2- greater than or equal to 10.4--are similar to those derived earlier for Wt RCs [Kleinfeld et al. (1985) Biochim. Biophys. Acta 809, 291-310] and may pertain to the quinone head group, per se.(ABSTRACT TRUNCATED AT 400 WORDS)

Citing Articles

Comparison of proton transfer paths to the Q and Q sites of the Rb. sphaeroides photosynthetic reaction centers.

Wei R, Zhang Y, Mao J, Kaur D, Khaniya U, Gunner M Photosynth Res. 2022; 152(2):153-165.

PMID: 35344134 DOI: 10.1007/s11120-022-00906-x.


The two last overviews by Colin Allen Wraight (1945-2014) on energy conversion in photosynthetic bacteria.

Maroti P, Govindjee Photosynth Res. 2015; 127(2):257-71.

PMID: 26216496 DOI: 10.1007/s11120-015-0175-0.


Colin A. Wraight, 1945-2014.

Govindjee , Prince R, Ort D Photosynth Res. 2015; 127(2):237-56.

PMID: 26202746 DOI: 10.1007/s11120-015-0174-1.


Stigmatellin probes the electrostatic potential in the QB site of the photosynthetic reaction center.

Gerencser L, Boros B, Derrien V, Hanson D, Wraight C, Sebban P Biophys J. 2015; 108(2):379-94.

PMID: 25606686 PMC: 4302209. DOI: 10.1016/j.bpj.2014.11.3463.


Second-site mutation at M43 (Asn→Asp) compensates for the loss of two acidic residues in the QB site of the reaction center.

Hanson D, Nance S, Schiffer M Photosynth Res. 2014; 32(2):147-53.

PMID: 24408285 DOI: 10.1007/BF00035949.