ESEEM studies of substrate water and small alcohol binding to the oxygen-evolving complex of photosystem II during functional turnover
Date
2006
Authors
Ahrling, Karin
Evans, Michael C W
Nugent, J H A
Ball, R J
Pace, Ronald
Journal Title
Journal ISSN
Volume Title
Publisher
American Chemical Society
Abstract
We report the first examination of exchangeable proton and MeOH interactions with the Mn catalytic cluster in photosystem II, under functional flash turnover conditions, using 2H ESEEM spectroscopy on the S 2 and S0 multiline states. Deuterium-labeled water (D 2O) and methyl d3-labeled methanol (DMeOH) are employed. It was discovered that a hyperfine resolved multiline S0 signal could be seen in the presence of D2O, the hyperfine structure of which depended on the presence or absence of methanol (MeOH). In the presence of DMeOH, significant dipolar coupling of the three methyl deuterons to the multiline centers in the S2 and S0 states was seen (S 2, 0.65, 0.39(2) MHz; and S0, 0.60, 0.37(2) MHz). These are consistent with direct binding of the methoxy fragment to Mn. Assuming terminal Mn-OMe ligation, the couplings indicated a spin projection coefficient (ρ) magnitude of ∼2 for the ligating Mn in both the S2 and S0 states, with inferred Mn-O distances of ∼1.9-2.0 Å. In the presence of D2O, four classes of exchangeable deuterons were identified by ESEEM in S2 and S0. Three of these classes (1, 2, and 4) exhibited populations and coupling strengths that were essentially constant under various conditions of sample preparation, illumination turnover, and small alcohol addition. Class 3 could be modeled with constant coupling but a highly variable deuteron population (n3 ∼ 0-10) depending in part on the preparation used. For all classes, the coupling parameters were very similar in S2 and S0. The favored interpretation is that the two strongest coupling classes (1 and 2) represent close binding of one water molecule to a single Mn which has an oxidation state of II in S 0 and III in S2, and p ∼ 2 in both cases. This water is not displaced by MeOH, but either the water or MeOH is singly deprotonated upon MeOH binding. Class 4 represents ∼2 water molecules which are not closely bound to Mn (Mn-deuteron distances of ∼3.7-4.7 Å). Class 3 probably represents protein matrix protons within ∼4 Å of the Mn in the cluster, which can be variably exchanged in different preparations.
Description
Keywords
Keywords: Alcohols; Deuterium; Methanol; Oxidation; Oxygen; Substrates; Deuteron population; Functional flash turnover; MeOH binding; Photosystems; Biochemistry; alcohol; oxygen; water; article; chemical binding; chemical structure; electron nuclear double resonanc
Citation
Collections
Source
Biochemistry
Type
Journal article
Book Title
Entity type
Access Statement
License Rights
DOI
10.1021/bi052146m
Restricted until
2037-12-31