N-Formylkynurenine as a Marker of High Light Stress in Photosynthesis

被引:59
作者
Dreaden, Tina M.
Chen, Jun
Rexroth, Sascha
Barry, Bridgette A.
机构
[1] Georgia Inst Technol, Sch Chem & Biochem, Atlanta, GA 30332 USA
[2] Georgia Inst Technol, Petit Inst Bioengn & Biosci, Atlanta, GA 30332 USA
基金
美国国家科学基金会;
关键词
EVOLVING PHOTOSYSTEM-II; BLUE NATIVE ELECTROPHORESIS; MEMBRANE-PROTEIN COMPLEXES; SITE-DIRECTED MUTAGENESIS; SINGLET OXYGEN; TRYPTOPHAN OXIDATION; CRYSTAL-STRUCTURE; D1; PROTEIN; CHLORIDE REQUIREMENT; RAMAN-SPECTROSCOPY;
D O I
10.1074/jbc.M110.212928
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Photosystem II (PSII) is the membrane protein complex that catalyzes the photo-induced oxidation of water at a manganese-calcium active site. Light-dependent damage and repair occur in PSII under conditions of high light stress. The core reaction center complex is composed of the D1, D2, CP43, and CP47 intrinsic polypeptides. In this study, a new chromophore formed from the oxidative post-translational modification of tryptophan is identified in the CP43 subunit. Tandem mass spectrometry peptide sequencing is consistent with the oxidation of the CP43 tryptophan side chain, Trp-365, to produce N-formylkynurenine (NFK). Characterization with ultraviolet visible absorption and ultraviolet resonance Raman spectroscopy supports this assignment. An optical assay suggests that the yield of NFK increases 2-fold (2.2 +/- 0.5) under high light illumination. A concomitant 2.4 +/- 0.5-fold decrease is observed in the steady-state rate of oxygen evolution under the high light conditions. NFK is the product formed from reaction of tryptophan with singlet oxygen, which can be produced under high light stress in PSII. Reactive oxygen species reactions lead to oxidative damage of the reaction center, D1 protein turnover, and inhibition of electron transfer. Our results are consistent with a role for the CP43 NFK modification in photoinhibition.
引用
收藏
页码:22632 / 22641
页数:10
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