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Chinese Academy of Sciences Institutional Repositories Grid
Directly probing redox-linked quinones in photosystem II membrane fragments via UV resonance Raman scattering

文献类型:期刊论文

作者Chen, Jun1,2; Yao, Mingdong1; Pagba, Cynthia V.3,4; Zheng, Yang1; Fei, Liping1; Feng, Zhaochi2; Barry, Bridgette A.3,4
刊名biochimica et biophysica acta-bioenergetics
出版日期2015-06-01
卷号1847期号:6-7页码:558-564
关键词Carbonyl bond Photosynthesis Proton transfer Electron transfer Lipid membrane Protein dynamics
英文摘要in photosynthesis, photosystem ii (psii) harvests sunlight with bound pigments to oxidize water and reduce quinone to quinol, which serves as electron and proton mediators for solar-to-chemical energy conversion. at least two types of quinone cofactors in psii are redox-linked: q(a), and q(b). here, we for the first time apply 257-nm ultraviolet resonance raman (uvrr) spectroscopy to acquire the molecular vibrations of plastoquinone (pq) in psii membranes. owing to the resonance enhancement effect, the vibrational signal of pq in psii membranes is prominent. a strong band at 1661 cm(-1) is assigned to ring c=c/c=0 symmetric stretch mode (nu 8a mode) of pq and a weak band at 469 cm(-1) to ring stretch mode. by using a pump-probe difference uvrr method and a sample jet technique, the signals of qa and qb can be distinguished. a frequency difference of 1.4 cm(-1) in nu 8a vibrational mode between qa and qb is observed, corresponding to similar to 86 mv redox potential difference imposed by their protein environment. in addition, there are other pqs in the psii membranes. a negligible anharmonicity effect on their combination band at 2130 cm(-1) suggests that the 'other pqs' are situated in a hydrophobic environment. the detection of the 'other pqs' might be consistent with the view that another functional pq cofactor (not q(a) or q(b)) exists in psii. this uvrr approach will be useful to the study of quinone molecules in photosynthesis or other biological systems. (c) 2015 elsevier b.v. all rights reserved.
WOS标题词science & technology ; life sciences & biomedicine
类目[WOS]biochemistry & molecular biology ; biophysics
研究领域[WOS]biochemistry & molecular biology ; biophysics
关键词[WOS]transform infrared-spectroscopy ; electron-transfer ; reaction centers ; spectra ; acceptor ; 1,4-benzoquinone ; reduction ; dynamics ; binding ; q(a)
收录类别SCI
语种英语
WOS记录号WOS:000355054900007
公开日期2016-05-09
源URL[http://cas-ir.dicp.ac.cn/handle/321008/146246]  
专题大连化学物理研究所_中国科学院大连化学物理研究所
作者单位1.Chinese Acad Sci, Dalian Inst Chem Phys, Dalian Natl Lab Clean Energy, Dalian 116023, Peoples R China
2.Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China
3.Georgia Inst Technol, Sch Chem & Biochem, Atlanta, GA 30332 USA
4.Georgia Inst Technol, Petit Inst Bioengn & Biosci, Atlanta, GA 30332 USA
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GB/T 7714
Chen, Jun,Yao, Mingdong,Pagba, Cynthia V.,et al. Directly probing redox-linked quinones in photosystem II membrane fragments via UV resonance Raman scattering[J]. biochimica et biophysica acta-bioenergetics,2015,1847(6-7):558-564.
APA Chen, Jun.,Yao, Mingdong.,Pagba, Cynthia V..,Zheng, Yang.,Fei, Liping.,...&Barry, Bridgette A..(2015).Directly probing redox-linked quinones in photosystem II membrane fragments via UV resonance Raman scattering.biochimica et biophysica acta-bioenergetics,1847(6-7),558-564.
MLA Chen, Jun,et al."Directly probing redox-linked quinones in photosystem II membrane fragments via UV resonance Raman scattering".biochimica et biophysica acta-bioenergetics 1847.6-7(2015):558-564.

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来源:大连化学物理研究所

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