کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
30760 | 44501 | 2007 | 8 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Formation and geminate quenching of singlet oxygen in purple bacterial reaction center
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موضوعات مرتبط
مهندسی و علوم پایه
مهندسی شیمی
بیو مهندسی (مهندسی زیستی)
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چکیده انگلیسی
The phosphorescence of singlet oxygen (1Xâ) photosensitized by the carotenoidless reaction center (RC) of Rhodobacter sphaeroides R26.1 has been investigated, using H2O and D2O as the suspending media. To enhance (under neutral conditions) the triplet quantum yield of the special pair P870 (P) by the radical pair mechanism, the quinone acceptor QA was removed by means of a chemical treatment. The phosphorescence signal fits the functional form P0[exp (ât/Ï) â exp(ât/ζ)], regardless of whether 1Xâ is sensitized by Pâ or Mâ (where the dagger denotes triplet excitation and M is a water-soluble molecule). The time constant ζ was identified with the decay time of 1Xâ; when Pâ is the sensitizer, one finds ζP(1)=3.3±0.3μs, and ζP(2)=34±3μs, where the superscripts 1 and 2 refer to H2O and D2O, respectively; the corresponding values for sensitization by Mâ (in the absence of RC) are ζM(1)=3.7±0.4μs, and ζM(2)=75±5μs. The addition of RC's to the solution of M in D2O reveals that the RC is a quencher of 1Xâ; however, for equal concentrations of the RC, ζP(2)<ζM(2), showing that 1Xâ is deactivated, after its entry into the suspending medium, mainly by the solvent or the same RC which acts as the sensitizer. The values of ÏP are similar in both solvents, ca. 2 μs, but this time constant does not figure in the disappearance of Pâ , which follows a bi-exponential course, α1exp(ât/Ï1) + α2exp(ât/Ï2). The time constants Ï1 and Ï2 (72 ± 5 μs and 12 ± 1 μs, respectively) as well as the factor α2 are insensitive to the oxygen content, and quenching of Pâ is manifested only through a threefold reduction in the magnitude of α1; these data imply the absence of dynamic quenching and heterogeneity of the RC. The mean lifetime of 1Xâ inside the protein matrix is identified with ÏP, and the absence of a prompt component in the phosphorescence signal rationalized by proposing that the radiative decay of 1Xâ within the RC is much slower than that in an aqueous environment.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Photochemistry and Photobiology B: Biology - Volume 87, Issue 2, 25 May 2007, Pages 105-112
Journal: Journal of Photochemistry and Photobiology B: Biology - Volume 87, Issue 2, 25 May 2007, Pages 105-112
نویسندگان
Juan B. Arellano, Yaser A. Yousef, Thor Bernt Melø, Samsun B.B. Mohamad, Richard J. Cogdell, K. Razi Naqvi,