Bibliothek

feed icon rss

Ihre E-Mail wurde erfolgreich gesendet. Bitte prüfen Sie Ihren Maileingang.

Leider ist ein Fehler beim E-Mail-Versand aufgetreten. Bitte versuchen Sie es erneut.

Vorgang fortführen?

Exportieren
Filter
  • Free radicals  (1)
  • S-states  (1)
  • conformational change  (1)
  • 1
    ISSN: 1573-5079
    Schlagwort(e): manganese cluster ; multiline signal ; oxygen evolution ; S-states ; water ligation
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie
    Notizen: Abstract A comparative study of X-band EPR and ENDOR of the S2 state of photosystem II membrane fragments and core complexes in the frozen state is presented. The S2 state was generated either by continuous illumination at T=200 K or by a single turn-over light flash at T=273 K yielding entirely the same S2 state EPR signals at 10 K. In membrane fragments and core complex preparations both the multiline and the g=4.1 signals were detected with comparable relative intensity. The absence of the 17 and 23 kDa proteins in the core complex preparation has no effect on the appearance of the EPR signals. 1H-ENDOR experiments performed at two different field positions of the S2 state multiline signal of core complexes permitted the resolution of four hyperfine (hf) splittings. The hf coupling constants obtained are 4.0, 2.3, 1.1 and 0.6 MHz, in good agreement with results that were previously reported (Tang et al. (1993) J Am Chem Soc 115: 2382–2389). The intensities of all four line pairs belonging to these hf couplings are diminished in D2O. A novel model is presented and on the basis of the two largest hfc's distances between the manganese ions and the exchangeable protons are deduced. The interpretation of the ENDOR data indicates that these hf couplings might arise from water which is directly ligated to the manganese of the water oxidizing complex in redox state S2.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 2
    ISSN: 1573-5079
    Schlagwort(e): conformational change ; detergent–protein interaction ; ENDOR/TRIPLE-spectroscopy ; pigment–protein interaction ; site-directed mutagenesis
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Biologie
    Notizen: Abstract The effects of detergents on the electronic structure of the oxidized primary donor P+ and the time constant τAP of the P+Q A − charge recombination at ambient temperatures have been investigated in native and mutant reaction centers (RCs) from Rhodobacter sphaeroides. It is shown that N-lauryl-N,N-dimethyl-3-ammonio-1-propane sulfonate (SB12) induces a transition to a second distinct conformation of the RC. In the case of the wild type and the mutant FY(M197), in which a hydrogen bond is introduced to the 2-acetyl group of the dimer half of P that is associated with the M-subunit of the RC, the conformational change causes a more asymmetric spin density distribution between the two bacteriochlorophyll moieties of P+ in favor of the L-half. For both types of RCs the time constant τAP depends on the SB12/RC ratio as does the position of the long-wavelength band of P, λmax. The increase of τAP by ∼30 ms and the shift of λmax from ∼866 nm to ∼851 nm are indicative for the conformational change. In addition, a smaller linear increase of τAP with increasing SB12/RC ratio is superimposed on the variation of τAP due to the conformational change. Similar effects of SB12 on the optical spectra as well as on τAP are also observed for the two heterodimer mutants HL(L173) and HL(M202), in which one of the bacteriochlorophylls of P is replaced by a bacteriopheophytin. There are no clear indications for a correlation of τAP with the localization of the positive charge in P+. Furthermore, it is concluded from the dependence of τAP on the SB12/RC ratio that the single-site mutations do not affect the standard free energy difference of the two conformations to a measurable extent.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 3
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 23 (1984), S. 173-194 
    ISSN: 0570-0833
    Schlagwort(e): ENDOR spectroscopy ; Spectroscopy ; Free radicals ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The name “ENDOR” has been known since biblical times and denotes a small town close to the Sea of Galilee (ca. 1000 B.C., 1 Sam. 28 : 7 ff). The acronym “ENDOR” (Electron Nuclear DOuble Resonance) characterizes the extension of electron spin resonance to electron-nuclear double resonance spectroscopy, a method that has opened up new dimensions for the investigation of complicated paramagnetic molecules. Only ENDOR spectoscopy, which has achieved technical perfection in the last decade, overcomes the resolution limitations of EPR spectroscopy, thus allowing interesting applications in the field of biochemistry. ENDOR investigations of the primary process of photosynthesis, of the mode of action of derivatives of vitamin E and K, and of the mechanism of the enzymatic catalysis of flavoenzymes in biological redox-chains have opened up new vistas. ENDOR and its extension to the triple resonance experiment TRIPLE offer, for example, the potential for a precise determination of hyperfine coupling constants, including their signs, which are frequently especially interesting. In addition to protons, a multiple of magnetic nuclei can be studied by ENDOR, such as e.g. 2H, 13C, and 14N. The ENDOR techniques is not restricted to monoradicals, but can also be applied to polyradicals in spin states of higher multiplicities (triplet, quartet, or quintet state). The experimental data accessible from ENDOR yield information about spin and charge density distributions, and about the geometrics of radicals and their internal dynamics; they also provide an excellent test for the accuracy of quantum mechanical calculations.
    Zusätzliches Material: 23 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
    BibTip Andere fanden auch interessant ...
Schließen ⊗
Diese Webseite nutzt Cookies und das Analyse-Tool Matomo. Weitere Informationen finden Sie hier...