Efficient conditions for the photoaccumulation of H-A in the photosynthetic reaction centre of Rhodobacter sphaeroides R26 with uniformly labelled bacteriopheophytin monitored by Fourier transform infrared difference spectroscopy

被引:7
作者
Egorova-Zachernyuk, TA
Remy, A
Shkuropatov, AY
Gast, P
Hoff, AJ
Gerwert, K
de Groot, HJM
机构
[1] Leiden Univ, Leiden Inst Chem, Gorlaeus Labs, NL-2300 RA Leiden, Netherlands
[2] Ruhr Univ Bochum, Lehrstuhl Biophys, D-44780 Bochum, Germany
[3] RAN, Inst Soil Sci & Photosynth, S-142292 Pushchino, Russia
[4] Leiden Univ, Huygens Lab, Dept Biophys, NL-2300 RA Leiden, Netherlands
关键词
bacteriopheophytin; bacterial reaction centres; electron transfer; isotope labelling; Fourier Transform Infra-red; Magic Angle Spinning NMR; photosynthesis;
D O I
10.1016/S0924-2031(99)00010-7
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The native bacteriopheophytins (BPheo) a at sites H-A and H-B in the reaction centre (RC) of Rhodobacter sphaeroides R26 have been exchanged with uniformly C-13, N-15 labelled BPheo a. Exchange at the H-A site was > 50% as monitored with light-induced FTIR-difference spectroscopy indicated by the shift of the band at 1590 cm(-1). The photoreduction of H-A has been monitored by light-induced FTIR-difference spectroscopy at 22 degrees C in the presence of reductant and mediator: either sodium dithionite and cytochrome c, or sodium dithionite and dyes (potassium indigotetrasulfonate, neutral red). New experimental conditions are described for Ha photoaccumulation, and light-induced FTIR-difference spectra characteristic of H-A(-) are reported. The H-A(-)/H-A FTIR-difference spectra of Rb. sphaeroides R26 RCs in which uniformly C-13, N-15 labelled BPheo a replaces the photoactive BPheo will allow the BPheo modes to be assigned and to be discriminated from those of the RC protein. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:347 / 352
页数:6
相关论文
共 20 条
[1]   STRUCTURE OF THE REACTION CENTER FROM RHODOBACTER-SPHAEROIDES R-26 - THE COFACTORS .1. [J].
ALLEN, JP ;
FEHER, G ;
YEATES, TO ;
KOMIYA, H ;
REES, DC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (16) :5730-5734
[2]  
[Anonymous], BIOPHYSICAL TECHNIQU, DOI [10.1007/0-306-47960-5_9, DOI 10.1007/0-306-47960-5_9]
[3]   STRUCTURE OF THE PHOTOCHEMICAL-REACTION CENTER OF A SPHEROIDENE-CONTAINING PURPLE BACTERIUM, RHODOBACTER-SPHAEROIDES-Y, AT 3 ANGSTROM RESOLUTION [J].
ARNOUX, B ;
GAUCHER, JF ;
DUCRUIX, A ;
REISSHUSSON, F .
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 1995, 51 :368-379
[4]   Electrostatic influence of Q(A) reduction on the IR vibrational mode of the 10a-ester C=O of H-A demonstrated by mutations at residues Glu L104 and Trp L100 in reaction centers from Rhodobacter sphaeroides [J].
Breton, J ;
Nabedryk, E ;
Allen, JP ;
Williams, JAC .
BIOCHEMISTRY, 1997, 36 (15) :4515-4525
[5]   ASYMMETRIC BINDING OF THE 1-C=0 AND 4-C=0 GROUPS OF Q(A) IN RHODOBACTER-SPHAEROIDES-R26 REACTION CENTERS MONITORED BY FOURIER-TRANSFORM INFRARED-SPECTROSCOPY USING SITE-SPECIFIC ISOTOPICALLY LABELED UBIQUINONE-10 [J].
BRUDLER, R ;
DEGROOT, HJM ;
VANLIEMT, WBS ;
STEGGERDA, WF ;
ESMEIJER, R ;
GAST, P ;
HOFF, AJ ;
LUGTENBURG, J ;
GERWERT, K .
EMBO JOURNAL, 1994, 13 (23) :5523-5530
[6]   LIGHT-INDUCED CHARGE SEPARATION IN RHODOPSEUDOMONAS-VIRIDIS REACTION CENTERS MONITORED BY FOURIER-TRANSFORM INFRARED DIFFERENCE SPECTROSCOPY - THE QUINONE VIBRATIONS [J].
BUCHANAN, S ;
MICHEL, H ;
GERWERT, K .
BIOCHEMISTRY, 1992, 31 (05) :1314-1322
[7]  
DEGROOT HJM, 1996, BIOPHYSICAL TECHNIQU, P299
[8]   THE PHOTOSYNTHETIC REACTION CENTER FROM THE PURPLE BACTERIUM RHODOPSEUDOMONAS-VIRIDIS [J].
DEISENHOFER, J ;
MICHEL, H .
EMBO JOURNAL, 1989, 8 (08) :2149-2170
[9]   Characterization of pheophytin ground states in Rhodobacter sphaeroides R26 photosynthetic reaction centers from multispin pheophytin enrichment and 2-D C-13 MAS NMR dipolar correlation spectroscopy [J].
EgorovaZachernyuk, TA ;
vanRossum, B ;
Boender, GJ ;
Franken, E ;
Ashurst, J ;
Raap, J ;
Gast, P ;
Hoff, AJ ;
Oschkinat, H ;
deGroot, HJM .
BIOCHEMISTRY, 1997, 36 (24) :7513-7519
[10]   STRUCTURE OF THE PHOTOSYNTHETIC REACTION-CENTER FROM RHODOBACTER-SPHAEROIDES AT 2.65-ANGSTROM RESOLUTION - COFACTORS AND PROTEIN-COFACTOR INTERACTIONS [J].
ERMLER, U ;
FRITZSCH, G ;
BUCHANAN, SK ;
MICHEL, H .
STRUCTURE, 1994, 2 (10) :925-936