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Journal ArticleDOI

Fourier transform infrared difference spectroscopy shows no evidence for an enolization of chlorophyll a upon cation formation either in vitro or during P700 photooxidation.

Eliane Nabedryk, +3 more
- 03 Apr 1990 - 
- Vol. 29, Iss: 13, pp 3242-3247
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TLDR
Molecular changes associated with the photooxidation of the primary electron donor P700 in photosystem I from cyanobacteria have been investigated with Fourier transform infrared (FTIR) difference spectroscopy and the 1718-cm-1 band in the difference spectrum of chlorophyll a is unambiguously assigned to the 9-keto carbonyl of the cation.
Abstract
Molecular changes associated with the photooxidation of the primary electron donor P700 in photosystem I from cyanobacteria have been investigated with Fourier transform infrared (FTIR) difference spectroscopy. Highly resolved signals are observed in the carbonyl stretching frequency region of the light-induced FTIR spectra. In order to assign and to interpret these signals, the FTIR spectra of isolated chlorophyll a and pyrochlorophyll a (lacking the 10a-ester carbonyl) in both their neutral and cation states were investigated. Comparison of the redox-induced FTIR difference spectra of these two model compounds demonstrates that upon chlorophyll a cation formation in tetrahydrofuran the 7c-ester carbonyl is essentially unperturbed while the 10a-ester carbonyl is upshifted from 1738 to 1751 cm-1. For the 9-keto group, the shift is from 1693 to 1718 cm-1 in chlorophyll a and from 1686 to 1712 cm-1 in pyrochlorophyll a. The 1718-cm-1 band in the difference spectrum of chlorophyll a is thus unambiguously assigned to the 9-keto carbonyl of the cation. Comparison of the light-induced FTIR difference spectrum associated with the photooxidation of P700 in vivo with the difference FTIR spectrum of chlorophyll a cation formation leads to the assignment of the frequencies of the 9-keto carbonyl group(s) at 1700 cm-1 in P700 and at 1717 cm-1 in P700+.(ABSTRACT TRUNCATED AT 250 WORDS)

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Citations
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Journal ArticleDOI

Infrared spectroscopy of proteins.

TL;DR: This review discusses the application of infrared spectroscopy to the study of proteins by focusing on the mid-infrared spectral region and theStudy of protein reactions by reaction-induced infrared difference spectroscopic.
Journal ArticleDOI

What vibrations tell us about proteins

TL;DR: This review deals with current concepts of vibrational spectroscopy for the investigation of protein structure and function, namely the amide I vibration of the polypeptide backbone that is used for secondary-structure analysis and some of the general aspects also apply to RamanSpectroscopy.
Journal ArticleDOI

Fourier transform infrared (FTIR) spectroscopy

TL;DR: This review presents basics of FTIR spectroscopy technique and provides specific important structural and functional information obtained from the analysis of the data from the photosystems, using this method.
Journal ArticleDOI

Energy transfer and trapping in photosystem I.

TL;DR: A direct comparison of the energy transfer and trapping properties of the PS I core complexes of cyanobacteria bear a large resemblance to the core complex of plants, and this results in a transmembrane electrochemical gradient that can be used to produce ATP.
Journal ArticleDOI

Photophysics of photosynthesis. Structure and spectroscopy of reaction centers of purple bacteria

TL;DR: In this article, a detailed account of investigations on the functioning of the reaction center protein with a number of optical and magnetic resonance spectroscopic techniques is presented, with emphasis on the relation between structure and function.
References
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Journal ArticleDOI

Examination of the secondary structure of proteins by deconvolved FTIR spectra.

TL;DR: Fourier transform ir (FTIR) spectra of 21 globular proteins have been obtained, revealing that the amide I band of each protein except casein consists of six to nine components, although all proteins do not exhibit components at every characteristic frequency.
Journal ArticleDOI

X-ray structure analysis of a membrane protein complex. Electron density map at 3 Å resolution and a model of the chromophores of the photosynthetic reaction center from Rhodopseudomonas viridis

TL;DR: In this paper, an atomic model of the prosthetic groups of the reaction center complex (4 bacteriochlorophyll b, 2 bacteriopheophytin b, 1 non-heme iron, 1 menaquinone, 4 heme groups) was built.
Journal ArticleDOI

Structure of the reaction center from Rhodobacter sphaeroides R-26: the cofactors

TL;DR: The three-dimensional structure of the cofactors of the reaction center of Rhodobacter sphaeroides R-26 has been determined by x-ray diffraction and refined at a resolution of 2.8 A with an R value of 26%.
Journal ArticleDOI

Pigment-protein interactions in the photosynthetic reaction centre from Rhodopseudomonas viridis.

TL;DR: An X‐ray structure analysis of the photosynthetic reaction centre from the purple bacterium Rhodopseudomonas viridis provides structural details of the pigment‐binding sites that may help to understand why only one branch of pigments is active in the light‐driven electron transfer.
Journal ArticleDOI

Structure of the reaction center from Rhodobacter sphaeroides R-26 and 2.4.1: protein-cofactor (bacteriochlorophyll, bacteriopheophytin, and carotenoid) interactions.

TL;DR: The three-dimensional structures of the cofactors and protein subunits of the reaction center (RC) from the carotenoidless mutant strain of Rhodobacter sphaeroides R-26 and the wild-type strain 2.4.1 have been determined by x-ray diffraction.
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