Please use this identifier to cite or link to this item: http://dspace.mediu.edu.my:8181/xmlui/handle/10261/4166
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dc.creatorYruela Guerrero, Inmaculada-
dc.creatorTomás Corruchaga, Raquel-
dc.creatorSanjuán, M. L.-
dc.creatorTorrado Plou, Elena-
dc.creatorAured Galve, María-
dc.creatorPicorel Castaño, Rafael-
dc.date2008-05-12T12:32:52Z-
dc.date2008-05-12T12:32:52Z-
dc.date1998-11-
dc.date.accessioned2017-01-31T01:14:34Z-
dc.date.available2017-01-31T01:14:34Z-
dc.identifierPhotochemistry and Photobiology 68(5): 725-737-
dc.identifier0031-8655-
dc.identifierhttp://hdl.handle.net/10261/4166-
dc.identifier10.1111/j.1751-1097.1998.tb02537.x-
dc.identifier.urihttp://dspace.mediu.edu.my:8181/xmlui/handle/10261/4166-
dc.descriptionThe definitive version is available at http://www.blackwell-synergy.com/-
dc.descriptionDifferent pigment extraction procedures and HPLC methods were tested to investigate the geometric configuration of the β-carotene in two forms of the photosystem II reaction center (Dl-D2-cytochrome (Cyt) b559) complex containing one and two β-carotene molecules per two pheophytin a. All the handling steps and HPLC analyses were done in darkness at room temperature and at 4°C. Two different pigment extracts were analyzed, a mixture of chlorophyll a, pheophytin a and 3-carotene, and the isolated p-carotene from that mixture. In both cases only the all-frans-β-carotene was detected. The chromatographic profiles were similar at both temperatures only differing in the retention times that were longer at 4°C. This result was independent of the concentration of photosynthetic starting material. Furthermore, no differences were observed between Dl-D2-Cyt b559 complexes with one and two p-carotene molecules per reaction center. The analysis of the β-carotene chromatographic peak indicated no 15-cis to all-fraws isom-erization occurred during the HPLC chromatography in our experimental conditions. Resonance Raman spectra were also recorded in the isolated Dl-D2-Cyt b559 complex at room and liquid nitrogen temperature with excitation at 514.5 nm from an Ar+ laser. Spectra of control preparations showed main bands at 1532, 1264, 1213, 1185, 1154 and 1003 cm−1 corresponding to the M-trans isomer and confirm previous results. The presence in the reaction center suspension of artificial electron acceptors such as silicomolybdate or 2,5-dibromo-3-methyl-6-iso-propyl-p-benzoquinone that are able to quench 3P680 did not modify the resonance Raman spectra of the native Dl-D2-Cyt b559 complex. The results suggest that no isomerization takes place during the laser irradiation.-
dc.descriptionThis work was supported by the Dirección General de Investigación Científica y Técnica (Grant PB95-0219) to R.P.-
dc.descriptionPeer reviewed-
dc.format1468673 bytes-
dc.formatapplication/pdf-
dc.languageeng-
dc.publisherBlackwell Publishing-
dc.rightsopenAccess-
dc.subjectphotosystem II-
dc.subjectreaction center-
dc.subjectbeta-caroteno-
dc.subjectHPLC-
dc.subjectresonance raman-
dc.titleThe configuration of beta-carotene in the photosystem II reaction center-
dc.typeArtículo-
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