Direct structural identification of polysaccharides from red algae by FTIR microspectrometry II: Identification of the constituents ofGracilaria verrucosa |
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Authors: | Sekkal Majda Declerck Christine Huvenne Jean-Pierre Legrand Pierre Sombret Bernard Verdus Marie-Claire |
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Affiliation: | (1) LASIR-CNRS UPR A 2631 L, Université des Sciences et Technologies de Lille, Bât C5, F-59655 Villeneuve d'Ascq Cedex, France;(2) Laboratorie de cytophysiologie végétale URA-CNRS, Université des Sciences et Technologies de Lille, Bât SN2, F-59655 Villeneuve d'Ascq Cedex, France |
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Abstract: | The use of the infrared microspectrometry analytical technique as a new tool for the identification of the polysaccharides contained in the red algaeGracilaria verrucosa has demonstrated that in addition to agar spectra, features of the other coexisting constituents can also be obtained. Indeed, the infrared spectra recorded previously, all exhibit two important bands at about 1645 and 1530cm–1. These two bands were not present in the infrared spectra of the extracted agars and they are expected to be due to the amide I and amide II protein vibrations. In order to confirm this supposition, we have applied some enzymatic treatments, firstly on the whole algae and secondly on the ground algae (the algae has been previously depigmented and then dehydrated). Agarase, xylanase and cellulase were successively carried out on the algae. The last resulting spectrum, i.e. the spectrum obtained from the fraction which has undergone the three treatments, has been identified to be characteristic of proteins. This spectrum contained, both the amide I and II vibrations and in addition, weak absorption at 1230 cm–1 due probably to the amide III, was observed. Additional weak bands in the 1400–1300 cm–1 due to the different skeletal modes of the proteins were also present in this spectrum.The infrared spectra also revealed that the use of the enzymatic treatments on the ground algae is more efficient than when it is carried out on the whole algae. |
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Keywords: | microscopy microspectrometry FTIR cell wall algae |
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