Comparative analysis of enzymatically digested κ-carrageenans, using liquid chromatography on ion-exchange and porous graphitic carbon columns coupled to an evaporative light scattering detector
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作者:
Antonopoulos, A
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机构:Univ Orleans, UMR CNRS 6005, Inst Chim Organ & Analyt, F-45067 Orleans 2, France
Antonopoulos, A
Herbreteau, B
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机构:Univ Orleans, UMR CNRS 6005, Inst Chim Organ & Analyt, F-45067 Orleans 2, France
Herbreteau, B
Lafosse, M
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机构:Univ Orleans, UMR CNRS 6005, Inst Chim Organ & Analyt, F-45067 Orleans 2, France
Lafosse, M
Helbert, W
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机构:Univ Orleans, UMR CNRS 6005, Inst Chim Organ & Analyt, F-45067 Orleans 2, France
Helbert, W
机构:
[1] Univ Orleans, UMR CNRS 6005, Inst Chim Organ & Analyt, F-45067 Orleans 2, France
[2] CNRS, UMR 1931, Lab Goemar, Biol Stn, F-29682 Roscoff, France
[3] Univ Lyon 1, UFR Chim Biochim, F-69622 Villeurbanne, France
Enzymatically digested K (A-G4S)-carrageenans, apart from their biological activities in plants, could be used as 'model' molecules to elucidate potential problems in nuclear magnetic resonance spectroscopy of carrageenans. Thus, oligosaccharides obtained from K-carrageenan by enzymatic digestion using K-carrageenase have been separated on silica and polymeric based ion-exchange and porous graphitic carbon (PGC) columns, coupled to an evaporative light scattering detector. Oligomers were separated on ion-exchange columns using a gradient of ammonium acetate as a developing ion, while analysis on PGC column presented an additional adjacent peak next to each main one, using a gradient of ammonium acetate in water/acetonitrile as a mobile phase. The phenomenon can be attributed to different retention mechanisms that govem the PGC surface. Furthermore, it has been demonstrated that acetonitrile can regulate the selectivity between the peaks raising hopes for preparative chromatography. (C) 2003 Elsevier B.V. All rights reserved.