Antonopoulos Aristotelis, Hardouin Julie, Favetta Patrick, Helbert William, Delmas Agnès F, Lafosse Michel
UMR CNRS 6005, Institut de Chimie Organique et Analytique, Université d'Orléans, BP 6759, 45067 Orléans Cedex 2, France.
Rapid Commun Mass Spectrom. 2005;19(16):2217-26. doi: 10.1002/rcm.2051.
Enzymatically digested oligosaccharides of kappa-, iota- and hybrid iota/nu-carrageenans were analysed using matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry in the negative-ion mode. nor-Harmane was used as matrix. Depending on the stock concentration and the laser intensity applied, the oligosaccharides exhibited losses of sulphate units (neutralised by the Na+ ion, and thus non-stable), leaving the primary backbone structure in most cases with only the deprotonated sulphate groups (carrying the negative charge, stable). This meant that kappa- and iota-oligosaccharides could not be easily distinguished from one another since they share the same primary backbone structure. However, for the hybrid iota/nu-oligosaccharides the primary backbone structure could be identified since the nu-carrageenan repeating unit differs from that of the kappa/iota-carrageenan unit. For all types of oligosaccharides, the results indicated cleavage of an anhydrogalactose unit from the non-reducing end. Specifically, for the hybrid oligosaccharides of iota/nu-carrageenans, this type of fragmentation means that the nu-carrageenan unit is not positioned on the non-reducing end of the hybrid oligosaccharides. Dehydration reactions, and exchange reactions of Na+ with K+ and Ca2+, were also observed.
采用基质辅助激光解吸/电离飞行时间质谱负离子模式,对κ-、ι-和杂交ι/ν-卡拉胶的酶解寡糖进行了分析。以去氢骆驼蓬碱作为基质。根据储备浓度和所施加的激光强度,寡糖表现出硫酸根单元的损失(被Na+离子中和,因此不稳定),在大多数情况下,仅留下带有负电荷且稳定的去质子化硫酸根基团的主链结构。这意味着κ-和ι-寡糖不易相互区分,因为它们具有相同的主链结构。然而,对于杂交ι/ν-寡糖,由于ν-卡拉胶重复单元与κ/ι-卡拉胶单元不同,因此可以鉴定出主链结构。对于所有类型的寡糖,结果表明从非还原端裂解出一个脱水半乳糖单元。具体而言,对于ι/ν-卡拉胶的杂交寡糖,这种类型的碎片化意味着ν-卡拉胶单元不在杂交寡糖的非还原端。还观察到了脱水反应以及Na+与K+和Ca2+的交换反应。