In vivo conversion of 6-O-sulfo-L-galactopyranosyl residues into 3,6-anhydro-L-galactopyranosyl residues in Gracilaria chilensis Bird, McLachlan et Oliveira

被引:16
作者
Hemmingson, JA
Furneaux, RH
Wong, H
机构
[1] Industrial Research Ltd., Gracefield Research Centre, Lower Hutt
关键词
agar biosynthesis; Gracilaria chilensis; precursor conversion;
D O I
10.1016/S0008-6215(96)00247-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The agar polysaccharides of the red seaweed Gracilaria chilensis Bird, McLachlan et Oliveira were labelled with the stable isotope C-13 by pulse feeding (NaHCO3)-C-13 to samples of this alga acclimatised to indoor culture. C-13 NMR spectroscopy of the labelled polysaccharides extracted from these samples has been used to demonstrate conversion in vivo of 6-O-sulfo-L-galactopyranosyl residues into 3,6-anhydro-L-galactopyranosyl residues. The 6-O-sulfo-L-galactopyranosyl residues can be linked to either 6-O-methyl-D-galactopyranosyl residues or D-galactopyranosyl residues. (C) 1996 Elsevier Science Ltd.
引用
收藏
页码:285 / 292
页数:8
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