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Volume 271,
Number 20,
Issue of May 17, 1996 pp. 11750-11755
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.
A
New Glycosaminoglycan from the Giant African Snail Achatina fulica
(Received for publication, December 19, 1995; and in revised form, February 16, 1996)
Yeong S.
Kim
,
You
Y.
Jo
,
Il M.
Chang
,
Toshihiko
Toida
,
Youmie
Park
,
Robert
J.
Linhardt
A new glycosaminoglycan has been isolated from the giant African
snail Achatina fulica. This polysaccharide had a molecular
weight of 29,000, calculated based on the viscometry, and a uniform
repeating disaccharide structure of
4)-2-acetyl,2-deoxy- -D-glucopyranose
(1 4)-2-sulfo- -L-idopyranosyluronic acid (1 .
This polysaccharide represents a new, previously undescribed
glycosaminoglycan. It is related to the heparin and heparan sulfate
families of glycosaminoglycans but is distinctly different from all
known members of these classes of glycosaminoglycans. The structure of
this polysaccharide, with adjacent N-acetylglucosamine and
2-sulfo-iduronic acid residues, also poses interesting questions about
how it is made in light of our current understanding of the
biosynthesis of heparin and heparan sulfate. This glycosaminoglycan
represents 3-5% of the dry weight of this snail's soft body
tissues, suggesting important biological roles for the survival of this
organism, and may offer new means to control this pest. Snail
glycosaminoglycan tightly binds divalent cations, such as copper(II),
suggesting a primary role in metal uptake in the snail. Finally, this
new polysaccharide might be applied, like the Escherichia coli K5 capsular polysaccharide, to the study of glycosaminoglycan
biosynthesis and to the semisynthesis of new glycosaminoglycan analogs
having important biological activities.

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Copyright © 1996 by the American Society for Biochemistry and Molecular Biology.
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