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Chain conformation and bioactivity of water‐soluble polysaccharide extracted from Rhizoma Panacis Japonici
Author(s) -
Huang Zhiping,
Ren Haibo,
Duan Xiaobo,
Zhang Lina
Publication year - 2010
Publication title -
biopolymers
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.556
H-Index - 125
eISSN - 1097-0282
pISSN - 0006-3525
DOI - 10.1002/bip.21364
Subject(s) - chemistry , radius of gyration , aqueous solution , intrinsic viscosity , dispersity , size exclusion chromatography , polysaccharide , chromatography , hydrodynamic radius , analytical chemistry (journal) , crystallography , polymer , nuclear chemistry , polymer chemistry , organic chemistry , micelle , enzyme
A water‐soluble α‐(1→4)‐ D ‐glucan heteropolysaccharide with 37% degree of branch extracted by base from Rhizoma Panacis Japonici , coded as RPS3, was fractionated into six fractions by the method of nonsolvent addition. Their weight‐average molecular mass ( M w ), polydispersity index ( M w / M n ), and radius of gyration (〈 s 2 〉 z 1/2 ) were determined with laser light scattering (LLS) and size exclusion chromatography combined with LLS. The structure of the fraction was determined by methylation analyses and 13 C NMR. The dependences of intrinsic viscosity ([η]) and 〈 s 2 〉 z 1/2 on M w were established as [η] = 0.71 M w 0.27 ± 0.01 (cm 3 /g) and 〈 s 2 〉 z 1/2 = 1.53 M w 0.27 ± 0.02 (nm) in the M w range from 5.62 × 10 4 to 3.05 × 10 6 (g/mol) for RPS3 in 0.15 M NaCl aqueous solution at 25°C. On the basis of the current theory of the polymer solution, the fractal dimension ( d f ), unperturbed chain dimension ( A ), and characteristic ratio ( C ∞ ) were calculated to be 3.0, 1.48 Å, and 15.1, respectively. The results revealed that the RPS3 chains existed as spherical conformation in the aqueous solution. Transmission electron microscope further provided the evidence of the sphere shape of the RPS3 and its fractionated molecules in water. In vitro cytotoxicity assay indicated that the fractions could inhibit the tumor cells and showed no harm to normal cells at low dose. The bioactivity was relative with molecular mass of the samples. © 2010 Wiley Periodicals, Inc. Biopolymers 93: 383–390, 2010. This article was originally published online as an acceptedpreprint. The “Published Online” date corresponds to the preprint version. You can request a copy of the preprint by emailing the Biopolymers editorial office atbiopolymers@wiley.com
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