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Search: WFRF:(Qi F.) > (2000-2004)

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  • Zhang, L. N., et al. (author)
  • Solution properties of antitumor sulfated derivative of alpha-(1 -> 3)-D-glucan from Ganoderma lucidum
  • 2000
  • In: Bioscience, biotechnology and biochemistry. - : Oxford University Press (OUP). - 0916-8451 .- 1347-6947. ; 64:10, s. 2172-2178
  • Journal article (peer-reviewed)abstract
    • Four fractions of a water-insoluble alpha-(1-->3)-D-glucan GL extracted from fruiting bodies of Ganoderma lucidum were dissolved in 0.25 M LiCl/DMsO, and then reacted with sulfur trioxide-pyridine complex at 80 degreesC to synthesize a series of water-soluble sulfated derivatives S-GL. The degree of substitution of DS was measured by using IR infrared spectra, elemental analysis, and C-13 NMR to be 1.2-1.6 in the non-selective sulfation. Weight-average molecular weight M, and intrinsic viscosity [eta] of the sulfated derivatives S-GL were measured by multi-angle laser light scattering and viscometry. The M-w value (2.4 x 10(4)) of sulfated glucan S-GL-1 was much lower than that (44.5 x 10(4)) of original alpha-(1-->3)-D-glucan GL-1. The Mark-Houwink equation and average value of characteristic ratio C-infinity for the S-GL in 0.2 M NaCl aqueous solution at 25 degreesC were found to be: [eta] =1.32 x 10(-3) M-w(1.06) (cm(3) g(-1)) and 16, respectively, in the M-w range from 1.1 x 10(4) to 2.4 x 10(4). It indicated that the sulfated derivatives of the alpha-(1-->3)-D-glucan in the aqueous solution behave as an expanded chain, owing to intramolecular hydrogen bonding or interaction between charge groups. Interestingly, two sulfated derivatives synthesized from the alpha-(1-->3)-D-glucan and curdlan, a beta-(1-->3)-D-glucan, all had significant higher antitumor activity against Ehrlich ascites carcinoma (EAC) than the originals. The effect of expanded chains of the sulfated glucan in the aqueous solution on the improvement of the antitumor activity could not be negligible.
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4.
  • Zhang, L. N., et al. (author)
  • Triple helix of beta-D-glucan from Lentinus Edodes in 0.5 M NaCl aqueous solution characterized by light scattering
  • 2001
  • In: Polymer journal. - : Springer Science and Business Media LLC. - 0032-3896 .- 1349-0540. ; 33:4, s. 317-321
  • Journal article (peer-reviewed)abstract
    • beta-(1 -->3)-D-glucan with (1 -->6) branching (L-FV-I) from Lentinus edodes in water was degraded into seven fractions of different molecular weights by ultrasonic irradiation. Weight-average molecular weight M,, radius of gyration (1/2)(5) and intrinsic viscosity [eta] of the beta -D-glucan and its fractions in 0.5 M NaCl aqueous solution and dimethylsulfoxide (DMSO) were studied by multi-angle laser light scattering (MALLS), GPC combined with MALLS, and viscometry. M, dependence of [eta] for the glucan in 0.5 M NaCl aqueous solution was represented approximately by [eta] =7.69 x 10(-6) M-w(1.32) (cm(3) g(-1)) at M-w from 1.87 X 10(5) to 1.20 X 10(6) at 25 degreesC. GPC chromatograms of the glucans in aqueous solution contained two peaks, a main peak corresponding to triple-stranded chains with molecular weight M-w,M-m, and small second peak corresponding to fragments of single chains with M-w,M-s (about 20 +/-5% content). Analysis of M-w,M-m and (1/2)(z,m) in term of the known theory for wormlike chains yielded 2180 +/- 100 nm(-1), 120 +/- 10 nm and 0.31 nm for molar mass per unit contour length M-L, persistence length q, and contour length h per main-chain glucose residue, respectively, which agree closely with theory data of triple-helical chains and reported parameters for triple-helix schizophyllan in 0.01 M NaOH aqueous solution. The ratios of M-w,M-m, in 0.5 M NaCl to M, in DMSO were calculated to be roughly 3. The predominant species of the glucan in 0.5 M NaCl aqueous solution exist as triple-helical chains with high rigidity, and in DMSO as single-flexible chains.
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5.
  • Zhang, L., et al. (author)
  • Transition from triple helix to coil of Lentinan in solution measured by SEC, viscometry, and C-13 NMR
  • 2002
  • In: Polymer journal. - : Springer Science and Business Media LLC. - 0032-3896 .- 1349-0540. ; 34:6, s. 443-449
  • Journal article (peer-reviewed)abstract
    • Lentinan, beta-(1 --> 3)-D-glucan with (1 --> 6) branching, was isolated from Lentinus edodes. Weight-average molecular weight M-w radius of gyration < s(2) > (1/2) and intrinsic viscosity [eta] of Lentinan in 0.2 M NaCl aqueous solution, dimethylsulfoxide (DMSO) and water/DMSO mixtures were measured by light scattering (LS), size exclusion chromatography (SEC) combined with LS, and viscometry. The results indicated that the glucan exists mainly as triple-helical chains in 0.2 M NaCl aqueous solution and water/DMSO mixtures with over 20 wt% water content, and as single-flexible chain in DMSO. The data from SEC-LS, viscosity and C-13 NMR measurements proved strongly that the helix-coil conformation transition occurred in a narrow range from 80 to 85 wt% DMSO aqueous solution, accompanying with obvious changes of M-w, < s(2) >(1/2)(z), [eta] as well as signals of C6 and C6(s). The transition of Lentinan in water/DMSO mixture was irreversible. The difference in C-13 NMR spectra for the triple-helical and coil conformations was the disappearance of the signals of C3 in beta-(1 --> 3)- linked backbone and the enhancement in relative intensities of glucose substituted C6s in the helix state, as well as the appearance of an asymmetric and broad peak of C6 in the intermediate of the conformation change. This suggests that the immobilization of the backbone by binding with intra and intermolecular hydrogen bonds resulted in the loss of the signals of its carbon atoms in the triple helix state. An overcoating cylinder model composed of the beta-(1 --> 3)- linked backbone as helix core and the side chains as rotatable overcoat was proposed to illustrate the triple-helical conformation and its transition in the solution.
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