Further data on the structure of brown seaweed fucans: relationships with anticoagulant activity

被引:251
作者
Chevolot, L
Foucault, A
Chaubet, F
Kervarec, N
Sinquin, C
Fisher, AM
Boisson-Vidal, C
机构
[1] IFREMER, Unite Rech Marine 2, F-44311 Nantes, France
[2] IFREMER, Lab Biochim & Mol Marines, F-44311 Nantes, France
[3] Univ Paris 13, Unite Rech Marine 2, F-93430 Villetaneuse, France
[4] Univ Paris 13, UMR CNRS 7540, Lab Rech Macromol, F-93430 Villetaneuse, France
[5] Univ Bretagne Occidentale, Serv RMN, F-29285 Brest, France
[6] Hop Necker Enfants Malad, Hematol Lab, F-75743 Paris, France
关键词
fucan structure; fucan NMR; anticoagulant activity; brown seaweed;
D O I
10.1016/S0008-6215(99)00127-5
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 composition, molecular weight (MW), anticoagulant activity and nuclear magnetic resonance spectra of various low-molecular-weight fucans (LMWFs) obtained by partial hydrolysis or radical depolymerization of a crude fucoidan extracted from the brown seaweed Ascophyllum nodosum are compared. Fucose units were found mainly sulfated at O-2, to a lesser extent at O-3, and only slightly at O-4, contrary to previously published results for fucoidans from other brown seaweeds, and fucose 2, 3-O-disulfate residues were observed for the first time. As the sulfation pattern excluded an alpha-(1 --> 2)-linked fucose backbone and a high proportion of alpha-(1 --> 4) linkages was found, it would appear that the concept of fucoidan structure needs to be revised. Anticoagulant activity is apparently related not only to MW and sulfation content, as previously determined, but also (and more precisely) to 2-O-sulfation and 2,3-O-disulfation levels. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:154 / 165
页数:12
相关论文
共 36 条
  • [1] Sulfated polysaccharides from the egg jelly layer are species-specific inducers of acrosomal reaction in sperms of sea urchins
    Alves, AP
    Mulloy, B
    Diniz, JA
    Mourao, PAS
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (11) : 6965 - 6971
  • [2] CARRAGEENANS .4. VARIATIONS IN STRUCTURE AND GEL PROPERTIES OF KAPPA-CARRAGEENAN AND CHARACTERISATION OF SULPHATE ESTERS BY INFRARED SPECTROSCOPY
    ANDERSON, NS
    DOLAN, TCS
    PENMAN, A
    REES, DA
    MUELLER, GP
    STANCIOF.DJ
    STANLEY, NF
    [J]. JOURNAL OF THE CHEMICAL SOCIETY C-ORGANIC, 1968, (05): : 602 - &
  • [3] BOISSON-VIDAL C, 1991, Drugs of the Future, V16, P539
  • [4] Boisson-Vidal C., 1995, Drugs of the Future, V20, P1237
  • [5] BRUHN T, 1995, P 8 INT S MAR NAT PR, P230
  • [6] INFRARED-ABSORPTION AND RAMAN-SCATTERING OF SULFATE GROUPS OF HEPARIN AND RELATED GLYCOSAMINOGLYCANS IN AQUEOUS-SOLUTION
    CABASSI, F
    CASU, B
    PERLIN, AS
    [J]. CARBOHYDRATE RESEARCH, 1978, 63 (JUN) : 1 - 11
  • [7] Preliminary report on fractionation of fucans by ion-exchange displacement centrifugal partition chromatography
    Chevolot, L
    Colliec-Jouault, S
    Foucault, A
    Ratiskol, J
    Sinquin, C
    [J]. JOURNAL OF CHROMATOGRAPHY B, 1998, 706 (01): : 43 - 54
  • [8] A LOW-MOLECULAR-WEIGHT FUCOIDAN FRACTION FROM THE BROWN SEAWEED PELVETIA-CANALICULATA
    COLLIEC, S
    BOISSONVIDAL, C
    JOZEFONVICZ, J
    [J]. PHYTOCHEMISTRY, 1994, 35 (03) : 697 - 700
  • [9] COLLIEC S, 1994, Patent No. 5321133
  • [10] CONTRERAS RR, 1988, CARBOHYD RES, V179, P411