Skip to main content
Log in

Antioxidant activity of different molecular weight sulfated polysaccharides from Ulva pertusa Kjellm (Chlorophyta)

  • Published:
Journal of Applied Phycology Aims and scope Submit manuscript

Abstract

Polysaccharides extracted from Ulva pertusa Kjellm (Chlorophyta) are a group of sulfated heteropolysaccharides, the ulvans. In this study, different molecular weight ulvans were prepared by H2O2 degradation and their antioxidant activities investigated including superoxide and hydroxyl radical scavenging activity, reducing power and metal chelating ability. The molecular weights of natural and degraded ulvans were 151.7, 64.5, 58.0, and 28.2 kDa, respectively, as determined by high performance gel permeation chromatography. Among the four samples, U3 (the lowest molecular weight sample) showed significant inhibitory effects on superoxide and hydroxyl radicals with IC50 values of 22.1 μ g mL−1 and 2.8 mg mL−1; its reducing power and metal chelating ability were also the strongest among the four samples. All the other samples also demonstrated strong activity against superoxide radicals. The results indicated that molecular weight had a significant effect on the antioxidant activity of ulvan with low molecular weight ulvan having stronger antioxidant activity.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Abbreviations

U:

polysaccharide extracted from U. pertusa (ulvan, Mw, 151.7 kDa)

U1 :

degraded ulvan of molecular weight 64.5 kDa

U2 :

degraded ulvan of molecular weight 58.0 kDa

U3 :

degraded ulvan of molecular weight 28.2 kDa

NBT:

nitro blue tetrazolium

PMS:

phenazine methosulfate

NADH:

nicotinamide adenine dinucleotide-reduced

EDTA:

ethylene diamine tetra-acetic acid

TCA:

trichloroacetic acid

TBA:

thiobarbituric acid

DR:

deoxyribose

HPGPC:

high performance gel permeation chromatography

GC:

gas liquid chromatography

References

  • Chen H, Wang K (1997) Function and structure of glycoconjugates. Shanghai University Press, Shanghai, China, 341pp. (in Chinese).

    Google Scholar 

  • Chen HX, Zhang M, Xie BJ (2005) Components and antioxidant activity of polysaccharide conjugate from green tea. Food Chem. 90: 17–21.

    Article  CAS  Google Scholar 

  • Cheng S, Wang JW, Fang L, Gao XD, Tan RX (2004) Free radical scavenging and antioxidant activities of EPS2, an exopolysaccharide produced by a marine filamentous fungus Keissleriella sp. YS 4108. Life Sci. 75: 1063–1073.

    Article  CAS  Google Scholar 

  • Colliec S, Boisson-Vidal C, Jozefonvicz J (1994) A low molecular weight fucoidan fraction from the brown seaweed Pelvetia canaliculata. Phytochem. 35: 697–700.

    Article  CAS  Google Scholar 

  • Council of Chinese Pharmacopoeia (1995) Chinese Pharmacopoeia. Chemistry Industry Press, Beijing, China. 36pp (in Chinese)

  • Dahl MK, Richardson T (1978) Photogeneration of superoxide anion in serum of bovine milk and in model systems containing riboflavin and amino acids. J. Dairy Sci. 61: 400-407.

    Article  Google Scholar 

  • Ferial HB, Mosstafa E, Corinne S, Catherine BV (2000) Relationship between sulfate group and biological activities of fucans. Thromb. Res. 100: 453–459.

    Article  Google Scholar 

  • Gordon MH (1990) The Mechanism of Antioxidant Action in vitro. In: Hudson BJF (ed.), Food Antioxiants. Elsevier Applied Science, London and New York. pp. 1–18.

    Google Scholar 

  • Halliwell B, Gutteridge JMC, Aruoma OI (1987) The deoxyribose method: A simple “test-tube” assay for determination of rate constants for reactions of hydroxyl radicals. Anal. Biochem. 165: 215–219.

    Article  PubMed  CAS  Google Scholar 

  • Halliwell B, Gutteridge JM, Cross CE (1992) Free radicals, antioxidants, and human disease: Where are we now? J. Lab. Clin. Med. 119: 598–620.

    CAS  Google Scholar 

  • Hettiarachchy NS, Glenn KC, Ghanasambandan R, Johnson MG (1996) Natural antioxidant extract from fenugreek (Trigonella foenumgraecum) for ground beef patties. J. Food Sci. 61: 516–519.

    Article  CAS  Google Scholar 

  • Hultin HO (1992) Lipid Oxidation in Muscle Foods via Redox Iron. In Angelo AJ (ed.) Lipid oxidation in food. American Chemical Society, Washington. pp. 105–113.

    Google Scholar 

  • Kanner J (1990) Nitric oxide, a super antioxidant. Free Radical Biol. Med. 9 (Suppl): 15.

    Google Scholar 

  • Kawai Y, Seno N, Anno K (1969) A modified method for chondrosulfatase assay. Anal. Biochem. 32: 314–321.

    Article  PubMed  CAS  Google Scholar 

  • Lahaye M (1998) NMR spectroscopic characterization of oligosaccharides from two Ulva rigida ulvan samples (Ulvales, Chlorophyta) deraded by a lyase. Carbohydr. Res. 314: 1–12.

    Article  PubMed  CAS  Google Scholar 

  • Lahaye M, Jegon D (1993) Chemical and physical-chemical characteristics of dietary fibers from Ulva lactuca (L.) Thuret and Enteromorpha compressa (L.) Grev. J. Appl. Phycol. 5: 195-200.

    Article  Google Scholar 

  • Lahaye M, Alvarez-Cable Cimadevilla E, Kuhlenkamp R, Quemener B, Lognoné V, Dion P (1999) Chemical composition and 13C-NMR spectroscopic characterisation of ulvans from Ulva(Ulvales, Chlorophyta). J. Appl. Phycol. 11: 1–7.

    Article  CAS  Google Scholar 

  • Lopes GKB, Schulman HM, Hermeslima M (1999) Polyphenol tannic acid inhibits hydroxyl radical formation from Fenton ions. Biochim. Biophys. Acta. 1472: 142–152.

    PubMed  CAS  Google Scholar 

  • Luo Q, Cai YZ, Yan J, Sun M, Corke H (2004) Hypoglycemic and hypolipidemic effects and antioxidant activity of fruit extracts from Lycium barbarum. Life Sci. 76: 137–149.

    Article  PubMed  CAS  Google Scholar 

  • Nishimiki M, Rao NA, Yagi K (1972) The occurrence of superoxide anion in the reaction of reduced phenazine methosulfate and molecular oxygen. Biochem. Biophys. Res. Commun. 46: 849–853.

    Article  Google Scholar 

  • Park PJ, Jung WK, Nam KS, Shahidi F, Kim SK (2001) Purification and characterization of antioxidative peptides from protein hydrolysate of lecithin-free egg yolk. J. Am. Oil Chem. Soc. 78: 651–656.

    Article  CAS  Google Scholar 

  • Pereira MS, Mulloy B, Mourao PAS (1999) Structure and anticoagulant activity of sulfated fucans. Comparison between the regular, repetitive, and linear fucans from echinoderms with the more heterogeneous and branched polymers from brown algae. J. Biol. Chem. 274: 7656–7667.

    Article  PubMed  CAS  Google Scholar 

  • Pin-Der D, Pin-Chan D, Gow-Chin Y (1999) Action of methanolic extract of mung bean hulls as inhibitors of lipid peroxidation and non-lipid oxidative damage. Food Chem. Toxicol. 37: 1055–1061.

    Article  Google Scholar 

  • Quemener B, Lahaye M, Bobin-Dubigeon C (1997) Sugar determination in ulvans by a chemical-enzymatic method coupled to high performance anion exchange chromatography. J. Appl. Phycol. 9: 179–188.

    Article  CAS  Google Scholar 

  • Ray B, Lahaye M (1995) Cell-wall polysaccharide from the marine green alga Ulva “rigida” (Ulvales, Chlorophyta). Extraction and chemical composition. Carbohydr. Res. 274: 251-261.

    Article  CAS  Google Scholar 

  • Shon MY, Kim TH, Sung NJ (2003) Antioxidants and free radical scavenging activity of Phellinus baumii (Phellinus of Hymenochaetaceae) extracts. Food Chem. 82: 593-597.

    Article  CAS  Google Scholar 

  • Smith C, Halliwell B, Aruoma OI (1992) Protection by albumin against the pro-oxidant actions of phenolic dietary components. Food Chem. Toxicol. 30: 483–489.

    Article  PubMed  CAS  Google Scholar 

  • Thibault JF (1979) Automatisation du dosage des substances pectiques par la méthode au méta-hydroxydiphényl. Lebensm. Wiss. Technol. 12: 247–251.

    CAS  Google Scholar 

  • Tsiapali E, Whaley S, Kalbfleisch J, Ensley HE, Browder IW, Williams DL (2001) Glucans exhibit weak antioxidant activity, but stimulate macrophage free radical activity. Free Radicals Biol. Med. 30: 393–402.

    Article  CAS  Google Scholar 

  • Wanita A, Loren L (1996) Antioxidant potential of 5-N-pentadecylresorcinol. J. Food Process. Pres. 20: 417-429.

    Article  Google Scholar 

  • Xing RE, Yu HH, Liu S, Zhang WW, Zhang QB, Li ZE, Li PC (2005) Antioxidant activity of differently regioselective chitosan sulfates in vitro. Bioorg. Med. Chem. 13: 1387–1392.

    Article  PubMed  CAS  Google Scholar 

  • Yamaguchi T, Takamura H, Matoba T, Terao J (1998) HPLC method for evaluation of the free radical-scavenging activity of foods by using 1,1-Diphenyl-2-picrylhydrazyl. Biosci. Biotechnol. Biochem. 62: 1201–1204.

    Article  PubMed  CAS  Google Scholar 

  • Yu PZ, L N, Liu XG, Zhou GF, Zhang QB, Li PC (2003a) Antihyperlipidemic effects of different molecular weight sulfated polysaccharides from Ulva pertusa (Chlorophyta). Pharmacol. Res. 48: 543–549.

    Article  CAS  Google Scholar 

  • Yu PZ, Zhang QB, Li N, Xu ZH, Wang YM, Li ZE (2003b) Polysaccharides from Ulva pertusa (Chlorophyta) and preliminary studies on their antihyperlipidemia activity. J. Appl. Phycol. 15: 21–27.

    Article  CAS  Google Scholar 

  • Zhang QB, Yu PZ, Li ZE, Zhang H, Xu Z, Li PC (2003) Antioxidant activities of sulfated polysaccharide fractions from Porphyra haitanesis. J. Appl. Phycol. 15: 305–310.

    Article  CAS  Google Scholar 

  • Zhang WJ (2003) Biochemical Technique of Glycoconjugates. Zhejiang University Press, Hangzhou, China. 38pp. (in Chinese)

    Google Scholar 

  • Zhou GF, Sun YP, Xin H, Zhang YN, Li ZE, Xu ZH (2004) In vivo antitumor and immunomodulation activities of different molecular weight lambda-carrageenans from Chondrus ocellatus. Pharmacol. Res. 50: 47–53.

    Article  PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Quanbin Zhang.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Qi, H., Zhao, T., Zhang, Q. et al. Antioxidant activity of different molecular weight sulfated polysaccharides from Ulva pertusa Kjellm (Chlorophyta). J Appl Phycol 17, 527–534 (2005). https://doi.org/10.1007/s10811-005-9003-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10811-005-9003-9

Key words

Navigation