Skip to main content
Log in

Paramylon (β-1,3-glucan) content in wild type and WZSL mutant of Euglena gracilis. Effects of growth conditions

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

Abstract

The effects of growth conditions on paramylon (a β-1,3-glucanreserve carbohydrate) content were examined in the photosyntheticwild-type and a spontaneous non-photosynthetic WZSL mutant of theunicellular flagellate Euglena gracilis. This carbohydrate is known toshow interesting applications in human and veterinary medicine, asimmunostimulant and immunopotentiator. For both strains, the synthesisof reserve depends mainly on the growth conditions, i.e. light or dark. Thehighest amount of paramylon is accumulated by the mutant (90% dryweight) under dark conditions and with glucose as the carbon source. Thesefindings are discussed in terms of feasibility of exploitation of both strainsas an alternative source of β-glucan, and of the importance of thechloroplast compartment in the synthesis of this compound.

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

References

  • Anderson DP, Siwicki AK (1994) Duration of protection against Aeromonas salmonicida in brook trout immunostimulated with glucan or chitosan by injection or immersion. Progres. Fish-Cult. 56: 258-261.

    Google Scholar 

  • Barras DR, Stone BA (1968) Carbohydrate composition and metabolism in Euglena. In Buetow DE (ed.), The Biology of Euglena, vol. II, Biochemistry. Academic Press, New York, pp. 149-191.

    Google Scholar 

  • Barsanti L, Bastianini A, Passarelli V, Tredici MR, Gualtieri P (2000) Fatty acid pattern in wild type and WZSL mutant of Euglena gracilis. Effects of carbon sources and growth conditions. J. appl. Phycol. 12.

  • Bates RC, Hulbert RE (1970) The effect of acetate on Euglena gracilis var. bacillaris as a function of environmental conditions. J. Protozool. 17: 134-138.

    Google Scholar 

  • Chen D, Ainsworth AJ (1992) Glucan administration potentiates immune defence mechanisms of channel catfish, Ictalurus punctatus Rafinesque. J. Fish Dis. 15: 295-304.

    Google Scholar 

  • Cramer M, Myers J (1952) Growth and photosynthetic characteristics of Euglena gracilis. Arch. Mikrobiol. 17: 384-402.

    Google Scholar 

  • Dwyer MR, Smillie RM (1970) A light-induced β-1,3-glucan breakdown associated with the differentiation of chloroplasts in Euglena gracilis. Biochim. Biophys. Acta 216: 392-401.

    Google Scholar 

  • Efthimiou S (1996) Dietary intake of β-1,3/1,6 glucans in juvenile dentex (Dentex dentex), Sparidae: effects on growth performance, mortalities and non-specific defence mechanisms. J. appl. Ichthyol. 12: 1-7.

    Google Scholar 

  • Eshleman JN, Danforth WF (1964) Some characteristics of ethanol metabolism in Euglena gracilis var. bacillaris. J. Protozool. 11: 394-399.

    Google Scholar 

  • Fruehauf JP, Bonnard GD, Herberman RB (1983) The effect of lentinan on production of interleukin-1 by human monocytes. Immunopharmacol. 5: 65-74.

    Google Scholar 

  • Gottlieb J (1850) Ueber eine neue, mit Starkmehl isomere Substanz. Ann Chem Pharm 75: 51-61.

    Google Scholar 

  • Gualtieri P, Barsanti L, Passarelli V, Verni F, Rosati G (1990) A look into the reservoir of Euglena gracilis: SEM investigations of the flagellar apparatus. Micr. Microsc. Acta 21: 131-138.

    Google Scholar 

  • Hayashi M, Toda K, Yoneji T, Sato O, Shozaburo K (1993) Dietary value of rotifers and Artemia enriched with Euglena gracilis for red sea bream. Nippon Suisan Gakkaishi 59: 1051-1058.

    Google Scholar 

  • Jeney D, Anderson DP (1993) Glucan injection or bath exposure given alone or in combination with a bacterin enhance the non-specific defence mechanism in rainbow trout (Oncorhyncus mykiss). Aquaculture 116: 315-329.

    Google Scholar 

  • Jorgensen JB, Robertsen B (1995) Yeast β-glucan stimulates respiratory burst activity of Atlantic salmon (Salmo salar L.) macrophages. Develop. Comp. Immunol. 19: 43-57.

    Google Scholar 

  • Kitaoka S, Hosotani K (1977) Studies on culture conditions for the determination of the nutritive value of Euglena gracilis protein and the general amino acid composition of the cells. Nogei-kagaku 51: 477-482.

    Google Scholar 

  • Koizumi N, Sakagami H, Utsumi A, Fujinaga S, Takeda M (1993) Anti-HIV (human immunodeficiency virus) activity of sulfated paramylon. Antiv. Res. 21: 1-14.

    Google Scholar 

  • Kondo Y, Kato A, Hojo H, Nozoe S, Takeuchi M, Ochi K (1992) Cytokine-related immunopotentiating activities of paramylon, a β-1,3-D-glucan from Euglena gracilis. J. Pharmacobio-Dyn. 15: 617-621.

    Google Scholar 

  • Kusmic C, Barsacchi R, Barsanti L, Gualtieri P, Passarelli V (1999) Euglena gracilis as source of the antioxidant vitamin E. Effects of culture conditions in the wild strain and in the natural mutant WZSL. J appl. Phycol. 10: 555-559.

    Google Scholar 

  • Murakami T, Ogawa H, Hayashi M, Yoshizumi H (1988) Effect of Euglena cells on blood pressure, cerebral and peripheral vascular changes and life-span in stroke-prone spontaneously hypertensive rats. J. Jpn. Soc. Nutr. Food Sci. 41: 115-125.

    Google Scholar 

  • Osumi M (1998) The ultrastructure of yeast: cell wall structure and formation. Micron 29: 207-233.

    Google Scholar 

  • Quesada LA, De Lustig ES, Marechal LR, Belocopitow E (1976) Antitumor activity of paramylon on sarcoma-180 in mice. Gann 67: 455-459.

    Google Scholar 

  • Rosati G, Barsanti L, Passareli V, Giambelluca A, Gualtieri P (1996) Ultrastructure of a novel non-photosynthetic Euglena mutant. Micron 27: 367-373.

    Google Scholar 

  • Schwartzbach SD, Schiff JA, Neil HD (1975) Events surroundings the early development of Euglena chloroplasts. V. Control of paramylon degradation. Plant Physiol. 56: 313-317.

    Google Scholar 

  • Sugawara I, Lee KC, Wong M (1984) Shizophyllan (SPG)-treated macrophages and anti-tumour activities against syngeneic and allogeneic tumour cells. I. Characteristics of SPG-treated macrophages. Cancer Immunol. Immunother. 16: 137-144.

    Google Scholar 

  • Sung HH, Kou GH, Song YL (1994) Vibriosis resistance induced by glucan treatment in tiger shrimp (Penaeus monodon) Fish Pathology 29: 11-17.

    Google Scholar 

  • Takeyama H, Kanamaru A, Yoshino Y, Kakuta H, Kawamura Y, Matsunaga T (1997) Production of antioxidant vitamins, β-carotene, vitamin C, vitamin E, by two-step culture of Euglena gracilis Z. Biotech. Bioengng 53: 185-190.

    Google Scholar 

  • Wang L, Behr SR, Newman RK, Newman CW (1997) Comparative cholesterol-lowering effects of barley β-glucan and barley oil in golden syrian hamsters. Nutrition Res. 17: 77-88.

    Google Scholar 

  • Wood PJ (1994) Evaluation of oat bran as a soluble fibre source. Characterization of oat β-glucan and its effects on glycaemic response. Carb. Pol. 25: 331-336.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Barsanti, L., Vismara, R., Passarelli, V. et al. Paramylon (β-1,3-glucan) content in wild type and WZSL mutant of Euglena gracilis. Effects of growth conditions. Journal of Applied Phycology 13, 59–65 (2001). https://doi.org/10.1023/A:1008105416065

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1008105416065

Navigation