Abstract
An hypothesis is presented that provitamin D (dehydrocholesterol and/or ergosterol) can act as a UV-B receptor in plants and algae. We also propose that the proportions between provitamins D, previtamins D, and vitamins D (D2 and D3), after calibration, can be used to evaluate UV-B exposure of phytoplankton and terrestrial vegetation.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Preview
Unable to display preview. Download preview PDF.
References
Arami, S., Hada, M. & Tada, M. 1997a. Near-UV-induced absorbance change and photochemical decomposition of ergosterol in the plasma membrane of the yeast Saccharornvice.s cerevesiae. Microbiology 143: 1665–1671.
Arami, S., Hada, M. & Tada, M. 1997b. Reduction of ATPase activity accompanied by photodecomposition of ergosterol by near-UV irradiation in plasma membranes prepared from Saccharomvices cerevesiae. Microbiology 143: 2465–2471.
Beggs, C. J. & Welhnann, E. 1994. Photocontrol of flavonoid biosynthesis. pp. 733–751. In: Kendrick, R. E. & Kronenberg, G. H. M. (eds), Photomorphogenesis in Plants, 2nd ed. Kluwer Academic Publishers, Dordrecht.
Björn, L. O. 1999. UV-B effects: Receptors and targets. pp. 793–803. In: Singhal, G. S. et al. (cds), Concepts of Photobiology. Narosa Publishing House, New Delhi.
Buchala, A. J. & Schmid, A, 1979. Vitamin D and its analogues as a new class of plant growth substances affecting rhizogencsis. Nature 280: 230–231.
Buchala, A. J. & Pythoud, F. 1988. Vitamin D and related compounds as plant growth substances. Physiol. Plant. 74: 391–396.
Buddecke, E. 1980. Grundriss der Biochemie ( 6. Aufl.). W. De Gruyter, Berlin.
Buffenstein, R., Skinner, D. C.. Yahav, S. D.. Mooilley, G. P., Cavaleros, M.. Zachcn, D., Ross, F. P. & Pettifor, J. M. 1991. Effect of oral cholecalciferol supplementation at physiological and supraphysiological doses in naturally vitamin D3 deficient subterranean damara mole rats (Crvptomvs damarensis). J. Endocrinol. 131: 197–202.
Cheplick, G. P. & Clay, K. 1988. Acquired chemical defenses of grasses: the role of fungal endophytes. Oikos 52: 309–318.
Clay, K. 1990. Fungal endophytes of grasses. Annu. Rev. Ecol. Syst. 21: 275–297.
Curino, A., Skliar, M. & Boland, R. 1998. Identification of 7-dehydrocholesterol, vitamin D3, 25(OH)-vitamin D3 and I.25(OH)2-vitamin D3 in Solarium g1aueophv1lum cultures grown in absence of light. Biochim. Biophys. Acta 1425: 485–492.
Feldman, D., Glorieux, F. H. & Pike, J. W. (eds) 1997. Vitamin D. Academic Press, New York.
Fries, L. 1984. D-vitamins and their precursors as growth regulators in axenically cultivated marine macroalgae. J. Phycol. 20: 62–66.
Galkin, O. N. & Terenetskaya, I.P. 1999. ‘Vitamin D’ biodosimeter: basic characteristics and potential applications. J. Photochem. Photobiol. B: Biol. 53: 12–19.
Gershengorn, M. C., Smith, A. R. H., Goulston, G., Goad, T.. J., Goodwon, T. W. & Haines, T. H. 1968. The sterols of Ochromona.s danica and Ochromonas malhamensis. Biochemistry 7: 1698–1706.
Gessner, M. O. & Schmitt, A. J. 1996. Use of solid-phase extraction to determine ergosterol concentrations in plant tissue colonized by fungi. Appt. Environ. Microbiol. 62: 415–419.
Grandmougin-Ferjani, A., Schuler-Muller, I. & Hartmann, M.-A. 1997. Sterol modulation of the plasma membrane H+-ATPase activity from corn roots reconstituted into soybean lipids. Plant Physiol. 113: 163–174.
Hannach, G. & Sigleo, A. C. 1998. Photoinduction of UV-absorbing compounds in six species of marine phytoplankton. Mar. Ecol. Progr. Ser. 174: 207–222.
Havinga, E. 1973. Vitamin D, example and challenge. Experientia 29: 1181–1193.
Hess, A. F. & Weinstock, M. 1924. Antirachitic properties imparted to inert fluids and green vegetables by ultraviolet radiation. J. Biol. Chem. 62: 301–313.
Holick, M. F. 1989. Phylogenetic and evolutionary aspects of vitamin D from phytoplankton to humans. pp. 7–43. In: Pang, P. K. T. & Schreibman, M. P. (eds), Vertebrate Endocrinology: Fundamentals and Biomedical Implications, volume 3. Regulation of Calcium and Phosphate. Academic Press, New York.
Holick, M. F. (ed.) 1999. Vitamin D: Molecular Biology, Physiology, and Clinical Applications (Nutrition and Health). Humana Press, Totowa, NJ 07512.
Horst R. L., Reinhard(T. A., Russell J. R. & Napoli J. L. 1984. The isolation of vitamin D) and vitamin D3 from Medicago satira (alfalfa plant). Arch. Biochcm. Biophys. 231: 67–71.
Hsiao, K. C. & Björn, L. O 1982. Aspects of photoinduction and carotenogenesis in the fungus Verticittiurtr agaricinurr. Physiologia Plantarum 54: 235–238.
Imbrie, C. W. & Murphy, T. M. 1982. UV-action spectrum (254–405 nm) for inhibition of a K+-stimulated adenosine triphosphatase from the plasma membrane of Rosa damascctrn. Photochem. Photobiol. 36: 537–542.
Imbrie, C. W. & Murphy, T. M. 1984. Photoinactivation of detergent-solubilized plasma membrane ATPase from Rosa darer ascena. Plant Physiol. 74: 617–621.
Jarvis, B. C. & Booth, A. 1981. Influence of indole-butyric acid, boron, sera -inositol, vitamin D2 and seedling age on adventitious root developmant in cuttings of Phaseolus aureus. Physiol. Plant. 53: 213–218.
MacLaughlin, J. A., Anderson, R. R. & Holick, M. F. 1982. Spectral character of sunlight modulates photosynthesis of previtamin D3 and its photoisomers in human skin. Science 216: 1001–1003.
Mellanby, E. 1918. The part played by an `accessory factor’ in the production of experimental rickets. J. Physiol. (London) 52: 11–14.
Moncousin, C. & Gaspar, T. 1983. Peroxidase as a marker for rooting improvement of Cvnara scolvmus L. cultured in vitro. Biocherr. Physiol. Pflanzen 178: 263–271.
Napoli J. L., Reeve L. E., Eisman J. A., Schnoes, H. K. & DeLuca, H. F. 1977. Solanum glaucophyllum as source of I,25-dihydroxyvitamin D3. J. Biol. Chem. 252: 2580–2583.
Nevo, E. 1995. Mammalian evolution underground. The ecological- genetic-phenetic interfaces. Acta Theriologica, Suppl. 3: 9–31.
Newsham, K. K., Lewis. G. C., Greenshade, P. D. & McLeod, A. R. 1998. Neotyphodium lolii, a fungal endophyte, reduces the fertility of Lolimn perenne exposed to elevated UV-B radiation. Ann. Bot. 81: 397–403.
Norman, T. C., Norman, A. W. 1993. Consideration of chemical mechanisms for the nonphotochemical production of vitamin D3 in biological systems. Bioorganic Med. Chem. Lett. 3: 1785–1788.
Patterson, G. W. 1971. The distribution of sterols in algae. Lipids 6: 120–127.
Patterson, G. W. 1974. Sterols of some green algae. Comparative Biochem. Physiol. 47B: 453–457.
Pfoerter, K. & Weber, J. P. 1972. Photochcmic der Vitamin D-Rcihe. 1. Kinetik und Quantenausbeuten der Ergosterinhestrahlung hei L=253,4 nm. Helvetica Chimica Acta 55: 921–937.
Pitcher, T. & Buffenstein, R. 1995. Intestinal calcium transport in mole-rats (Cryptomys darnarensis and Heterocephalus glaber) is independent of both genomic and non-genomic vitamin D mediation. Exp. Physiol. 80: 597–608.
Pitcher. T., Buffenstein, R., Keegan, J. D., Moodley, G. P. & Yahav, S. 1992. Dietary calcium content, calcium balance and mode of uptake in a subterranean mammal, the damara mole-rat. J. Nutrition 122: 108–114.
Pitcher, T., Sergeev, I. N. & Buffenstein, R. 1994. Vitamin D metabolism in the damara mole-rat is altered by exposure to sunlight, yet mineral metabolism is unaffected. J. Endocrinolol. 143: 367–374.
Pitcher, T., Pettifor, J. M. & Buffenstein, R. 1994. The effect of dietary calcium content and oral vitamin D3 supplementation on mineral homeostasis in a subterranean mole-rat, Cryptomys damaren.ris. Bone Mineral. 27: 145–157.
Portwich, A. & Garcia-Pichel, F. 2000. A novel prokaryotic UVB photoreceptor in the cyanobacterium Chlorogloeopsis PCC 6912. Photochem. Photohiol. 71: 493–498.
Pottier, R. H. & Russell, D. A. 1991. Quantum yield of a photochemical reaction. pp. 45–57. In: Valenzano, D. P., Pottier, R. H., Mathis, P., Douglas, R. H. (eds) Photobiological Techniques. Plenum Press, New York, pp. xiv+381.
Prema, T. P. & Raghuramulu, N. 1994. Free vitamin D3 metabolites in Cestrum diurnum leaves. Phytochemistry 37: 677–681.
Prema, T. P. & Raghuramulu, N. 1996. Vitamin D3 and its metabolites in the tomato plant. Phytochemistry 42: 617–620.
Rambeck W. A., Kreutzberg O., Bruns-Droste C. & Zucker, H. 1981. Vitamin D-like activity of Trisetum flavescens. Z. Pllanzenphysiol. 104: 9–16.
Redlin, S. C. & Carris, L. M. (eds) 1996. Endophytic fungi in grasses and woody plants: Systematics, ecology and evolution. The American Phytopathological Association (APS Press), St. Paul, Minnesota.
Schuler, I., Milon, A., Nakatani, Y., Ourisson, G., Albrecht, A.-M., Beneviste, P. & Hartmann, M.-A. 1991. Differential effects of plant sterols on water permeability and on acyl chain ordering of soybean phosphatidylcholine hilayers. Proc. Nat. Acad. Sci. USA 88: 6926–6930.
Siegel, M. C., Latch, G. C.M. & Johnson, M. C. 1987. Fungal endophytes of grasses. Annu. Rev. Phytopathol. 25: 293–315.
Steenbock, H. & Black, A. 1924. The induction of growth-promoting and calcifying properties in a ration by exposure to ultra-violet light. J. Biol. Chem. 61: 405–422.
Stem, A. I., Schiff, J. A. & Klein, H. P. 1960. Isolation of ergosterol from Euglena graeilis; distribution among mutant strains. J. Protozool. 7: 52–55.
Sugisaki, N., Welcher, M. & Monder, C. 1974. Lack of vitamin D3 synthesis by goldfish (Carassius auratus L.). Comp. Biochem. Physiol. 49B: 647–653.
Sunita Rao, D. & Raghuramulu, N. 1996a. Food chain as origin of vitamin Din fish. Comp. Biochem. Physiol. 1 14A: 15–19.
Sunita Rao, D. & Raghuramulu, N. 1996b. Lack of vitamin D3 synthesis in Tilapia mossamhica from cholesterol and acetate. Comp. Biochem. Physiol. 114A: 21–25.
Wasserman R. H. 1975. Vitamin D-like substances in Solammm malacoxvlon and other calcinogenic plants. Nutr. Rev. 33: 1–5.
Wasserman, R. H., Henion, J. D., Haussier, M. R. & McCain, T. A. 1976. Calcinogenic factor in Solarium malac2rylon: Evidence that it is 1,25-dihydroxyvitamin D3-glycoside. Science 194: 853–855.
Webb, A. R., Kline, L. & Holick, M. F. 1988. Influence of season and latitude on on the cutaneous synthesis of vitamin D3: Exposure to winter sunlight in Boston and Edmonton will not promote vitamin D3 synthesis in human skin. J. Clin. Endocrinol. Metabolism 67: 373–378.
Zucker, H., Stark, H. & Rambeck, W. 1980. Light-dependent synthesis of cholecalciferol in a green plant. Nature 283: 68–69.
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2001 Springer Science+Business Media Dordrecht
About this chapter
Cite this chapter
Björn, L.O., Wang, T. (2001). Is provitamin D a UV-B receptor in plants?. In: Rozema, J., Manetas, Y., Björn, LO. (eds) Responses of Plants to UV-B Radiation. Advances in Vegetation Science, vol 18. Springer, Dordrecht. https://doi.org/10.1007/978-94-017-2892-8_1
Download citation
DOI: https://doi.org/10.1007/978-94-017-2892-8_1
Publisher Name: Springer, Dordrecht
Print ISBN: 978-90-481-5353-4
Online ISBN: 978-94-017-2892-8
eBook Packages: Springer Book Archive