Enhancing Biosynthesis of Flavonol Protective Biomaterials Using FLS Transgenic Plants

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Flavonol synthase (FLS) gene encodes an enzyme that is involved in conversion substrates into flavonols, quercetin and kaempferol. These substances are a subgroup of flavonoids which have an important role in both plant and human health. Many environmental factors such as temperature, pH and UV-A radiation have been studied and presented relationship with flavonoid synthesis. In this experiment, the combination of visible and UV-A lights was used as factors for elevating flavonoid biosynthesis of wild type (WT) plant and two lines of FLS transgenic plant under tissue culture condition. Both transgenic lines significantly enhanced the accumulation of quercetin and kaempferol substances nearly one fold higher than WT plant did. The photosynthetic pigment levels of chlorophyll A, chlorophyll B and carotenoid in transgenic lines are in the range 45.20-46.88, 16.34-17.04 and 13.63-13.46, while those of WT plants are 35.93, 13.18 and 10.55 (µg/g FW), respectively. Therefore, FLS transgenic plants containing high flavonol content showed a better in the protection photosynthetic pigments by less reductions of chlorophyll and carotenoid pigments.

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29-32

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June 2017

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© 2017 Trans Tech Publications Ltd. All Rights Reserved

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[1] S.A. Aherne, N.M. OʹBrien, Dietary flavonols: chemistry, food content, and metabolism, Nutrition. 18 (2002) 75-81.

DOI: 10.1016/s0899-9007(01)00695-5

Google Scholar

[2] K. Ishige, D. Schubert, Y. Sagara, Flavonoids protect neuronal cells from oxidative stress by three distinct mechanisms, Free Radic Biol Med. 30 (2001) 433-446.

DOI: 10.1016/s0891-5849(00)00498-6

Google Scholar

[3] S. Kanthang, K. Sompornpailin, Increasing plant flavonoid biomaterials in response to UV-A light, Adv Mat Res. 802 (2013) 74-78.

DOI: 10.4028/www.scientific.net/amr.802.74

Google Scholar

[4] P.W. Barnes, M.A. Tobler, K. Keefover-Ring, S.D. Flint, A. E. Barkley, R. J. Ryel, R. L. Lindroth, Rapid modulation of ultraviolet shielding in plants is influenced by solar ultraviolet radiation and linked to alteration in flavonoids, Plant Cell Environ. 39 (2016).

DOI: 10.1111/pce.12609

Google Scholar

[5] S. Chirumbolo, The role of quercetin, flavonols and flavones in modulating inflammatory cell function, In flamm Allergy Drug Targets. 9 (2010) 263-285.

DOI: 10.2174/187152810793358741

Google Scholar

[6] K. Rashed, A. Ćirić, J. Glamočlija, M. Soković, Antibacterial and antifungal activities of methanol extract and phenolic compounds from Diospyros virginiana L, Ind Crop Prod. 59 (2014) 210-215.

DOI: 10.1016/j.indcrop.2014.05.021

Google Scholar

[7] D.A. Okoth, H.Y. Chenia, N.A. Koorbanally, Antibacterial and antioxidant activities of flavonoids from Lannea alata (Engl. ) Engl. (Anacardiaceae), Phytochem Lett. 6 (2013) 476-481.

DOI: 10.1016/j.phytol.2013.06.003

Google Scholar

[8] R.M. Desentis-Mendoza , H. Hernández-Sánchez , A. Moreno , E.R. del-C, L. Chel-Guerrero, J. Tamariz, M.E. Jaramillo-Flores, Enzymatic polymerization of phenolic compounds using Laccase and Tyrosinase from Ustilago maydis, Biomacromolecules. 7 (2006).

DOI: 10.1021/bm060159p

Google Scholar

[9] G. Agati, S. Biricolti, L. Guidi, F. Ferrini, A. Fini, M. Tattini, The biosynthesis of flavonoids is enhanced similarity by UV radiation and root zone salinity in L. vulgre leaves, J Plant Physiol. 168 (2011) 204-212.

DOI: 10.1016/j.jplph.2010.07.016

Google Scholar

[10] T. Murashige, F. Skoog, A revised medium for rapid growth and bioassays with tobacco tissue cultures, Physiol. Plantarum. 15 (1962) 473-497.

DOI: 10.1111/j.1399-3054.1962.tb08052.x

Google Scholar

[11] J.B. Harborne, Phytochemical Methods: A guide to modern techniques of plant analysis. Chapman and Hall. London. UK. (1998).

Google Scholar

[12] K. Sompornpailin, S. Kanthang, Tobacco randomly inserted TT8 differenly enhance light signals and flavonoid accumulation, Pak. J. Bot. 47 (2015) 1303-1309.

Google Scholar

[13] C. Reiss, Experiments in Plant Physiology, New Jersey: Prentice-Hall, (1994).

Google Scholar

[14] J. Li, T.M. Ou-Lee, R. Raba, R.G. Amundson, R.L. Last, Arabidopsis flavonoid mutants are hypersensitive to UV-B irradiation, Plant Cell. 5 (1993) 171-179.

DOI: 10.1105/tpc.5.2.171

Google Scholar

[15] B. Winkel-Shirley, Biosynthesis of flavonoids and effects of stress, Plant Biology. 5 (2002) 218-223.

DOI: 10.1016/s1369-5266(02)00256-x

Google Scholar

[16] M.L.F. Ferreyra, S.P. Rius, P. Casati, Flavonoids: biosynthesis, biological function, and biotechnological applications, Front. Plant Sci. 3 (2012) 1-15.

DOI: 10.3389/fpls.2012.00222

Google Scholar

[17] E.M. Middleton, A.H. Teramura, The role of flavonol glycosides and carotenoids in protecting soybean from ultraviolet-B damage, Plant Physiol. 103 (1993) 741-752.

DOI: 10.1104/pp.103.3.741

Google Scholar

[18] L.G. Landry, C.C.S. Chapple, R.L. Last, Arabidopsis mutants lacking phenolic sunscreens exhibit enhanced ultraviolet-B injury and oxidative damage, Plant Physiol. 109 (1995) 1159-1166.

DOI: 10.1104/pp.109.4.1159

Google Scholar

[19] G. Agati, G. Stefano, S. Biricolti, M. Tattini, Mesophyll distribution of antioxidant flavonoids in Ligustrum vulgare leaves under contrasting sunlight irradiance, Ann. Bot. 104 (2009) 853-861.

DOI: 10.1093/aob/mcp177

Google Scholar

[20] P.M. Mullineaux, S. Karpinski, Signal transduction in response to excess light: getting out of the chloroplast, Curr Opin Plant Biol. 5 (2002) 43-48.

DOI: 10.1016/s1369-5266(01)00226-6

Google Scholar