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IDENTIFICATION OF PHENOL COMPOUNDS IN BROCCOLI (BRASSICA OLERACEA L. VAR. ITALICA) BY UPLC/UV-MS/MS

DOI: https://doi.org/10.29296/25877313-2019-03-08
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Issue: 
3
Year: 
2019

D.A. Potapova Post-graduate Student, Pharmaceutical Natural Sciences Department, Institute of Pharmacy, Sechenov First State Medical University (Moscow) E-mail: 79166851211@ya.ru T.D. Rendyuk Ph.D. (Pharm.), Associate Professor, Pharmaceutical Natural Sciences Department, Institute of Pharmacy, Sechenov First State Medical University (Moscow)

Vegetables of Brassicaceae family, especially broccoli, are known to play an important role in human nutrition due to their phytochemicals, such as vitamins, minerals, glucosinolates, and phenolic compounds. In particular, it has been shown that broccoli potentially exert inhibitory activity against chronic diseases like cancer. Phenols such as flavonoids and hydroxycinnamic acid derivatives are widely distributed in plants and are important biologically active constituents. Risk of age-related diseases decreased in several epidemiologic studies, and the concept that flavonoids and other phenolic compounds are responsible is supported by some animal and in vitro studies. Flavonoids have powerful antioxidant activities, being able to scavenge a wide range of reactive oxygen, nitrogen, and chlorine species, such as superoxide, hydroxyl radical, peroxyl radicals. Glucosinolates are sulfur- and nitrogen-containing plant secondary metabolites. These have a common core structure containing a thioglucose group linked to a sulfonated aldoxime moiety and a variable side chain derived from amino acids. Sinapic acid is widespread in the plant kingdom and derivatives of sinapic acid are characteristic compounds in plants Brassica. Its shows antioxidant, antimicrobial, anti-inflammatory, anticancer, and anti-anxiety activity. This study identified phenolic compounds and glucosinalates from broccoli. These compounds were extracted from ethanolic extract of broccoli and characterized using ultra-performance liquid chromatography with photodiode array and triple-quadrupole mass spectrometry detector (UPLC-UV-MS/MS). Sinapic acid and several sinapoyl conjugates and compounds from class glucosinolate were identified based on retention time, UV spectra, MS fragmentation pattern. Compounds were identified in broccoli: sinapic acid derivatives: 1,2-disinapoylgentiobioside, 1-sinapoyl-2-feruloylgentiobioside, 1,2,2’-trisinapoylgentiobioside, 1,2’-disinapoyl-2-feruloylgentiobioside; glucosinolates: 4-methoxyglucobrassicin, neoglucobrassicin. This study showed that broccoli could be considered as good sources of food polyphenols. And could be conclusion about the prospects of broccoli as medicinal plant raw material was made.

Keywords: 
broccoli
phenol compounds
glucosinolates
UPLC

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References: 
  1. Cartea M.E., Velasco P. Glucosinolates in Brassica foods: bioavailability in food and significance for human health // Phytochem Rev. 2008. V. 7. P. 213–229.
  2. Traka M., Mithen R. Glucosinolates, isothiocyanates and human health // Phytochem Rev. 2009. V. 8. P. 269–282.
  3. Jahangir M., Kim H.K., Choi Y.H., Verpoorte R. Health-affecting compounds in Brassicaceae // Compr. Rev. Food Sci. Food Saf. 2009. V. 8. P. 31–43.
  4. Jeffery E.H., Araya M. Physiological effects of broccoli consumption // Phytochem Rev. 2009. V. 8. P. 283–298.
  5. Manchali A., Murthy K.N.C., Patil B.S. Crucial facts about health benefits of popular cruciferous vegetables // J. Funct Foods. 2012. V. 4. P. 94–106.
  6. Liu R.H. Health-promoting components of fruits and vegetables in the diet // Adv. Nutr. 2013. V. 4. P. 384S–392S.
  7. Chen S., Andreasson E. Update on glucosinolate metabolism and transport // Plant Physiol. Biochem. 2001. V. 39. P. 743–758.
  8. Halkier B.A., Gershenzon J. Biology and biochemistry of glucosinolates // Annu. Rev. Plant Biol. 2006. V. 57. P. 303–333.
  9. Bones A.M., Rossiter J.T. The myrosinase-glucosinolate system, its organisation and biochemistry // Physiol. Plant. 1996. V. 97. P. 194–208.
  10. Rask L., Andréasson E., Ekbom B., Eriksson S., Pontoppidan B., Meijer J. Myrosinase: gene family evolution and herbivore defense in Brassicaceae // Plant Mol. Biol. 2000. V. 42. P. 93–113.
  11. Wittstock U., Agerbirk N., Stauber E.J., Olsen C.E., M. Hippler, Mitchell-Olds T., Gershenzon J., Vogel H. Successful herbivore attack due to metabolic diversion of a plant chemical defense // PNAS. 2004. V. 101. P. 4859–4864.
  12. Fahey J.W., Zalcmann A.T., Talalay P. The chemical diversity and distribution of glucosinolates and isothiocyanates among plants // Phytochemistry. 2001. V. 56. P. 5–51.
  13. Baenas N, et al. Selecting sprouts of Brassicaceae for optimum phytochemical composition // J. Agric. Food Chem. 2012. V. 60. P. 11409–11420.
  14. Halliwell B., Rafter J., Jenner A. Health promotion by flavonoids, tocopherols, tocotrienols, and other phenols: direct or indirect effects? Antioxidant or not? // Am. J. Clin. Nutr. 2005. V. 81. P. 268S–276S.
  15. Mouradov A., Spangenberg G. Flavonoids: A metabolic network mediating plants adaptation to their real estate // Front Plant Sci. 2014. V. 5. P. 620.
  16. Ferreyra M.L.F, Rius S.P., Casati P. Flavonoids: Biosynthesis, biological functions, and biotechnological applications // Front Plant Sci. 2012. V. 3. P. 222.
  17. Niciforovic N., Abramovic H. Sinapic acid and its derivatives: natural sources and bioactivity // Compr. Rev. Food Sci. Food Saf. 2014. V. 13. № 1. P. 34–51.
  18. Yokozawa T., Kim H.Y., Cho E.J., Choi J.S., Chung H.Y. Antioxidant effects of isorhamnetin 3,7-di-O-beta-D-glucopyranoside isolated from mustard leaf (Brassica juncea) in rats with streptozotocin-induced diabetes // J. Agric. Food Chem. 2002. V. 50. P. 5490–5495.