ANTHOCYANINS IN LILAC FLOWERS SYRINGA VULGARIS

UDC 543.544.123:543.51:577.13

Keywords: anthocyanins, flowers, Syringa vulgaris, reversed-phase HPLC, electronic absorption spectra, mass spectrometry

Abstract

Anthocyanins from flowers of common lilac (Syringa vulgaris L.) of various color intensities and shades of lilac color from nine samples purchased at the Belgorod market were studied using reverse-phase high-performance liquid chromatography. To determine the structure of anthocyanins, we used the analysis of electronic absorption spectra recorded in the cuvette of a diode array detector and the analysis of mass spectra obtained by electrospray ionization with partial fragmentation. As a result, it was found that in all the studied samples the main component was delphinidin-3-rutinoside (84–90% by peak areas in the chromatogram). The level of cyanidin-3-rutinoside biosynthesis was significantly lower (6–19.6%). Among the minor compounds, delphinidin-3-glucoside and petunidin-3-glucoside were found. Among the unusual compounds, pyranoanthocyanin, built on the basis of delphinidin-3-rutinoside due to condensation with pyruvic acid, was found in a number of studied samples, but the reasons for its appearance have not yet been established. The total content of anthocyanins is low and amounts to 0.020–0.120 g per 100 g of fresh material (depending on the color intensity of the original plant material) in terms of cyanidin-3-glucoside. By drying flowers on a cut branch, air-dried material was obtained containing 0.100–0.300 g per 100 g of anthocyanins.

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Author Biographies

Irina Petrovna Blinova, Belgorod State National Research University

кандидат химических наук, доцент, доцент кафедры общей химии

Viktor Ivanovich Deyneka, Belgorod State National Research University

доктор химических наук, профессор, профессор кафедры общей химии

Yaroslava Yur'yevna Salasiina, Belgorod State National Research University

кандидат химических наук, старший преподаватель кафедры общей химии

Yelena Yur'yevna Oleynits, Belgorod State National Research University

ассистент кафедры общей химии

Lyudmila Aleksandrovna Deyneka, Belgorod State National Research University

кандидат химических наук, доцент, доцент кафедры общей химии

References

Tóth G., Barabás C., Tóth A., Kéry Á., Béni S., Boldizsár I., Varga E., Noszál B. Biomed. Chromatogr., 2016, vol. 30, pp. 923–932. DOI: 10.1002/bmc.3630.

Deeva A.M., Shabunya P.S., Fatykhova S.A., Zubarev A.V., Reshetnikov V.N., Spiridovich E.V. Fiziologiya rasteniy, 2022, vol. 69, no. 2, pp. 161–170. DOI: 10.31857/S001533032202004X. (in Russ.).

Deineka V.I., Sidorov A.N., Deineka L.A., Kostenko M.O., Blinova I.P. Russ. J. Phys. Chem. A, 2016, vol. 90, no. 4, pp. 861–863. DOI: 10.1134/S0036024416040075.

Welch C.R., Wu Q., Simon J.E. Curr. Anal. Chem., 2008, vol. 4, pp. 75–101. DOI: 10.2174/157341108784587795.

Khoo H.E., Azlan A., Tang S.T., Lim S.M. Food Nutr. Res., 2017, vol. 61, article 1361779. DOI: 10.1080/16546628.2017.1361779.

Fossen T., Cabrita L., Andersen Ø.M. Food Chem., 1998, vol. 63, no. 4, pp. 435–440. DOI: 10.1016/S0308-8146(98)00065-X.

Castañeda-Ovando A., Pacheco-Hernández M., Páez-Hernández M.E., Rodríguez J.A., Galán-Vidal C.A. Food Chem., 2009, vol. 113, pp. 859–871. DOI: 10.1016/j.foodchem.2008.09.001

Deng R.-X., Yuan H., Liu P., Yin W.-P., Wang X.-S., Zhao T.-Z. Biochem. System. Ecol., 2010, vol. 38, pp. 813–815. DOI: 10.1016/j.bse.2010.08.004.

Su G., Cao Y., Li C., Yu X., Gao X., Tu P., Chai X. Chem. Central J., 2015, vol. 9, article 2. DOI: 10.1186/s13065-015-0079-2.

Woźniak M., Michalak B., Wyszomierska J., Dudek M.K., Kiss A.K. Front Pharmacol., 2018, vol. 9, article 349. DOI: 10.3389/fphar.2018.00349.

Mlcek J., Rop O. Trends Food Sci. Technol., 2011, vol. 22, pp. 561–569. DOI: 10.1016/j.tifs.2011.04.006

Deineka V.I., Sidorov A.N., Chulkov A.N., Deineka L.A. J. Anal. Chem., 2017, vol. 72, no. 14, pp. 1441–1445. DOI: 10.1134/S1061934817140040.

Giusti M.M., Wrolstad R.E. Curr. Prot. Food Anal. Chem., 2001, pp. F1.2.1–F1.2.13. DOI: 10.1002/0471142913.faf0102s00.

Deyneka L.A., Shaposhnik Ye.I., Gostishchev D.A., Deyneka V.I., Sorokopudov V.N., Selemenev V.F. Sorbtsionnyye i khromatograficheskiye protsessy, 2009, vol. 9, no. 4, pp. 529–536. (in Russ.).

Zhao Xu. He X.-M., Liud F.., Duan C.-Q., He F. Food Chem., 2022, vol. 391, article 133255. DOI: 10.1016/j.foodchem.2022.133255.

Harborne J.B. Biochem. J., 1958, vol. 70, pp. 22–28. DOI: 10.1042/bj0700022.

Deyneka V.I., Salasina Ya.Yu., Blinova I.P., Deyneka L.A., Varushkina S.M., Chulkov A.N., Selemenev V.F. Sor-btsionnyye i khromatograficheskiye protsessy, 2021, vol. 21, vol. 2, pp. 187–195. DOI: 10.17308/sorpchrom.2021.21/3353. (in Russ.).

He F., Liang N.-N., Mu L., Pan Q.-H., Wang J., Reeves M.J., Duan C.-Q. Molecules, 2012, vol. 17, pp. 1483–1519. DOI: 10.3390/molecules17021483.

Published
2023-10-02
How to Cite
1. Blinova I. P., Deyneka V. I., Salasiina Y. Y., Oleynits Y. Y., Deyneka L. A. ANTHOCYANINS IN LILAC FLOWERS SYRINGA VULGARIS // chemistry of plant raw material, 2023. № 3. P. 127-132. URL: http://journal.asu.ru/cw/article/view/11638.
Section
Low-molecular weight compounds