Anthocyanins in Lilac Flowers Syringa vulgaris

IF 1.1 4区 化学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
I. P. Blinova, V. I. Deyneka, Ya. Yu. Salasina, E. Yu. Oleinits, L. A. Deineka
{"title":"Anthocyanins in Lilac Flowers Syringa vulgaris","authors":"I. P. Blinova,&nbsp;V. I. Deyneka,&nbsp;Ya. Yu. Salasina,&nbsp;E. Yu. Oleinits,&nbsp;L. A. Deineka","doi":"10.1134/S1068162024070069","DOIUrl":null,"url":null,"abstract":"<p><b>Objective:</b> This study aims to determine the structure of anthocyanins of common lilac flowers (<i>Syringa vulgaris</i> L.) of various color intensities and shades of lilac color from nine samples purchased at the Belgorod market by investigation of solute retention regularities of the compounds, peculiarities of their electronic absorption spectra as well as mass-spectra fixtures. <b>Methods:</b> Reversed-phase HPLC with a diode array as well as mass spectra detection by electrospray ionization with partial fragmentation were used. <b>Results and Discussion:</b> 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 in the samples was rather low in the region of 0.020–0.120 g per 100 g of fresh material (depending on the color intensity of the original plant material) expressed as cyanidin-3-glucoside. <b>Conclusions:</b> By drying flowers on a cut branch, air-dried material was obtained containing 0.100–0.300 per 100 g of anthocyanins.</p>","PeriodicalId":758,"journal":{"name":"Russian Journal of Bioorganic Chemistry","volume":"50 7","pages":"2813 - 2817"},"PeriodicalIF":1.1000,"publicationDate":"2024-12-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Russian Journal of Bioorganic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1134/S1068162024070069","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Objective: This study aims to determine the structure of anthocyanins of common lilac flowers (Syringa vulgaris L.) of various color intensities and shades of lilac color from nine samples purchased at the Belgorod market by investigation of solute retention regularities of the compounds, peculiarities of their electronic absorption spectra as well as mass-spectra fixtures. Methods: Reversed-phase HPLC with a diode array as well as mass spectra detection by electrospray ionization with partial fragmentation were used. Results and Discussion: 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 in the samples was rather low in the region of 0.020–0.120 g per 100 g of fresh material (depending on the color intensity of the original plant material) expressed as cyanidin-3-glucoside. Conclusions: By drying flowers on a cut branch, air-dried material was obtained containing 0.100–0.300 per 100 g of anthocyanins.

Abstract Image

求助全文
约1分钟内获得全文 求助全文
来源期刊
Russian Journal of Bioorganic Chemistry
Russian Journal of Bioorganic Chemistry 生物-生化与分子生物学
CiteScore
1.80
自引率
10.00%
发文量
118
审稿时长
3 months
期刊介绍: Russian Journal of Bioorganic Chemistry publishes reviews and original experimental and theoretical studies on the structure, function, structure–activity relationships, and synthesis of biopolymers, such as proteins, nucleic acids, polysaccharides, mixed biopolymers, and their complexes, and low-molecular-weight biologically active compounds (peptides, sugars, lipids, antibiotics, etc.). The journal also covers selected aspects of neuro- and immunochemistry, biotechnology, and ecology.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信