Isolation and characterization of catechol derivatives from Semecarpus anacardium seeds and their antibacterial potential in in vitro

Ramalingam Sundaram , Karuppiah Muthu , Subramani Nagaraj , Palanivelu Shanthi , Panchanatham Sachdanandam
{"title":"Isolation and characterization of catechol derivatives from Semecarpus anacardium seeds and their antibacterial potential in in vitro","authors":"Ramalingam Sundaram ,&nbsp;Karuppiah Muthu ,&nbsp;Subramani Nagaraj ,&nbsp;Palanivelu Shanthi ,&nbsp;Panchanatham Sachdanandam","doi":"10.1016/j.bionut.2013.12.001","DOIUrl":null,"url":null,"abstract":"<div><p><span>The aim of the present investigation was to isolate and identify the phytochemicals from </span><em>Semecarpus anacardium</em><span> seeds and evaluate their activity against Gram positive and Gram negative bacterial strains (</span><span><em>Bacillus subtilis</em></span> MTCC 441, <span><em>Staphylococcus aureus</em></span> MTCC 96, <em>Escherichia coli</em> MTCC 1689 and <span><em>Proteus vulgaris</em></span><span><span> MTCC 742 using well diffusion method). The phytochemicals were isolated using silica gel<span><span> column chromatography and characterized as </span>catechol derivatives by spectroscopic analyses. The </span></span>antimicrobial activity<span><span> of the isolated catechol derivatives I-IV varied according to the dose and bacterial strains tested. Among the four catechol derivatives, catechol derivatives I and IV showed prominent antibacterial activity against both the positive and negative human </span>pathogenic organisms<span> compared to catechol derivatives II, III and tetracycline<span> – a reference antibiotic drug. From these findings, it can be concluded that catechol derivatives I and IV possessed methyl group (CH3) in aromatic ring and no double bond in the aliphatic side chain which was not present in catechol derivatives II and III and they possessed double bonds in the aliphatic side chain and no methyl group in the aromatic ring. These may be the possible reason for showing more inhibitory activity of catechol derivatives I and IV. These results showed the effectiveness of catechol derivatives against tested bacterial strains. Further work is necessary to explore these antimicrobial compounds, which are useful in clinical applications.</span></span></span></span></p></div>","PeriodicalId":100182,"journal":{"name":"Biomedicine & Preventive Nutrition","volume":"4 2","pages":"Pages 177-180"},"PeriodicalIF":0.0000,"publicationDate":"2014-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.bionut.2013.12.001","citationCount":"7","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomedicine & Preventive Nutrition","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2210523913000743","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 7

Abstract

The aim of the present investigation was to isolate and identify the phytochemicals from Semecarpus anacardium seeds and evaluate their activity against Gram positive and Gram negative bacterial strains (Bacillus subtilis MTCC 441, Staphylococcus aureus MTCC 96, Escherichia coli MTCC 1689 and Proteus vulgaris MTCC 742 using well diffusion method). The phytochemicals were isolated using silica gel column chromatography and characterized as catechol derivatives by spectroscopic analyses. The antimicrobial activity of the isolated catechol derivatives I-IV varied according to the dose and bacterial strains tested. Among the four catechol derivatives, catechol derivatives I and IV showed prominent antibacterial activity against both the positive and negative human pathogenic organisms compared to catechol derivatives II, III and tetracycline – a reference antibiotic drug. From these findings, it can be concluded that catechol derivatives I and IV possessed methyl group (CH3) in aromatic ring and no double bond in the aliphatic side chain which was not present in catechol derivatives II and III and they possessed double bonds in the aliphatic side chain and no methyl group in the aromatic ring. These may be the possible reason for showing more inhibitory activity of catechol derivatives I and IV. These results showed the effectiveness of catechol derivatives against tested bacterial strains. Further work is necessary to explore these antimicrobial compounds, which are useful in clinical applications.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
半猕猴桃种子儿茶酚衍生物的分离鉴定及其体外抗菌潜力
本研究的目的是通过孔扩散法分离鉴定半仙人掌种子中的植物化学物质,并评价其对革兰氏阳性和革兰氏阴性菌株(枯草芽孢杆菌MTCC 441、金黄色葡萄球菌MTCC 96、大肠杆菌MTCC 1689和普通变形杆菌MTCC 742)的抑菌活性。通过硅胶柱层析分离得到植物化学物质,并通过光谱分析鉴定为儿茶酚衍生物。分离的儿茶酚衍生物I-IV的抑菌活性随剂量和菌株的不同而变化。在四种儿茶酚衍生物中,与儿茶酚衍生物II、III和参考抗生素四环素相比,儿茶酚衍生物I和IV对阳性和阴性人类病原微生物均表现出显著的抗菌活性。由此可见,儿茶酚衍生物I和IV在芳香环上具有甲基(CH3)而在脂肪侧链上没有双键,而儿茶酚衍生物II和III则没有,它们在脂肪侧链上具有双键而在芳香环上没有甲基。这可能是儿茶酚衍生物I和IV表现出更强抑制活性的原因。这些结果表明儿茶酚衍生物对被试菌株的有效性。这些抗菌化合物在临床应用中具有重要意义,需要进一步的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Antioxidative potential of chrysin, a flavone in streptozotocin–nicotinamide-induced diabetic rats Antidiabetic therapeutics from natural source: A systematic review Insignificant viability of the granules of probiotic and prebiotic with skimmed milk powder Protective role of Solanum trilobatum (Solanaeace) against benzo(a)pyrene-induced lung carcinogenesis in Swiss albino mice Molecular docking, isolation and biological evaluation of Rhizophora mucronata flavonoids as anti-nociceptive agents
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1