Lorenzo Camarda, Talya Dayton, Vita Di Stefano, Rosa Pitonzo, Domenico Schillaci
{"title":"乳香属几种油胶树脂精油的化学成分及抑菌活性研究","authors":"Lorenzo Camarda, Talya Dayton, Vita Di Stefano, Rosa Pitonzo, Domenico Schillaci","doi":"10.1002/adic.200790068","DOIUrl":null,"url":null,"abstract":"<p>The chemical composition of <i>Boswellia carteri</i> (Somalia), <i>B. papyrifera</i> (Ethiopia), <i>B. serrata</i> (India) and <i>B. rivae</i> (Ethiopia) oleogum resin essential oils was investigated using GC-MS to identify chemotaxonomy marker components. Total ion current peak areas gave good approximations to relative concentrations based on GC-MS peak areas.</p><p><i>B. carteri</i> and <i>B. serrata</i> oleogum resin oils showed similar chemical profiles, with isoincensole and isoincensole acetate as the main diterpenic components.</p><p>Both n-octanol and n-octyl acetate, along with the diterpenic components incensole and incensole acetate, were the characteristic compounds of <i>B. papyrifera</i> oleogum resin oil. Hydrocarbon and oxygenated monoterpenes were the most abundant classes of compounds identified in the <i>B. rivae</i> oleogum resin oil.</p><p>The antimicrobial activities of the essential oils were individually evaluated against different microorganisms including fungi, Gram-positive and Gram-negative bacteria strains.</p><p>The essential oils with the best activity against fungal strains were those obtained from <i>B. carteri</i> and <i>B. papyrifera</i> with MIC values as low as 6.20 μg/ml. The essential oil of <i>B. rivae</i> resin showed the best activity against <i>C. albicans</i> with a MIC value of 2.65 μg/ml.</p>","PeriodicalId":8193,"journal":{"name":"Annali di chimica","volume":"97 9","pages":"837-844"},"PeriodicalIF":0.0000,"publicationDate":"2007-07-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/adic.200790068","citationCount":"133","resultStr":"{\"title\":\"Chemical Composition and Antimicrobial Activity of Some Oleogum Resin Essential Oils from Boswellia SPP. (Burseraceae)\",\"authors\":\"Lorenzo Camarda, Talya Dayton, Vita Di Stefano, Rosa Pitonzo, Domenico Schillaci\",\"doi\":\"10.1002/adic.200790068\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The chemical composition of <i>Boswellia carteri</i> (Somalia), <i>B. papyrifera</i> (Ethiopia), <i>B. serrata</i> (India) and <i>B. rivae</i> (Ethiopia) oleogum resin essential oils was investigated using GC-MS to identify chemotaxonomy marker components. Total ion current peak areas gave good approximations to relative concentrations based on GC-MS peak areas.</p><p><i>B. carteri</i> and <i>B. serrata</i> oleogum resin oils showed similar chemical profiles, with isoincensole and isoincensole acetate as the main diterpenic components.</p><p>Both n-octanol and n-octyl acetate, along with the diterpenic components incensole and incensole acetate, were the characteristic compounds of <i>B. papyrifera</i> oleogum resin oil. Hydrocarbon and oxygenated monoterpenes were the most abundant classes of compounds identified in the <i>B. rivae</i> oleogum resin oil.</p><p>The antimicrobial activities of the essential oils were individually evaluated against different microorganisms including fungi, Gram-positive and Gram-negative bacteria strains.</p><p>The essential oils with the best activity against fungal strains were those obtained from <i>B. carteri</i> and <i>B. papyrifera</i> with MIC values as low as 6.20 μg/ml. The essential oil of <i>B. rivae</i> resin showed the best activity against <i>C. albicans</i> with a MIC value of 2.65 μg/ml.</p>\",\"PeriodicalId\":8193,\"journal\":{\"name\":\"Annali di chimica\",\"volume\":\"97 9\",\"pages\":\"837-844\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2007-07-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1002/adic.200790068\",\"citationCount\":\"133\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Annali di chimica\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/adic.200790068\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annali di chimica","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/adic.200790068","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Chemical Composition and Antimicrobial Activity of Some Oleogum Resin Essential Oils from Boswellia SPP. (Burseraceae)
The chemical composition of Boswellia carteri (Somalia), B. papyrifera (Ethiopia), B. serrata (India) and B. rivae (Ethiopia) oleogum resin essential oils was investigated using GC-MS to identify chemotaxonomy marker components. Total ion current peak areas gave good approximations to relative concentrations based on GC-MS peak areas.
B. carteri and B. serrata oleogum resin oils showed similar chemical profiles, with isoincensole and isoincensole acetate as the main diterpenic components.
Both n-octanol and n-octyl acetate, along with the diterpenic components incensole and incensole acetate, were the characteristic compounds of B. papyrifera oleogum resin oil. Hydrocarbon and oxygenated monoterpenes were the most abundant classes of compounds identified in the B. rivae oleogum resin oil.
The antimicrobial activities of the essential oils were individually evaluated against different microorganisms including fungi, Gram-positive and Gram-negative bacteria strains.
The essential oils with the best activity against fungal strains were those obtained from B. carteri and B. papyrifera with MIC values as low as 6.20 μg/ml. The essential oil of B. rivae resin showed the best activity against C. albicans with a MIC value of 2.65 μg/ml.