α-Linalool - a marker compound of forged/synthetic sweet basil (Ocimum basilicum L.) essential oils

被引:16
作者
Radulovic, Niko S. [1 ]
Blagojevic, Polina D. [1 ]
Miltojevic, Ana B. [1 ]
机构
[1] Univ Nis, Dept Chem, Fac Sci & Math, Nish 18000, Serbia
关键词
Ocimum basilicum L; Lamiaceae; sweet basil; -linalool; multivariate statistical analysis; forged; synthetic oil; SOLID-PHASE MICROEXTRACTION; CHEMICAL-COMPOSITION; HS-SPME; GC-MS; COMPONENTS; FLOWERS; LEAVES;
D O I
10.1002/jsfa.6175
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
BACKGROUND Ocimum basilicum L. (sweet basil) is known to occur as several chemotypes or cultivars that differ in their essential oil composition. The surprising discovery of 3,7-dimethylocta-1,7-dien-3-ol, the rare isomer of the well-known monoterpene alcohol -linalool (3,7-dimethylocta-1,6-dien-3-ol), in samples of Serbian basil oil provoked an investigation of the origin of -linalool in these samples. Three scenarios were considered, namely (a) the existence of a new natural chemotype, (b) an artefactual formation during the isolation procedure and (c) the case of a synthetic/forged oil. RESULTS Noteworthy amounts (15.1-16.9%) of pure -linalool were isolated from a commercial sample of basil oil, and detailed spectral analyses (MS, IR, H-1 and C-13 NMR) unequivocally confirmed its identity. The analysis by GC and GC/MS of an additional 20 samples of different O. basilicum oils commercially available on the Serbian market or isolated from plant material cultivated in Serbia resulted in the identification of 149 compounds. The obtained compositional data were compared using multivariate statistical analysis to reveal the possible existence of a new basil chemotype. CONCLUSION The results of the chemical and statistical analyses give more pro arguments for the synthetic/forged oil hypothesis and suggest that -linalool could be used as a marker compound of such O. basilicum oils. (c) 2013 Society of Chemical Industry
引用
收藏
页码:3292 / 3303
页数:12
相关论文
共 41 条
[1]  
Adams R., 2007, IDENTIFICATION ESSEN
[2]  
[Anonymous], 2013, THE PLANT LIST
[3]   Antimicrobial activity of essential oils from Tunisian aromatic plants [J].
Bouzouita, N ;
Kachouri, F ;
Hamdi, M ;
Chaabouni, MM .
FLAVOUR AND FRAGRANCE JOURNAL, 2003, 18 (05) :380-383
[4]   De novo synthesis of monoterpenes by Saccharomyces cerevisiae wine yeasts [J].
Carrau, FM ;
Medina, K ;
Boido, E ;
Farina, L ;
Gaggero, C ;
Dellacassa, E ;
Versini, G ;
Henschke, PA .
FEMS MICROBIOLOGY LETTERS, 2005, 243 (01) :107-115
[5]  
CAS, 2007, SCIFINDER SCHOL VERS
[6]   Comparative essential oil composition of flowers, leaves and stems of basil (Ocimum basilicum L.) used as herb [J].
Chalchat, Jean-Claude ;
Oezcan, Mehmet Musa .
FOOD CHEMISTRY, 2008, 110 (02) :501-503
[7]   Solid-phase microextraction of volatile components from natural grassland plants [J].
Cornu, A ;
Carnat, AP ;
Martin, B ;
Coulon, JB ;
Lamaison, JL ;
Berdague, JL .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2001, 49 (01) :203-209
[8]   ALKYLATION OF LINALOOL AT CARBON-8 (AND CARBON-6) [J].
CUVIGNY, T ;
JULIA, M ;
ROLANDO, C .
JOURNAL OF ORGANOMETALLIC CHEMISTRY, 1988, 344 (01) :9-28
[9]   Chemical Composition and in Vitro Antimicrobial and Mutagenic Activities of Seven Lamiaceae Essential Oils [J].
De Martino, Laura ;
De Feo, Vincenzo ;
Nazzaro, Filomena .
MOLECULES, 2009, 14 (10) :4213-4230
[10]   Application of HS-SPME and GC-MS to characterization of volatile compounds emitted from osmanthus flowers [J].
Deng, CH ;
Song, GX ;
Hu, YM .
ANNALI DI CHIMICA, 2004, 94 (12) :921-927