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Antimicrobial activity profiles of the two enantiomers of limonene and carvone isolated from the oils of Mentha spicata and Anethum sowa
Author(s) -
Aggarwal K. K.,
Khanuja S. P. S.,
Ahmad Ateeque,
Santha Kumar T. R.,
Gupta Vivek K.,
Kumar Sushil
Publication year - 2001
Publication title -
flavour and fragrance journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.393
H-Index - 70
eISSN - 1099-1026
pISSN - 0882-5734
DOI - 10.1002/ffj.1040
Subject(s) - carvone , mentha spicata , anethum graveolens , limonene , chemistry , monoterpene , essential oil , terpenoid , terpene , antimicrobial , enantiomer , botany , traditional medicine , stereochemistry , food science , organic chemistry , biology , medicine
The antimicrobial activity of the essential oils of Mentha spicata L. and Anethum sowa Roxb. (Indian dill) were studied. The major chemical constituents of the hydrodistilled essential oils and their major isolates from cultivated M. spicata and A. sowa were identified by IR, 1 H‐ and 13 C‐NMR and GC: ( S )‐(−)‐limonene (27.3%) and ( S )‐(−)‐carvone (56.6%) (representing 83.9% of the spearmint oil) and ( R )‐(+)‐limonene (21.4%), dihydrocarvone (5.0%), ( R )‐(+)‐carvone (50.4%) and dillapiole (17.7%) (together 76.9% in Indian dill oil), respectively. In vitro bioactivity evaluation of the isolated oil components revealed that both the optical isomers of carvone were active against a wide spectrum of human pathogenic fungi and bacteria tested. ( R )‐(+)‐limonene showed comparable bioactivity profile over the ( S )‐(−)‐isomer. The activity of these monoterpene enantiomers was found to be comparable to the bioactivity of the oils in which they occurred. Copyright © 2001 John Wiley & Sons, Ltd.