Hj. Bouwmeester et al., ENANTIOMERIC COMPOSITION OF CARVONE, LIMONENE, AND CARVEOLS IN SEEDS OF DILL AND ANNUAL AND BIENNIAL CARAWAY VARIETIES, Journal of agricultural and food chemistry, 43(12), 1995, pp. 3057-3064
The enantiomeric compositions of limonene, carvone, and carveols were
determined in hydrodistillates and hexane extracts of seeds of dill an
d annual and biennial caraway. A range of varieties and accessions of
several harvest years was investigated to gain insight into genetic va
riation and differences between years. Both enantiomers of limonene, c
arvone, and cis- and trans-carveol were detected in the two caraway ty
pes and, except for (-)-cis-carveol, also in dill. The enantiomeric co
mpositions of the two caraway types were similar, but dill had a highe
r (-)/total limonene ratio than either caraway type. Due to less compl
ete extraction, the calculated seed contents of all compounds and thei
r enantiomers were lower for hydrodistilled than for hexane-extracted
seeds except for (-)-carvone content, which was significantly higher f
or hydrodistilled seeds, possibly as a result of conversions during ex
traction. Also, monoterpene composition was altered by hydrodistillati
on: the more polar carvone was extracted more efficiently than the apo
lar limonene. Total monoterpene content in biennial caraway was higher
than in the two annual species. The contents of all carveol isomers a
nd (-)/total limonene and (-)/total carvone ratios decreased with stor
age time between harvest and analysis. The correlations between enanti
omers of limonene and carvene and the implications for the pathways of
limonene and carvene formation in dill and caraway are discussed. As
the enantiomeric composition of carvene is similar for dill and annual
and biennial caraway, all three are equally suited as carvene supplie
rs for sprouting inhibition in potatoes.