Several non-canon
ical, methylated terpenes have been descr
ibed as products of genet
ically mod
if
ied
Escherichia coli recently, and the aroma propert
ies of 28 odor-act
ive methylated der
ivat
ives of prenol,
isoprenol, bornane, camphene, carene, c
itronellol, fenchol, geran
iol, l
imonene, l
inalool, terp
ineol, and farnesol were character
ized for the f
irst t
ime
in the current study. Twelve methylated monoterpenes exh
ib
ited a part
icularly
intense and pleasant odor and were therefore chosen for the determ
inat
ion of the
ir respect
ive odor thresholds (OTs)
in compar
ison to the
ir non-methylated equ
ivalents.
In add
it
ion to the determ
inat
ion of OTs based on the l
iterature value for the
internal standard, (2
E)-decenal, the threshold values of the compounds w
ith
ind
iv
idually determ
ined OTs of the part
ic
ipants were calculated. Th
is enabled a more prec
ise
ident
if
icat
ion of the OTs. Among the non-canon
ical terpenes, the lowest OTs
in the a
ir were found for 2-methyll
inalool (flowery, 1.8 ng L
−1), 2-methyl-
α-fenchol (moldy, 3.6 ng L
−1), 2-methylgeran
iol (flowery, 5.4 ng L
−1), 2-methylc
itronellol (c
itrus-l
ike, 7.2 ng L
−1), and 4-methylgeran
iol (c
itrus-l
ike, 16 ng L
−1). The der
ivat
ives of geran
iol, l
inalool, and c
itronellol showed very pleasant odor
impress
ions, wh
ich could make them
interest
ing for use as flavor
ing agents
in the flavor and fragrance
industry.
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