posted on 2015-10-07, 00:00authored byMichael Backes, Katja Obst, Juliane Bojahr, Anika Thorhauer, Natacha Roudnitzky, Susanne Paetz, Katharina
V. Reichelt, Gerhard E. Krammer, Wolfgang Meyerhof, Jakob P. Ley
Sensory
screening of a series of naturally occurring N-cinnamoyl
derivatives of substituted phenethylamines revealed that
rubemamine (9, from Chenopodium album) and rubescenamine (10, from Zanthoxylum
rubsecens) elicit strong intrinsic umami taste in
water at 50 and 10 ppm, respectively. Sensory tests in glutamate-
and nucleotide-containing bases showed that the compounds influence
the whole flavor profile of savory formulations. Both rubemamine (9) and rubescenamine (10) at 10–100 ppm
dose-dependently positively modulated the umami taste of MSG (0.17–0.22%)
up to threefold. Among the investigated amides, only rubemamine (9) and rubescenamine (10) are able to directly
activate the TAS1R1-TAS1R3 umami taste receptor. Moreover, both compounds
also synergistically modulated the activation of TAS1R1-TAS1R3 by
MSG. Most remarkably, rubemamine (9) was able to further
positively modulate the IMP-enhanced TAS1R1-TAS1R3 response to MSG
∼1.8-fold. Finally, armatamide (11), zanthosinamide
(13), and dioxamine (14), which lack intrinsic
umami taste in vivo and direct receptor response in vitro, also positively
modulated receptor activation by MSG about twofold and the IMP-enhanced
MSG-induced TAS1R1-TAS1R3 responses approximately by 50%. In sensory
experiments, dioxamine (14) at 25 ppm in combination
with 0.17% MSG exhibited a sensory equivalent to 0.37% MSG.