Umami, one of the five basic tastes, is described as a pleasant 'brothy' or 'meaty' perception. The umami intensity mirrors the content of nitrogen which refers to amino acids in foods. 1-3 Quantities of researches have approved that there are three receptors involved in umami perception process, consisting of heterodimer T1R1/T1R3, 4,5 metabotropic glutamate receptor 1 (mGluR1), 6 metabotropic glutamate receptor 4 (mGluR4) 7 and their variants. 8,9 All the mentioned receptors belong to G protein-coupled receptors (GPCRs) and co-regulate the generation of umami taste signals. T1R1/T1R3 exhibits species-dependent differences in ligand specificity; human T1R1/T1R3 specifically responds to L-glutamate, whereas mouse T1R1/T1R3 responds more strongly to other L-amino acids than to L-glutamate, 10 which makes monosodium glutamate (MSG) an excellent ligand for umami receptor activation. Moreover, disodium inosinate (IMP) is a potentiator of T1R1/T1R3 activation but is not a potentiator at other putative umami receptors. 11 mGluR1 and mGluR4 are other umami receptors in taste buds, which are specifically elicited by glutamate and certain analogs. 9 Some studies indicated that mGluRs in the taste receptor cells of mice also respond to L-amino acid and IMP. 12 The synergism between L-glutamate and 5'-purine nucleotides is a hallmark of umami modality. In general, umami taste induced by the synergism is the main umami taste since most daily foods contain various umami substances such as MSG and disodium inosinate (IMP). At molecular level, it was assumed that umami synergism occurred at T1R1/T1R3. Several studies found that mice lost synergistic effect of MSG and IMP when T1R1 or T1R3 was knockout. 13-15 Hence, T1R1/T1R3 was considered as the primary umami receptor