Cairoli Paola, Pieraccini Stefano, Sironi Maurizio, Morelli Carlo F, Speranza Giovanna, Manitto Paolo
Dipartimento di Chimica Organica e Industriale, Università degli Studi di Milano, via Venezian 21, I-20133 Milano, Italy.
J Agric Food Chem. 2008 Feb 13;56(3):1043-50. doi: 10.1021/jf072803c. Epub 2008 Jan 9.
A number of N2-alkyl and N2-acyl derivatives of guanosine 5'-phosphate (GMP) have been synthesized and tested for their synergistic effect with monosodium L-glutamate (MSG), the prototypical substance imparting umami taste to savory-based foods. Capacities to enhance the taste intensity of MSG (gamma values) were estimated through subjective comparisons of MSG/nucleotide mixtures in water with appropriate solutions of MSG alone. Assuming beta = gamma[nucleotide]/gamma[IMP], beta values of the N2-substituted GMPs were found in the range 1.2-5.7. Such values appear to be related to the chain length of the substituent in the 2-position of the purine nucleus and dependent on the replacement of a CH 2 group with an S atom and/or with an alpha-CO group. These findings indicate that the exocyclic NHR group of the guanine moiety is actively implicated in the synergism between GMP derivatives and MSG. Theoretical calculations suggest that an anti conformation is probably assumed by ribonucleotide molecules interacting with umami receptors.
已经合成了多种5'-磷酸鸟苷(GMP)的N2-烷基和N2-酰基衍生物,并测试了它们与L-谷氨酸钠(MSG)的协同作用,MSG是赋予咸味食品鲜味的典型物质。通过将水中的MSG/核苷酸混合物与单独的适当MSG溶液进行主观比较,估计了增强MSG味道强度的能力(γ值)。假设β = γ[核苷酸]/γ[IMP],发现N2-取代的GMP的β值在1.2-5.7范围内。这些值似乎与嘌呤核2位上取代基的链长有关,并取决于用S原子和/或α-CO基团取代CH2基团。这些发现表明,鸟嘌呤部分的环外NHR基团积极参与了GMP衍生物与MSG之间的协同作用。理论计算表明,与鲜味受体相互作用的核糖核苷酸分子可能呈反式构象。