L-theanine
compound / compound-l-theanine
L-テアニン
L-theanine. Its effect on bitter-ligand response in hTAS2R16-expressing cells has been tested.
On this page (7 sections)
Reading the bitterness
L-theanine has been reported to inhibit, partially in a noncompetitive manner, the response of this receptor to its bitter ligand salicin in an assay using hTAS2R16-expressing HEK293T cells. Quantitatively, when theanine was added up to a highest concentration of 100 mM, the maximum response to salicin alone decreased by 55%, and the half-maximal effect concentration (EC50) increased 2- to 3-fold. This effect is also seen with other umami compounds (glutamate dimer and inosinate), and is not an action specific to theanine. Note that this result is from calcium response in heterologously expressed receptors, not human sensory testing, and extrapolation to the bitterness of tea or dishes overall cannot be confirmed within the scope of this collection.
In electronic tongue measurements targeting the major galloylated catechins of green tea (EGCG, ECG, GCG), umami amino acids including theanine have been reported to inhibit, in a concentration-dependent manner, the electronic tongue response to the bitterness intensity of these catechins. Theanine, together with glutamate, interacts more strongly with galloylated catechins than aspartate does, and hydrogen bonding is reported to be the main interactive force.
In a sensory and compositional analysis of green tea extracted 3 times in succession, some amino acids including L-theanine (glutamate and lysine) showed positive correlation with bitter and astringent attributes of the 1st infusion (the extract evaluated as having the strongest bitterness and astringency), together with catechins, gallic acid, and caffeine. On the other hand, the authors of the same study also argue that amino acids as a whole contribute to a fresh and sweet taste and have a role in mitigating bitterness.
Sources for this overview
Suppression of hTAS2R16 Signaling by Umami Substances
Checked for this overview: Used as the basis for the report that salicin response is inhibited noncompetitively / Used as the basis for the quantitative value of 55% reduction at 100 mM
Checked for this overview: Used as the basis for concentration-dependent inhibition of galloylated catechin bitterness by electronic tongue
Three Successive Infusions: Scientific Insights Into a Traditional Green Tea Drinking Custom
Checked for this overview: Positive correlation between 1st-infusion bitterness and astringency and theanine concentration, with mitigation theory also noted
Follow the connections
L-theanine →antagonizes→ TAS2R16
epigallocatechin gallate →— electronic-tongue bittern…→ L-theanine
L-theanine →— perceived bitterness is a…→ green tea infusion →— sensory attribute→ bitterness
Structured claims — open a section to read each claim's confidence, evidence and limits
Sensory (2)
Scope: Electronic tongue measurement targeting major galloylated catechins of green tea (EGCG, ECG, GCG). Tested with theanine, glutamate, and aspartate
Note: Glutamate and aspartate have also been reported to inhibit the electronic tongue response to bitterness intensity in a concentration-dependent manner. This is based on electronic tongue (instrument) response values, not confirmation by human sensory panel. Theanine and glutamate interact more strongly with galloylated catechins than aspartate does, and hydrogen bonding is reported to be the main interactive force.
Show data
compound-egcg —has_e_tongue_bitterness_reduced_by→ compound-l-theanineScope: Layer: food. Green tea extracted in 3 successive infusions (GT1-GT3), five-taste sensory evaluation by electronic tongue, Pearson correlation analysis, and PLSR.
Show data
compound-l-theanine —has_perceived_bitterness_associated_with→ ingredient-green-teaMechanism and receptors (1)
Scope: The same hTAS2R16-expressing cell system
Note: Reported as partial, non-surmountable antagonism. Not extrapolated to the overall bitterness of tea or dishes.
Show data
compound-l-theanine —antagonizes→ receptor-tas2r16