MCGRANE SCOTT (GB)
TAYLOR ANDREW (GB)
MCGRANE SCOTT (GB)
| WO2005053421A2 | 2005-06-16 |
| US4267195A | 1981-05-12 | |||
| US20030232407A1 | 2003-12-18 | |||
| US3524747A | 1970-08-18 | |||
| JP2000253847A | 2000-09-19 | |||
| US20060286276A1 | 2006-12-21 | |||
| US20060286275A1 | 2006-12-21 | |||
| US3524747A | 1970-08-18 |
DATABASE WPI Week 200944, Derwent World Patents Index; AN 2009-H44303, XP002697329
YOSHII K ET AL: "Synergistic effects of 5'-nucleotides on rat taste responses to various amino acids", BRAIN RESEARCH, ELSEVIER, AMSTERDAM, NL, vol. 367, no. 1-2, 5 March 1986 (1986-03-05), pages 45 - 51, XP024279385, ISSN: 0006-8993, [retrieved on 19860305], DOI: 10.1016/0006-8993(86)91577-5
YOSHI ET AL., SYN ERGISTIC EFFECTS OF 5'-NUCLEOTIDES ON RAT TASTE RESPONSES TO VARIOUS AMINO ACIDS, BRAIN RESEARCH, vol. 367, 1986, pages 45 - 51
| CLAIMS: 1. Use of one or more nucleotides, one or more amino acids selected from the group consisting of glycine, asparagine, alanine, cysteine, histidine, leucine, methionine, phenylalanine, serine, tryptophan and tyrosine and one or more furanones for increasing the palatability of a foodstuff to a companion animal. 2. The use according to claim 1, wherein the one or more nucleotides is/are selected from the group consisting of CMP, XMP, UMP, AMP, GMP and IMP. 3. The use according to claim 3, wherein the one or more nucleotides is a mixture of GMP and IMP. 4. The use according to any one of claims 1 to 4, wherein the one or more furanones is/are a compound according to formula I or formula II Formula I Formula II wherein each Ri and R2 are independently selected from hydrogen or Ci_6 alkyl, preferably hydrogen, methyl or ethyl; R3 is hydrogen, hydroxyl or Ci_6 alkyl, preferably methyl; P is hydrogen, hydroxyl or Ci_6 alkyl, preferably hydroxyl; R5 is hydrogen, hydroxyl, Ci_6 alkyl, Ci_6 alkoxy, 5 or 6 membered saturated heterocycle or -OC(0)R7, preferably hydroxyl, -OCH3, -OCH2CH3, -OC(0)CH3, methyl or pyrrolidine; Re is hydrogen or Ci_6 alkyl, preferably hydrogen or methyl; R7 is Ci_6 alkyl, preferably methyl. 5. The use according to any one of claims 1 to 5, wherein the one or more furanone is selected from the group consisting of furaneol, homofuraneol, sotolon, norfuraneol, abhexon, mesifuranone or dimethoxyfuranone, as defined in Table 1. 6. The use according to any one of claims 1 to 5, wherein the nucleotide, the amino acid and the furanone are in addition to any nucleotides, amino acids and furanones that may be found in any meat, vegetable or dairy component of the foodstuff. 7. The use according to any one of claims 1 to 6, wherein the one or more nucleotide is present in an amount of less than 100 mM. 8. The use according to any one of claims 1 to 8, wherein the one or more amino acid is present at an amount of less than 1M. 9. The use according to any one of claims 1 to 8, wherein the one or more furanone is present at an amount of less than 40ppm. 10. One or more nucleotides, one or more amino acids selected from the group consisting of glycine, alanine, cysteine, histidine, leucine, methionine, phenylalanine, serine, tryptophan and tyrosine and one or more furanones for use in increasing the acceptance of a pet foodstuff in a companion animal. 11. A nucleotide, an amino acid or a furanone for use according to claim 9, wherein the acceptance is a preference for a foodstuff comprising the nucleotide, amino acid and furanone over a foodstuff that does not comprise a nucleotide, an amino acid and a furanone. 12. A pet foodstuff comprising one or more nucleotides, one or more amino acids selected from the group consisting of glycine, alanine, cysteine, histidine, leucine, methionine, phenylalanine, serine, tryptophan and tyrosine, and one or more furanones. 13. A pet foodstuff according to claim 12, wherein the one or more nucleotide, the one or more amino acid and the one or more furanone are in a combination selected from the group consisting of: 14. A method for increasing acceptance of a foodstuff in a companion animal comprising allowing the animal access to a foodstuff comprising at least one nucleotide, at least one amino acid selected from the group consisting of glycine, alanine, cysteine, histidine, leucine, methionine, phenylalanine, serine, tryptophan and tyrosine and one or more furanones as defined in any one of claims 12 or 13. 15. A process of preparing a pet foodstuff comprising at least one nucleotide, at least one amino acid selected from the group consisting of glycine, alanine, cysteine, histidine, leucine, methionine, phenylalanine, serine, tryptophan and tyrosine, and one or more furanones the process comprising the steps of adding and mixing at least one nucleotide, at least one amino acid and one or more furanones with a pet foodstuff. 16. A process of preparing a pet foodstuff according to claim 15, wherein the process comprises combining one or more pet food ingredient; the at least one amino acid; the at least one nucleotide, wherein the amino acid, one or more furanones, nucleotide and furanones are added together or separately, and wherein the amino acid, the nucleotide and the furanones together provide no more than 30 wt% of the dry matter that is contained in the foodstuff. 17. A process according to any one of claims 15 or 16, wherein the one or more pet food ingredients include one or more of the edible materials selected from meat, animal fat, blood plasma, marrowbone, vegetable protein, vegetable fat, milk protein, grains and starch, wherein the one or more edible ingredients provide at least 60 wt % of the dry matter that is contained in the pet foodstuff. 18. A method for increasing the palatability of a foodstuff, the method comprising adding to a foodstuff during or after manufacture at least one nucleotide, at least one amino acid selected from the group consisting of glycine, alanine, cysteine, histidine, leucine, methionine, phenylalanine, serine, tryptophan and tyrosine, and one or more furanones. 19. A pet foodstuff produced by the methods of claims 15 to 18. |
The present invention relates to the use of one or more nucleotides, one or more amino acids selected from the group consisting of glycine, asparagine, alanine, cysteine, histidine, leucine, methionine, phenylalanine, serine, tryptophan and tyrosine and one or more furanones for increasing the palatability of a foodstuff to a companion animal. The invention also relates to a pet foodstuff or supplement comprising one or more nucleotides, one or more amino acids selected from the group consisting of glycine, asparagine, alanine, cysteine, histidine, leucine, methionine, phenylalanine, serine, tryptophan and tyrosine and one or more furanones, and also to a method of increasing the palatability of a foodstuff to a companion animal.
It is well known that many feline and canine companion animals are fussy with their food. An animal will often refuse to eat a foodstuff that it has been accepting over some time, or refuse to eat any more than a minimal amount of a foodstuff. Part of this phenomenon can be driven by subtle changes in the sensory profile of the raw materials. These changes might not be perceived by the human consumer, but due to a difference in the olfactory and gustatory systems, feline and canine companion animals may well perceive these differences. These sensory differences can be due to natural variation of the raw materials used or when materials are in short supply and have to be substituted with alternatives. This can be very frustrating for the owner and can result in the owner perceiving that the animal is unhappy and not enjoying its food. An animal may also fail to ingest its required amount of essential nutrients if not consuming an adequate amount of food available to it. Therefore, it can clearly be seen that there exists a need for a way to encourage companion animals to eat the foodstuff with which it is provided. Many solutions have been suggested to overcome this problem. Most commercially available pet foods are provided in a range of different flavours and/or textures. However, the companion animal owner will know that often a companion animal will suddenly, for no clear reason, refuse the flavour that the owner perceives to be its most preferred. Much research has been carried out on the flavour preferences of companion animals, by offering them a choice of different foodstuffs. The present inventors have taken this research further by studying the key taste receptor in cat, the umami receptor, (umami flavour is also referred to as savoury or meat flavour) and identifying the associated taste mechanisms. They have looked at a range of compounds, volatile and non-volatile, that are found in naturally occurring foodstuffs and established the interactions of these compounds and therefore developed a combination for optimal taste. Of particular interest and importance has been a focus on compounds that interact with and are perceived via the umami receptor.
Surprisingly, the inventors have found that companion animals show a strong and consistent preference for certain combinations of compounds, whether presented to the animals in water, a gel or in a model foodstuff. The present invention therefore relates to a use of a combination of compounds that is highly desirable to a companion animal for increasing palatability of a foodstuff to a companion animal. The companion animal is preferably a mammalian companion animal.
When a companion animal eats its recommended amount of (main meal) foodstuff each day, the animal will receive its required level of vitamins and minerals, and thus is highly likely to remain healthy and happy. Furthermore, the owner is satisfied that the animal is eating well. The inventors have identified certain volatile and non-volatile compounds that are present in natural products that particularly appeal to companion animals in
combination. Non-volatile compounds relate to taste, (i.e. they are detected on the tongue); volatile compounds relate to aroma, and are compounds that affect the smell of the food, (i.e. compounds detected in the nose); and some compounds fall within both categories. The combination of both taste and aroma give the food its flavour. Flavour, as used herein, therefore encompasses both the taste and aroma of a foodstuff. The invention, therefore, provides as a first aspect the use of one or more nucleotides, one or more amino acids selected from the group consisting of glycine, asparagine, alanine, cysteine, histidine, leucine, methionine, phenylalanine, serine, tryptophan and tyrosine and one or more furanones for increasing the palatability of a foodstuff to a companion animal and, therefore, for use in ensuring an adequate intake of food stuff by a companion animal. The amino acid may be selected from the group consisting of histidine, alanine and glycine. The nucleotide may be selected from the group consisting of adenosine monophosphate (AMP), guanosine monophosphate (GMP), inosine monophosphate (IMP), uridine monophosphate (UMP), cytidine monophosphate (CMP), xanthosine monophosphate (XMP) or a mixture of two or more thereof. The nucleotide may be AMP, GMP, or IMP or a mixture thereof. The nucleotide may be GMP alone, or IMP alone, or a mixture of
IMP and GMP. The nucleotide may be a mixture of GMP and IMP from about 1% to about 99% of GMP and of from about 1% to about 99% of IMP, more preferably, of from about 20% to about 80% of GMP and of from about 20% to about 80% of IMP or a mixture of about 50% GMP and about 50% IMP.
The amino acid is selected from the group consisting of glycine, asparagine, alanine, cysteine, histidine, leucine, methionine, phenylalanine, serine, tryptophan and tyrosine or a mixture of 2, 3, 4, 5, 6, 7, 8, 9, 10 or 11 thereof. Suitably, the amino acid may be selected from the group consisting of histidine, glycine and alanine. The amino acid is preferably in the L-amino acid form.
The furanone is suitably as set out in formula I or formula II, below, optionally substituted by hydroxyl, Ci_ 6 alkyl, Ci_ 6 alkoxy.
Formula I Formula II
Each P i and R 2 are independently selected from hydrogen or Ci_ 6 alkyl, preferably hydrogen, methyl or ethyl;
P 3 is hydrogen, hydroxyl or Ci_ 6 alkyl, preferably methyl;
P is hydrogen, hydroxyl or Ci_ 6 alkyl, preferably hydroxyl;
Pv 5 is hydrogen, hydroxyl, Ci_ 6 alkyl, Ci_ 6 alkoxy, 5 or 6 membered saturated heterocycle or -OC(0)Pv 7 , preferably hydroxyl, -OCH 3 , -OCH 2 CH 3 , -OC(0)CH 3 , methyl or pyrrolidine; Re is hydrogen or Ci_ 6 alkyl, preferably hydrogen or methyl;
R 7 is Ci_6 alkyl, preferably methyl.
The furanone may be selected from the group consisting of the furanones set out in Table 1 , or a mixture of 2, 3, 4, 5, 6, 7, 8, 9, 10, 1 1 or 12 thereof. Suitably, the furanone is furaneol, homofuraneol, sotolon, norfuraneol, abhexon, mesifuranone, dimethoxyfuranone, or norfuraneol, as defined in Table 1. Alternatively, the furanone may be selected from the group consisting of furaneol, sotolon and abhexon, as defined herein in Table 1.
Table 1
Optionally, the invention may also include the use of a pyrophosphate, such as tetra potassium pyrophosphate or a disodium pyrophosphate. Polyphosphates may be included in the composition also, such as sodium tripolyphosphate. The pyrophosphates and/or polyphosphates may be present in the composition at a concentration of ImM or above. Suitably, the concentration of pyrophosphate and/or polyphosphate may be 5mM, lOmM, 15mM, 20mM, 25mM, 30mM, 40mM, 50mM, lOOmM or 500mM. The invention includes a composition comprising one or more nucleotides, one or more amino acids and one or more furanones, as herein defined, for use in increasing the palatability of a foodstuff to a companion animal. The composition may also comprise a pyrophosphate and/or polyphosphate as herein defined. The one or more amino acids selected from the group consisting of glycine, asparagine, alanine, cysteine, histidine, leucine, methionine, phenylalanine, serine, tryptophan and tyrosine may be present (individually or as a combination) in an amount of less than 1M, ImM to 1M, 250mM to 1M, 5mM to 500mM, lOmM to lOOmM, lOmM to 50mM or 20mM to 50mM. The amount of amino acid may be less than 200mM, less than lOOmM, less than 20mM or less than lOmM. The amino acid(s) may be present in an amount of 25mM.
The one or more nucleotides may be present (individually or as a combination) in an amount of less than lOOmM, O. lmM to lOOmM, 0.5mM to 50mM, ImM to 20mM or 5mM to lOmM. The nucleotide may be present in an amount of greater than ImM or greater than 2.5mM. The nucleotide may be present in an amount of less than 50mM, less than
20mM or less than lOmM. Most preferably, the one or more nucleotides may be present in an amount of ImM to lOOmM, such as 5mM, or 2mM. The nucleotide(s) may be present in an amount of 5mM. The one or more furanones may be present (individually or as a combination) at a concentration of greater than 0.005ppm, 0.00 lppm to 40ppm, 0.005ppm to 20ppm, 0.00 lppm to 5ppm, lppm to lOppm or 2ppm to 5ppm. The furanone(s) may be present in an amount less than 40ppm. The furanone(s) may be present in an amount of 4ppm. The one or more nucleotides, the one or more amino acids and the one or more furanones for use in the invention are in addition to those found naturally in meat, vegetable or dairy products that may form part of a food stuff. The nucleotide(s) amino acid(s) and furanone(s) may be added to a pet food during or after manufacture. The nucleotide(s), amino acid(s) and furanone(s) are added in order to enhance or optimise the flavour profile of the basic meat (or other macronutrient) ingredients of the pet food.
The companion animal is preferably a feline animal (cat), or a canine animal (dog) although it may also be a guinea pig, a rabbit, bird or a horse. The invention also provides as a second aspect a pet foodstuff comprising one or more nucleotides, one or more amino acids selected from the group consisting of glycine, asparagine, alanine, cysteine, histidine, leucine, methionine, phenylalanine, serine, tryptophan and tyrosine, and one or more furanones. The foodstuff may be packaged, wherein the packaging carries written or graphic information indicating that the pet foodstuff is meant to be consumed by a cat or a dog, or a guinea pig, a rabbit, a bird or a horse. The suitable and preferred features of the first aspect also apply to the second aspect, mutatis mutandis.
The combination of nucleotide, amino acid and furanone may be any set out in Table 2. The mixture of GMP to IMP may be of from 1 to 99:99 to 1, preferably from 20 to 80:80 to 20, or about 50:50 in all combinations including GMP and IMP in Table 2, provided of course that the total amount of the combination is 100%. The preferred levels of alanine, histidine and/or glycine and GMP, IMP, GMP/IMP and AMP are as stated above.
Table 2
GMP from about 1% to Alanine Abhexon about 99% and IMP from
about 1% to about 99%
IMP Alanine Abhexon
GMP Alanine Abhexon
AMP Alanine Abhexon
GMP from about 1% to Alanine Mesifuranone about 99% and IMP from
about 1% to about 99%
IMP Alanine Mesifuranone
GMP Alanine Mesifuranone
AMP Alanine Mesifuranone
GMP from about 1% to Alanine Sotolon about 99% and IMP from
about 1% to about 99%
IMP Alanine Sotolon
GMP Alanine Sotolon
AMP Alanine Sotolon
GMP from about 1% to Asparagine Furaneol about 99% and IMP from
about 1% to about 99%
IMP Asparagine Furaneol
GMP Asparagine Furaneol
AMP Asparagine Furaneol
GMP from about 1% to Asparagine Norfuraneol about 99% and IMP from
about 1% to about 99%
IMP Asparagine Norfuraneol
GMP Asparagine Norfuraneol
AMP Asparagine Norfuraneol GMP from about 1% to Asparagine Homofuraneol about 99% and IMP from
about 1% to about 99%
IMP Asparagine Homofuraneol
GMP Asparagine Homofuraneol
AMP Asparagine Homofuraneol
GMP from about 1% to Asparagine Abhexon about 99% and IMP from
about 1% to about 99%
IMP Asparagine Abhexon
GMP Asparagine Abhexon
AMP Asparagine Abhexon
GMP from about 1% to Asparagine Mesifuranone about 99% and IMP from
about 1% to about 99%
IMP Asparagine Mesifuranone
GMP Asparagine Mesifuranone
AMP Asparagine Mesifuranone
GMP from about 1% to Asparagine Sotolon about 99% and IMP from
about 1% to about 99%
IMP Asparagine Sotolon
GMP Asparagine Sotolon
AMP Asparagine Sotolon
GMP from about 1% to Cysteine Furaneol about 99% and IMP from
about 1% to about 99%
IMP Cysteine Furaneol
GMP Cysteine Furaneol
AMP Cysteine Furaneol GMP from about 1% to Cysteine Norfuraneol about 99% and IMP from
about 1% to about 99%
IMP Cysteine Norfuraneol
GMP Cysteine Norfuraneol
AMP Cysteine Norfuraneol
GMP from about 1% to Cysteine Homofuraneol about 99% and IMP from
about 1% to about 99%
IMP Cysteine Homofuraneol
GMP Cysteine Homofuraneol
AMP Cysteine Homofuraneol
GMP from about 1% to Cysteine Abhexon about 99% and IMP from
about 1% to about 99%
IMP Cysteine Abhexon
GMP Cysteine Abhexon
AMP Cysteine Abhexon
GMP from about 1% to Cysteine Mesifuranone about 99% and IMP from
about 1% to about 99%
IMP Cysteine Mesifuranone
GMP Cysteine Mesifuranone
AMP Cysteine Mesifuranone
GMP from about 1% to Cysteine Sotolon about 99% and IMP from
about 1% to about 99%
IMP Cysteine Sotolon
GMP Cysteine Sotolon
AMP Cysteine Sotolon GMP from about 1% to Glycine Furaneol about 99% and IMP from
about 1% to about 99%
IMP Glycine Furaneol
GMP Glycine Furaneol
AMP Glycine Furaneol
GMP from about 1% to Glycine Norfuraneol about 99% and IMP from
about 1% to about 99%
IMP Glycine Norfuraneol
GMP Glycine Norfuraneol
AMP Glycine Norfuraneol
GMP from about 1% to Glycine Homofuraneol about 99% and IMP from
about 1% to about 99%
IMP Glycine Homofuraneol
GMP Glycine Homofuraneol
AMP Glycine Homofuraneol
GMP from about 1% to Glycine Abhexon about 99% and IMP from
about 1% to about 99%
IMP Glycine Abhexon
GMP Glycine Abhexon
AMP Glycine Abhexon
GMP from about 1% to Glycine Mesifuranone about 99% and IMP from
about 1% to about 99%
IMP Glycine Mesifuranone
GMP Glycine Mesifuranone
AMP Glycine Mesifuranone GMP from about 1% to Glycine Sotolon about 99% and IMP from
about 1% to about 99%
IMP Glycine Sotolon
GMP Glycine Sotolon
AMP Glycine Sotolon
GMP from about 1% to Histidine Furaneol about 99% and IMP from
about 1% to about 99%
IMP Histidine Furaneol
GMP Histidine Furaneol
AMP Histidine Furaneol
GMP from about 1% to Histidine Norfuraneol about 99% and IMP from
about 1% to about 99%
IMP Histidine Norfuraneol
GMP Histidine Norfuraneol
AMP Histidine Norfuraneol
GMP from about 1% to Histidine Homofuraneol about 100% and IMP from
about 1% to about 99%
IMP Histidine Homofuraneol
GMP Histidine Homofuraneol
AMP Histidine Homofuraneol
GMP from about 1% to Histidine Abhexon about 99% and IMP from
about 1% to about 99%
IMP Histidine Abhexon
GMP Histidine Abhexon
AMP Histidine Abhexon GMP from about 1% to Histidine Mesifuranone about 99% and IMP from
about 1% to about 99%
IMP Histidine Mesifuranone
GMP Histidine Mesifuranone
AMP Histidine Mesifuranone
GMP from about 1% to Histidine Sotolon about 99% and IMP from
about 1% to about 99%
IMP Histidine Sotolon
GMP Histidine Sotolon
AMP Histidine Sotolon
GMP from about 1% to Leucine Furaneol about 99% and IMP from
about 1% to about 99%
IMP Leucine Furaneol
GMP Leucine Furaneol
AMP Leucine Furaneol
GMP from about 1% to Leucine Norfuraneol about 99% and IMP from
about 1% to about 99%
IMP Leucine Norfuraneol
GMP Leucine Norfuraneol
AMP Leucine Norfuraneol
GMP from about 1% to Leucine Homofuraneol about 99% and IMP from
about 1% to about 99%
IMP Leucine Homofuraneol
GMP Leucine Homofuraneol
AMP Leucine Homofuraneol GMP from about 1% to Leucine Abhexon about 99% and IMP from
about 1% to about 99%
IMP Leucine Abhexon
GMP Leucine Abhexon
AMP Leucine Abhexon
GMP from about 1% to Leucine Mesifuranone about 99% and IMP from
about 1% to about 99%
IMP Leucine Mesifuranone
GMP Leucine Mesifuranone
AMP Leucine Mesifuranone
GMP from about 1% to Leucine Sotolon about 99% and IMP from
about 1% to about 99%
IMP Leucine Sotolon
GMP Leucine Sotolon
AMP Leucine Sotolon
GMP from about 1% to Methionine Furaneol about 99% and IMP from
about 1% to about 99%
IMP Methionine Furaneol
GMP Methionine Furaneol
AMP Methionine Furaneol
GMP from about 1% to Methionine Norfuraneol about 99% and IMP from
about 1% to about 99%
IMP Methionine Norfuraneol
GMP Methionine Norfuraneol
AMP Methionine Norfuraneol GMP from about 1% to Methionine Homofuraneol about 99% and IMP from
about 1% to about 99%
IMP Methionine Homofuraneol
GMP Methionine Homofuraneol
AMP Methionine Homofuraneol
GMP from about 1% to Methionine Abhexon about 99% and IMP from
about 1% to about 99%
IMP Methionine Abhexon
GMP Methionine Abhexon
AMP Methionine Abhexon
GMP from about 1% to Methionine Mesifuranone about 99% and IMP from
about 1% to about 99%
IMP Methionine Mesifuranone
GMP Methionine Mesifuranone
AMP Methionine Mesifuranone
GMP from about 1% to Methionine Sotolon about 99% and IMP from
about 1% to about 99%
IMP Methionine Sotolon
GMP Methionine Sotolon
AMP Methionine Sotolon
GMP from about 1% to Phenylalanine Furaneol about 99% and IMP from
about 1% to about 99%
IMP Phenylalanine Furaneol
GMP Phenylalanine Furaneol
AMP Phenylalanine Furaneol GMP from about 1% to Phenylalanine Norfuraneol about 99% and IMP from
about 1% to about 99%
IMP Phenylalanine Norfuraneol
GMP Phenylalanine Norfuraneol
AMP Phenylalanine Norfuraneol
GMP from about 1% to Phenylalanine Homofuraneol about 99% and IMP from
about 1% to about 99%
IMP Phenylalanine Homofuraneol
GMP Phenylalanine Homofuraneol
AMP Phenylalanine Homofuraneol
GMP from about 1% to Phenylalanine Abhexon about 99% and IMP from
about 1% to about 99%
IMP Phenylalanine Abhexon
GMP Phenylalanine Abhexon
AMP Phenylalanine Abhexon
GMP from about 1% to Phenylalanine Mesifuranone about 99% and IMP from
about 1% to about 99%
IMP Phenylalanine Mesifuranone
GMP Phenylalanine Mesifuranone
AMP Phenylalanine Mesifuranone
GMP from about 1% to Phenylalanine Sotolon about 99% and IMP from
about 1% to about 99%
IMP Phenylalanine Sotolon
GMP Phenylalanine Sotolon
AMP Phenylalanine Sotolon
GMP from about 1% to Serine Furaneol about 99% and IMP from about 1% to about 99%
IMP Serine Furaneol
GMP Serine Furaneol
AMP Serine Furaneol
GMP from about 1% to Serine Norfuraneol about 99% and IMP from
about 1% to about 99%
IMP Serine Norfuraneol
GMP Serine Norfuraneol
AMP Serine Norfuraneol
GMP from about 1% to Serine Homofuraneol about 99% and IMP from
about 1% to about 99%
IMP Serine Homofuraneol
GMP Serine Homofuraneol
AMP Serine Homofuraneol
GMP from about 1% to Serine Abhexon about 99% and IMP from
about 1% to about 99%
IMP Serine Abhexon
GMP Serine Abhexon
AMP Serine Abhexon
GMP from about 1% to Serine Mesifuranone about 99% and IMP from
about 1% to about 99%
IMP Serine Mesifuranone
GMP Serine Mesifuranone
AMP Serine Mesifuranone
GMP from about 1% to Serine Sotolon about 99% and IMP from
about 1% to about 99% IMP Serine Sotolon
GMP Serine Sotolon
AMP Serine Sotolon
GMP from about 1% to Tryptophan Furaneol about 99% and IMP from
about 1% to about 99%
IMP Tryptophan Furaneol
GMP Tryptophan Furaneol
AMP Tryptophan Furaneol
GMP from about 1% to Tryptophan Norfuraneol about 99% and IMP from
about 1% to about 99%
IMP Tryptophan Norfuraneol
GMP Tryptophan Norfuraneol
AMP Tryptophan Norfuraneol
GMP from about 1% to Tryptophan Homofuraneol about 99% and IMP from
about 1% to about 99%
IMP Tryptophan Homofuraneol
GMP Tryptophan Homofuraneol
AMP Tryptophan Homofuraneol
GMP from about 1% to Tryptophan Abhexon about 99% and IMP from
about 1% to about 99%
IMP Tryptophan Abhexon
GMP Tryptophan Abhexon
AMP Tryptophan Abhexon
GMP from about 1% to Tryptophan Mesifuranone about 99% and IMP from
about 1% to about 99%
IMP Tryptophan Mesifuranone
GMP Tryptophan Mesifuranone AMP Tryptophan Mesifuranone
GMP from about 1% to Tryptophan Sotolon about 99% and IMP from
about 1% to about 99%
IMP Tryptophan Sotolon
GMP Tryptophan Sotolon
AMP Tryptophan Sotolon
GMP from about 1% to Tyrosine Furaneol about 100% and IMP from
about l% to 100%
IMP Tyrosine Furaneol
GMP Tyrosine Furaneol
AMP Tyrosine Furaneol
GMP from about 1% to Tyrosine Norfuraneol about 99% and IMP from
about 1% to about 99%
IMP Tyrosine Norfuraneol
GMP Tyrosine Norfuraneol
AMP Tyrosine Norfuraneol
GMP from about 1% to Tyrosine Homofuraneol about 99% and IMP from
about 1% to about 99%
IMP Tyrosine Homofuraneol
GMP Tyrosine Homofuraneol
AMP Tyrosine Homofuraneol
GMP from about 1% to Tyrosine Abhexon about 99% and IMP from
about 1% to about 99%
IMP Tyrosine Abhexon
GMP Tyrosine Abhexon
AMP Tyrosine Abhexon GMP from about 1% to Tyrosine Mesifuranone about 99% and IMP from
about 1% to about 99%
IMP Tyrosine Mesifuranone
GMP Tyrosine Mesifuranone
AMP Tyrosine Mesifuranone
GMP from about 1% to Tyrosine Sotolon about 99% and IMP from
about 1% to about 99%
IMP Tyrosine Sotolon
GMP Tyrosine Sotolon
AMP Tyrosine Sotolon
UMP Alanine Furaneol
XMP Alanine Furaneol
CMP Alanine Furaneol
UMP Alanine Norfuraneol
XMP Alanine Norfuraneol
CMP Alanine Norfuraneol
UMP Alanine Homofuraneol
XMP Alanine Homofuraneol
CMP Alanine Homofuraneol
UMP Alanine Abhexon
XMP Alanine Abhexon
CMP Alanine Abhexon
UMP Alanine Mesifuranone
XMP Alanine Mesifuranone
CMP Alanine Mesifuranone
UMP Alanine Sotolon
XMP Alanine Sotolon
CMP Alanine Sotolon
UMP Asparagine Furaneol
XMP Asparagine Furaneol CMP Asparagine Furaneol
UMP Asparagine Norfuraneol
XMP Asparagine Norfuraneol
CMP Asparagine Norfuraneol
UMP Asparagine Homofuraneol
XMP Asparagine Homofuraneol
CMP Asparagine Homofuraneol
UMP Asparagine Abhexon
XMP Asparagine Abhexon
CMP Asparagine Abhexon
UMP Asparagine Mesifuranone
XMP Asparagine Mesifuranone
CMP Asparagine Mesifuranone
UMP Asparagine Sotolon
XMP Asparagine Sotolon
CMP Asparagine Sotolon
UMP Cysteine Furaneol
XMP Cysteine Furaneol
CMP Cysteine Furaneol
UMP Cysteine Norfuraneol
XMP Cysteine Norfuraneol
CMP Cysteine Norfuraneol
UMP Cysteine Homofuraneol
XMP Cysteine Homofuraneol
CMP Cysteine Homofuraneol
UMP Cysteine Abhexon
XMP Cysteine Abhexon
CMP Cysteine Abhexon
UMP Cysteine Mesifuranone
XMP Cysteine Mesifuranone
CMP Cysteine Mesifuranone
UMP Cysteine Sotolon XMP Cysteine Sotolon
CMP Cysteine Sotolon
UMP Glycine Furaneol
XMP Glycine Furaneol
CMP Glycine Furaneol
UMP Glycine Norfuraneol
XMP Glycine Norfuraneol
CMP Glycine Norfuraneol
UMP Glycine Homofuraneol
XMP Glycine Homofuraneol
CMP Glycine Homofuraneol
UMP Glycine Abhexon
XMP Glycine Abhexon
CMP Glycine Abhexon
UMP Glycine Mesifuranone
XMP Glycine Mesifuranone
CMP Glycine Mesifuranone
UMP Glycine Sotolon
XMP Glycine Sotolon
CMP Glycine Sotolon
UMP Histidine Furaneol
XMP Histidine Furaneol
CMP Histidine Furaneol
UMP Histidine Norfuraneol
XMP Histidine Norfuraneol
CMP Histidine Norfuraneol
UMP Histidine Homofuraneol
XMP Histidine Homofuraneol
CMP Histidine Homofuraneol
UMP Histidine Abhexon
XMP Histidine Abhexon
CMP Histidine Abhexon UMP Histidine Mesifuranone
XMP Histidine Mesifuranone
CMP Histidine Mesifuranone
UMP Histidine Sotolon
XMP Histidine Sotolon
CMP Histidine Sotolon
UMP Leucine Furaneol
XMP Leucine Furaneol
CMP Leucine Furaneol
UMP Leucine Norfuraneol
XMP Leucine Norfuraneol
CMP Leucine Norfuraneol
UMP Leucine Homofuraneol
XMP Leucine Homofuraneol
CMP Leucine Homofuraneol
UMP Leucine Abhexon
XMP Leucine Abhexon
CMP Leucine Abhexon
UMP Leucine Mesifuranone
XMP Leucine Mesifuranone
CMP Leucine Mesifuranone
UMP Leucine Sotolon
XMP Leucine Sotolon
CMP Leucine Sotolon
UMP Methionine Furaneol
XMP Methionine Furaneol
CMP Methionine Furaneol
UMP Methionine Norfuraneol
XMP Methionine Norfuraneol
CMP Methionine Norfuraneol
UMP Methionine Homofuraneol
XMP Methionine Homofuraneol CMP Methionine Homofuraneol
UMP Methionine Abhexon
XMP Methionine Abhexon
CMP Methionine Abhexon
UMP Methionine Mesifuranone
XMP Methionine Mesifuranone
CMP Methionine Mesifuranone
UMP Methionine Sotolon
XMP Methionine Sotolon
CMP Methionine Sotolon
UMP Phenylalanine Furaneol
XMP Phenylalanine Furaneol
CMP Phenylalanine Furaneol
UMP Phenylalanine Norfuraneol
XMP Phenylalanine Norfuraneol
CMP Phenylalanine Norfuraneol
UMP Phenylalanine Homofuraneol
XMP Phenylalanine Homofuraneol
CMP Phenylalanine Homofuraneol
UMP Phenylalanine Abhexon
XMP Phenylalanine Abhexon
CMP Phenylalanine Abhexon
UMP Phenylalanine Mesifuranone
XMP Phenylalanine Mesifuranone
CMP Phenylalanine Mesifuranone
UMP Phenylalanine Sotolon
XMP Phenylalanine Sotolon
CMP Phenylalanine Sotolon
UMP Serine Furaneol
XMP Serine Furaneol
CMP Serine Furaneol
UMP Serine Norfuraneol XMP Serine Norfuraneol
CMP Serine Norfuraneol
UMP Serine Homofuraneol
XMP Serine Homofuraneol
CMP Serine Homofuraneol
UMP Serine Abhexon
XMP Serine Abhexon
CMP Serine Abhexon
UMP Serine Mesifuranone
XMP Serine Mesifuranone
CMP Serine Mesifuranone
UMP Serine Sotolon
XMP Serine Sotolon
CMP Serine Sotolon
UMP Tryptophan Furaneol
XMP Tryptophan Furaneol
CMP Tryptophan Furaneol
UMP Tryptophan Norfuraneol
XMP Tryptophan Norfuraneol
CMP Tryptophan Norfuraneol
UMP Tryptophan Homofuraneol
XMP Tryptophan Homofuraneol
CMP Tryptophan Homofuraneol
UMP Tryptophan Abhexon
XMP Tryptophan Abhexon
CMP Tryptophan Abhexon
UMP Tryptophan Mesifuranone
XMP Tryptophan Mesifuranone
CMP Tryptophan Mesifuranone
UMP Tryptophan Sotolon
XMP Tryptophan Sotolon
CMP Tryptophan Sotolon UMP Tyrosine Furaneol
XMP Tyrosine Furaneol
CMP Tyrosine Furaneol
UMP Tyrosine Norfuraneol
XMP Tyrosine Norfuraneol
CMP Tyrosine Norfuraneol
UMP Tyrosine Homofuraneol
XMP Tyrosine Homofuraneol
CMP Tyrosine Homofuraneol
UMP Tyrosine Abhexon
XMP Tyrosine Abhexon
CMP Tyrosine Abhexon
UMP Tyrosine Mesifuranone
XMP Tyrosine Mesifuranone
CMP Tyrosine Mesifuranone
UMP Tyrosine Sotolon
XMP Tyrosine Sotolon
CMP Tyrosine Sotolon
It should be noted that taurine is not included as an amino acid in respect of the invention. In fact, taurine is an organic sulfonic acid and lacks the carboxyl group which is characteristic of amino acids i.e. there is no COOH group. However in the art, such as described in US 2006/0286276 and US 2006/286275, taurine is often described as an amino acid, which is incorrect. Since taurine does not contain a carboxyl group it is postulated that it does not fit in the same way into the binding site of the umami receptor as does an amino acid as defined by the invention. The invention also relates to, as a third aspect, a composition comprising one or more nucleotides, one or more amino acids selected from the group consisting of glycine, asparagine, alanine, cysteine, histidine, leucine, methionine, phenylalanine, serine, tryptophan and tyrosine and one or more furanones for use in increasing the acceptance and/or ensuring adequate intake of a foodstuff in a companion animal. Increasing the palatability leads to increased enjoyment and acceptance of the foodstuff to the animal. Increased acceptance and enjoyment helps to overcome the fussiness of a companion animal with regard to food. Since the animal accepts and enjoys the foodstuff in accordance with the invention, it is more likely to reach its required daily calorie and nutrient intake.
The composition may be for use in increasing the appetising appeal of a foodstuff to an animal in order to encourage an animal to eat a healthy amount of foodstuff. Thus, the use of a composition comprising one or more nucleotides, one or more amino acids selected from the group consisting of glycine, asparagine, alanine, cysteine, histidine, leucine, methionine, phenylalanine, serine, tryptophan and tyrosine and one or more furanones in increasing the appetising appeal of a foodstuff; in encouraging a healthy intake of a foodstuff; in ensuring the required intake of nutrients and calories in a companion animal, is included in the present invention. By healthy level it is meant an amount that enables the animal to maintain or achieve an intake contributing to its overall general health in terms of micronutrients, macronutrients and calories. By this it is meant that an animal may eat sufficient calories and receive a nutritionally complete diet without needing to eat excess calories and thus maintaining a healthy balance, such as set out in the "Mars Petcare Essential Nutrient Standards".
As mentioned above, the umami receptor has been studied as a target for flavour compounds. Many studies relating to the activation of the umami receptor focus on the human umami receptor. However, surprisingly the inventors have found that the umami receptor of humans differs in sequence to that of certain companion animals as shown in Figure 18. Moreover, even though certain companion animals have shown preferences according to the art to particular amino acids, these preferences differ from animal to animal. Therefore, it is not possible to predict from work carried out in humans whether a companion animal would have the same response to the same amino acids. In the human umami receptor, the key active site residues involved in glutamate and IMP binding have been identified by in silico modelling and by site-directed mutagenesis. These studies show that the key residues are at positions H71, T149, SI 72, D192, Y220, E301 S306 and S385 and the residues are highly conserved in other species. A comparison of the human, pig, mouse and cat sequences showed only two changes in these particular residues (pig L220 and mouse A385).
The high level of conservation in these active site residues does not fit well with the different amino acid specificity for the umami receptor in the species studied. A study on pig umami receptors identified other residues in the active site that were reported as being important in binding. The amino acids in these locations were conserved between humans and pigs (R277, R307 and H308). On the basis of this similarity, pig umami was proposed as a model for human umami. However, the pig umami receptor showed a wide amino acid specificity (glutamate, alanine, asparagine, glutamine, serine and threonine) compared to the usual glutamate and aspartate ligands that are associated with human umami receptor activation. A report that used some other amino acids (glycine, alanine, serine) at high concentrations (up to 1M) suggested that these compounds delivered a umami sensation in humans but the effect was only monitored using sensory analysis and no receptor studies were reported. Thus it seems that the range of amino acids that activate the human umami receptor are very limited compared to other species and that the residues identified so far do not satisfactorily explain the difference in amino acid specificity between the pig and human umami receptors. The invention also provides a method of enhancing the umami flavour/taste of a foodstuff, the method comprising adding to or including in the foodstuff one or more nucleotides, one or more amino acids consisting of glycine, asparagine, alanine, cysteine, histidine, leucine, methionine, phenylalanine, serine, tryptophan and tyrosine and one or more furanones. By enhancing it is meant that the umami flavour is detected more strongly/more intensely by the animal. It is thought that the addition of an amino acid strengthens the binding of a nucleotide to the umami receptor or vice versa. The addition of a furanone synergistically increases the umami flavour potency. The present invention also provides a method of increasing an animal's preference for a foodstuff, the method comprising the addition of a nucleotide, an amino acid selected from the group consisting of glycine, asparagine, alanine, cysteine, histidine, leucine, methionine, phenylalanine, serine, tryptophan and tyrosine and a furanone to the foodstuff. Also provided is a method of enhancing the umami flavour of a foodstuff, the method comprising the addition of a nucleotide, an amino acid selected from the group consisting of glycine, asparagine, alanine, cysteine, histidine, leucine, methionine, phenylalanine, serine, tryptophan and tyrosine and a furanone to the foodstuff. A method of increasing the meaty (savoury) flavour of a foodstuff is also achieved by the use of a nucleotide, an amino acid selected from the group consisting of (glycine, asparagine, alanine, cysteine, histidine, leucine, methionine, phenylalanine, serine, tryptophan and tyrosine) and a furanone as described herein. The combination of the three components enables them to work in synergy to enhance umami flavour perception.
As a further aspect, the invention relates to a process for producing a pet foodstuff comprising one or more nucleotides, one or more amino acids selected from the group consisting of glycine, asparagine, alanine, cysteine, histidine, leucine, methionine, phenylalanine, serine, tryptophan and tyrosine and one or more furanones, the method comprising the steps of adding and mixing one or more nucleotides, one or more amino acids selected from the group consisting of glycine, asparagine, alanine, cysteine, histidine, leucine, methionine, phenylalanine, serine, tryptophan and tyrosine and one or more furanones with a pet foodstuff. The addition and/or mixing may be carried out prior to, during or after formulating, processing or packaging the foodstuff. The addition and/or mixing of the nucleotide, amino acid and furanone may be sequential or simultaneous.
All features of all aspects apply to all other aspects, mutatis mutandis.
The inventors have found that the addition of one or more nucleotides, one or more amino acids selected from the group consisting of glycine, asparagine, alanine, cysteine, histidine, leucine, methionine, phenylalanine, serine, tryptophan and tyrosine and one or more furanones to a pet food product significantly increases the preference of a companion animal for the foodstuff. The animals show a strong preference for a foodstuff or water comprising one or more nucleotides, one or more amino acids selected from the group consisting of glycine, asparagine, alanine, cysteine, histidine, leucine, methionine, phenylalanine, serine, tryptophan and tyrosine and one or more furanones over a foodstuff or water having none, or one or two of these compounds. This overcomes the difficulties associated with fussy animals and ensures an animal eats the entirety of the recommended daily amount of foodstuff provided to it, resulting in the health and wellbeing of the animal as well as the peace of mind of the owner.
The advantage, therefore, of a three component mixture for inclusion in a foodstuff is several-fold: an animal will be encouraged to eat the foodstuff on a consistent and long term basis; the synergistic effect means that a lower amount of each of the ingredients needs to be included in a foodstuff, meaning cost effective use of each of the nucleotide, amino acid and furanone. Without wishing to be bound by theory, the present inventors believe that the umami taste receptor on the tongue of an animal can detect a nucleotide and an amino acid (importantly, selected from the group consisting of glycine, asparagine, alanine, cysteine, histidine, leucine, methionine, phenylalanine, serine, tryptophan and tyrosine) at different binding sites and thus, the effect of combining both a nucleotide and such an amino acid in the composition provides more than an additive effect of each component individually to the animal. This effect is further amplified by the addition of a furanone. The umami receptor is a heterodimeric transmembrane protein receptor and is also referred to in the art as TlRl/TlR3. The present application shows that through in silico modelling of a non-human umami receptor and in vitro assays using a non-human umami receptor the inventors have found that the amino acids of the present invention, namely glycine, asparagine, alanine, cysteine, histidine, leucine, methionine, phenylalanine, serine, tryptophan and tyrosine are each able to bind to and activate the umami receptor to different extents.
Further modelling of the cat umami receptor identified two other positions in the active site (170 and 302) that contained very different residues between human and other species and could potentially modify the access of amino acids to the binding site and also modify the binding behaviour of amino acids. It appears that the binding of one of the amino acids of the invention may change the conformation of the umami receptor allowing it more contact with a bound nucleotide. As can be seen in Figure 17, the receptor could be described in terms of a Venus Fly Trap, wherein the binding site consists of a structure similar to 'jaws', which close upon being bound by the compounds according to the invention. Once the amino acid has bound within the "jaws" of the receptor, the receptor may be more amenable to the binding of the nucleotide. It can be said that the amino acid potentially optimises the molecular environment for nucleotide binding. It is hypothesised that amino acid ligands have a primary binding site in the T1R1 active site but they also make interactions with other residues around the active site. The nature and extent of the interactions depends on the functional groups present in the amino acid side chain e.g. carboxyl, amino or hydrophobic groups. Thus changes in other residues in the active site are postulated as a possible reason for the different amino acid binding specificities observed between species. Furthermore, it is postulated that once the amino acid and nucleotide have bound, the furanone interacts synergistically to increase the umami flavour perception. This interaction may occur by cross talk between binding sites or during the transduction and neural processes.
The flytrap domain consists of two lobes, an upper lobe and a lower lobe that are connected by a region known as the hinge, (Figure 17). The flytrap transitions from an open confirmation to a closed conformation upon binding of an amino acid and/or nucleotide.
In silico modelling and in vitro testing by the inventors has shown that the amino acid binds near to the hinge region of the flytrap and the nucleotide binds at a region more distal to the hinge, but still remains between the lobes of the jaws. Thus, it appears that the amino acid first binds allowing the nucleotide to have a stronger connection with the receptor. Without the presence of the amino acid, the nucleotide seems to bind within the flytrap jaws but further away from the hinge region of the receptor. In the absence of the amino acid, the nucleotide does not appear to fit as tightly into the jaws/ binding site as when the amino acid (in accordance with the invention) is present.
Thus, the nucleotide and the amino acid (selected from those listed herein) appear to work together in a coordinated manner in order to assist each other in binding to the umami receptor and increasing the perception of both compounds by the animal on the taste receptor when they are delivered together in a composition. Again, without wishing to be bound by theory, it appears that the amino acid selected from the group consisting of glycine, asparagine, alanine, cysteine, histidine, leucine, methionine, phenylalanine, serine, tryptophan and tyrosine, and the nucleotide encourage each other in binding to the umami receptor. The umami flavour perception created from the nucleotide and amino acid binding is further increased by the presence of a furanone which acts in a synergistic manner.
The amino acids selected from the group consisting of glycine, asparagine, alanine, cysteine, histidine, leucine, methionine, phenylalanine, serine, tryptophan and tyrosine all have in common an uncharged side chain, and it should be noted that this list does not include cyclic amino acids, spyro amino acids or alpha disubstituted amino acids. Furthermore, the types of amino acids that interact in a complementary fashion with nucleotides in this way to increase the perception of such compounds by an animal, include aromatic, polar, lipohilic or small saturated ring amino acids.
As mentioned above, in addition to in silico modelling of the feline umami receptor, sequence alignments of the human, cat and dog receptors have been performed. Interestingly, the human sequence alignment shows that two amino acids at position 170 and 302 (numbered in relation to the human T1R1 receptor) are found as alanine residues in human, whereas these positions are glutamate and aspartate in the other species. Additionally, the feline umami receptor does not bind aspartate or glutamate, which are natural ligands for the human T1R1/T1R3 receptor. Therefore, due to these significant differences, it would not be expected by the skilled person that compounds that are known to bind to the human receptor would affect the umami receptor of other animals as described herein. It is noted that Yoshi et al, (Synergistic Effects of 5 '-Nucleotides on Rat Taste Responses to Various Amino Acids, Brain Research, 367 (1986) 45-51), conclude that a synergistic effect is seen between the amino acids and nucleotides. However, the experiments described were not carried out in vivo, but rather utilised in vitro nerve signalling.
Notably, it was assumed that a nerve response was concluded to be a positive response. However, as it is well known in the art, a nerve response can also be a negative response for an animal i.e. in vivo a nerve response could be a negative taste perception. Further, it can be seen that the amino acids discovered to be most responsive are not those that correlate to the information provided by the present invention. This is almost certainly due to the 'artificial' environment in which the amino acids were tested by Yoshi et al.
US patent US3524747 describes the addition of a minimum of seven amino acids to a foodstuff to impart a "meaty" flavour. However, although a combination of seven amino acids could be contemplated by the present invention, the knowledge obtained by the inventors (that certain amino acids with a nucleotide and a furanone enhances palatability) enables fewer than seven amino acids to be utilised to increase the palatability of a foodstuff.
It is notable that none of the prior art known to the inventors contemplates the use of a nucleotide and amino acid, (particularly, an amino acid selected from the group consisting of glycine, asparagine, alanine, cysteine, histidine, leucine, methionine, phenylalanine, serine, tryptophan and tyrosine) together with a furanone for enhancing the flavour of a foodstuff for a companion animal. As mentioned, these particular amino acids are thought to enhance the nucleotide binding to umami receptor working in a synergistic way, whereas other amino acids do not appear to bind to the umami receptor.
The nucleotide, amino acid and furanone according to the present invention may be incorporated into any product which an animal, such as a dog or a cat, may consume in its diet. Thus, the invention covers standard food products, supplements, pet food, drinks, snacks and treats. The food product is preferably a cooked product. It may incorporate meat or animal derived material (such as beef, chicken, turkey, lamb, blood plasma, marrowbone etc. or two or more thereof). The food stuff alternatively may be meat free (preferably including a meat substitute such as soya, maize gluten or a soya product) in order to provide a protein source. The product may contain additional protein sources such as soya protein concentrate, milk proteins, gluten etc. The product may also contain a starch source, such as gelatinised starch, such as one or more grains (e.g. wheat, corn, rice, oats, barely etc) or may be starch free. A typical dry commercial cat and dog food contains about 10-70% crude protein, about 10-60% fat and the remainder being carbohydrate, including dietary fibre and ash. A typical wet, or moist product contains (on a dry matter basis) about 40% fat, 50% protein and the remainder being fibre and ash. The present invention is particularly relevant for a pet foodstuff as herein described which is sold as a diet, foodstuff or supplement for a cat or dog. In the present text the terms "domestic" dog and "domestic" cat mean dogs and cats, in particular Felis domesticus and Canis domes ticus. Preferably, the pet foodstuff will meet the macronutrient requirements of an animal preferably a ratio of protein: fat: carbohydrate of approximately 50:40: 10 for feline animals and 30:60: 10 for a canine animal.
As can be seen from the examples, below, it has been surprisingly found that an amino acid selected from the group consisting of glycine, asparagine, alanine, cysteine, histidine, leucine, methionine, phenylalanine, serine, tryptophan and tyrosine, a nucleotide and a furanone of the invention provide a greater than additive effect when presented to an animal. In other words, the preference of a companion animal for the combination of a nucleotide, an amino acid selected from the group consisting of glycine, asparagine, alanine, cysteine, histidine, leucine, methionine, phenylalanine, serine, tryptophan and tyrosine and a furanone is greater than an additive effect of the preference for any or each of the individual compounds. The addition of a furanone increases this preference to a greater extent. That is, inclusion of a furanone increases preference by more than the additive effect of the preference for the furanone alone.
Thus, the unexpected benefit of the combination of one or more nucleotides, one or more amino acids and one or more furanones is increased palatability. Without wishing to be bound by theory, the present inventors believe that this is due to the conformation and positioning of the binding sites of the umami receptor for a nucleotide, amino acid and the enhancing effect of furanone, as described above. The invention will now be described in reference to the following Figures and Examples in which:
Figure 1 shows the results of a difference test of a composition comprising 25mM histidine + 2.5mM IMP with a composition comprising 25mM histidine;
Figure 2 shows the results of a difference test of a composition comprising 25mM histidine + 2.5mM IMP with a composition comprising 2.5mM IMP;
Figure 3 shows the results of a difference test of a composition comprising 25mM alanine + 2.5mM GMP with a composition comprising 25mM alanine; Figure 4 shows the results of a difference test of a composition comprising 25mM alanine + 2.5mM GMP with a composition comprising 2.5mM GMP;
Figure 5 shows the results of a difference test of a composition comprising 25mM glycine + 2.5mM AMP with a composition comprising 25mM glycine;
Figure 6 shows the results of a difference test of a composition comprising 25mM glycine + 2.5mM AMP with a composition comprising 2.5mM AMP;
Figure 7 shows the results of a difference test of a composition comprising 25mM histidine + 2.5mM IMP/GMP + 4000ppb (4ppm) furaneol with a composition comprising 2.5mM IMP/GMP + 4000ppb (4ppm) furaneol;
Figure 8 shows the results of a difference test of a composition comprising 2.5mM
IMP/GMP + 4ppm furaneol with a composition comprising 2.5mM IMP/GMP;
Figure 9 shows the results of a difference test of a composition comprising 25mM histidine + 1.25mM IMP/GMP + 4ppm furaneol with a composition comprising 25mM histidine + 1.25mM IMP/GMP;
Figure 10 shows the results of a difference test of a gel composition comprising 25mM histidine + 2ppm furaneol with a gel composition comprising 25mM histidine;
Figure 11 shows the results of a difference test of a composition comprising 25mM histidine + 2.5mM GMP + 4ppm furaneol with a composition comprising 25mM histidine + 2.5mM GMP;
Figure 12 shows the results of a difference test of a composition comprising 25mM histidine + 2.5mM GMP + 5ppb sotolon with a composition comprising 25mM histidine + 2.5mM GMP;
Figure 13 shows the results of a difference test of a pet food comprising 25mM histidine + 2.5mM IMP/GMP + 4ppm furaneol with a pet food comprising a conventional reaction flavour system.
Figure 14 shows the resulting dose response curves of each amino acid of the invention that were screened in vitro for their ability to activate the T1R1/T1R3 receptor in the presence of 0.2mM IMP. The corresponding EC 50 values are shown in the table.
Figure 15 shows the dose response curves of nucleotides of the invention that were screened in vitro for their ability to activate the T1R1/T1R3 receptor in the presence of 20mM alanine. The corresponding EC 50 values are shown in the table.
Figure 16 shows the predicted structure of the T1R1/T1R3 umami receptor.
Figure 17 shows a schematic of the predicted structure of the umami receptor; and Figure 18 shows a sequence alignment of the human, feline, canine, mouse and rat umami receptors.
Examples
All amino acids used in the examples were of the L-form. Ajitide is a 50:50 mixture of GMP:IMP.
Example 1
Cats were allowed access to water containing 25mM histidine + 2.5mM IMP and to water containing 25mM histidine.
The methodology used a 2-bottle choice test with 24 cats (the final number of cats for each test can vary due to data being discarded by spillage, etc.). Cats were housed individually during trial periods and had free access to water available between testing periods. The test involved a choice test between the tastant/ mixture at a given concentration dissolved in deionised water versus deionised water only or another tastant/ mixture. Control was made for positional bias (e.g. AJ B exposure 1 and B/ A exposure 2) and evaporation loss. The testing time was 36 hours (i.e. 18 hours per day, allowing a two-day crossover).
Following two consecutive days of each testing, cats had two consecutive days of rest. Cats were offered a dry diet as a single meal at the start of the test period for one hour, calculated to meet the individual requirements for each cat.
The results are shown in the table below, and in Figure 1.
Analysis of Intake g
ANOVA Table for Fixed Effects
Table of Mean Product Difference, Standard Error & 95% Confidence Intervals
Intake of the combination of histidine + IMP, was on average 25.74g more that the intake of histidine alone, and shows a clear preference for the combination over histidine alone.
Example 2
Cats were allowed access to water containing 25mM histidine + 2.5mM IMP and to water containing 2.5mM IMP alone.
The results are shown in the table below, and in Figure 2.
Analysis of Intake g
ANOVA Table for Fixed Effects
Table of Mean Product Difference, Standard Error & 95% Confidence Intervals
Intake of the combination of histidine + IMP, was on average 38.81g more that the intake of IMP alone, which is a significant difference and shows a clear preference for the combination over IMP alone. The results of examples 1 and 2 together show that a combination of histidine and IMP is preferable to either of the compounds alone. Example 3
A difference test was carried out as described in Example 1 to compare a composition containing 25mM alanine + 2.5mM GMP with a composition containing 25mM alanine only.
The results are shown in the table below and in Figure 3.
Analysis of Intake g
AN OVA Table for Fixed Effects
Table of Mean Product Difference, Standard Error & 95% Confidence Intervals
It can be seen that the intake of the combination of alanine + GMP was, on average, 55.62g more than the intake of water containing alanine alone which is a significant difference. This shows that the animals prefer the combination of alanine + GMP to alanine alone.
Example 4
The difference test was carried out as described in example 2; however the composition containing 25mM alanine + 2.5mM GMP was compared with a composition containing 2.5mM GMP only.
The results are shown in the table below and in Figure 4.
Analysis of Intake g
ANOVA Table for Fixed Effects
Table of Mean Product Difference, Standard Error & 95% Confidence Intervals
It can be seen that the intake of GMP + alanine was, on average, 56.16g more than the intake of GMP alone, which is a significant difference, and shows that the animals significantly prefer the combination of alanine + GMP to GMP alone.
The results of Example 3 and 4 together show that a combination of alanine + GMP is preferable to either of the compounds alone. Example 5
A difference test was carried out as described in Example 1 to compare a composition containing 25mM glycine + 2.5mM AMP with a composition comprising 25mM glycine only. The results are shown in the table below and in Figure 5.
Analysis of Intake g
ANOVA Table for Fixed Effects
Table of Mean Product Difference, Standard Error & 95% Confidence Intervals It can be seen that the intake of glycine + AMP was, on average, 23.79g more than the intake of glycine alone. This shows that the animals significantly prefer the combination of glycine + AMP to glycine alone.
Example 6
The difference test was carried out as described in Example 4; however the composition containing 25mM glycine + 2.5mM AMP, was compared with a composition containing 2.5mM AMP only.
The results are shown in the table below, and in Figure 6.
Analysis of Intake g
AN OVA Table for Fixed Effects
Table of Mean Product Difference, Standard Error & 95% Confidence Intervals It can be seen that the intake of glycine + AMP was, on average, 36.63g more than the intake of AMP, and shows that the animals significantly prefer the combination of glycine + AMP to AMP alone.
The results of Examples 5 and 6 together show that a combination of glycine + AMP is preferable to either of the compounds alone.
Example 7
A difference test was carried out as described in Example 1 to compare a composition containing 25mM histidine + 2.5mM IMP/GMP (Ajitide) + 4ppm furaneol, with a composition comprising 2.5mM IMP/GMP (Ajitide) + 4ppm furaneol only. The results are shown in the table below and in Figure 7.
Analysis of Intake g
ANOVA Table for Fixed Effects
Table of Mean Product Difference, Standard Error & 95% Confidence Intervals It can be seen that the intake of histidine + IMP/GMP(Aji) + furaneol was, on average, 63.07g more than the intake of IMP/GMP + furaneol, and shows that the animals significantly prefer the combination of histidine + IMP/GMP + furaneol to IMP/GMP + furaneol. Example 8
A difference test was carried out as described in Example 1 to compare a composition containing 2.5mM IMP/GMP (Ajitide) + 4ppm furaneol, with a composition comprising 2.5mM IMP/GMP (Ajitide) only. The results are shown in the table below and in Figure 8.
Analysis of Intake g
ANOVA Table for Fixed Effects
Table of Mean Product Difference, Standard Error & 95% Confidence Intervals
It can be seen that the intake of IMP/GMP(Aji) + furaneol was, on average, 69.29g more than the intake of IMP/GMP (Aji) alone, and shows that the animals significantly prefer the combination of IMP/GMP (Aji) + furaneol to IMP/GMP (Aji) alone.
Example 9
A difference test was carried out as for Example 6, however, a composition containing 25mM histidine + 1.25mM IMP/GMP(Aji) + 4ppm furaneol, with a composition comprising 25mM histidine + 1.25mM IMP/GMP (Aji) only.
The results are shown below and in figure 9.
Analysis of Intake g ANOVA Table for Fixed Effects
Table of Mean Product Difference, Standard Error & 95% Confidence Intervals It can be seen that the intake of histidine + IMP/GMP + furaneol was on average 34.29g more than the intake of histidine + IMP/GMP, and thus shows that the animals significantly preferred the combination of histidine + IMP/GMP + furaneol to histidine + IMP/GMP.
Example 10
Cats were allowed access to gelatine gel containing either 25mM histidine + 2ppm furaneol or a gel comprising 25mM histidine only). The methodology used a 2-bowl choice test with 30 cats (the final number of cats for each test can vary due to data being discarded by spillage, etc.). Cats were housed individually during trial periods and had free access to water available between testing periods. The test involved a choice test between the tastant/ mixture at a given concentration dissolved in a gelatine gel versus another tastant/ mixture. Control was made for positional bias (e.g. AJ B exposure 1 and B/ A exposure 2). The testing time was 1 hour (i.e. 30 minutes per day, allowing a two- day crossover). Following two consecutive days of each testing, cats had two consecutive days of rest. Cats were offered a dry diet as a single meal prior to the start of the test period for 30 minutes, calculated to meet the individual requirements for each cat.
The results are shown below and in figure 10.
Analysis of Intake (g)
ANOVA Table for Fixed Effects
Table of Mean Product Difference, Standard Error & 95% Confidence Intervals It can be seen that the intake of histidine + furaneol was an average 29.84g more than the intake of histidine alone, and thus shows that the animals significantly prefer the combination of histidine + furaneol to histidine alone. This example also shows that a preference effect can be seen whether the base composition is water or a gel matrix.
Example 11
A difference test was carried out as described in Example 1 to compare a composition containing 25mM histidine + 2.5mM GMP + 4ppm furaneol, with a composition comprising 2.5mM GMP + 25mM histidine only.
The results are shown in the table below and in Figure 11.
ANOVA Table for Fixed Effects
Table of Mean Product Difference, Standard Error & 95% Confidence Intervals It can be seen that the intake of histidine + GMP + furaneol was, on average, 31.61g more than the intake of GMP + histidine, and shows that the animals significantly prefer the combination of histidine + GMP + furaneol to GMP + histidine.
Example 12
A difference test was carried out as described in Example 1 to compare a composition containing 25mM histidine + 2.5mM GMP + 5ppm sotolon, with a composition comprising 2.5mM GMP + 25mM histidine only.
The results are shown in the table below and in Figure 12. ANOVA Table for Fixed Effects
Table of Mean Product Difference, Standard Error & 95% Confidence Intervals
It can be seen that the intake of histidine+ GMP + sotolon was, on average, 8.85g more than the intake of GMP + histidine, and shows that the animals prefer the combination of histidine + GMP + sotolon to GMP + histidine.
Example 13
A difference test was carried out as previously described; however the compositions were a wet cat food either comprising histidine + IMP/GMP (Ajitide) + furaneol or a conventional reaction flavour system. The pet food comprising histidine +IMP/GMP + furaneol was preferred by the cats. Results are shown in Figure 13.
Example 14
In vitro screening was carried out in order to establish which amino acids bind and activate the umami receptor. Results are shown in Figure 14. Example 15
In vitro screening was carried out in order to establish which nucleotides bind and activate the umami receptor. Results are shown in Figure 15.