felinine
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Felinine, also known as ''(R)-2-amino-3-(4-hydroxy-2-methylbutan-2-ylthio)propanoic acid'', is a chemical compound and
amino acid Amino acids are organic compounds that contain both amino and carboxylic acid functional groups. Although hundreds of amino acids exist in nature, by far the most important are the alpha-amino acids, which comprise proteins. Only 22 alpha a ...
found in cat urine and a precursor via microbial lyase of the putative cat pheromone and
thiol In organic chemistry, a thiol (; ), or thiol derivative, is any organosulfur compound of the form , where R represents an alkyl or other organic substituent. The functional group itself is referred to as either a thiol group or a sulfhydryl gro ...
called 3-mercapto-3-methylbutan-1-ol (MMB). Felinine is excreted by selected Felidae species including bobcats, Chinese desert cats, the
kodkod The kodkod (''Leopardus guigna'') (), also called guiña, is the smallest felid species native to the Americas. It lives primarily in central and southern Chile, as well as marginally in adjoining areas of Argentina. Since 2002, it has been liste ...
, and domestic cats.


Biosynthesis

Felinine synthesis starts in the liver through a
condensation reaction In organic chemistry, a condensation reaction is a type of chemical reaction in which two molecules are combined to form a single molecule, usually with the loss of a small molecule such as water. If water is lost, the reaction is also known as a ...
of
glutathione Glutathione (GSH, ) is an antioxidant in plants, animals, fungi, and some bacteria and archaea. Glutathione is capable of preventing damage to important cellular components caused by sources such as reactive oxygen species, free radicals, pe ...
and
isopentenyl pyrophosphate Isopentenyl pyrophosphate (IPP, isopentenyl diphosphate, or IDP) is an isoprenoid precursor. IPP is an intermediate in the classical, HMG-CoA reductase pathway (commonly called the mevalonate pathway) and in the ''non-mevalonate'' MEP pathway of i ...
to form 3-methylbutanolglutathionine (3-MBG). Then, kidney epithelia tissue secretes ''γ''-glutamyl transpeptidase (''γ''-GTP). ''γ''-GTP converts 3-MBG to 3-methylbutanol-cysteinylglycine (MBCG). Next, a majority of MBCG is hydrolyzed to felinine and glycine by
carboxylesterase The enzyme carboxylesterase (or carboxylic-ester hydrolase, EC 3.1.1.1; systematic name carboxylic-ester hydrolase) catalyzes reactions of the following form: :a carboxylic ester + H2O \rightleftharpoons an alcohol + a carboxylate Most enzymes fr ...
5A, or cauxin.
Cauxin Cauxin is a carboxylesterase that is excreted in large amounts in cat urine. There is also evidence that it can serve as a peptide hydrolase in the production of cat pheromone precursors. Cauxin has a mass of 70 kilodaltons and is composed of 545 ...
specifically works by hydrolyzing the dipeptide (felinylglycine) in MBCG to increase the concentration of urinary felinine. The leftover MBCG is converted to felinine and secreted into the cells where it is acetylated and transported to fecal material. Therefore, high concentration of felinine is present in urine while a minor concentration of N-acetylfelinine is present in cat excrement. # Glutathione + Isopentenyl Pyrophosphate → 3-MBG # 3-MBG + ''γ''-GTP → MBCG #* MBCG + Cauxin → Felinine +
Glycine Glycine (symbol Gly or G; ) is an amino acid that has a single hydrogen atom as its side chain. It is the simplest stable amino acid ( carbamic acid is unstable), with the chemical formula NH2‐ CH2‐ COOH. Glycine is one of the proteinog ...
, or #* MBCG → N-Acetylfelinine Urine of domestic cats may contain a series of felinine-containing compounds including free felinine, acetylfelinine, felinylglycine and 3-MBG. Cysteine also plays a role in the synthesis of felinine. For one, the
amino acid Amino acids are organic compounds that contain both amino and carboxylic acid functional groups. Although hundreds of amino acids exist in nature, by far the most important are the alpha-amino acids, which comprise proteins. Only 22 alpha a ...
is commonly present in many enzymes. Also, it is one of the few precursors for glutathione. Glutathione is converted to 3-MBG, and so cysteine has an important role in the early steps of synthesis. # Cysteine + Glycine + Glutamate → Glutathione  


Uses

A precursor for mercaptan is 3-mercapto-3-methylbutanol (MMB). MMB is a chemical which gives a strong odor to cat urine. This smell is likely used for communicating amongst cats as well as scaring away predators and rivals. That is, the smell can mark their territory amongst other male cats and attract a female mate.


Felinine Variables

Felinine excretion is regulated by levels of testosterone, and so its concentration is dependent on the sex and age of the cat. For instance, cats with high levels of testosterone produce higher levels of 3-MBG. Consequently, non neutered males have significantly higher concentrations of felinine in their urine than females and neutered males. Furthermore, cauxin is a carboxylesterase enzyme which hydrolyzes 3-methylbutanol-cysteinylglycine (MBCG) into felinine. Thus, felinine is dependent upon cauxin, and cauxin is excreted most in male cats above the age of three months. Therefore, older cats, compared to young kittens, have higher concentrations of felinine. Also, long hair cats have less cysteine to go around as the amino acid is also used for protein structures found in hair. Thus, long haired cats make less felinine than short haired cats. The presence of urea in cat urine has been found to react with the felinine in the urine. After synthetic felinine was incubated in urea, none of it was recovered, suggesting a degradation or modification of felinine. However, evidence suggests that the interaction does not stem from a nucleophilic reaction. It has been found that dietary supplementation with amino acids other than cysteine impact felinine excretion. This is most likely caused by the presence of arginine, which is believed to inhibits synthesis of MBG, which decreases felinine excretion.


See also

* Cat pheromone


References

Sulfur amino acids {{biochem-stub