Felinine
Names
IUPAC name
(2R)-2-Amino-3-[(3-hydroxy-1,1-dimethylpropyl)thio]propanoic acid
Identifiers
3D model (JSmol)
2250979
ChEBI
ChemSpider
UNII
  • InChI=1S/C8H17NO3S/c1-8(2,3-4-10)13-5-6(9)7(11)12/h6,10H,3-5,9H2,1-2H3,(H,11,12)/t6-/m0/s1 checkY
    Key: IFERABFGYYJODC-LURJTMIESA-N checkY
  • InChI=1/C8H17NO3S/c1-8(2,3-4-10)13-5-6(9)7(11)12/h6,10H,3-5,9H2,1-2H3,(H,11,12)/t6-/m0/s1
    Key: IFERABFGYYJODC-LURJTMIEBQ
  • O=C(O)[C@@H](N)CSC(CCO)(C)C
Properties
C8H17NO3S
Molar mass 207.29 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Infobox references

Felinine, also known as (R)-2-amino-3-(4-hydroxy-2-methylbutan-2-ylthio)propanoic acid, is an amino acid found in cat urine and a precursor via microbial lyase of the putative cat pheromone and thiol called 3-mercapto-3-methylbutan-1-ol (MMB).[1] [2][3] Felinine is excreted by some Felidae species, including bobcats, Chinese desert cats, the kodkod, and domestic cats.

Biosynthesis

Felinine synthesis starts in the liver through a condensation reaction of glutathione and isopentenyl pyrophosphate to form 3-methylbutanolglutathionine (3-MBG).[4] 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 5A, or cauxin.[5] Cauxin specifically works by hydrolyzing the dipeptide (felinylglycine) in MBCG to increase the concentration of urinary felinine.[6] 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.[5]

  1. Glutathione + Isopentenyl Pyrophosphate → 3-MBG
  2. 3-MBG + γ-GTP → MBCG
    • MBCG + Cauxin → Felinine + Glycine, or
    • MBCG → N-Acetylfelinine

Urine of domestic cats may contain a series of felinine-containing compounds including free felinine, acetylfelinine, felinylglycine and 3-MBG.[7]

Cysteine also plays a role in the synthesis of felinine. For one, the amino acid 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.[8]

  1. 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.[9]

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.[10] 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.[11]

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.[12]

The 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.[13]

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 inhibit synthesis of MBG, which decreases felinine excretion.[14]

See also

References

  1. ↑ Discovery of felinine: Westall, R. G. "Amino acids and other ampholytes of urine. II. Isolation of a new sulfur-containing amino acid from cat urine" Biochemical Journal (1953), 55, 244-8.
  2. ↑ W.H. Hendriks; P.J. Moughan; M.F. Tarttelin; A.D. Woolhouse (1995). "Felinine: a urinary amino acid of Felidae". Comp. Biochem. Physiol. 112B (4): 581–588. doi:10.1016/0305-0491(95)00130-1. PMID 8590373.
  3. ↑ P. David Josephy (28 January 2006). Molecular Toxicology. Oxford University. p. 376. ISBN 978-0-19-977145-5. Retrieved 29 July 2013.
  4. ↑ K.J. Rutherfurd; S.M. Rutherfurd; P.J. Moughan; W.H. Hendriks (January 2002). "Isolation and Characterization of a Felinine-containing Peptide from the Blood of the Domestic Cat (Felis catus)". J. Biol. Chem. 277 (1): 114–119. doi:10.1074/jbc.M107728200. PMID 11698402.
  5. 1 2 Futsuta, Ayami; Hojo, Wataru; Miyazaki, Tamako; Yamashita, Tetsuro; Miyazaki, Masao (January 2018). "LC–MS/MS quantification of felinine metabolites in tissues, fluids, and excretions from the domestic cat (Felis catus)". Journal of Chromatography B. 1072: 94–99. doi:10.1016/j.jchromb.2017.11.006. PMID 29145026.
  6. ↑ M. Miyazaki; T. Yamashita; Y. Suzuki; Y. Saito; S. Soeta; H. Taira; A. Suzuki (October 2006). "A major urinary protein of the domestic cat regulates the production of felinine, a putative pheromone precursor". Chem. Biol. 13 (10): 1071–1079. doi:10.1016/j.chembiol.2006.08.013. PMID 17052611.
  7. ↑ W.H. Hendriks; D.R.K. Harding; K.J. Rutherfurd-Markwick (2004). "Isolation and characterisation of renal metabolites of g-glutamylfelinylglycine in the urine of the domestic cat (Felis catus)". Comp. Biochem. Phys. 139 (2): 245–251. doi:10.1016/j.cbpc.2004.07.007. PMID 15465671.
  8. ↑ Hendriks, W.H; Rutherfurd, S.M; Rutherfurd, K.J (July 2001). "Importance of sulfate, cysteine and methionine as precursors to felinine synthesis by domestic cats (Felis catus)". Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology. 129 (3): 211–216. doi:10.1016/S1532-0456(01)00196-X. PMID 11461837.
  9. ↑ Futsuta, Ayami; Hojo, Wataru; Miyazaki, Tamako; Yamashita, Tetsuro; Miyazaki, Masao (January 2018). "LC–MS/MS quantification of felinine metabolites in tissues, fluids, and excretions from the domestic cat (Felis catus)". Journal of Chromatography B. 1072: 94–99. doi:10.1016/j.jchromb.2017.11.006. PMID 29145026.
  10. ↑ Miyazaki, Masao; Yamashita, Tetsuro; Suzuki, Yusuke; Saito, Yoshihiro; Soeta, Satoshi; Taira, Hideharu; Suzuki, Akemi (October 2006). "A Major Urinary Protein of the Domestic Cat Regulates the Production of Felinine, a Putative Pheromone Precursor". Chemistry & Biology. 13 (10): 1071–1079. doi:10.1016/j.chembiol.2006.08.013. PMID 17052611.
  11. ↑ Miyazaki, Masao; Yamashita, Tetsuro; Suzuki, Yusuke; Saito, Yoshihiro; Soeta, Satoshi; Taira, Hideharu; Suzuki, Akemi (October 2006). "A Major Urinary Protein of the Domestic Cat Regulates the Production of Felinine, a Putative Pheromone Precursor". Chemistry & Biology. 13 (10): 1071–1079. doi:10.1016/j.chembiol.2006.08.013. PMID 17052611.
  12. ↑ Hagen-Plantinga, E. A.; Bosch, G.; Hendriks, W. H. (June 2014). "Felinine excretion in domestic cat breeds: a preliminary investigation". Journal of Animal Physiology and Animal Nutrition. 98 (3): 491–496. doi:10.1111/jpn.12097. PMID 23819478.
  13. ↑ Rutherfurd, S. M.; Kitson, T. M.; Woolhouse, A. D.; McGrath, M. C.; Hendriks, W. H. (2007-07-31). "Felinine stability in the presence of selected urine compounds". Amino Acids. 32 (2): 235–242. doi:10.1007/s00726-006-0369-z. ISSN 0939-4451. PMID 16868647. S2CID 2045082.
  14. ↑ Hendriks, Wouter H.; Rutherfurd-Markwick, Kay J.; Weidgraaf, Karin; Hugh Morton, R.; Rogers, Quinton R. (2008-10-08). "Urinary felinine excretion in intact male cats is increased by dietary cystine". The British Journal of Nutrition. 100 (4): 801–809. doi:10.1017/S0007114508945165. ISSN 1475-2662. PMID 18341755. S2CID 26079809.
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