Mimosine

Mimosine
Names
	IUPAC name (2S)-2-Amino-3-(3-hydroxy-4-oxopyridin-1-yl)propanoic acid
	Other names leucenol
Identifiers
CAS Number	500-44-7 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:29063 ;
ChEMBL	ChEMBL251433 ;
ChemSpider	3728 ;
DrugBank	DB01055 ;
ECHA InfoCard	100.007.187
PubChem CID	3862;
UNII	Z46B1LUI5N ;
	InChI InChI=1S/C8H10N2O4/c9-5(8(13)14)3-10-2-1-6(11)7(12)4-10/h1-2,4-5,12H,3,9H2,(H,13,14) Key: WZNJWVWKTVETCG-UHFFFAOYSA-N ; InChI=1/C8H10N2O4/c9-5(8(13)14)3-10-2-1-6(11)7(12)4-10/h1-2,4-5,12H,3,9H2,(H,13,14) Key: WZNJWVWKTVETCG-UHFFFAOYAK;
	SMILES O=C(O)C(N)CN/1/C=C\C(=O)C(\O)=C\1;
Properties
Chemical formula	C8H10N2O4
Molar mass	198.178 g·mol−1
Melting point	291 °C (556 °F; 564 K)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	verify (what is ?)
	Infobox references

Mimosine or leucenol is a toxic non-protein amino acid chemically similar to tyrosine, that was first isolated from Mimosa pudica. It occurs in a few other Mimosa spp. and all members of the closely related genus Leucaena.

This compound, also known as leucenol, was first isolated from the seeds of Leucaena glauca Benth.,[1] and was later investigated by Adams and coworkers.[2]

Properties

Mimosine melts with decomposition. The hydrochloride salt melts at 174.5–175.0 °C with decomposition; the hydrobromide decomposes at 179.5 °C, and the hydroiodide decomposes at 183.0–183.5 °C. Mimosine only forms monobasic acids, but the methyl ester forms a dihydrochloride, C₇H₉O₂N₂(COOMe)•2 HCl•½ H₂O, mp. 175–6 °C.

Biological effects

Mimosine arrests dividing cells in the late G1 phase by inhibiting DNA replication initiation.[3] In ruminants, mimosine is degraded to 3,4- and 2,3-dihydroxypyridone (3,4- and 2,3-DHP).

Although toxicosis has occurred in Australia, Papua New Guinea, Africa and Florida, it has not been recorded in any other tropical and subtropical regions. Goats in Burma lost hair when fed a diet containing 50% of Leucaena. Goats and cattle in Hawaii are able to degrade the 3,4-DHP ruminally. Tolerance might be related to the presence or absence of microbes tolerant to mimosine and 3,4-DHP. It is known that at least Australian goats do not share the abilities of their Hawaiian counterparts.

Bickel and Wibaut[4] found in feeding experiments with rats and mice that leucenol is probably the toxic constituent of Leucaena glauca seeds, but they did not observe with these animals the loss of hair which seems to occur when these seeds are fed to cattle.[5] Aung from Myanmar isolated the new subspecies of Klebsiella pneumonae that can degrade mimosine.[6]

Some rhizobia are known to produce rhizomimosinase, which consumes pyridoxal 5′-phosphate to degrade mimosine into 3,4-dihydroxypyridone, pyruvate, and ammonium.[7] A similar enzyme, mimosinase, is produced by Leucaena leucocephala.[8]

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References

Mascré (1937). Comptes Rendus. 204: 890. Missing or empty |title= (help)
Adams, Roger; Cristol, Stanley J.; Anderson, Arthur A.; Albert, Alfred A. (1945). "The Structure of Leucenol. I". J. Am. Chem. Soc. 67: 89–92. doi:10.1021/ja01217a032.
T. Krude Exp. Cell Res. Volume 247, Issue 1, 1999, Pages 148-159
Rec. Trav. Chim., 1946, 65 65; Wibaut, Helv. Chim. Acta, 1946, 29 1669; (with Kleipol), Rec. Trav. Chim., 1947, 66 24, 459.
Mascré; Ottenwälder (1941). Bull. Sci. Pharmacol. 3 (3): 65. Missing or empty |title= (help)
http://tropicalgrasslands.info/index.php/tgft/article/viewFile/38/11
Negi VS, Bingham JP, Li QX, Borthakur D. (2013). "midD-encoded 'rhizomimosinase' from Rhizobium sp. strain TAL1145 is a C–N lyase that catabolizes L-mimosine into 3-hydroxy-4-pyridone, pyruvate and ammonia". Amino Acids. 44 (6): 1537–47. doi:10.1007/s00726-013-1479-z. PMID 23462928.CS1 maint: uses authors parameter (link)
Negi VS, Bingham J-P, Li QX, Borthakur D. (2014). "A Carbon–Nitrogen Lyase from Leucaena leucocephala Catalyzes the First Step of Mimosine Degradation". Plant Physiology. 164 (2): 922–934. doi:10.1104/pp.113.230870. PMC 3912116. PMID 24351687.CS1 maint: uses authors parameter (link)

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[1] Mascré (1937). Comptes Rendus. 204: 890. Missing or empty |title= (help)

[2] Adams, Roger; Cristol, Stanley J.; Anderson, Arthur A.; Albert, Alfred A. (1945). "The Structure of Leucenol. I". J. Am. Chem. Soc. 67: 89–92. doi:10.1021/ja01217a032.

[3] T. Krude Exp. Cell Res. Volume 247, Issue 1, 1999, Pages 148-159

[4] Rec. Trav. Chim., 1946, 65 65; Wibaut, Helv. Chim. Acta, 1946, 29 1669; (with Kleipol), Rec. Trav. Chim., 1947, 66 24, 459.

[5] Mascré; Ottenwälder (1941). Bull. Sci. Pharmacol. 3 (3): 65. Missing or empty |title= (help)

[6] ttp://tropicalgrasslands.info/index.php/tgft/article/viewFile/38/11

[7] Negi VS, Bingham JP, Li QX, Borthakur D. (2013). "midD-encoded 'rhizomimosinase' from Rhizobium sp. strain TAL1145 is a C–N lyase that catabolizes L-mimosine into 3-hydroxy-4-pyridone, pyruvate and ammonia". Amino Acids. 44 (6): 1537–47. doi:10.1007/s00726-013-1479-z. PMID 23462928.CS1 maint: uses authors parameter (link)

[8] Negi VS, Bingham J-P, Li QX, Borthakur D. (2014). "A Carbon–Nitrogen Lyase from Leucaena leucocephala Catalyzes the First Step of Mimosine Degradation". Plant Physiology. 164 (2): 922–934. doi:10.1104/pp.113.230870. PMC 3912116. PMID 24351687.CS1 maint: uses authors parameter (link)