'Methionine' is an α-
amino acid with the
chemical formula HO
2CCH(NH
2)CH
2CH
2SCH
3. This
essential amino acid is classified as
nonpolar. Together with
cysteine, methionine is one of two
sulfur-containing proteinogenic amino acids. Its derivative
S-adenosyl methionine (SAM) serves as a
methyl donor. Methionine in an intermediate in the biosynthesis of cysteine,
carnitine, and
taurine,
lecithin,
phosphatidylcholine, and other
phospholipids. Improper conversion of methionine can lead to
atherosclerosis.
Methionine is one of only two amino acids encoded by a single codon (AUG) in the standard
genetic code (
tryptophan, encoded by UGG, is the other). The codon AUG is also significant, in that it carries the "Start" message for a
ribosome that signals the initiation of protein
translation from mRNA. As a consequence, methionine is incorporated into the N-terminal position of all
proteins in
eukaryotes and
archaea during translation, although it is usually removed by
post-translational modification.
Biosynthesis
As an essential amino acid, methionine is not synthesized in humans, hence we must ingest methionine or methionine-containing proteins. In plants and microorganisms, methionine is synthesized via a pathway that uses both
aspartic acid and
cysteine. First, aspartic acid is converted via β-aspartyl-semialdehyde into homoserine, introducing the pair of contiguous methylene groups. Homoserine converts to ''O''-succinyl
homoserine, which then reacts with cysteine to produce
cystathionine, which is cleaved to yield
homocysteine. Subsequent methylation of the
thiol group by
folates affords methionine. Both
cystathionine-γ-synthase and
cystathionine-β-lyase require
Pyridoxyl-5'-phosphate as a
cofactor, whereas
homocysteine methyltransferase requires
Vitamin B12 as a cofactor.
[1]
Enzymes involved in methionine biosynthesis:
#
aspartokinase
# β-aspartate semialdehyde
dehydrogenase
# homoserine dehydrogenase
# homoserine
acyltransferase
# cystathionine-γ-
synthase
# cystathionine-β-
lyase
#
methionine synthase (in mammals, this step is performed by
homocysteine methyltransferase)
Other biochemical pathways
Although mammals cannot synthesize methionine, they can still utilize it in a variety of biochemical pathways:
Methionine is converted to
S-adenosylmethionine (SAM) by (1)
methionine adenosyltransferase. SAM serves as a methyl-donor in many (2)
methyltransferase reactions and is converted to
S-adenosylhomocysteine (SAH). (3)
adenosylhomocysteinase converts SAH to
homocysteine.
There are two fates of
homocysteine.
★ First, methionine can be regenerated from homocysteine via (4)
methionine synthase. It can also be remethylated using
glycine betaine (NNN-trimethyl glycine) to methionine via the enzyme
Betaine-homocysteine methyltransferase (E.C.2.1.1.5, BHMT). BHMT makes up to 1.5% of all the soluble protein of the liver, and recent evidence suggests that it may have a greater influence on methionine and homocysteine homeostasis than Methionine sythase.
★ Alternatively, homocysteine can be converted to cysteine. (5)
cystathionine-β-synthase (a PLP-dependent enzyme) combines homocysteine and serine to produce
cystathionine. Instead of degrading
cystathionine via
cystathionine-β-lyase as in the biosynthetic pathway, cystathionine is broken down to
cysteine and
α-ketobutyrate via (6)
cystathionine-γ-lyase. (7)
α-ketoacid dehydrogenase converts α-ketobutyrate to
propionyl-CoA, which is metabolized to
succinyl-CoA in a three-step process (see
propionyl-CoA for pathway).
Synthesis
Racemic methionine can be synthesized from diethyl sodium phthalimidomalonate by alkylation with chloroethylmethylsulfide (ClCH
2CH
2SCH
3) followed by hydrolysis and decarboxylation.
[2]
Dietary aspects
High levels of methionine can be found in sesame seeds, Brazil nuts, fish, meats, and some other plant seeds. Most fruit and vegetables contain very little; however, some have significant amounts, such as spinach, potatoes, and boiled corn. DL-methionine is sometimes added as an ingredient to
pet foods. Methionine, cysteine and soy protein heated in a small amount of water creates a meat like aroma.
See also
★
Allantoin
★
Formylmethionine
References
1. Nelson, D. L.; Cox, M. M. "Lehninger, Principles of Biochemistry" 3rd Ed. Worth Publishing: New York, 2000. ISBN 1-57259-153-6.
2.
External links
★
Foods containing methionine
★
Computational Chemistry Wiki