The invention concerns a method for preparing a compound of formula (I) and its use for producing
methionine and analogs thereof wherein formula (I) is (I) in which X is selected from S and Se; R1 is selected from H,
alkyl groups,
aryl groups and alkylaryl groups; R2 is selected from OH, NR5R6 where R5 and R6 are identical or different and are selected from H and
alkyl groups; and R3 is C(O)NR7R8 where R7 and R8 are identical or different and are selected from H and
alkyl groups; which method comprising the reaction of a compound of formula (II) in which X, R1 and R2 are as defined above for the compound of formula (I); and R4 is CN; in the presence of an
enzyme having a
nitrile hydratase activity and comprising at least an α-
subunit and a β-
subunit, said α-
subunit being defined by SEQ ID No: 1 and said β-subunit being defined by SEQ ID No: 2, wherein said α-subunit has at least one
mutation selected from the group consisting of Leu6, Ile13, Ala19, Thr36, Asp40, Ala43, Asn48, Arg71, Asp92, Met94, Phe126, Gly148 and Val204, and / or said β-subunit has at least one
mutation selected from the group consisting of Val4, Thr10, Val24, Phe37, Phe41, Met46, Leu48, Phe51, His79, Gln96, Pro107, Glu108, Phe118, Leu127, Arg160, Leu186, Ala200, Gly205, Pro206, Ser212, Tyr215, Ala230 and Ala231, said
amino acid in said position(s) being replaced by anyone of
alanine,
arginine,
asparagine,
aspartic acid,
cysteine,
glutamic acid,
glutamine,
glycine,
histidine,
isoleucine,
leucine,
lysine,
methionine,
phenylalanine,
proline,
serine,
threonine,
tryptophan,
tyrosine, or
valine.