Process for the enzymatic preparation of an amide from a nitrile
Disclosed herein are cyanide-tolerant nitrile hydratases especially from Pseudomonas putida or Pseudomonas marginalis strains which exhibit increased cyanide tolerance. Also disclosed are methods of preparing amides from nitriles in the presence of cyanides and polynucleotide sequences coding for cyanide-tolerant nitrile hydratases.
1. A process for the enzymatic preparation of an amide from a nitrile, which comprises contacting a compound comprising a nitrile group with a polypeptide having nitrile hydratase activity thereby converting the nitrile to the corresponding amide, wherein said polypeptide
a) comprises the amino acid sequence of SEQ ID NO: 2, 3, or 5,
b) is encoded by a polynucleotide comprising the nucleotide sequence of SEQ ID NO: 1 or 4, or
c) is encoded by a polynucleotide which hybridizes with the complementary sequence of the nucleotide sequence of SEQ ID NO: 1 or 4 under stringent conditions, where stringent conditions mean washing in 5XSSC at a temperature of from 50 to 65° C.;
or microorganism which produces the polypeptide, or a lysate thereof.
2. The process as claimed in claim 1 , wherein resting cells of the microorganism are employed.
3. The process as claimed in claim 1 , wherein the polypeptide is purified.
4. The process as claimed in claim 1 , wherein the polypeptide is derived from microorganisms of the genus Pseudomonas.
5. The process as claimed in claim 4 , wherein the polypeptide is derived from employed microorganisms of the species Pseudomonas putida or Pseudomonas marginalis.
6. The process as claimed in claim 5 , wherein the employed microorganisms are deposited under the numbers DSM 16275 and DSM 16276.
7. The process as claimed in claim 1 , wherein the compound has the general formula (I) or (II)
where
X is OH, H, alkyl, or NH 2 ;
R is H, saturated alkyl radical having 1 to 12 C atoms, branched or unbranched, optionally NH 2 -substituted, unsaturated alkyl radicals having a double bond and 1 to 12 C atoms, branched or unbranched, cycloalkyl groups having 3 to 6 C atoms, or alkylene radicals substituted by alkylthio groups, where alkyl here corresponds to a C 1 to C 3 radical, and alkylene corresponds to a divalent C 3 to C 8 radical,
R′ is H, or an alkyl having 1 to 3 C atoms,
R″ is a mono- or binuclear unsaturated ring having 6 to 12 C atoms, optionally substituted by one or two alkyl groups (C 1 -C 3 ), Cl, Br, F, or an alkyl nitrile radical having 1 to 6 C atoms.
8. The process as claimed in claim 7 , wherein the compound is converted in the presence of hydrocyanic acid or a salt of hydrocyanic acid.
9. The process as claimed in claim 8 , wherein the conversion is carried out in the presence of an initial concentration of more than 0.5 mol % cyanide to 3 mol % cyanide, based on the compound employed.
10. The process as claimed in claim 1 , wherein 2-amino-4-methylthiobutyronitrile is employed as the compound.
11. The process as claimed in claim 1 , wherein 2-hydroxy-4-methylthiobutyronitrile is employed as the compound.
12. The process as claimed in claim 1 , wherein 2-hydroxy-2-methylpropionitrile is employed as the compound.
13. The process as claimed in claim 1 , wherein the amide or the solution comprising the amide is separated from the microorganism, and the amide is hydrolyzed to the corresponding acid.
14. The process as claimed in claim 1 , wherein the amide or the solution comprising the amide is separated from the microorganism, and the amide is hydrolyzed with alkali metal or alkaline earth metal hydroxides to the salts of the corresponding carboxylic acids.
15. The process as claimed in claim 14 , wherein MHA amide is hydrolyzed with calcium hydroxide, and the calcium salt is obtained.
16. The process as claimed in claim 1 , wherein
a) the microorganism is of the genus Pseudomonas and is fermented to obtain the polypeptide or a protein fraction comprising the polypeptide, and
b) transferring the polypeptide or the protein fraction into a medium which comprises the compound.
17. The process as claimed in claim 16 , wherein the compound has the general formula (I) or (II)
where
X is OH, H, alkyl, or NH 2 ;
R is H, saturated alkyl radical having 1 to 12 C atoms, branched or unbranched, optionally NH 2 -substituted, unsaturated alkyl radicals having a double bond and 1 to 12 C atoms, branched or unbranched, cycloalkyl groups having 3 to 6 C atoms, or alkylene radicals substituted by alkylthio groups, where alkyl here corresponds to a C 1 to C 3 radical, and alkylene corresponds to a divalent C 3 to C 8 radical,
R′ is H, or an alkyl having 1 to 3 C atoms,
R″ is a mono- or binuclear unsaturated ring having 6 to 12 C atoms, optionally substituted by one or two alkyl groups (C 1 -C 3 ), Cl, Br, F, or an alkyl nitrile radical having 1 to 6 C atoms.