Method for the microbiological isomerisation of alpha-hydroxy carboxylic acids
The present invention relates to a method for the microbiological isomerization of alpha-hydroxycarboxylic acids using an alpha-hydroxycarboxylic acid racemase, the enzymes used for this method and microorganisms which express a suitable racemase activity, a screening method for microorganisms with alpha-hydroxycarboxylic acid racemase activity, the nucleic acid sequences encoding this enzyme, expression vectors, recombinant microorganisms which express this racemase, and methods for the production or isolation of a protein with alpha-hydroxycarboxylic acid racemase activity.
1. A method for the microbiological isomerization of alpha-hydroxycarboxylic acids of the formula I
where
R is straight-chain or branched C 2 -C 8 alkyl or C 2 -C 8 alkenyl or —(CH 2 ) n -Cyc, where n is an integer of 0 to 4, and Cyc is an unsubstituted or mono- or polysubstituted, mono- or binuclear carbo- or heterocyclic ring,
wherein said method comprises isomerizing a substrate consisting essentially of a first stereoisomer of an alpha-hydroxycarboxylic acid of the formula (I) with an enzyme in a reaction medium to obtain a second stereoisomer or an isomer mixture comprising the first stereoisomer and the second stereoisomer,
wherein the enzyme is contained in an extract of a microorganism or present in intact cells of a microorganism which express the enzyme, wherein said microorganism is selected from the group consisting of the strains L. paracasei DSM 15755, L. paracasei DSM 15751 , L. delbrueckii DSM 15754 , L. sakei DSM 15753 and L. oris DSM 15752, and wherein said microorganism is capable of racemizing at least one compound selected from the group consisting of (R) and/or (S) form of phenyl lactate, 4-fluorophenyl lactate, 2-hydroxy-4-phenylbutyric acid, 2-hydroxy-4-methylpentanecarboxylic acid and 2-hydroxy-3-methylbutyric acid.
2. The method of claim 1 , wherein the second stereoisomer is removed from the isomer mixture and the remaining part of the isomer mixture is subjected to a further isomerization step.
3. The method of claim 1 , wherein the isomer mixture is subjected to a subsequent chemical or enzymatic stereoselective reaction and a reaction mixture is obtained, wherein the reaction mixture obtained is subjected to a further isomerization step.
4. The method of claim 1 , wherein the isomerization reaction is coupled with a subsequent chemical or enzymatic, enantioselective reaction, during which the second stereoisomer is removed from the reaction medium.
5. The method of claim 3 , wherein the subsequent chemical or enzymatic, enantioselective reaction is an esterification or an amidation of the alpha-hydroxycarboxylic acid.
6. A method for the microbiological isomerization of alpha-hydroxycarboxylic acids of the formula I
where
R is straight-chain or branched C 2 -C 8 alkyl or C 2 -C 8 alkenyl or —(CH 2 ) n -Cyc, where n is an integer of 0 to 4, and Cyc is an unsubstituted or mono- or polysubstituted, mono- or binuclear carbo- or heterocyclic ring,
wherein said method comprises
(i) screening and obtaining a microorganism of the genus Lactobacillus that is capable of racemizing at least one compound selected from the group consisting of (R) and/or (S) form of phenyl lactate, 4-fluorophenyl lactate, 2-hydroxy-4-phenylbutyric acid, 2-hydroxy-4-methylpentanecarboxylic acid and 2-hydroxy-3-methylbutyric acid,
(ii) isomerizing a substrate consisting essentially of a first stereoisomer of an alpha-hydroxycarboxylic acid of the formula (I) with an enzyme in a reaction medium to obtain a second stereoisomer or an isomer mixture comprising the first stereoisomer and the second stereoisomer, wherein the enzyme is contained in an extract of said microorganism or present in intact cells of said microorganism which express the enzyme, wherein said microorganism is selected from the group consisting of the strains L. paracasei DSM 15755, L. paracasei DSM 15751 , L. delbrueckii DSM 15754 , L. sakei DSM 15753 and L. oris DSM 15752.
7. The method of claim 6 , wherein the second stereoisomer is removed from the isomer mixture and the remaining part of the isomer mixture is subjected to a further isomerization step.
8. The method of claim 6 , wherein the isomer mixture is subjected to a subsequent chemical or enzymatic stereoselective reaction and a reaction mixture is obtained, wherein the reaction mixture obtained is subjected to a further isomerization step.
9. The method of claim 6 , wherein the isomerization reaction is coupled with a subsequent chemical or enzymatic, enantioselective reaction, during which the second stereoisomer is removed from the reaction medium.
10. The method of claim 8 , wherein the subsequent chemical or enzymatic, enantioselective reaction is an esterification or an amidation of the alpha-hydroxycarboxylic acid.