Enzymatic production of glycolic acid
View Patent ↗Various methods are provided for the enzymatic production of glycolic acid from glycolonitrile. These methods include: 1) use of Acidovorax facilis 72W nitrilase mutants having improved nitrilase activity for converting glycolonitrile to glycolic acid, and 2) methods to improve catalyst stability and/or productivity. The methods to improve catalyst stability/productivity include use of reaction stabilizers, running the reactions under substantially oxygen free conditions, and controlling the concentration of substrate in the reaction mixture.
1. A process to produce glycolic acid from glycolonitrile comprising:
a) contacting glycolonitrile in a suitable aqueous reaction mixture with an enzyme catalyst comprising a polypeptide having nitrilase activity, said polypeptide having an amino acid sequence of SEQ ID NO: 6 with an amino acid substitution selected from the group consisting of:
1) a substitution at amino acid residue 168 with lysine, methionine, threonine or valine; and
2) a substitution at amino acid residue 201 with glutamine, glycine, histidine, lysine, asparagine, serine, alanine, cysteine, or threonine;
whereby glycolic acid is produced; and
b) recovering the glycolic acid produced in (a) in the form of a salt or acid; wherein said enzyme catalyst provides at least a 1.5-fold increase in nitrilase activity relative to the nitrilase activity of the Acidovorax facilis 72W nitrilase when converting glycolonitrile to glycolic acid under identical reaction conditions.
2. The process of claim 1 wherein said amino acid sequence is selected from the group consisting of SEQ ID NOs: 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, and 32.
3. The process of claim 1 wherein the enzyme catalyst is an improved nitrilase catalyst providing at least about a 2-fold improvement in nitrilase activity when converting glycolonitrile to glycolic acid relative to the activity of the A. facilis 72W (ATCC 55746) nitrilase under identical reaction conditions.
4. The process of claim 2 wherein the enzyme catalyst is an improved nitrilase catalyst providing at least about a 4-fold improvement in nitrilase activity when converting glycolonitrile to glycolic acid relative to the activity of the A. facilis 72W (ATCC 55746) nitrilase under identical reaction conditions.
5. The process of claim 1 wherein the enzyme catalyst is in the form of whole microbial cells, permeabilized microbial cells, one or more cell components of a microbial cell extract, partially purified enzyme, or purified enzyme.
6. The process of claim 5 wherein said whole microbial cell is a transformed microbial host cell recombinantly expressing said polypeptide.
7. The process of claim 5 wherein the transformed microbial host cell is selected from the group consisting of Comamonas sp., Corynebacterium sp., Brevibacterium sp., Rhodococcus sp., Azotobacter sp., Citrobacter sp., Enterobacter sp., Clostridium sp., Klebsiella sp., Salmonella sp., Lactobacillus sp., Aspergillus sp., Saccharomyces sp., Zygosaccharomyces sp., Pichia sp., Kluyveromyces sp., Candida sp., Hansenula sp., Dunaliella sp., Debaryomyces sp., Mucor sp., Torulopsis sp., Methylobacteria sp., Bacillus sp., Escherichia sp., Pseudomonas sp., Rhizobium sp., and Streptomyces sp.
8. The process of claim 7 wherein the transformed microbial host cell is Escherichia coli.
9. The process of claim 8 wherein the transformed microbial host cell is an Escherichia coli strain selected from the group consisting of E. coli MG1655 having international depository number ATCC 47076 and E. coli FM5 having international depository number ATCC 53911.
10. The process of any one of claims 1 – 9 wherein the enzyme catalyst is immobilized in or on a soluble or insoluble support.
11. The process of claim 1 wherein the concentration of ammonium glycolate produced in the aqueous reaction mixture is about 0.02 wt % to about 90 wt %
12. The process of claim 11 wherein the concentration of ammonium glycolate produced in the aqueous reaction mixture is about 0.02 wt % to about 40 wt %.
13. The process of claim 10 wherein the glycolonitrile concentration in the aqueous reaction mixture is in the range of about 5 mM to about 1 M.
14. The process of claim 13 wherein the glycolonitrile concentration in the aqueous reaction mixture is maintained by continuous or aliquot addition.
15. The process of claim 1 wherein the pH in the aqueous reaction mixture is maintained between about 5.5 and about 7.7.
16. The process of claim 1 wherein the enzymatic conversion of glycolonitrile to glycolic acid occurs under substantially oxygen free conditions.
17. The process of claim 1 wherein the aqueous reaction mixture further comprises a stabilizer selected form the group consisting of potassium thiosulfate and sodium dithionite at a concentration of less than 5 wt %.
18. The process of claim 1 wherein the enzyme catalyst is a recycled enzyme catalyst.
19. The process of claim 1 wherein the enzyme catalyst provides a catalyst productivity of at least 300 grams of glycolic acid per gram of dry cell weight enzyme catalyst.
20. The process of claim 19 wherein the enzyme catalyst provides a catalyst productivity of at least 450 grams of glycolic acid per gram of dry cell weight enzyme catalyst.
21. The process of claim 20 wherein the enzyme catalyst provides a catalyst productivity of at least 1000 grams of glycolic acid per gram of dry cell weight enzyme catalyst.