Methods for making simvastatin and intermediates
View Patent ↗The invention provides synthetic chemical and chemoenzymatic methods of producing simvastatin and various intermediates. In one aspect, enzymes such as hydrolases, e.g., esterases, are used in the methods of the invention.
1. A method for the preparation of simvastatin comprising a homodiacylation process comprising:
(a) enzymatic hydrolysis of lovastatin, lovastatin acid or a salt of lovastatin acid with an esterase enzyme to form a triol acid,
wherein the esterase has a sequence having at least about 90% sequence identity to SEQ ID NO:2, SEQ ID NO:4 or SEQ ID NO:6;
(b) forming a diol lactone from the triol acid by lactonization;
(c) acylating the 4-position (4′-OH) and 8-position (8′-OH) on the lactone ring of the diol lactone by chemical acylation to form a 4,8-diacetyl lactone; and
(d) removing selectively the acyl group at the 4′ position by enzymatic hydrolysis, thereby making simvastatin.
2. A method for preparing 4-acetyl lactone comprising enzymatic hydrolysis of lovastatin with an esterase enzyme to make a triol acid or a salt of a triol acid, followed by lactonization of the triol acid to make a diol lactone, followed by regioselective enzymatic acylation of the diol lactone on the 4-position (4′-OH) of the lactone ring to make 4-acetyl lactone,
wherein the esterase has a sequence having at least about 90% sequence identity to SEQ ID NO:2, SEQ ID NO:4 or SEQ ID NO:6.
3. A method for preparing 4-acetyl-simvastatin comprising enzymatic hydrolysis of lovastatin with an esterase enzyme to make a triol acid or a salt of a triol acid, followed by lactonization of the triol acid to make a diol lactone, followed by regioselective enzymatic acylation of the diol lactone on the 4-position (4′-OH) of the lactone ring to make 4-acetyl lactone, followed by regioselective enzymatic acylation of the 4-acetyl lactone on the 8-position (8′-OH) of the lactone to make 4-acetyl-simvastatin,
wherein the esterase has a sequence having at least about 90% sequence identity to SEQ ID NO:2, SEQ ID NO:4 or SEQ ID NO:6.
4. A method for the preparation of a triol acid or a salt of a triol acid from lovastatin with an esterase enzyme comprising:
(a) providing a lovastatin, lovastatin or a salt of lovastatin, and an esterase enzyme; and
(b) contacting the lovastatin, lovastatin or a salt of lovastatin with the esterase under conditions wherein the esterase catalyzes the hydrolysis of the lovastatin to a triol acid or a salt of a triol acid,
wherein the esterase has a sequence having at least about 90% sequence identity to SEQ ID NO:2, SEQ ID NO:4 or SEQ ID NO:6.
5. A kit comprising (a) reagents and at least one esterase enzyme for practicing the methods of claim 1 , wherein the esterase has a sequence having at least about 90% sequence identity to SEQ ID NO:2, SEQ ID NO:4 or SEQ ID NO:6; and
(b) instructions for practicing the methods of claim 1 .
6. The method of claim 1 , wherein at least one step is performed in a separate reaction vessel.
7. The method of claim 6 , wherein at least two steps are performed in separate reaction vessels.
8. The method of claim 1 , wherein at least one step is performed with a cell extract, or at least one step is performed in a whole cell.
9. The method of claim 1 , further comprising crystallization of the simvastatin.
10. The method of claim 9 , further comprising re-crystallization of the simvastatin.
11. The method of claim 1 , further comprising re-lactonization to provide simvastatin with a desired purity.
12. The method of claim 1 , wherein at least one hydrolysis reaction is carried out by an esterase:
(a) encoded by a nucleic acid having at least sequence identity to SEQ ID NO:1, or enzymatically active fragments thereof;
(b) encoded by a nucleic acid having at least sequence identity to SEQ ID NO:3, or enzymatically active fragments thereof; or
(c) encoded by a nucleic acid having at least sequence identity to SEQ ID NO:5, or enzymatically active fragments thereof.
13. The method of claim 1 , wherein at least one hydrolysis reaction is carried out by an esterase having a sequence at least about sequence identity to SEQ ID NO:2, SEQ ID NO:4 or SEQ ID NO:6, or enzymatically active fragments thereof.
14. The method of claim 1 , wherein the method further comprises enzymatic hydrolysis of lovastatin to make a triol acid or a salt of a triol acid.
15. The method of claim 14 , wherein the method further comprises lactonization of the triol acid and enzymatic acylation of the 4-postion (4′-OH) of the lactone ring to make a 4-acyl lactone.
16. The method of claim 15 , wherein the method further comprises enzymatic acylation of the 4-acyl lactone to make a 4-acetyl-simvastatin.
17. The method of claim 16 , wherein the method further comprises regioselective enzymatic hydrolysis of the 4-acetyl-simvastatin to make simvastatin.
18. The method of claim 4 , wherein the esterase has a sequence at least about sequence identity to SEQ ID NO:2, SEQ ID NO:4 or SEQ ID NO:6.
19. The method of claim 1 , wherein enzymatic hydrolysis reaction is carried out by an esterase having a sequence as set forth in SEQ ID NO:2, SEQ ID NO:4 or SEQ ID NO:6.
20. The method of claim 2 , wherein enzymatic hydrolysis reaction is carried out by an esterase having a sequence as set forth in SEQ ID NO:2, SEQ ID NO:4 or SEQ ID NO:6.
21. The method of claim 3 , wherein enzymatic hydrolysis reaction is carried out by an esterase having a sequence as set forth in SEQ ID NO:2, SEQ ID NO:4 or SEQ ID NO:6.
22. The method of claim 4 , wherein enzymatic hydrolysis reaction is carried out by an esterase having a sequence as set forth in SEQ ID NO:2, SEQ ID NO:4 or SEQ ID NO:6.