Process for producing pravastatin sodium salt using streptomyces flavidovirens dsm 14455

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We claim:

1. A strain of Strepomyces flavidovirens deposited at Deutsche Sammlung von Mikro-organismen und Zelikulturen GmbH under accession number DSM 14455.

2. A microbial process for preparing a compound of formula I ##STR00003## from a substrate compound of general formula II, ##STR00004## wherein R represents an alkali metal or ammonium ion, comprising steps of (i) preparing a seed inoculum of astrain of Streptomyces flavidovirens that 6.beta.-hydroxylates a compound of formula II, (ii) transferring the seed inoculum to a production medium, (iii) subjecting the production medium to fermentation, (iv) feeding a substrate of Formula II in theproduction medium at different intervals, (v) controlling the pH during fermentation by feeding a carbon source in the production medium, (vi) fermenting the substrate until bioconversion to Pravastatin is complete, (vii) extracting Pravastatin from theproduction medium, and (viii) isolating Pravastatin sodium salt.

3. The process of claim 2, wherein the strain of Streptomyces flavidovirens is the Strepbomyces flavidovirens strain deposited with DSMZ (Deutsche Sammlung von Mikro-organismen und Zellkulturen GmbH) under accession number DSMZ 14455.

4. The process of claim 2 wherein the inoculum used for the seed is a spore suspension or a vegetative mycelium.

5. The process of claim 2 wherein the substrate is compactin, a compactin salt or a compactin derivative.

6. The process of claim 2 wherein the seed inoculum comprises malt extract and peptone.

7. The process of claim 2 further comprising a step of incubating the seed inoculum.

8. The process of claim 7 wherein the seed medium is incubated between about 25 and 35.degree. C. for about 40 to 55 hours.

9. The process of claim 2 wherein constituents of the production medium are selected from the group consisting of dextrose monohydrate, peptone and yeast extract.

10. The process of claim 2 further comprising a step of incubating the production medium.

11. The process of claim 10 wherein the production medium is incubated between about 24 and 35.degree. C. for about 48 to 148 hours.

12. The process of claim 2 wherein the carbon source is selected from a saccharide or glycerol.

13. The process of claim 12 wherein the carbon source is dextrose.

14. The process of claim 2 wherein the step of isolating Pravastatin sodium salt comprises converting Pravastatin isolated from the cell broth to its dibenzylamide salt.

15. The process of claim 14 wherein the dibenzylamide salt is converted to Pravastatin sodium salt by reaction with sodium caprylate.

16. The process of claim 2 wherein in the step of extracting Pravastatin from the whole cell broth, Pravastatin is obtained in its lactone form.

17. The process of claim 2 wherein in the step of extracting Pravastatin from the whole cell broth, Pravastatin is obtained as its lactone form, and the step of isolating Pravastatin sodium salt comprises converting the lactone to Pravastatinacid.

18. The process of claim 17 wherein converting the lactone to Pravastatin acid comprises contacting the lactone with a methanolic solution of sodium hydroxide.

19. The process of claim 17 wherein Pravastatin acid is further converted to Pravastatin sodium salt by reaction with sodium caprylate.

20. The process of claim 17 wherein Pravastatin acid is further converted to Pravastatin sodium salt by reaction with sodium acetate.

21. The process of claim 17 wherein Pravastatin acid is further converted to Pravastatin dibenzylamide salt by reaction with dibenzylamine.

22. The process of claim 21 wherein Pravastatin dibenzylamide salt is further converted to Pravastatin sodium salt by reaction with sodium caprylate.

23. A composition comprising a strain Streptomyces flavidovirens DSM 14455 and compactin, a compactin salt or a compactin derivative.