Synthesis of (S)- and (R)-3-hydroxy acids using cells or purified (S)-3-hydroxycarboxylate oxidoreductase from Clostridium tyrobutyricum and the NADP(H) regeneration system of Clostridium thermoaceticum

[1]  H. Simon,et al.  Purification and characterization of an (S)-3-hydroxycarboxylate oxidoreductase from Clostridium tyrobutyricum , 1994, Applied Microbiology and Biotechnology.

[2]  M. Kula,et al.  Studies on the distribution and regulation of microbial keto ester reductases , 1992, Applied Microbiology and Biotechnology.

[3]  Yasushi Kawai,et al.  Stereochemical control of microbial reduction. 17. A method for controlling the enantioselectivity of reductions with bakers' yeast , 1991 .

[4]  P. Adlercreutz.  Asymmetric reduction of ketones with enzymes from acetic acid bacteria , 1991, Biotechnology Letters.

[5]  W. König,et al.  Cyclodextrins as chiral stationary phases in capillary gas chromatography. Part V: Octakis(3‐O‐butyryl‐2,6‐di‐O‐pentyl)‐γ‐cyclodextrin , 1989 .

[6]  C. Laane,et al.  Purification of intracellular enzymes from whole bacterial cells using reversed micelles , 1987 .

[7]  G. Whitesides,et al.  Regeneration of nicotinamide cofactors for use in organic synthesis , 1987, Applied biochemistry and biotechnology.

[8]  J. Kovar,et al.  Purification and properties of D-3-hydroxybutyrate dehydrogenase from Paracoccus denitrificans , 1985 .

[9]  J. Bader,et al.  Unconventional and effective methods for the regeneration of NAD(P) H in microorganisms or crude extracts of cells , 1984 .

[10]  E. Santaniello,et al.  Chiral synthesis of a component of Amanita muscaria, (−)-4-hydroxypyrrolidin-2-one, and assessment of its absolute configuration , 1984 .

[11]  T. Atkinson,et al.  The rapid purification of 3-hydroxybutyrate dehydrogenase and malate dehydrogenase on triazine dye affinity matrices. , 1982, The Biochemical journal.

[12]  D. Seebach,et al.  SYNTHESIS OF OPTICALLY ACTIVE 2‐METHYL‐ AND 2‐ETHYL‐1,6‐DIOXASPIRO(4.4)NONANE AND ‐(4.5)DECANE PHEROMONES FROM A COMMON CHIRAL PRECURSOR , 1981 .

[13]  J. Bader,et al.  The activities of hydrogenase and enoate reductase in two Clostridium species, their interrelationship and dependence on growth conditions , 1980, Archives of Microbiology.

[14]  H. Krebs,et al.  Purification and properties of crystalline 3-hydroxybutyrate dehydrogenase from Rhodopseudomonas spheroides. , 1967, The Biochemical journal.

[15]  M. Simonyi.  Problems and Wonders of Chiral Molecules , 1995 .

[16]  H. Simon,et al.  Application of High Enzyme Activities Present in Clostridium Thermoaceticum for the Efficient Regeneration of NADPH, NADP+, NADH AND NAD+ , 1994 .

[17]  Y. Naoshima,et al.  Control of the enantioselectivity of the bioreduction with immobilized bakers' yeast in a hexane solvent system , 1992 .

[18]  R. Holt,et al.  Biotransformations using clostridia: stereospecific reductions of a β-keto ester , 1992 .

[19]  A. Fauve,et al.  Regiospecificity and Enantiospecificity in Microbiological Reduction of Acyclic β-Diketones , 1990 .

[20]  N. Oguni,et al.  Complete stereoselective synthesis of chiral intermediates for thienamycin and related antibiotics , 1988 .

[21]  J. Bader,et al.  [28] Electroenzymatic and electromicrobial reduction: Preparation of chiral compounds , 1987 .

[22]  G. Whitesides,et al.  Synthesis of ribulose 1,5-bisphosphate: routes from glucose 6-phosphate (via 6-phosphogluconate) and from adenosine monophosphate (via ribose 5-phosphate). , 1982, Methods in enzymology.