U.S. patents available from 1976 to present.
U.S. patent applications available from 2005 to present.

Process for producing optically active ଱-substituted organic acid and microorganism and enzyme used therefor

Patent 5283193 Issued on February 1, 1994. Estimated Expiration Date: Icon_subject November 27, 2011. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

Process of preparing L and D ଱-amino acids by enzyme treatment of DL-଱-amino acid amide
Patent #: 4080259
Issued on: 03/21/1978
Inventor: Boesten ,   et al.

Process for preparing L-଱-methylphenyl alanines
Patent #: 4443548
Issued on: 04/17/1984
Inventor: Oshima ,   et al.

Optically active substituted butyramide, and process for the optical separation of substituted butyramide Patent #: 4812403
Issued on: 03/14/1989
Inventor: Boesten ,   et al.

Inventors

Assignee

Application

No. 799879 filed on 11/27/1991

US Classes:

435/280Resolution of optical isomers or purification of organic compounds or composition containing same

Examiners

Primary: Lee, Lester L.

Attorney, Agent or Firm

Foreign Patent References

  • 54-14668 JP. 06/13/1979
  • 61-56086 JP. 03/13/1986
  • 61-88894 JP. 05/13/1986
  • 62-282089 JP. 12/13/1986
  • 62-55098 JP. 03/13/1987
  • 8607386 WO. 12/13/1986

International Class

C12P 007/40

Foreign Application Priority Data

1988-06-27 JP

Abstract

A process for producing an optically active ଱-substituted organic acid represented by formula (II), comprising the steps of (a) treating a racemic substituted nitrile or amide represented by formula (I) with a microorganism selected from the group consisting of the microorganisms of genuses Alcaligenes, Pseudomonas, Rhodopseudomonas, Corynebacterium, Acinetobacter, Bacillus, Mycobacterium, Rhodococcus and Candida, or preparations thereof; and (b) recovering the resulting optically active u-substituted organic acid represented by formula (II): ##STR1## wherein R1 and R2 each represent a halogen atom, a hydroxyl group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted alkoxy group, a substituted or unsubstituted aryl group, a substituted or unsubstituted aryloxy group or a substituted or unsubstituted heterocyclic group with the proviso that R1 and R2 are different from each other; and X represents a nitrile group or an amido group, ##STR2## wherein R1 and R2 are as defined above.

Other References

  • Fukuda, Y. et al, J. Ferment. Technol., 51:393-397 (1973
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