D-amino acid dehydrogenase and method of making D-amino acids

Chemistry: molecular biology and microbiology – Micro-organism – tissue cell culture or enzyme using process... – Preparing alpha or beta amino acid or substituted amino acid...

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

C435S189000, C435S190000

Reexamination Certificate

active

07550277

ABSTRACT:
Polypeptides capable of catalyzing the reductive amination of a 2-ketoacid to its corresponding D-amino acid are provided. The polypeptides can be prepared by mutagenesis of, e.g., a diaminopimelate dehydrogenase. Also provided is a method of making a D-amino acid using a catalytically active polypeptide, wherein a 2-ketoacid is allowed to contact the polypeptide in the presence of a nicotinamide cofactor and ammonia or an ammonia source.

REFERENCES:
patent: 5798234 (1998-08-01), Engel et al.
patent: 2003/0207436 (2003-11-01), Osabe et al.
patent: 62 205790 (1987-09-01), None
patent: WO 91/05870 (1991-05-01), None
patent: WO 01/62948 (2001-08-01), None
patent: WO 2005/017171 (2005-02-01), None
Bommarius, A. S. et al.; “Biocatalysis to amino acid-based chiral pharmaceuticals-examples and perspectives”; Journal of Molecular Catalysis B: Enzymatic 5; (1998); pp. 1-11.
Zhao, H. et al.; “Directed evolution of enzymes and pathways for industrial biocatalysis”; Current Opinion in Biotechnology; (2002): 13; pp. 104-110.
Farinas, E. T. et al.; “Directed enzyme evolution”; Current Opinion in Biotechnology; (2001); 12, pp. 545-551.
Uchiyama, H. et al.; “Directed Evolution to Improve the Thermostability of Prolyl Endopeptidase”; The Japanese Biochemical Society; (2000); vol. 128, No. 3; pp. 441-447.
Matsumura, I. et al.; “In vitro Evolution of Beta-glucuronidase into a Beta-galactosidase Proceeds Through Non-specific Intermediates”; J. Mol. Biol.; (2001); 305, pp. 331-339.
May, O. et al.; “Inverting enantioselectivity by directed evolution of hydantoinase for imroved production of L-methionine”; Nature Biotechnology; (2000); vol. 18, pp. 317-320.
Schmid, A. et al.; “The use of enzymes in the chemical industry in Europe”; Current Opinion in Biotechnology, (2002); 13; pp. 359-366.
Wakayama, M. et al.; “Production of D-amino acids by N-acyl-D-amino acid amidohydrolase and its structure and function”; Journal of Molecular Catalysis B: Enzymatic 23; (2003); pp. 71-85.
Mor, A. et al.; “Identification of a D-Alanine-containing Polypeptide Precursor for the Peptide Opioid, Dermorphin”; The Journal of Biological Chemistry; (1991); vol. 266, No. 10, Issue of Apr. 5, pp. 6264-6270.
Pritsker, M. et al.; “A synthetic all D-amino acid peptide corresponding to the N-terminal sequence of HIV-1 gp41 recognizes the wild-type fusion peptide in the membrane and inhibits HIV-1 envelope glycoprotein-mediated cell fusion”; Proc. National. Academy of Sciences USA; (1998) vol. 95, pp. 7287-7292.
Bommarius, A. S. et al.; “Comparison of Different Chemoenzymatic Process Routes to Enantiomerically Pure Acids”; Chimia 55; (2001); 50-59.
Pietzsch, M. et al.; “A New Racemase for 5-Monosubstituted Hydantoins”; Annals New York Academy of Sciences 672; (1992); pp. 478-483.
Cirilli, M. et al.; “The three-dimensional structure of the ternary complex ofCorynebacterium glutamicumdiaminopimelate dehydrogenase-NADPH-L-2-amino-6-methylene-pimelate”; Protein Science; (2000); 9:pp. 2034-2037.
Brunhuber, N. M. W. et al.; “The Biochemistry and Enzymology of Amino Acid Dehydrogenases”; Critical Reviews in Biochemistry and Molecular Biology; (1994); 29(6), pp. 415-467.
Krix, G. et al.; “Enzymatic reduction of α-keto acids leading to L-amino acids, D- or L-hydroxy acids”; Journal of Biotechnology; (1997); 53; pp. 29-39.
Cooper, A. J. .L. et al.; “Synthesis and Properties of the α-Keto Acids”; Chemical Reviews; (1983); vol. 83, No. 3, pp. 321-358.
Galkin, A. et al.; “Synthesis of Optically Active Amino Acids from α-Keto Acids withEscherichia coliCells Expressing Heterologous Genes”; Applied and Environmental Microbiology; Dec. (1997); vol. 63, No. 12, pp. 4651-4656.
Vedha-Peters K., et al.; “Creation of a Broad-Range and Highly Stereoselective D-Amino Acid Dehydrogenase for the One-Step Synthesis of D-amino acids” Journal of the American Chemical Society; (2006); vol. 128, No. 33, pp. 10923-10929.
Kazlauskas, R.; “Engineering a multipurpose catalyst.” Nature Chemical Biology; (Oct. 2006), vol. 2, No. 10, pp. 514-515.
International Search Report and Written Opinion from Applicants' counterpart PCT Application, No. PCT/US2006/011772.

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

D-amino acid dehydrogenase and method of making D-amino acids does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with D-amino acid dehydrogenase and method of making D-amino acids, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and D-amino acid dehydrogenase and method of making D-amino acids will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-4144090

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.