IP Library Granted Patent US 12,331,325
Granted Patent B2
US 12,331,325 · App. 18/459,797 · Granted Jun 17, 2025

Engineered transaminase polypeptides

Inventors: Scott J. Novick (Palo Alto, CA); Nikki Dellas (San Carlos, CA)
Assignee: Codexis, Inc.
C12N9/1096
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Quick Facts
Patent No.
US 12,331,325
App. No.
18/459,797
Granted
Jun 17, 2025
Kind
B2
Abstract

The present disclosure provides engineered transaminase polypeptides useful for the synthesis of chiral amine compounds under industrially relevant conditions. The disclosure also provides polynucleotides encoding the engineered transaminase polypeptides, host cells capable of expressing the engineered transaminases, and methods of using the engineered transaminases for the production of chiral amine compounds.

Claims (11)

1. An engineered polynucleotide encoding an engineered transaminase having an amino acid sequence of at least 85% identity to SEQ ID NO: 8, or a functional fragment thereof, and a set of substitutions at positions 21/163/323/408, in said amino acid sequence , wherein the positions of said substitutions are numbered with reference to SEQ ID NO: 8 and wherein the engineered transaminase exhibits an increased enzymatic activity relative to an engineered transaminase having the amino acid sequence set forth in SEQ ID NO:8.

2. The polynucleotide of claim 1 , wherein said polynucleotide encodes an engineered transaminase having a polypeptide sequence and further comprising at least one substitution or set of substitutions at one or more positions selected from: 5, 18/23/149/260/383/395/401/416, 18/23/149/383, 18/163/164, 163/315/316, 23/56/86/149/163/164/383/401/416, 23/86, 23/149/260, 23/149/284/383/395, 23/163/164/383, 23/163/164/401/416, 24, 42, 42/110, 42/187/272, 42/187/324/363/366, 42/187/353, 42/272/291, 42/272/291/363, 42/272/324/363/366, 42/272/363/410, 42/272/410, 42/291/313/363/410, 42/291/363, 42/291/363/366, 42/353, 42/363, 46, 66, 77, 86/149/163/164/383/395/401, 86/149/395, 86/163/164/260/383, 86/383,107, 110, 110/187, 110/187/253/410, 134, 138, 149/164/260/383/395/401, 149/260/383, 149/416, 163/259/323, 163/259/408, 163/315/316, 164/260/401, 164/316/383/401, 167, 186, 187, 187/253/363/366, 187/272/324/363/410, 187/272/363, 187/272/363/366/410, 187/291, 189, 191, 195, 199, 203, 210, 211, 248, 259/307, 260/395/401, 272, 272/353, 272/363/366, 272/410, 277, 291, 305, 309, 315, 342, 343, 351, 354, 358, 361, 362, 363, 363/366, 365, 367, 383, 383/401, 383/416/422, 385, 388, 389, 392, 395, 396, 401, 404, 405, 410, 416, 417, 439, 443, 447, 450, and 451, and wherein the amino acid positions are numbered with reference to SEQ ID NO:8.

3. The polynucleotide of claim 1 , wherein the polynucleotide encodes an engineered transaminase having a polypeptide sequence has at least 90% sequence identity to SEQ ID NO: 8, wherein said engineered transaminase further comprises at least one substitution or substitution set in said polypeptide sequence at one or more positions selected from: 18/23/149/383, 272, 291, and 383, and wherein the amino acid positions are numbered with reference to SEQ ID NO:8.

4. The polynucleotide of claim 1 , wherein said polynucleotide sequence is operably linked to a control sequence.

5. The polynucleotide of claim 1 , wherein said polynucleotide sequence is codon optimized.

6. An expression vector comprising at least one polynucleotide sequence of claim 1 .

7. A host cell comprising at least one expression vector of claim 6 .

8. A host cell comprising at least one polynucleotide sequence of claim 1 .

9. A method of producing an engineered transaminase in a host cell, comprising culturing the host cell of claim 8 , under suitable conditions, such that at least one engineered transaminase is produced.

10. The method of claim 9 , further comprising recovering at least one engineered transaminase from the culture and/or host cell.

11. The method of claim 10 , further comprising the step of purifying said at least one engineered transaminase.

Assignments (1)
SECURITY INTEREST Recorded Feb 15, 2024
From: CODEXIS, INC.
To: INNOVATUS LIFE SCIENCES LENDING FUND I, LP, AS COLLATERAL AGENT
Reel/Frame 066600/0650 →
Continuity (3)
Division 17223677 · Apr 6, 2021
Provisional Application 63008047 · Apr 10, 2020
Related Publication 20240002816A1 · Jan 4, 2024
References Cited (246)
US 4518692A · Rozzell · 1985 [cited by applicant]
US 4600692A · Wood et al. · 1986 [cited by applicant]
US 4826766A · Rozzell · 1989 [cited by applicant]
US 4950606A · Stirling et al. · 1990 [cited by applicant]
US 5169780A · Stirling et al. · 1992 [cited by applicant]
US 5300437A · Stirling et al. · 1994 [cited by applicant]
US 5316943A · Kidman et al. · 1994 [cited by applicant]
US 5605793A · Stemmer · 1997 [cited by applicant]
US 5811238A · Stemmer et al. · 1998 [cited by applicant]
US 5830721A · Stemmer et al. · 1998 [cited by applicant]
US 5834252A · Stemmer et al. · 1998 [cited by applicant]
US 5837458A · Minshull et al. · 1998 [cited by applicant]
US 5928905A · Stemmer et al. · 1999 [cited by applicant]
US 6096548A · Stemmer · 2000 [cited by applicant]
US 6117679A · Stemmer · 2000 [cited by applicant]
US 6132970A · Stemmer · 2000 [cited by applicant]
US 6165793A · Stemmer · 2000 [cited by applicant]
US 6180406B1 · Stemmer · 2001 [cited by applicant]
US 6197558B1 · Fotheringham · 2001 [cited by applicant]
US 6251674B1 · Tobin et al. · 2001 [cited by applicant]
US 6265201B1 · Wackett et al. · 2001 [cited by applicant]
US 6277638B1 · Stemmer · 2001 [cited by applicant]
US 6287861B1 · Stemmer et al. · 2001 [cited by applicant]
US 6287862B1 · delCardayre et al. · 2001 [cited by applicant]
US 6291242B1 · Stemmer · 2001 [cited by applicant]
US 6297053B1 · Stemmer · 2001 [cited by applicant]
US 6303344B1 · Patten et al. · 2001 [cited by applicant]
US 6309883B1 · Minshull et al. · 2001 [cited by applicant]
US 6319713B1 · Patten et al. · 2001 [cited by applicant]
US 6319714B1 · Crameri et al. · 2001 [cited by applicant]
US 6323030B1 · Stemmer · 2001 [cited by applicant]
US 6326204B1 · delCardayre et al. · 2001 [cited by applicant]
US 6335160B1 · Patten et al. · 2002 [cited by applicant]
US 6335198B1 · delCardayre et al. · 2002 [cited by applicant]
US 6337186B1 · Krebber · 2002 [cited by applicant]
US 6344356B1 · Stemmer · 2002 [cited by applicant]
US 6352859B1 · delCardayre et al. · 2002 [cited by applicant]
US 6355484B1 · Patten et al. · 2002 [cited by applicant]
US 6358740B1 · Patten et al. · 2002 [cited by applicant]
US 6358742B1 · Stemmer · 2002 [cited by applicant]
US 6365377B1 · Patten et al. · 2002 [cited by applicant]
US 6365408B1 · Stemmer · 2002 [cited by applicant]
US 6368861B1 · Crameri et al. · 2002 [cited by applicant]
US 6372497B1 · Stemmer · 2002 [cited by applicant]
US 6376246B1 · Crameri et al. · 2002 [cited by applicant]
US 6379964B1 · delCardayre et al. · 2002 [cited by applicant]
US 6387702B1 · Stemmer · 2002 [cited by applicant]
US 6391552B2 · Stemmer · 2002 [cited by applicant]
US 6391640B1 · Minshull et al. · 2002 [cited by applicant]
US 6395547B1 · Stemmer · 2002 [cited by applicant]
US 6406855B1 · Patten et al. · 2002 [cited by applicant]
US 6406910B1 · Patten et al. · 2002 [cited by applicant]
US 6413745B1 · Patten et al. · 2002 [cited by applicant]
US 6413774B1 · Stemmer · 2002 [cited by applicant]
US 6420175B1 · Stemmer · 2002 [cited by applicant]
US 6423542B1 · Crameri et al. · 2002 [cited by applicant]
US 6426224B1 · Crameri et al. · 2002 [cited by applicant]
US 6436675B1 · Welch et al. · 2002 [cited by applicant]
US 6444468B1 · Stemmer et al. · 2002 [cited by applicant]
US 6455253B1 · Patten et al. · 2002 [cited by applicant]
US 6479652B1 · Crameri et al. · 2002 [cited by applicant]
US 6482647B1 · Stemmer · 2002 [cited by applicant]
US 6483011B1 · Stemmer et al. · 2002 [cited by applicant]
US 6484105B2 · Zhang · 2002 [cited by applicant]
US 6489146B2 · Stemmer et al. · 2002 [cited by applicant]
US 6500617B1 · Stemmer et al. · 2002 [cited by applicant]
US 6500639B2 · Subramanian · 2002 [cited by applicant]
US 6506602B1 · Stemmer · 2003 [cited by applicant]
US 6506603B1 · Stemmer · 2003 [cited by applicant]
US 6518065B1 · Stemmer · 2003 [cited by applicant]
US 6519065B1 · Colbourne et al. · 2003 [cited by applicant]
US 6521453B1 · Crameri et al. · 2003 [cited by applicant]
US 6528311B1 · delCardayre et al. · 2003 [cited by applicant]
US 6537746B2 · Arnold et al. · 2003 [cited by applicant]
US 6573098B1 · Stemmer · 2003 [cited by applicant]
US 6576467B1 · Stemmer · 2003 [cited by applicant]
US 6579678B1 · Patten et al. · 2003 [cited by applicant]
US 6586182B1 · Patten et al. · 2003 [cited by applicant]
US 6605430B1 · Affholter et al. · 2003 [cited by applicant]
US 6602986B1 · Stemmer et al. · 2003 [cited by applicant]
US 6613514B2 · Patten et al. · 2003 [cited by applicant]
US 6653072B1 · Patten et al. · 2003 [cited by applicant]
US 6686515B1 · Lassner et al. · 2004 [cited by applicant]
US 6703240B1 · Stemmer et al. · 2004 [cited by applicant]
US 6716631B1 · delCardayre et al. · 2004 [cited by applicant]
US 6825001B2 · Wackett et al. · 2004 [cited by applicant]
US 6902922B2 · Ness et al. · 2005 [cited by applicant]
US 6917882B2 · Selifonov et al. · 2005 [cited by applicant]
US 6946296B2 · Patten et al. · 2005 [cited by applicant]
US 6961664B2 · Selifonov et al. · 2005 [cited by applicant]
US 6995017B1 · Stemmer · 2006 [cited by applicant]
US 7024312B1 · Selifonov et al. · 2006 [cited by applicant]
US 7058515B1 · Selifonov et al. · 2006 [cited by applicant]
US 7105297B2 · Minshull et al. · 2006 [cited by applicant]
US 7148054B2 · delCardayre et al. · 2006 [cited by applicant]
US 7169592B2 · Yamada et al. · 2007 [cited by applicant]
US 7220566B2 · Ness et al. · 2007 [cited by applicant]
US 7288375B2 · Stemmer et al. · 2007 [cited by applicant]
US 7384387B1 · Raillard et al. · 2008 [cited by applicant]
US 7399627B2 · Emalfarb et al. · 2008 [cited by applicant]
US 7421347B2 · Selifonov et al. · 2008 [cited by applicant]
US 7430477B2 · Selifonov et al. · 2008 [cited by applicant]
US 7462469B2 · Bass et al. · 2008 [cited by applicant]
US 7534564B2 · Patten et al. · 2009 [cited by applicant]
US 7620500B2 · Mundorff et al. · 2009 [cited by applicant]
US 7620502B2 · Selifonov et al. · 2009 [cited by applicant]
US 7629170B2 · delCardayre et al. · 2009 [cited by applicant]
US 7702464B1 · Emig et al. · 2010 [cited by applicant]
US 7747391B2 · Gustafsson et al. · 2010 [cited by applicant]
US 7747393B2 · Fox · 2010 [cited by applicant]
US 7751986B2 · Gustafsson et al. · 2010 [cited by applicant]
US 7776598B2 · Patten et al. · 2010 [cited by applicant]
US 7783428B2 · Gustafsson et al. · 2010 [cited by applicant]
US 7795030B2 · Minshull et al. · 2010 [cited by applicant]
US 7853410B2 · Selifonov et al. · 2010 [cited by applicant]
US 7868138B2 · Stemmer et al. · 2011 [cited by applicant]
US 7873477B1 · Gustafsson et al. · 2011 [cited by applicant]
US 7873499B2 · Selifonov et al. · 2011 [cited by applicant]
US 7904249B2 · Selifonov et al. · 2011 [cited by applicant]
US 7957912B2 · Selifonov et al. · 2011 [cited by applicant]
US 7981614B2 · Stemmer et al. · 2011 [cited by applicant]
US 8014961B2 · Bass et al. · 2011 [cited by applicant]
US 8029988B2 · Crameri et al. · 2011 [cited by applicant]
US 8048674B2 · Minshull et al. · 2011 [cited by applicant]
US 8058001B2 · Crameri et al. · 2011 [cited by applicant]
US 8076138B2 · delCardayre et al. · 2011 [cited by applicant]
US 8108150B2 · Mundorff et al. · 2012 [cited by applicant]
US 8170806B2 · Selifonov et al. · 2012 [cited by applicant]
US 8224580B2 · Mundorff et al. · 2012 [cited by applicant]
US 8293507B2 · Savile et al. · 2012 [cited by applicant]
US 8377681B2 · delCardayre et al. · 2013 [cited by applicant]
US 8383346B2 · Colbeck et al. · 2013 [cited by applicant]
US 8457903B1 · Emig et al. · 2013 [cited by applicant]
US 8504498B2 · Fox · 2013 [cited by applicant]
US 8589085B2 · Selifonov et al. · 2013 [cited by applicant]
US 8762066B2 · Fox · 2014 [cited by applicant]
US 8768871B2 · Fox · 2014 [cited by applicant]
US 9388395B2 · Nazor et al. · 2016 [cited by applicant]
US 9593326B2 · Clark et al. · 2017 [cited by applicant]
US 9714437B2 · Chan et al. · 2017 [cited by applicant]
US 20060195947A1 · Davis et al. · 2006 [cited by applicant]
US 20070259410A1 · Donaldson et al. · 2007 [cited by applicant]
US 20080220990A1 · Fox · 2008 [cited by applicant]
US 20090312196A1 · Colbeck et al. · 2009 [cited by applicant]
US 20150045562A1 · Crowe et al. · 2015 [cited by applicant]
US 20170283781A1 · Nazor et al. · 2017 [cited by applicant]
EP 137280B1 · 1992 [cited by applicant]
WO 9522625A1 · 1995 [cited by applicant]
WO 9533836A1 · 1995 [cited by applicant]
WO 9600787A1 · 1996 [cited by applicant]
WO 970078A1 · 1997 [cited by applicant]
WO 9735966A1 · 1997 [cited by applicant]
WO 9827230A1 · 1998 [cited by applicant]
WO 0042651A1 · 2000 [cited by applicant]
WO 0175767A2 · 2001 [cited by applicant]
WO 2005005633A2 · 2005 [cited by applicant]
WO 2008127646A2 · 2008 [cited by applicant]
WO 2009008908A2 · 2009 [cited by applicant]
WO 2009152336A1 · 2009 [cited by applicant]
WO 2010081053A2 · 2010 [cited by applicant]
WO 2011005477A1 · 2011 [cited by applicant]
WO 2011017551A1 · 2011 [cited by applicant]
WO 2011159910A2 · 2011 [cited by applicant]
WO 2012024104A2 · 2012 [cited by applicant]
WO 2012177527A1 · 2012 [cited by applicant]
WO 2014099730A1 · 2014 [cited by applicant]
WO 2018231462A1 · 2018 [cited by applicant]
WO 2019055498A1 · 2019 [cited by applicant]
WO 2020210613A1 · 2020 [cited by applicant]
Fransceus. J Ind Microbiol Biotechnol. May 2017;44(4-5):687-695. [cited by examiner]
Sanavia. Computational and Structural Biotechnology Journal, vol. 18, 2020, pp. 1968-1979. [cited by examiner]
Stemmer, W., “DNA Shuffling by Random Fragmentation and Reassembly: In vitro Recombination for Molecular Evolution,” Proc. Natl. Acad. Sci. USA, 91:10747-10751 (1994). [cited by applicant]
Stemmer, W.P.C., “Rapid evolution of a protein in vitro by DNA shuffling”, Nature, 370:389-391 (1994). [cited by applicant]
Stenico, M., et al., “Codon usage in Caenorhabditis elegans: delineation of translational selection and mutational biases,” Nucl. Acids Res. 22(13):2437-46 [1994]. [cited by applicant]
Takahashi, T., et al., “Efficient gene disruption in the koji-mold Aspergillus sojae using a novel variation of the positive-negative method,” Mol. Gen. Genom., 272: 344-352 [2004]. [cited by applicant]
Tiwari, S., et al., “Prediction of probable genes by Fourier analysis of genomic sequences,” Comput. Appl. Biosci. 13(3):263-270 [1997]. [cited by applicant]
Truppo, M.D., et al., “Development of an Improved Immobilized CAL-B for the Enzymatic Resolution of a Key Intermediate to Odanacatib,” Organic Process Research & Development, 15:1033-1035 (2011). [cited by applicant]
Uberbacher, E.C., et al., “Discovering and Understanding Genes in Human DNA Sequence Using GRAIL,” Methods Enzymol., 266:259-281 [1996]. [cited by applicant]
Van Ophem, P.W., et al., “Substrate inhibition of D-amino acid transaminase and protection by salts and by reduced nicotinamide adenine dinucleotide: isolation and initial characterization of a pyridoxo intermediate rel… [cited by applicant]
Villa-Komaroff, L., et al., “A bacterial clone synthesizing proinsulin,” Proc. Natl Acad. Sci. USA, 75:3727-3731 (1978). [cited by applicant]
Wada, K., et al., “Codon usage tabulated from the GenBank genetic sequence data,” Nucl. Acids Res., 20:2111-2118 [1992]. [cited by applicant]
Wells, J.A., et al., “Cassette mutagenesis: an efficient method for generation of multiple mutations at defined sites,” Gene, 34:315-323 (1985). [cited by applicant]
Wilson, I.A., et al., “The structure of antigenic determinant in a protein,” Cell, 37:767-778 [1984]. [cited by applicant]
Wright, F., “The ‘effective number of codons’ used in a gene,” Gene 87:23-29 [1990]. [cited by applicant]
Yi, S., et al., “Covalent immobilization of omega-transaminase from Vibrio fluvialis JS17 on chitosan beads,” Process Biochemistry 42(5): 895-898 (2007). [cited by applicant]
Yonaha, K., et al., “Distribution of ω-Amino Acid : Pyruvate Transaminase and Aminobutyrate : α-Ketoglutarate Transaminase in Microorganisms,” Agric. Biol. Chem., 47 (10):2257-2265 [1983]. [cited by applicant]
You, B., et al., “Gene-specifc disruption in the fillamentous fungus [cited by applicant]
Yun, H., et al., “ω-Amino Acid:Pyruvate Transaminase from Alcaligenes denitrificans Y2k-2: a New Catalyst for Kinetic Resolution of β-Amino Acids and Amines ,” Appl. Environ. Microbiol., 70:2529-2534 [2004]. [cited by applicant]
Zhang, J-H., et al., “Directed evolution of a fucosidase from a galactosidase by DNA shuffling and screening ,” Proc. Nat. Acad. Sci., U.S.A., 94:4504-4509 (1997). [cited by applicant]
GenBank Accession No. ABA47738.1 dated Jan. 31, 2014. [cited by applicant]
GenBank Accession No. AEA39183.1 dated Apr. 4, 2011. [cited by applicant]
GenBank Accession No. AM902716.1 dated Feb. 27, 2015. [cited by applicant]
GenBank Accession No. BAK39753.1 dated Feb. 16, 2012. [cited by applicant]
NCBI Accession No. YP_002257813 dated Aug. 27, 2013. [cited by applicant]
International Search Report from corresponding PCT application No. PCT/US2021/025967 mailed Nov. 8, 2021. [cited by applicant]
Studer, R.A., et al., “Residue mutations and their impact on protein structure and function: detecting beneficial and pathogenic changes,” Biochem. J., 449:581-594 [2013]. [cited by applicant]
Altschul, S., et al., “Basic local alignment search tool,” J. Mol. Biol., 215: 403-410 (1990). [cited by applicant]
Altschul, S.F., et al., “Gapped BLAST and PSI-BLAST: a new generation of protein database search programs,” Nucleic Acids Res., 25(17):3389-3402 (1997). [cited by applicant]
Beaucage, S.L., et al., “Deoxynucleoside phosphoamidites—A new class of key intermediates for deoxypolynucleotide synthesis,” Tetrahedron Letters, 22(20):1859-62 (1981). [cited by applicant]
Blaiseau, P-L., et al., “Primary structure of a chitinase-encoding gene (chi1) from the filamentous fungus [cited by applicant]
Boel, E., et al., “Two different types of intervening sequences in the glucoamylase gene from Aspergillus niger,” EMBO J., 3:1581-85 [1984]. [cited by applicant]
Botstein, D., et al., “Strategies and applications of in vitro mutagenesis,” Science, 229(4719):1193-1201 [1985]. [cited by applicant]
Carter, P., “Site-directed mutagenesis,” Biochem. J., 237:1-7 (1986). [cited by applicant]
Chaveroche, M., et al., “A rapid method for efficient gene replacement in the filamentous fungus [cited by applicant]
Cho, Y., et al., “A high throughput targeted gene disruption method for Alternaria brassicicola functional genomics using linear minimal element (LME) constructs,” Mol Plant Microbe Interact, 19(1):7-15 [2006]. [cited by applicant]
Christians, F.C., et al., “Directed evolution of thymidine kinase for AZT phosphorylation using DNA family shuffling,” Nat. Biotechnol., 17:259-264 (1999). [cited by applicant]
Combier, J.-P., et al., “Agrobacterium tumefaciens-mediated transformation as a tool for insertional mutagenesis in the symbiotic ectomycorrhizal fungus [cited by applicant]
Crameri, A., et al., “DNA shuffling of a family of genes from diverse species accelerates directed evolution”, Nature, 391:288-291 (1998). [cited by applicant]
Crameri, A., et al., “Improved green fluorescent protein by molecular evolution using DNA shuffling,” Nat. Biotechnol., 14(3):315-319 (1996). [cited by applicant]
Crameri, A., et al., “Molecular evolution of an arsenate detoxification pathway by DNA shuffling,” Nat. Biotechnol., 15 (5):436-438 (1997). [cited by applicant]
Dale, S.J., et al., “Oligonucleotide-directed random mutagenesis using the phosphorothioate method,” Methods Mol. Biol., 57:369-74 (1996). [cited by applicant]
De Boer, H.A., et al., “The tac promoter: A functional hybrid derived from the trp and lac promoters,” Proc. Natl Acad. Sci. USA, 80: 21-25 (1983). [cited by applicant]
Ehrlich, S.D., “Dna cloning in Bacillus subtilis,” Proc Natl Acad Sci. USA, 75:1433 (1978). [cited by applicant]
Eisenberg, D., et al., “Analysis of Membrane and Surface Protein Sequences with the Hydrophobic Moment Plot,” J. Mol. Biol., 179:125-142 [1984]. [cited by applicant]
Firon, A., et al., “Identification of Essential Genes in the Human Fungal Pathogen Aspergillus fumigatus by Transposon Mutagenesis,” Eukaryot. Cell, 2(2):247-55 [2003]. [cited by applicant]
Guo, Z., et al., “3′-End-Forming Signals of Yeast mRNA,” Mol. Cell. Biol., 15(11):5983-5990 [1995]. [cited by applicant]
Henaut and Danchin in Neidhardt et al. [eds.], [cited by applicant]
Henikoff, S., et al., “Amino acid substitution matrices from protein blocks,” Proc. Natl. Acad. Sci. USA, 89:10915-10919 [1992]. [cited by applicant]
Hong, J., et al., “Cloning and functional expression of thermostable beta-glucosidase gene from Thermoascus aurantiacus,” Appl. Microbiol. Biotechnol, 73:1331-1339 [2007]. [cited by applicant]
Hwang, B.-Y., et al., “High-throughput screening method for the identification of active and enantioselective ω-transaminases”, Enzyme and Microbial Technology, 34:429-436 [2004]. [cited by applicant]
Iwasaki, A., et al., “Microbial synthesis of (R)- and (S)-3,4-dimethoxyamphetamines through stereoselective transamination,” Biotech. Lett., 25:1843-1846 [2003]. [cited by applicant]
Iwasaki, A., et al., “Microbial synthesis of chiral amines by (R)-specific transamination with [cited by applicant]
Koszelewski, D., et al., “Immobilization of omega-transaminases by encapsulation in a sol-gel/celite matrix,” Journal of Molecular Catalysis B: Enzymatic, 63: 39-44 (2010). [cited by applicant]
Kramer, B., et al., “Different base/base mismatches are corrected with different efficiencies by the methyl-directed DNA mismatch-repair system of [cited by applicant]
Lathe, R., et al., “Plasmid and bacteriophage vectors for excision of intact inserts,” Gene, 57:193-201 (1987). [cited by applicant]
Limon, C., et al., “Primary structure and expression pattern of the 33-kDa chitinase gene from the nucoparasitic fungus [cited by applicant]
Ling, M., et al., “Approaches to DNA Mutagenesis:An Overview,” Anal. Biochem., 254:157-78 (1997). [cited by applicant]
Martin, A.R., et al., “Characterization of free and immobilized (S)-aminotransferase for acetophenone production,” Applied Microbiology and Biotechnology, 76(4): 843-851 (2007). [cited by applicant]
Maruyama, J., “Multiple gene disruptions by marker recycling with highly efficient gene-targeting background (delta-ligD) in Aspergillus oryzae,” Biotechnol Lett., 30:1811-1817 [2008]. [cited by applicant]
Mateo, C., et al., “Epoxy sepabeads: a novel epoxy support for stabilization of industrial enzymes via very intense multipoint covalent attachment,” Biotechnology Progress 18(3):629-34 (2002). [cited by applicant]
Matthes, H.W.D., et al., “Simultaneous rapid chemical synthesis of over one hundred oligonucleotides on a microscale,” EMBO J., 3(4):801-05 (1984). [cited by applicant]
McInerney, J.O., “GCUA: general codon usage analysis,” Bioinformatics, 14(4):372-73 [1998]. [cited by applicant]
Minshull, J., et al., “Protein evolution by molecular breeding,” Curr. Op. Chem. Biol., 3(3):284-290 (1999). [cited by applicant]
Nakamura, Y., et al., “Codon usage tabulated from international DNA sequence databases: status for the year 2000,” Nucl. Acids Res., 28:292 [2000]. [cited by applicant]
Needleman, S., et al., “A general method applicable to the search for similarities in the amino acid sequence of two proteins,” J. Mol. Biol. 48:443-453 (1970). [cited by applicant]
Nunberg, J.H., et al., “Molecular Cloning and Characterization of the Glucoamylase Gene of Aspergillus awamori,” Mol. Cell Biol., 4(11):2306-2315 [1984]. [cited by applicant]
Parry, N.J., et al., “Biochemical characterization and mechanism of action of a thermostablebeta-glucosidase purified from Thermoascus aurantiacus,” Biochem. J., 353:117-127 [2001]. [cited by applicant]
Pearson, W.R., “Improved tools for biological sequence comparison,” Proc. Nat'l. Acad. Sci. USA, 85:2444-2448 (1988). [cited by applicant]
Porath, J., “Immobilized metal ion affinity chromatography,” Protein Expression and Purification, 3:263-281 (1992). [cited by applicant]
Romanos, M.A., et al., “Foreign gene expression in yeast: a review,” Yeast 8:423-488 [1992]. [cited by applicant]
Savile, C.K., et al., “Biocatalytic asymmetric synthesis of chiral amines from ketones applied to sitagliptin manufacture,” Science 329(5989):305-9 (2010). [cited by applicant]
Shin, J.S., et al., “Comparison of the omega-transaminases from different microorganisms and application to production of chiral amines,” Biosci. Biotechnol. Biochem. 65:1782-1788 (2001). [cited by applicant]
Shin, J.S., et al., “Purification, characterization, and molecular cloning of a novel amine:pyruvate transaminase from Vibrio fluvialis JS17,” Appl. Microbiol. Biotechnol., 61(5-6):463-471 [2003]. [cited by applicant]
Simonen, M., et al., “Protein Secretion in [cited by applicant]
Smith, M., “In vitro mutagenesis,” Ann. Rev. Genet., 19:423-462 (1985). [cited by applicant]
Smith, T., et al., “Comparison of Biosequences,” Adv. Appl. Math, 2:482-489 (1981). [cited by applicant]