At the dated check, the references listed below either did not resolve in
Crossref or DataCite, or carried a retraction notice. Each one is shown with the
registry record that put it there.
The 365 checked references that resolve
resolves10.1039/C6GC02003HNew enzymatic methods for the synthesis of primary α-aminonitriles and unnatural α-amino acids by oxidative cyanation of primary amines with
<scp>d</scp>
-amino acid oxidase from porcine kidney
resolves10.1039/C6GC01922FBiocatalytic stereoinversion of
<scp>d</scp>
-para-bromophenylalanine in a one-pot three-enzyme reaction
resolves10.3390/biom3040741Biocatalytic Synthesis of Chiral Alcohols and Amino Acids for Development of Pharmaceuticals
resolves10.1021/ja00386a035O-Sulfated .beta.-lactam hydroxamic acids (monosulfactams). Novel monocyclic .beta.-lactam antibiotics of synthetic origin
resolves10.1097/00001721-199601000-00009Effects of inogatran, a new low-molecular-weight thrombin inhibitor, in rat models of venous and arterial thrombosis, thrombolysis and bleeding time
resolves10.1039/b919599hRecent advances in the catalytic asymmetric synthesis of β-amino acids
resolves10.1002/bit.26198Metabolic engineering of <i>Escherichia coli</i> for microbial production of L‐methionine
resolves10.1021/cs500535dEfficient Synthesis of Non-Natural <scp>l</scp>-2-Aryl-Amino Acids by a Chemoenzymatic Route
resolves10.1002/adsc.201100923Enzymatic Synthesis of Chiral Phenylalanine Derivatives by a Dynamic Kinetic Resolution of Corresponding Amide and Nitrile Substrates with a Multi‐Enzyme System
resolves10.1016/j.tetlet.2014.01.044High yield synthesis of d-phenylglycine and its derivatives by nitrilase mediated dynamic kinetic resolution in aqueous-1-octanol biphasic system
resolves10.1016/j.ccr.2007.09.012Chemo-enzymatic deracemization methods for the preparation of enantiopure non-natural α-amino acids
resolves10.1002/adsc.201700356NAD(P)H‐Dependent Dehydrogenases for the Asymmetric Reductive Amination of Ketones: Structure, Mechanism, Evolution and Application
resolves10.1002/biot.200900110Biocatalytic asymmetric amination of carbonyl functional groups – a synthetic biology approach to organic chemistry
resolves10.1016/S0167-4838(99)00192-2The NAD-dependent glutamate dehydrogenase from the hyperthermophilic archaeon Pyrobaculum islandicum: cloning, sequencing, and expression of the enzyme gene
resolves10.1016/j.molcatb.2014.03.010Stereoselective synthesis of l-tert-leucine by a newly cloned leucine dehydrogenase from Exiguobacterium sibiricum
resolves10.1007/s10295-016-1738-6Construction and evaluation of a novel bifunctional phenylalanine–formate dehydrogenase fusion protein for bienzyme system with cofactor regeneration
resolves10.1002/adsc.200700013Preparation of an Amino Acid Intermediate for the Dipeptidyl Peptidase IV Inhibitor, Saxagliptin, using a Modified Phenylalanine Dehydrogenase
resolves10.1016/j.bej.2014.08.003Efficient synthesis of l-tert-leucine through reductive amination using leucine dehydrogenase and formate dehydrogenase coexpressed in recombinant E. coli
resolves10.1021/ja0603960Creation of a Broad-Range and Highly Stereoselective<scp>d</scp>-Amino Acid Dehydrogenase for the One-Step Synthesis of<scp>d</scp>-Amino Acids
resolves10.1128/AEM.02234-12A Novel
<i>meso</i>
-Diaminopimelate Dehydrogenase from Symbiobacterium thermophilum: Overexpression, Characterization, and Potential for
<scp>d</scp>
-Amino Acid Synthesis
resolves10.1016/j.jmb.2004.10.063The First Crystal Structure of Hyperthermostable NAD-dependent Glutamate Dehydrogenase from Pyrobaculum islandicum
resolves10.1016/j.jmb.2008.01.091Three-Dimensional Structures of Apo- and Holo-l-Alanine Dehydrogenase from Mycobacterium tuberculosis Reveal Conformational Changes upon Coenzyme Binding
resolves10.1107/S0907444997009980Crystallization of NAD<sup>+</sup>-dependent phenylalanine dehydrogenase from<i>Nocardia sp239</i>
resolves10.1006/jmbi.1996.0900Crystal structure of glutamate dehydrogenase from the hyperthermophilic eubacterium Thermotoga maritima at 3.0 Å resolution
resolves10.1016/j.jsb.2011.10.006Crystal structure of NAD+-dependent Peptoniphilus asaccharolyticus glutamate dehydrogenase reveals determinants of cofactor specificity
resolves10.1021/bi982244qPhenylalanine Dehydrogenase from <i>Rhodococcus sp.</i> M4: High-Resolution X-ray Analyses of Inhibitory Ternary Complexes Reveal Key Features in the Oxidative Deamination Mechanism<sup>,</sup>
resolves10.1021/bi000494c<i>Rhodococcus</i> <scp>l</scp>-Phenylalanine Dehydrogenase: Kinetics, Mechanism, and Structural Basis for Catalytic Specifity<sup>,</sup>
resolves10.1002/prot.340120109Subunit assembly and active site location in the structure of glutamate dehydrogenase
resolves10.1007/BF00508114Leucine dehydrogenase from Bacillus sphaericus. Optimized production conditions and an efficient method for its large-scale purification
resolves10.1007/BF01088008Screening of thermostable leucine and alanine dehydrogenases in thermophilicBacillus strains
resolves10.1021/bi00425a026Gene cloning and sequence determination of leucine dehydrogenase from Bacillus stearothermophilus and structural comparison with other NAD(P)+-dependent dehydrogenases
resolves10.1099/00221287-135-5-1305Purification and Characterization of Leucine Dehydrogenase from the Thermophile 'Bacillus caldolyticus'
resolves10.1111/j.1432-1033.1994.tb18869.xThe purification, characterization, cloning and sequencing of the gene for a halostable and thermostable leucine dehydrogenase from <i>Thermoactinomyces intermedius</i>
resolves10.1007/BF00169940Gene cloning, purification, and characterization of thermostable and halophilic leucine dehydrogenase from a halophilic thermophile, Bacillus licheniformis TSN9
resolves10.1007/s002539900290Investigating expression systems for the stable large-scale production of recombinant L -leucine-dehydrogenase from Bacillus cereus in Escherichia coli
resolves10.1111/j.1470-8744.1989.tb00063.xOverproduction of thermostable leucine dehydrogenase of Bacillus stearothermophilus and its one‐step purification from recombinant cells of Escherichia coli
resolves10.1016/j.molcatb.2012.06.018A psychrophilic leucine dehydrogenase from Sporosarcina psychrophila: Purification, characterization, gene sequencing and crystal structure analysis
resolves10.1002/elsc.201500092A cold‐adapted leucine dehydrogenase from marine bacterium <i>Alcanivorax dieselolei</i>: Characterization and <scp>l</scp><i>‐tert</i>‐leucine production
resolves10.1007/s10529-016-2053-zExpression, purification and characterization of a thermostable leucine dehydrogenase from the halophilic thermophile Laceyella sacchari
resolves10.1021/jm970494jMatrix Metalloproteinase Inhibitors: A Structure−Activity Study
resolves10.1128/AEM.63.12.4651-4656.1997Synthesis of optically active amino acids from alpha-keto acids with Escherichia coli cells expressing heterologous genes
resolves10.1002/elsc.200402162From Enzymes to “Designer Bugs” in Reductive Amination: A New Process for the Synthesis of L‐<i>tert</i>‐Leucine Using a Whole Cell‐Catalyst
resolves10.1021/op0501702A “Second-Generation Process” for the Synthesis of <scp>l</scp>-Neopentylglycine: Asymmetric Reductive Amination Using a Recombinant Whole Cell Catalyst
resolves10.1007/s00253-016-7371-5Directed evolution of leucine dehydrogenase for improved efficiency of l-tert-leucine synthesis
resolves10.1038/srep30462Construction of a tunable multi-enzyme-coordinate expression system for biosynthesis of chiral drug intermediates
resolves10.1002/bit.260271118Improvement for <scp>L</scp>‐leucine production in a continuously operated enzyme membrane reactor
resolves10.1002/bit.260231213Continuous enzymatic transformation in an enzyme membrane reactor with simultaneous NAD(H) regeneration
resolves10.1016/0045-2068(90)90033-2Synthesis of l-β-hydroxyvaline from α-keto-β-hydroxyisovalerate using leucine dehydrogenase from Bacillus species
resolves10.1021/op2003562Preparation of (<i>S</i>)-1-Cyclopropyl-2-methoxyethanamine by a Chemoenzymatic Route Using Leucine Dehydrogenase
resolves10.1002/jlcr.1496Stereoselective synthesis of L‐[<sup>15</sup>N] amino acids with glucose dehydrogenase and galactose mutarotase as NADH regenerating system
resolves10.1080/00397919808006866Practical Synthesis of Methyl Z-2-(N-Acetylamino) but-2-Enoate. An Intermediate to D- and L-2-Aminobutyric Acid
resolves10.1007/s10529-013-1424-yA one-pot system for production of l-2-aminobutyric acid from l-threonine by l-threonine deaminase and a NADH-regeneration system based on l-leucine dehydrogenase and formate dehydrogenase
resolves10.1007/s10529-015-1957-3A recyclable biotransformation system for l-2-aminobutyric acid production based on immobilized enzyme technology
resolves10.1016/j.procbio.2017.01.022Development of a multi-enzymatic desymmetrization and its application for the biosynthesis of l -norvaline from dl -norvaline
resolves10.1016/j.jbiotec.2014.10.026A novel d-mandelate dehydrogenase used in three-enzyme cascade reaction for highly efficient synthesis of non-natural chiral amino acids
resolves10.1093/protein/10.6.687Construction of a new leucine dehydrogenase with preferred specificity for NADP+ by site-directed mutagenesis of the strictly NAD+-specific enzyme
resolves10.1007/BF00425806Isolation and characterization of a bacterium possessing L-phenylalanine dehydrogenase activity
resolves10.1007/BF00253523Isolation of l-phenylalanine dehydrogenase from Rhodococcus sp. M4 and its application for the production of l-phenylalanine
resolves10.1016/S0021-9258(18)61119-6Novel phenylalanine dehydrogenases from Sporosarcina ureae and Bacillus sphaericus. Purification and characterization.
resolves10.1271/bbb.59.1994Nucleotide Sequencing of Phenylalanine Dehydrogenase Gene from<i>Bacillus badius</i>IAM 11059
resolves10.1007/BF00277534Purification, characterization and regulation of a monomeric l-phenylalanine dehydrogenase from the facultative methylotroph Nocardia sp. 239
resolves10.1128/jb.173.13.3943-3948.1991Distribution, purification, and characterization of thermostable phenylalanine dehydrogenase from thermophilic actinomycetes
resolves10.1007/s002030050564Thermostable phenylalanine dehydrogenase from a mesophilic Microbacterium sp. strain DM 86-1
resolves10.1007/BF00253645l-Phenylalanine dehydrogenase from Brevibacterium sp. for production of l-phenylalanine by reductive amination of phenylpyruvate
resolves10.1021/jo00308a012Enantioselective synthesis of (S)-amino acids by phenylalanine dehydrogenase from Bacillus sphaericus: use of natural and recombinant enzymes
resolves10.1016/j.jbiotec.2009.03.005Efficient screening for new amino acid dehydrogenase activity: Directed evolution of Bacillus sphaericus phenylalanine dehydrogenase towards activity with an unsaturated non-natural amino acid
resolves10.1016/0014-5793(95)00804-IAlteration in relative activities of phenylalanine dehydrogenase towards different substrates by site‐directed mutagenesis
resolves10.1021/bi020196aSingle Amino Acid Substitution in <i>Bacillus sphaericus</i> Phenylalanine Dehydrogenase Dramatically Increases Its Discrimination between Phenylalanine and Tyrosine Substrates
resolves10.1046/j.1432-1033.2003.03852.xKinetic analysis of phenylalanine dehydrogenase mutants designed for aliphatic amino acid dehydrogenase activity with guidance from homology‐based modelling
resolves10.1039/b406364cEnantioselective synthesis of non-natural amino acids using phenylalanine dehydrogenases modified by site-directed mutagenesis
resolves10.1016/j.jbiotec.2006.08.008Phenylalanine dehydrogenase mutants: Efficient biocatalysts for synthesis of non-natural phenylalanine derivatives
resolves10.1039/b510816kEngineered phenylalanine dehydrogenase in organic solvents: homogeneous and biphasic enzymatic reactions
resolves10.1016/j.enzmictec.2006.10.021An engineered mutant, L307V of phenylalanine dehydrogenase from Bacillus sphaericus: high activity and stability in organic-aqueous solvent mixtures and utility for synthesis of non-natural l-amino acids
resolves10.3109/10242420009015258Phenylalanine Dehydrogenase Catalyzed Reductive Amination of 6-(1′,3′-Dioxolan-2′-YL)-2-Keto-Hexanoic Acid to 6-(1′,3′-Dioxolan-2′-YL)-2S-Aminohexanoic Acid with Nadh Regeneration and Enzyme and Cofactor Retention
resolves10.1016/0045-2068(91)90041-MEnzyme-catalyzed asymmetric synthesis of (S)-2-amino-4-phenylbutanoic acid and (R)-2-hydroxy-4-phenylbutanoic acid
resolves10.1016/j.bej.2010.08.010Synthesis of l-homophenylalanine via integrated membrane bioreactor: Influence of pH on yield
resolves10.1016/j.molcatb.2012.11.014Immobilization of phenylalanine dehydrogenase onto Eupergit CM for the synthesis of (S)-2-amino-4-phenylbutyric acid
resolves10.1007/s00253-013-5117-1Enhancement of biocatalytic efficiency by increasing substrate loading: enzymatic preparation of l-homophenylalanine
resolves10.1021/cs4011919Microparticle-Based Strategy for Controlled Release of Substrate for the Biocatalytic Preparation of <scp>l</scp>-Homophenylalanine
resolves10.1021/ol702470jChemoenzymatic Synthesis of (<i>S</i>)-Hexafluoroleucine and (<i>S</i>)-Tetrafluoroleucine
resolves10.1002/bit.21501Biotransformation of <scp>D</scp>‐methionine into <scp>L</scp>‐methionine in the cascade of four enzymes
resolves10.1021/sb400093xDevelopment of an NADPH-Dependent Homophenylalanine Dehydrogenase by Protein Engineering
resolves10.1007/BF02418236Isolation and characterization of a gene encoding meso-diaminopimelate dehydrogenase fromGlycine max
resolves10.1021/bi961628iThree-Dimensional Structure of<i> meso</i>-Diaminopimelic Acid Dehydrogenase from <i>Corynebacterium glutamicum</i><sup>,</sup>
resolves10.1021/bi9727949Substrate and Inhibitor Binding Sites in <i>Corynebacterium glutamicum</i> Diaminopimelate Dehydrogenase<sup>,</sup>
resolves10.1002/adsc.201600682Single‐Biocatalyst Synthesis of Enantiopure <scp>d</scp>‐Arylalanines Exploiting an Engineered <scp>d</scp>‐Amino Acid Dehydrogenase
resolves10.1128/AEM.01049-13Engineering the
<i>meso</i>
-Diaminopimelate Dehydrogenase from Symbiobacterium thermophilum by Site Saturation Mutagenesis for
<scp>d</scp>
-Phenylalanine Synthesis
resolves10.1021/op400013eEnzymatic Preparation of an<i>R</i>-Amino Acid Intermediate for a γ-Secretase Inhibitor
resolves10.1007/s00253-013-4902-1Efficient synthesis of d-branched-chain amino acids and their labeled compounds with stable isotopes using d-amino acid dehydrogenase
resolves10.1021/acscatal.5b01132Chemoenzymatic Synthesis of Optically Pure <scp>l</scp>- and <scp>d</scp>-Biarylalanines through Biocatalytic Asymmetric Amination and Palladium-Catalyzed Arylation
resolves10.1186/2191-0855-1-43Highly stable meso-diaminopimelate dehydrogenase from an Ureibacillus thermosphaericus strain A1 isolated from a Japanese compost: purification, characterization and sequencing
resolves10.1007/s10529-012-0952-1Creation of a thermostable NADP+-dependent d-amino acid dehydrogenase from Ureibacillus thermosphaericus strain A1 meso-diaminopimelate dehydrogenase by site-directed mutagenesis
resolves10.1107/S1399004715003673Structural insight into the thermostable NADP<sup>+</sup>-dependent<i>meso</i>-diaminopimelate dehydrogenase from<i>Ureibacillus thermosphaericus</i>
resolves10.1128/AEM.00491-17Structure-Based Engineering of an Artificially Generated NADP
<sup>+</sup>
-Dependent
<scp>d</scp>
-Amino Acid Dehydrogenase
resolves10.1002/cbic.201300691Structural and Mutational Studies on the Unusual Substrate Specificity of <i>meso</i>‐Diaminopimelate Dehydrogenase from <i>Symbiobacterium thermophilum</i>
resolves10.1002/cbic.201402632Structural Analysis Reveals the Substrate‐Binding Mechanism for the Expanded Substrate Specificity of Mutant <i>meso</i>‐Diaminopimelate Dehydrogenase
resolves10.1128/AEM.00476-17A Newly Determined Member of the
<i>meso</i>
-Diaminopimelate Dehydrogenase Family with a Broad Substrate Spectrum
resolves10.1002/cbic.201700493Sustainable and Continuous Synthesis of Enantiopure <scp>l</scp>‐Amino Acids by Using a Versatile Immobilised Multienzyme System
resolves10.1006/jmbi.1994.0126Crystal Structure of the Closed Form of Chicken Cystosolic Aspartate Aminotransferase at 1.9 Å Resolution
resolves10.1128/AEM.72.2.1588-1594.2006Functional and Structural Characterization of Thermostable<scp>d</scp>-Amino Acid Aminotransferases from<i>Geobacillus</i>spp
resolves10.1128/JB.180.16.4319-4323.1998Characterization of the Genes Encoding
<scp>d</scp>
-Amino Acid Transaminase and Glutamate Racemase, Two
<scp>d</scp>
-Glutamate Biosynthetic Enzymes of
<i>Bacillus sphaericus</i>
ATCC 10208
resolves10.1128/jb.177.2.336-342.1995Staphylococcus haemolyticus contains two D-glutamic acid biosynthetic activities, a glutamate racemase and a D-amino acid transaminase
resolves10.1016/j.enzmictec.2016.10.002A Novel highly thermostable branched-chain amino acid aminotransferase from the crenarchaeon Vulcanisaeta moutnovskia
resolves10.1016/j.jbiotec.2016.06.004Pichia pastoris mutants as host strains for efficient secretion of recombinant branched chain aminotransferase (BCAT)
resolves10.1016/j.abb.2016.08.009Experimental and computational studies on the unusual substrate specificity of branched-chain amino acid aminotransferase from Thermoproteus uzoniensis
resolves10.1111/febs.12609The specificity and kinetic mechanism of branched‐chain amino acid aminotransferase from <i>Escherichia coli</i> studied with a new improved coupled assay procedure and the enzyme's potential for biocatalysis
resolves10.1016/S0167-4838(01)00136-4Recombinant tyrosine aminotransferase from Trypanosoma cruzi: structural characterization and site directed mutagenesis of a broad substrate specificity enzyme
resolves10.1074/jbc.272.35.21932Active-site Arg → Lys Substitutions Alter Reaction and Substrate Specificity of Aspartate Aminotransferase
resolves10.1186/1471-2105-10-273The B6 database: a tool for the description and classification of vitamin B6-dependent enzymatic activities and of the corresponding protein families
resolves10.1021/bi00030a002Crystal Structure of a D-Amino Acid Aminotransferase: How the Protein Controls Stereoselectivity
resolves10.1021/bi010384lStructures of <i>Escherichia coli</i> Branched-Chain Amino Acid Aminotransferase and Its Complexes with 4-Methylvalerate and 2-Methylleucine: Induced Fit and Substrate Recognition of the Enzyme<sup>,</sup>
resolves10.1006/jmbi.1998.1869Crystal structures of Paracoccus denitrificans aromatic amino acid aminotransferase: a substrate recognition site constructed by rearrangement of hydrogen bond network
resolves10.1002/prot.24233Crystal structure of the ω‐aminotransferase from <i>Paracoccus denitrificans</i> and its phylogenetic relationship with other class III amino‐ transferases that have biotechnological potential
resolves10.1107/S0907444999006630Crystallization and preliminary crystallographic analysis of the <i>Escherichia coli</i> tyrosine aminotransferase
resolves10.1021/bi952138dThe Reaction Catalyzed by <i>Escherichia coli</i> Aspartate Aminotransferase Has Multiple Partially Rate-Determining Steps, While That Catalyzed by the Y225F Mutant Is Dominated by Ketimine Hydrolysis
resolves10.1021/bi001403eStrain Is More Important Than Electrostatic Interaction in Controlling the p<i>K</i><sub>a</sub> of the Catalytic Group in Aspartate Aminotransferase<sup>,</sup>
resolves10.1016/S0040-4039(99)01302-7A new access to alkyl-α-ketoglutaric acids, precursors of glutamic acid analogues by enzymatic transamination. Application to the synthesis of (2S,4R)-4-propyl-glutamic acid
resolves10.1021/jm050597zChemoenzymatic Synthesis of a Series of 4-Substituted Glutamate Analogues and Pharmacological Characterization at Human Glutamate Transporters Subtypes 1−3
resolves10.1016/j.tetlet.2005.10.156Synthesis of the constrained glutamate analogues (2S,1′R,2′R)- and (2S,1′S,2′S)-2-(2′-carboxycyclobutyl)glycines L-CBG-II and L-CBG-I by enzymatic transamination
resolves10.1021/jm060822sStereoselective Chemoenzymatic Synthesis of the Four Stereoisomers of <scp>l</scp>-2-(2-Carboxycyclobutyl)glycine and Pharmacological Characterization at Human Excitatory Amino Acid Transporter Subtypes 1, 2, and 3
resolves10.1021/jm800091eChemo-Enzymatic Synthesis of (2<i>S</i>,4<i>R</i>)-2-Amino-4-(3-(2,2-diphenylethylamino)-3-oxopropyl)pentanedioic Acid: A Novel Selective Inhibitor of Human Excitatory Amino Acid Transporter Subtype 2
resolves10.1021/jm800092xChemo-Enzymatic Synthesis of a Series of 2,4-<i>Syn</i>-Functionalized (<i>S</i>)-Glutamate Analogues: New Insight into the Structure−Activity Relation of Ionotropic Glutamate Receptor Subtypes 5, 6, and 7
resolves10.1021/jm301433mChemoenzymatic Synthesis of New 2,4-<i>syn</i>-Functionalized (<i>S</i>)-Glutamate Analogues and Structure–Activity Relationship Studies at Ionotropic Glutamate Receptors and Excitatory Amino Acid Transporters
resolves10.1021/jo070805qChemoenzymatic Synthesis of Glutamic Acid Analogues: Substrate Specificity and Synthetic Applications of Branched Chain Aminotransferase from <i>Escherichia coli</i>
resolves10.1021/op025518xNonproteinogenic α-Amino Acid Preparation Using Equilibrium Shifted Transamination
resolves10.3109/10242422.2011.638373Asymmetric synthesis of<scp>l</scp>-6-hydroxynorleucine from 2-keto-6-hydroxyhexanoic acid using a branched-chain aminotransferase
resolves10.1016/j.molcatb.2010.05.014Asymmetric synthesis of l-tert-leucine and l-3-hydroxyadamantylglycine using branched chain aminotransferase
resolves10.1128/AEM.56.1.1-6.1990Stereospecific production of the herbicide phosphinothricin (glufosinate) by transamination: isolation and characterization of a phosphinothricin-specific transaminase from Escherichia coli
resolves10.1128/AEM.56.1.7-12.1990Stereospecific production of the herbicide phosphinothricin (glufosinate) by transamination: cloning, characterization, and overexpression of the gene encoding a phosphinothricin-specific transaminase from Escherichia coli
resolves10.1128/AEM.62.10.3794-3799.1996Stereospecific production of the herbicide phosphinothricin (glufosinate): purification of aspartate transaminase from Bacillus stearothermophilus, cloning of the corresponding gene, aspC, and application in a coupled transaminase process
resolves10.1002/cctc.201300571Biocatalytic Asymmetric Synthesis of Unnatural Amino Acids through the Cascade Transfer of Amino Groups from Primary Amines onto Keto Acids
resolves10.1016/j.molcatb.2015.07.011Biocatalytic cascade reactions for asymmetric synthesis of aliphatic amino acids in a biphasic reaction system
resolves10.1002/bit.10526Simultaneous synthesis of enantiomerically pure (<i>S</i>)‐amino acids and (<i>R</i>)‐amines using coupled transaminase reactions
resolves10.1016/j.molcatb.2003.07.006Simultaneous synthesis of enantiomerically pure (S)-amino acids and (R)-amines using α/ω-aminotransferase coupling reactions with two-liquid phase reaction system
resolves10.1002/bit.10661Asymmetric synthesis of <scp>L</scp>‐homophenylalanine by equilibrium‐shift using recombinant aromatic <scp>L</scp>‐amino acid transaminase
resolves10.1002/bit.20902Engineering aromatic <scp>L</scp>‐amino acid transaminase for the asymmetric synthesis of constrained analogs of <scp>L</scp>‐phenylalanine
resolves10.1016/S1381-1177(02)00011-5Application of a thermostable glutamate racemase from Bacillus sp. SK-1 for the production of d-phenylalanine in a multi-enzyme system
resolves10.1134/S0003683815060095Screening, characterization and utilization of D-amino acid aminotransferase to obtain D-phenylalanine
resolves10.1021/op800149qEnzymatic Preparation of a<scp>d</scp>-Amino Acid from a Racemic Amino Acid or Keto Acid
resolves10.1016/j.tetasy.2006.07.034Asymmetric synthesis of nonproteinogenic amino acids with l-amino acid transaminase: synthesis of (2S)-2-amino-4-oxo-4-phenylbutyric and (3E,2S)-2-amino-4-phenylbutenoic acids
resolves10.1021/bp990044fEnhanced Conversion Rate of L-Phenylalanine by Coupling Reactions of Aminotransferases and Phosphoenolpyruvate Carboxykinase in Escherichia coli K-12
resolves10.1002/cbic.200700601Efficient Asymmetric Synthesis of Chiral Amines by Combining Transaminase and Pyruvate Decarboxylase
resolves10.1016/S0968-0896(99)00153-4Engineering of a novel biochemical pathway for the biosynthesis of l-2-aminobutyric acid in Escherichia coli K12
resolves10.1007/s00253-011-3127-4Removal of l-alanine from the production of l-2-aminobutyric acid by introduction of alanine racemase and d-amino acid oxidase
resolves10.1002/bit.22178Simultaneous synthesis of 2‐phenylethanol and <scp>L</scp>‐homophenylalanine using aromatic transaminase with yeast Ehrlich pathway
resolves10.1016/j.jbiosc.2016.06.013Cosynthesis of l-homophenylalanine and 2-phenylethanol by recombinant Saccharomyces cerevisiae expressing aspartate aminotransferase from Escherichia coli BL21(DE3)
resolves10.1023/A:1010308506263Chemo-enzymatic synthesis of 3-(2-naphthyl)- L-alanine by an aminotransferase from the extreme thermophile, Thermococcus profundus
resolves10.1007/BF03026244Asymmetric synthesis of unnaturall-amino acids using thermophilic aromaticl-amino acid transaminase
resolves10.1002/btpr.272Asymmetrically simultaneous synthesis of <scp>L</scp>‐homophenylalanine and <i>N</i><sup>6</sup>‐protected‐2‐oxo‐6‐amino‐hexanoic acid by engineered <i>Escherichia coli</i> aspartate aminotransferase
resolves10.1039/c2gc35615eω-Transaminase-catalyzed kinetic resolution of chiral amines using l-threonine as an amino acceptor precursor
resolves10.1002/anie.201406571Chiral Amine Synthesis Using ω‐Transaminases: An Amine Donor that Displaces Equilibria and Enables High‐Throughput Screening
resolves10.1002/chem.201603188A New Generation of Smart Amine Donors for Transaminase‐Mediated Biotransformations
resolves10.1002/adsc.201000601One‐Pot Conversion of <scp>L</scp>‐Threonine into <scp>L</scp>‐Homoalanine: Biocatalytic Production of an Unnatural Amino Acid from a Natural One
resolves10.1039/c3ob40495aω-Transaminase-catalyzed asymmetric synthesis of unnatural amino acids using isopropylamine as an amino donor
resolves10.1002/adsc.201400185Deracemization of Amino Acids by Coupling Transaminases of Opposite Stereoselectivity
resolves10.1128/AEM.01533-15Active-Site Engineering of ω-Transaminase for Production of Unnatural Amino Acids Carrying a Side Chain Bulkier than an Ethyl Substituent
resolves10.1007/s00253-013-4846-5Active site model of (R)-selective ω-transaminase and its application to the production of d-amino acids
resolves10.1039/c2ob07161dDeracemization of unnatural amino acid: homoalanine using d-amino acid oxidase and ω-transaminase
resolves10.1128/AEM.02119-06Cloning and Characterization of a Novel β-Transaminase from<i>Mesorhizobium</i>sp. Strain LUK: a New Biocatalyst for the Synthesis of Enantiomerically Pure β-Amino Acids
resolves10.1128/AEM.02525-12Biochemical Properties and Crystal Structure of a β-Phenylalanine Aminotransferase from Variovorax paradoxus
resolves10.1016/j.enzmictec.2016.02.013Biochemical characterization of thermostable ω-transaminase from Sphaerobacter thermophilus and its application for producing aromatic β- and γ-amino acids
resolves10.1039/C3CC44864AEnzymatic synthesis of chiral γ-amino acids using ω-transaminase
resolves10.1128/AEM.70.4.2529-2534.2004ω-Amino Acid:Pyruvate Transaminase from
<i>Alcaligenes denitrificans</i>
Y2k-2: a New Catalyst for Kinetic Resolution of β-Amino Acids and Amines
resolves10.1002/biot.201500181Asymmetric synthesis of aromatic β‐amino acids using ω‐transaminase: Optimizing the lipase concentration to obtain thermodynamically unstable β‐keto acids
resolves10.1007/s10529-016-2271-4Biotransformation of β-keto nitriles to chiral (S)-β-amino acids using nitrilase and ω-transaminase
resolves10.1002/bit.24962Production of non‐proteinogenic amino acids from α‐keto acid precursors with recombinant <i>Corynebacterium glutamicum</i>
resolves10.1021/bi200497yStructural Basis for the Catalytic Mechanism of Aspartate Ammonia Lyase
resolves10.1016/j.bmc.2014.06.035Bacterial Anabaena variabilis phenylalanine ammonia lyase: A biocatalyst with broad substrate specificity
resolves10.1016/j.abb.2005.04.012Purification, cloning, and functional expression of phenylalanine aminomutase: The first committed step in Taxol side-chain biosynthesis
resolves10.1002/anie.201410670Synthesis of <scp>D</scp>‐ and <scp>L</scp>‐Phenylalanine Derivatives by Phenylalanine Ammonia Lyases: A Multienzymatic Cascade Process
resolves10.1021/jacs.5b07326The Bacterial Ammonia Lyase EncP: A Tunable Biocatalyst for the Synthesis of Unnatural Amino Acids
resolves10.1002/cctc.201000435Asymmetric Synthesis of (<i>S</i>)‐2‐Indolinecarboxylic Acid by Combining Biocatalysis and Homogeneous Catalysis
resolves10.1021/jo901833yPhenylalanine Aminomutase-Catalyzed Addition of Ammonia to Substituted Cinnamic Acids: a Route to Enantiopure α- and β-Amino Acids
resolves10.1002/anie.201106372Mechanism‐Inspired Engineering of Phenylalanine Aminomutase for Enhanced β‐Regioselective Asymmetric Amination of Cinnamates
resolves10.1021/bi102067rMechanistic, Mutational, and Structural Evaluation of a <i>Taxus</i> Phenylalanine Aminomutase
resolves10.1021/bi049053+Crystal Structure of Phenylalanine Ammonia Lyase: Multiple Helix Dipoles Implicated in Catalysis
<sup>,</sup>
resolves10.1021/bi061774gDiscovery of Two Cyanobacterial Phenylalanine Ammonia Lyases: Kinetic and Structural Characterization<sup>,</sup>
resolves10.1002/anie.201311061Phenylalanine Ammonia Lyase Catalyzed Synthesis of Amino Acids by an MIO‐Cofactor Independent Pathway
resolves10.1371/journal.pone.0085943Expression and Properties of the Highly Alkalophilic Phenylalanine Ammonia-Lyase of Thermophilic Rubrobacter xylanophilus
resolves10.1007/s10529-013-1140-7Cloning, expression and characterization of phenylalanine ammonia-lyase from Rhodotorula glutinis
resolves10.1128/AEM.42.5.773-778.1981Production of
<scp>l</scp>
-Phenylalanine from
<i>trans</i>
-Cinnamic Acid with
<i>Rhodotorula glutinis</i>
Containing
<scp>l</scp>
-Phenylalanine Ammonia-Lyase Activity
resolves10.1007/BF00253308Novel stabilization of phenylalanine ammonia-lyase catalyst during bioconversion of trans-cinnamic acid to l-phenylalanine
resolves10.1016/0141-0229(87)90137-2Biotransformation of trans-cinnamic acid to l-phenylalanine: Optimization of reaction conditions using whole yeast cells
resolves10.1002/jlcr.2580241106Synthesis of specifically labelled L‐phenylalanines using phenylalanine ammonia lyase activity
resolves10.1111/j.1472-765X.2008.02364.xInfluence of amino acids, organic solvents and surfactants for phenylalanine ammonia lyase activity in recombinant Escherichia coli
resolves10.1007/s12010-012-9738-0Cross-Linked Enzyme Aggregates of Phenylalanine Ammonia Lyase: Novel Biocatalysts for Synthesis of L-Phenylalanine
resolves10.1007/BF01021641Synthesis of L-phenylalanine analogs byRhodotorula glutinis. Bioconversion of cinnamic acids derivatives
resolves10.1002/cjoc.19950130308Red yeast catalyzed amination of olefinic bonds and synthesis of optically pure <i>S</i>‐amino acids
resolves10.1016/S0141-0229(96)00013-0Stabilization of phenylalanine ammonia lyase containing Rhodotorula glutinis cells for the continuous synthesis of l-phenylalanine methyl ester/96/
resolves10.1006/abbi.1998.0860The Behavior of Substrate Analogues and Secondary Deuterium Isotope Effects in the Phenylalanine Ammonia-Lyase Reaction
resolves10.1002/ejoc.200500902Chemoenzymatic One‐Pot Synthesis of Enantiopure <scp>L</scp>‐Arylalanines from Arylaldehydes
resolves10.1016/j.tet.2015.12.063Telescopic one-pot condensation-hydroamination strategy for the synthesis of optically pure L-phenylalanines from benzaldehydes
resolves10.1039/C6CY00855KIntensified biocatalytic production of enantiomerically pure halophenylalanines from acrylic acids using ammonium carbamate as the ammonia source
resolves10.1021/acs.orglett.6b02559Synthesis of Enantiomerically Pure Ring-Substituted <scp>l</scp>-Pyridylalanines by Biocatalytic Hydroamination
resolves10.1016/j.tet.2016.06.026Engineering of phenylalanine ammonia lyase from Rhodotorula graminis for the enhanced synthesis of unnatural l-amino acids
resolves10.1016/j.btre.2014.06.001Mechanism-based site-directed mutagenesis to shift the optimum pH of the phenylalanine ammonia-lyase from Rhodotorula glutinis JN-1
resolves10.1039/C7OB00562HExpanding the substrate scope of phenylalanine ammonia-lyase from
<i>Petroselinum crispum</i>
towards styrylalanines
resolves10.1074/jbc.M411215200Cloning, Heterologous Expression, and Characterization of a Phenylalanine Aminomutase Involved in Taxol Biosynthesis
resolves10.1002/cbic.200800568Enzymatic Synthesis of Enantiopure α‐ and β‐Amino Acids by Phenylalanine Aminomutase‐Catalysed Amination of Cinnamic Acid Derivatives
resolves10.1021/bi7003685The Structure of <scp>l</scp>-Tyrosine 2,3-Aminomutase from the C-1027 Enediyne Antitumor Antibiotic Biosynthetic Pathway<sup>,</sup>
resolves10.1021/ja0762689The Mechanism of MIO-Based Aminomutases in β-Amino Acid Biosynthesis
resolves10.1002/bip.21500Probing the active site of MIO‐dependent aminomutases, key catalysts in the biosynthesis of β‐amino acids incorporated in secondary metabolites
resolves10.1002/adsc.201600894Kinetic Resolution of Aromatic β‐Amino Acids Using a Combination of Phenylalanine Ammonia Lyase and Aminomutase Biocatalysts
resolves10.1093/nar/13.6.2063Cloning and nucleotide sequence of the aspartase gene of<i>Escherichia coli W</i>
resolves10.1128/jb.173.12.3831-3845.1991Cloning, nucleotide sequence, and expression of the Bacillus subtilis ans operon, which codes for L-asparaginase and L-aspartase
resolves10.1093/jb/mvg012Thermostable Aspartase from a Marine Psychrophile, Cytophaga sp. KUC-1: Molecular Characterization and Primary Structure
resolves10.1006/abbi.1999.1186Purification and Characterization of Thermostable Aspartase fromBacillussp. YM55-1
resolves10.1021/cb3002792Catalytic Mechanisms and Biocatalytic Applications of Aspartate and Methylaspartate Ammonia Lyases
resolves10.1252/jcej.17.647A stabilization of aspartase activity of immobilized Escherichia coli cells by temperature-raising operation.
resolves10.1007/s00449-012-0732-2Immobilized l-aspartate ammonia-lyase from Bacillus sp. YM55-1 as biocatalyst for highly concentrated l-aspartate synthesis
resolves10.1007/BF00499507Continuous production of L-alanine from fumarate in a two-stage membrane reactor
resolves10.1016/S0141-0229(00)00149-6Selective production of L-aspartic acid and L-phenylalanine by coupling reactions of aspartase and aminotransferase in Escherichia coli
resolves10.1016/S0141-0229(03)00206-0Efficient production of l-phenylalanine catalyzed by a coupled enzymatic system of transaminase and aspartase
resolves10.1002/chem.200801407Biocatalytic Enantioselective Synthesis of <i>N</i>‐Substituted Aspartic Acids by Aspartate Ammonia Lyase
resolves10.1016/j.molcatb.2015.02.007Nitrilase-catalyzed hydrolysis of 3-aminopropionitrile at high concentration with a tandem reaction strategy for shifting the reaction to β-alanine formation
resolves10.1006/bbrc.2000.3472Enhancement of the Activity of -Aspartase from Escherichia coli W by Directed Evolution
resolves10.1007/s00253-011-3615-6Characterization of a thermostable methylaspartate ammonia lyase from Carboxydothermus hydrogenoformans
resolves10.1074/jbc.M111180200The Structure of 3-Methylaspartase from Clostridium tetanomorphum Functions via the Common Enolase Chemical Step
resolves10.1016/S0040-4039(00)96139-2Stereochemical course of the enzymic amination of chloro- and bromo- fumaric acid by 3-methylaspartate ammonia-lyase
resolves10.1271/bbb.58.223Occurrence of 3-Methylaspartate Ammonia-lyase in Facultative Anaerobes and Their Application to Synthesis of 3-Substituted (<i>S</i>)-Aspartic Acids
resolves10.1016/S0040-4020(01)87795-4Enantiospecific synthesis of 3-substituted aspartic acids via enzymic amination of substituted fumaric acids
resolves10.1016/S0957-4166(00)80221-9Syntheses of (2S,3R)- and (2S,3R)[3-2h]- 3-methylaspartic acid: slow substrates for a syn-elimination reaction catalysed by methylaspartase.
resolves10.1038/nchem.1338Engineering methylaspartate ammonia lyase for the asymmetric synthesis of unnatural amino acids
resolves10.1002/cctc.201200906Enantioselective Synthesis of N‐Substituted Aspartic Acids Using an Engineered Variant of Methylaspartate Ammonia Lyase
resolves10.1002/chem.201301832Kinetic Resolution and Stereoselective Synthesis of 3‐Substituted Aspartic Acids by Using Engineered Methylaspartate Ammonia Lyases
resolves10.1002/cctc.201500318Chemoenzymatic Synthesis of <i>ortho</i>‐, <i>meta</i>‐, and <i>para</i>‐Substituted Derivatives of <scp>L</scp>‐<i>threo</i>‐3‐Benzyloxyaspartate, An Important Glutamate Transporter Blocker
resolves10.1039/C7OB00305FRapid chemoenzymatic route to glutamate transporter inhibitor
<scp>l</scp>
-TFB-TBOA and related amino acids
resolves10.1007/s00253-005-1934-1Recombinant production of serine hydroxymethyl transferase from Streptococcus thermophilus and its preliminary evaluation as a biocatalyst
resolves10.1016/j.molcatb.2008.05.002Screening of microorganisms producing α-methylserine hydroxymethyltransferase, purification of the enzyme, gene cloning, and application to the enzymatic synthesis of α-methyl-l-serine
resolves10.1016/j.molcatb.2008.06.007Gene cloning, purification, and characterization of α-methylserine aldolase from Bosea sp. AJ110407 and its applicability for the enzymatic synthesis of α-methyl-l-serine and α-ethyl-l-serine
resolves10.1007/s00253-015-7218-5Threonine aldolases: perspectives in engineering and screening the enzymes with enhanced substrate and stereo specificities
resolves10.1007/s00253-010-2751-8Threonine aldolases—screening, properties and applications in the synthesis of non-proteinogenic β-hydroxy-α-amino acids
resolves10.1080/10826068.2011.583975OPTIMAL PRODUCTION OF L-<i>threo</i>-2,3-DIHYDROXYPHENYLSERINE (L-<i>threo</i>-DOPS) ON A LARGE SCALE BY DIASTEREOSELECTIVITY-ENHANCED VARIANT OF L-THREONINE ALDOLASE EXPRESSED IN<i>Escherichia coli</i>
resolves10.1111/febs.12581On the catalytic mechanism and stereospecificity of
<i>
<scp>E</scp>
scherichia coli
</i>
<scp>l</scp>
‐threonine aldolase
resolves10.1021/bi020393+X-ray Structures of Threonine Aldolase Complexes: Structural Basis of Substrate Recognition<sup>,</sup>
resolves10.1016/j.tet.2007.06.013Synthesis of γ-halogenated and long-chain β-hydroxy-α-amino acids and 2-amino-1,3-diols using threonine aldolases
resolves10.1007/s10529-009-0125-zDiastereoselective synthesis of l-threo-3,4-dihydroxyphenylserine by low-specific l-threonine aldolase mutants
resolves10.1021/ja9720422Enzymatic Synthesis of β-Hydroxy-α-amino Acids Based on Recombinant <scp>d</scp>- and <scp>l</scp>-Threonine Aldolases
resolves10.1007/s002539900301Gene cloning and overproduction of low-specificity d -threonine aldolase from Alcaligenes xylosoxidans and its application for production of a key intermediate for parkinsonism drug
resolves10.1021/ja036707dConversion of a PLP-Dependent Racemase into an Aldolase by a Single Active Site Mutation
resolves10.1371/journal.pone.0124056The Crystal Structure of D-Threonine Aldolase from Alcaligenes xylosoxidans Provides Insight into a Metal Ion Assisted PLP-Dependent Mechanism
resolves10.1002/chem.200800031Serine Hydroxymethyl Transferase from <i>Streptococcus thermophilus</i> and <scp>L</scp>‐Threonine Aldolase from <i>Escherichia coli</i> as Stereocomplementary Biocatalysts for the Synthesis of β‐Hydroxy‐α,ω‐diamino Acid Derivatives
resolves10.1002/anie.200602529Stereoselectivity and Expanded Substrate Scope of an Engineered PLP‐Dependent Aldolase
resolves10.1002/anie.200700710Enhancing Activity and Controlling Stereoselectivity in a Designed PLP‐Dependent Aldolase
resolves10.1007/s00253-015-6803-yExpanding the threonine aldolase toolbox for the asymmetric synthesis of tertiary α-amino acids
resolves10.1016/0040-4039(96)00430-3Kinetic and thermodynamic control of L-Threonine aldolase catalyzed reaction and its application to the synthesis of mycestericin D
resolves10.1016/j.tetasy.2008.12.029The first enantioselective synthesis of imino-deoxydigitoxose and protected imino-digitoxose by using l-threonine aldolase-catalyzed aldol condensation
resolves10.1021/acs.oprd.5b00192Development of a Two-Step, Enantioselective Synthesis of an Amino Alcohol Drug Candidate
resolves10.1074/jbc.273.27.16678A Novel Metal-activated Pyridoxal Enzyme with a Unique Primary Structure, Low Specificity d-Threonine Aldolase fromArthrobacter sp. Strain DK-38
resolves10.1002/chir.1180Application of <scp>L</scp>‐threonine aldolase‐catalyzed reaction to the preparation of protected 3R,5R‐dihydroxy‐<scp>L</scp>‐homoproline as a mimetic of idulonic acid
resolves10.1016/S0040-4039(98)01567-6Application of l-threonine aldolase-catalyzed reaction for the preparation of a peptidic mimetic of RNA: A leading compound of Vero-toxin inhibitors
resolves10.1002/anie.200604142Overcoming Thermodynamic and Kinetic Limitations of Aldolase‐Catalyzed Reactions by Applying Multienzymatic Dynamic Kinetic Asymmetric Transformations
resolves10.1002/chem.200701643De‐racemization of Enantiomers versus De‐epimerization of Diastereomers—Classification of Dynamic Kinetic Asymmetric Transformations (DYKAT)
resolves10.1002/adsc.200700051Synthesis of Aromatic 1,2‐Amino Alcohols Utilizing a Bienzymatic Dynamic Kinetic Asymmetric Transformation
resolves10.1007/s00253-014-6333-zDevelopment of a growth-dependent selection system for identification of l-threonine aldolases
resolves10.1007/s10529-008-9885-0Enhanced synthesis of l-threo-3,4-dihydroxyphenylserine by high-density whole-cell biocatalyst of recombinant l-threonine aldolase from Streptomyces avelmitilis
resolves10.1271/bbb.80274Gene Cloning of α-Methylserine Aldolase from<i>Variovorax paradoxus</i>and Purification and Characterization of the Recombinant Enzyme
resolves10.1128/AEM.00677-08Purification and Gene Cloning of α-Methylserine Aldolase from
<i>Ralstonia</i>
sp. Strain AJ110405 and Application of the Enzyme in the Synthesis of α-Methyl-
<scp>l</scp>
-Serine
resolves10.1002/anie.201411484Engineered <scp>L</scp>‐Serine Hydroxymethyltransferase from <i>Streptococcus thermophilus</i> for the Synthesis of α,α‐Dialkyl‐α‐Amino Acids
resolves10.1016/j.jbiotec.2007.05.008Towards preparative asymmetric synthesis of β-hydroxy-α-amino acids: l-allo-Threonine formation from glycine and acetaldehyde using recombinant GlyA
resolves10.1007/s00726-010-0637-9Preparation of optically active β-hydroxy-α-amino acid by immobilized Escherichia coli cells with serine hydroxymethyl transferase activity
checked 2026-08-24 — re-checked daily as this page is visited;
titles and statuses come from Crossref and DataCite and are not part of the signed record
Both snippets point at the live badge image and link back to this page. The
badge re-renders from the daily check, so an embed never goes stale by more than a day of visits.