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Crystal Structure of a Novel N-Substituted L-Amino Acid Dioxygenase from Burkholderia ambifaria AMMDThe case for an early biological origin of DNAGenetic approaches to dissect the mechanisms of two distinct pathways of cell cycle-coupled cytokinesis in Dictyostelium.Characteristics and biotechnology applications of aliphatic amino acid hydroxylases belonging to the Fe(II)/α-ketoglutarate-dependent dioxygenase superfamily.Novel Enzyme Family Found in Filamentous Fungi Catalyzing trans-4-Hydroxylation of L-Pipecolic Acid.Construction of microbial platform for an energy-requiring bioprocess: practical 2'-deoxyribonucleoside production involving a C-C coupling reaction with high energy substrates.Expression, purification, crystallization and preliminary X-ray analysis of 4-hydroxy-3-methyl-2-keto-pentanoate aldolase (asHPAL) from Arthrobacter simplex strain AKU 626Improvement of NADPH-dependent bioconversion by transcriptome-based molecular breeding.Engineering a short-chain dehydrogenase/reductase for the stereoselective production of (2S,3R,4S)-4-hydroxyisoleucine with three asymmetric centers.A novel family of bacterial dioxygenases that catalyse the hydroxylation of free L-amino acids.A novel L-isoleucine metabolism in Bacillus thuringiensis generating (2S,3R,4S)-4-hydroxyisoleucine, a potential insulinotropic and anti-obesity amino acid.Metabolic engineering of Escherichia coli to produce (2S, 3R, 4S)-4-hydroxyisoleucine.Two laccase isoenzymes and a peroxidase of a commercial laccase-producing basidiomycete, Trametes sp. Ha1.A novel l-isoleucine hydroxylating enzyme, l-isoleucine dioxygenase from Bacillus thuringiensis, produces (2S,3R,4S)-4-hydroxyisoleucine.Improvement of a direct electron transfer-type fructose/dioxygen biofuel cell with a substrate-modified biocathode.Characterization of a novel l-amino acid oxidase with protein oxidizing activity from Penicillium steckii AIU 027.Functional coupling between vanillate-O-demethylase and formaldehyde detoxification pathway.Engineering of the cytochrome P450 monooxygenase system for benzyl maltol hydroxylation.Attempt to simultaneously generate three chiral centers in 4-hydroxyisoleucine with microbial carbonyl reductases.L-leucine 5-hydroxylase of Nostoc punctiforme is a novel type of Fe(II)/α-ketoglutarate-dependent dioxygenase that is useful as a biocatalyst.New nucleoside hydrolase with transribosylation activity from Agromyces sp. MM-1 and its application for enzymatic synthesis of 2'-O-methylribonucleosides.Production of dicarboxylic acids from novel unsaturated fatty acids by laccase-catalyzed oxidative cleavage.A novel nucleoside hydrolase from Lactobacillus buchneri LBK78 catalyzing hydrolysis of 2'-O-methylribonucleosides.Trehalose accumulation enhances tolerance of Saccharomyces cerevisiae to acetic acid.Enzymatic synthesis of 2'-O-methylribonucleosides with a nucleoside hydrolase family enzyme from Lactobacillus buchneri LBK78.Production of a pharmaceutical intermediate via biohydroxylation using whole cells of Rhodococcus rubropertinctus N82.A novel Fe(II)/α-ketoglutarate-dependent dioxygenase from Burkholderia ambifaria has β-hydroxylating activity of N-succinyl l-leucine.Imidase catalyzing desymmetric imide hydrolysis forming optically active 3-substituted glutaric acid monoamides for the synthesis of gamma-aminobutyric acid (GABA) analogsCharacterization and application of a L-specific amino acid oxidase from Rhodococcus sp. AIU LAB-3Breeding of a cyclic imide-assimilating bacterium, Pseudomonas putida s52, for high efficiency production of pyruvateStructural optimization of SadA, an Fe(II)- and α-ketoglutarate-dependent dioxygenase targeting biocatalytic synthesis of N-succinyl-L-threo-3,4-dimethoxyphenylserine
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P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Makoto Hibi
@ast
Makoto Hibi
@en
Makoto Hibi
@es
Makoto Hibi
@nl
Makoto Hibi
@sl
type
label
Makoto Hibi
@ast
Makoto Hibi
@en
Makoto Hibi
@es
Makoto Hibi
@nl
Makoto Hibi
@sl
prefLabel
Makoto Hibi
@ast
Makoto Hibi
@en
Makoto Hibi
@es
Makoto Hibi
@nl
Makoto Hibi
@sl
P1053
L-6422-2017
P106
P1153
35316076300
P31
P3829
P496
0000-0002-6714-9008