ライフサイエンスコーパス: alcohol dehydrogenase

1 cess is catalyzed by an ene-reductase and an alcohol dehydrogenase.

2 d using tryptic digests of yeast enolase and alcohol dehydrogenase.

3 g of light by beta- and gamma-crystallin and alcohol dehydrogenase.

4 s the hydride ion, whose paradigm example is alcohol dehydrogenase.

5 in vertebrates, in addition to a specialized alcohol dehydrogenase.

6 er, namely dihydrofolate reductase and liver alcohol dehydrogenase.

7 e chaperone-like activity against denaturing alcohol dehydrogenase.

8 on the oxidation of benzyl alcohol by yeast alcohol dehydrogenase.

9 m as a consequence of ethanol metabolism via alcohol dehydrogenase.

10 gnated VA cells, that constitutively express alcohol dehydrogenase.

11 uit that comprises glucose dehydrogenase and alcohol dehydrogenase.

12 o-atRA formation is mediated by a microsomal alcohol dehydrogenase.

13 unctional acetaldehyde-CoA dehydrogenase and alcohol dehydrogenase.

14 idium thermocellum bifunctional acetaldehyde/alcohol dehydrogenase.

15 models for C-H activation in the context of alcohol dehydrogenase.

16 hibitors selectively inhibit GSNOR among the alcohol dehydrogenases.

17 itous or overlapping activities of redundant alcohol dehydrogenases.

18 itamin that serves as a cofactor in numerous alcohol dehydrogenases.

19 nzyme classes, lipoxygenases and prokaryotic alcohol dehydrogenases.

20 r characteristics to well known medium-chain alcohol dehydrogenases.

21 erved in the proton relay system for class I alcohol dehydrogenases.

22 th a fourth gene whose product is similar to alcohol dehydrogenases.

23 nzyme families, dihydrofolate reductases and alcohol dehydrogenases.

24 -keto reductases and three genes that encode alcohol dehydrogenases.

25 t controls C-H activation in the prokaryotic alcohol dehydrogenases.

26 Mouse alcohol dehydrogenase 1 (Adh1) gene expression occurs at

27 In Schizosaccharomyces pombe, alcohol dehydrogenase 1 (Adh1) is an abundant zinc-requi

28 to produce acetaldehyde, which is reduced by alcohol dehydrogenase 1 (Adh1) to ethanol, which accumul

29 downregulation of Sub1C and upregulation of Alcohol dehydrogenase 1 (Adh1), indicating that Sub1A-1

30 In yeast, Adh1 (alcohol dehydrogenase 1) is an abundant zinc-binding pro

31 els, of EtOH-metabolizing enzymes, including alcohol dehydrogenase 1, aldehyde dehydrogenase 1A1, and

32 clear (internal transcribed spacer, ITS; and alcohol dehydrogenase 1A, Adh) and plastid (trnT-trnL sp

33 notyped for the alcohol-metabolizing enzymes alcohol dehydrogenase 1B (ADH-1B; rs1229984) and alcohol

34 A coding variant in alcohol dehydrogenase 1B (ADH1B) (rs1229984) that leads

35 hol dehydrogenase 1B (ADH-1B; rs1229984) and alcohol dehydrogenase 1c (ADH-1C; rs698).

36 Variants in the alcohol dehydrogenase 1C (ADH1C) gene may modify the ass

37 to investigate whether a polymorphism in the alcohol dehydrogenase 1c (ADH1C) gene modifies the assoc

38 Human alcohol dehydrogenase 4 (ADH4) is one of the key enzymes

39 oise responses and enables identification of alcohol dehydrogenase 5 (ADH5) as an enzyme that regulat

40 genous formaldehyde is removed by the enzyme alcohol dehydrogenase 5 (ADH5/GSNOR), and Adh5(-/-) mice

41 a specific SNO-CoA reductase encoded by the alcohol dehydrogenase 6 (ADH6) gene and show that deleti

42 BAC sequences surrounding the gene encoding alcohol dehydrogenase A (AdhA) from four cotton genomes:

43 act alpha-, beta-, and gamma-crystallins and alcohol dehydrogenase, a protein used in aggregation stu

44 mber of oxidoreductases, including XoxF-type alcohol dehydrogenases, a type II secretion system, and

45 ol oxidases (AAO) and the intracellular aryl-alcohol dehydrogenases (AAD) were also produced after ex

46 Here, we demonstrate that Abeta-binding alcohol dehydrogenase (ABAD) is a direct molecular link

47 Abeta binding alcohol dehydrogenase (ABAD) is an NAD-dependent mitocho

48 Amyloid-beta (Abeta) peptide-binding alcohol dehydrogenase (ABAD), an enzyme present in neuro

49 Amyloid-beta peptide (Abeta) binding alcohol dehydrogenase (ABAD), an enzyme present in neuro

50 , also known as amyloid beta-peptide-binding alcohol dehydrogenase (ABAD), has been implicated in the

51 ted with increased level of Abeta binding to alcohol dehydrogenase (ABAD).

52 6 plants were shown to have limited cinnamyl alcohol dehydrogenase activity (CAD; EC 1.1.1.195), the

53 Inhibition of alcohol dehydrogenase activity abolished this reduction,

54 in, red-pigmented stems, low CAD and sinapyl alcohol dehydrogenase activity, low lignin contents, and

55 LDH the redox balance is maintained through alcohol dehydrogenase activity.

56 on alcohol metabolism because inhibition of alcohol dehydrogenase (ADH) activity blunted ChREBP EtOH

57 The relationships between some alcohol dehydrogenase (ADH) and aldehyde dehydrogenase (

58 h two steps of oxidative catabolism in which alcohol dehydrogenase (ADH) and aldehyde dehydrogenase (

59 nt HepG2 cells (VL-17A cells), which express alcohol dehydrogenase (ADH) and CYP2E1.

60 ting partially unfolded betaL crystallin and alcohol dehydrogenase (ADH) and significantly less effec

61 ing proteins [superoxide dismutase (SOD) and alcohol dehydrogenase (ADH) as protein models] showed th

62 ctrochemical transistor (OECT) modified with alcohol dehydrogenase (ADH) as the sensor.

63 r we designed and investigated bioanode with alcohol dehydrogenase (ADH) catalysing oxidation of glyc

64 Alcohol dehydrogenase (ADH) deficiency results in decrea

65 ty of the approach by genetically dissecting alcohol dehydrogenase (ADH) enzyme activity.

66 ously reported elevations in hepatic Class 1 alcohol dehydrogenase (ADH) expression in ethanol-fed ra

67 internal standard to absolutely quantify the alcohol dehydrogenase (ADH) expression level in a human

68 The alcohol dehydrogenase (ADH) family of enzymes catalyzes

69 FurX is a tetrameric Zn-dependent alcohol dehydrogenase (ADH) from Cupriavidus necator JMP

70 he structure of the recombinant medium chain alcohol dehydrogenase (ADH) from the hyperthermophilic a

71 aturally occurring tandem duplication of the Alcohol dehydrogenase (Adh) gene exhibits 2.6-fold great

72 al reduction of codon bias in the Drosophila alcohol dehydrogenase (Adh) gene led to a significant de

73 We aimed to test whether alcohol dehydrogenase (ADH) gene variants were associate

74 cated on chromosome 4q, in the region of the alcohol dehydrogenase (ADH) genes, affected risk for alc

75 ously reported associations of AD with seven alcohol dehydrogenase (ADH) genes.

76 study focuses on the population genetics of alcohol dehydrogenase (Adh) in cactophilic Drosophila.

77 l blood mononuclear cell (PBMC) responses to alcohol dehydrogenase (ADH) in patients with alcohol-rel

78 rthern blotting analyses to demonstrate that alcohol dehydrogenase (ADH) is downregulated in Candida

79 Liver alcohol dehydrogenase (ADH) is increased by physiologica

80 Histidine-51 in horse liver alcohol dehydrogenase (ADH) is part of a hydrogen-bonded

81 Alcohol dehydrogenase (ADH) is the principal ethanol-met

82 ed to Arabidopsis roots with the Arabidopsis alcohol dehydrogenase (Adh) promoter (Adh::TaPCS1/cad1-3

83 tion removing acetaldehyde produced from the alcohol dehydrogenase (ADH) reaction was shown to improv

84 in derived from the still extant short-chain alcohol dehydrogenase (ADH) through retroposition, provi

85 anol biosensor through the immobilization of alcohol dehydrogenase (ADH) via Nafion entrapment, with

86 The enzymes lactate dehydrogenase (LDH) and alcohol dehydrogenase (ADH) were used as markers of gene

87 sequence data for orthologous regions of the Alcohol dehydrogenase (Adh), Alcohol dehydrogenase relat

88 ocused on oxidations in mammals catalyzed by alcohol dehydrogenase (ADH), aldehyde dehydrogenase (ALD

89 alcohol-metabolizing enzyme, hepatic Class I alcohol dehydrogenase (ADH), and this mechanism involves

90 er disease (ALD) have antibodies directed to alcohol dehydrogenase (ADH), anti-ADH titers being assoc

91 ing to the Old Yellow Enzyme family) with an alcohol dehydrogenase (ADH), applying the in situ substr

92 Sequences were analyzed from the Alcohol dehydrogenase (Adh), big brain (bib), and timele

93 N-Heptylformamide, a potent inhibitor of alcohol dehydrogenase (ADH), decreased the conversion of

94 e nicotinamide ring of the coenzyme bound to alcohol dehydrogenase (ADH), may facilitate hydride tran

95 y was to determine whether class I and/or IV alcohol dehydrogenase (ADH), medium chain ADHs that can

96 siren1 and siren2 are novel alcohol dehydrogenase (Adh)-derived chimeric genes in th

97 cytochromes P450 from the CYP71 clan and an alcohol dehydrogenase (ADH).

98 ession of keto-acid decarboxylases (KDC) and alcohol dehydrogenase (ADH).

99 We then analyzed the relation of maternal alcohol dehydrogenase (ADH)1B genotype (rs1229984) with

100 th monoenzymatic [utilizing a single enzyme, alcohol dehydrogenase (ADH)] and bienzymatic (anchoring

101 Mammalian alcohol dehydrogenases (ADH) form a complex enzyme syste

102 tosan, glassy carbon, platinum) and enzymes (alcohol dehydrogenase, ADH; lactate dehydrogenase, LDH;

103 Previous genetic studies have revealed that alcohol dehydrogenase Adh1 is required for efficient cle

104 The ability of class I alcohol dehydrogenase (ADH1) and class IV alcohol dehydr

105 e dehydrogenase (ALDH2) and the super-active alcohol dehydrogenase (ADH2) alleles may promote hepatic

106 ith the oxidation of geraniol to geranial by alcohol dehydrogenase ADH3, followed by the enantioselec

107 I alcohol dehydrogenase (ADH1) and class IV alcohol dehydrogenase (ADH4) to metabolize retinol to re

108 Here, we resurrect digestive alcohol dehydrogenases (ADH4) from our primate ancestors

109 ucted by insertion of the gene for bacterial alcohol dehydrogenase (AdhA) into the archaeon Pyrococcu

110 tes of histidine phosphorylation on aldehyde-alcohol dehydrogenase (AdhE) and pyruvate kinase (PykF)

111 d that substitution of bifunctional aldehyde/alcohol dehydrogenase (AdhE2) with separate butyraldehyd

112 A was reduced to yield 1-hexanol by aldehyde/alcohol dehydrogenase (AdhE2).

113 Aldehyde/alcohol dehydrogenases (ADHEs) are bifunctional enzymes

114 in coding and non-coding regions of class IB alcohol dehydrogenase (ADHIB) and evaluated for altered

115 1D1V2; tabersonine 3-oxygenase (T3O)] and an alcohol dehydrogenase [ADHL1; tabersonine 3-reductase (T

116 ose of bacterial and archaeal homotetrameric alcohol dehydrogenases (ADHs) and also to the mammalian

117 hyde by a distinct family of metal-dependent alcohol dehydrogenases (ADHs).

118 acterization of two cDNAs encoding zebrafish alcohol dehydrogenases (ADHs).

119 ysis, identified and cloned a novel cinnamyl alcohol dehydrogenase allele (SbCAD2) that has an 8-bp d

120 Only slow ethanol metabolizers (alcohol dehydrogenase alleles [ADH1B*1] carriers) signif

121 ly involved in natural product metabolism-an alcohol dehydrogenase and a cytochrome P450-produces une

122 Hepatic alcohol dehydrogenase and aldehyde dehydrogenase activit

123 for enzymes that metabolise alcohol, such as alcohol dehydrogenase and aldehyde dehydrogenase; those

124 oiled-coil cross-links, and (2) it expresses alcohol dehydrogenase and aldo-keto reductase activity n

125 Similarity also exists between liver alcohol dehydrogenase and cAMP-dependent protein kinase

126 lin, and in vitro chaperone target proteins, alcohol dehydrogenase and citrate synthase.

127 VL-17A cells (HepG2 cells overexpressing alcohol dehydrogenase and cytochrome P450-2E1) were expo

128 Applications to hydride transfer in liver alcohol dehydrogenase and dihydrofolate reductase result

129 ere we report that in HepG2 cells expressing alcohol dehydrogenase and hepatocytes of ethanol-fed rat

130 Here, in both HepG2 cells overexpressing alcohol dehydrogenase and in rat hepatocytes, we found t

131 d crySI, were found to reduce aggregation of alcohol dehydrogenase and insulin, which demonstrates th

132 D(+) and N(tz)ADH to be substrates for yeast alcohol dehydrogenase and lactate dehydrogenase, respect

133 the alcohol-metabolizing enzymes, cytosolic alcohol dehydrogenase and mitochondrial aldehyde dehydro

134 ar starvation results in a weak induction of alcohol dehydrogenase and other anaerobic genes.

135 Two proteins, liver alcohol dehydrogenase and parvalbumin, and the tryptopha

136 nded networks], the activation of C-H bonds [alcohol dehydrogenase and soybean lipoxygenase (SLO) as

137 s discussed in the context of a thermophilic alcohol dehydrogenase and soybean lipoxygenase-1.

138 biquitous nature of beta-oxidation, aldehyde/alcohol dehydrogenase and thioesterase enzymes has the p

139 tive analogues of the aldehyde substrates of alcohol dehydrogenases and are useful for structure-func

140 reactions that employ esterases, lipases or alcohol dehydrogenases and gold(I) or ruthenium(II) comp

141 iscent of the NAD(+)-dependent mechanisms of alcohol dehydrogenases and sirtuins and the RNA-mediated

142 e thermal aggregation of beta(H) crystallin, alcohol dehydrogenase, and citrate synthase in vitro.

143 ffect was only seen in cell lines expressing alcohol dehydrogenase, and inhibition of ethanol oxidati

144 de 3-phosphate dehydrogenase, transaldolase, alcohol dehydrogenase, and phosphoenolpyruvate carboxyki

145 te aminotransferase, citrate synthase, liver alcohol dehydrogenase, and the catalytic subunit of cAMP

146 hol dissolution into carboxylic acid through alcohol dehydrogenase, and voltage-regulated H(+) channe

147 KIEs in solution are compared to those with alcohol dehydrogenases, and sources of the observed "puz

148 that the EutD phosphotransacetylase and EutG alcohol dehydrogenase are important to maintain metaboli

149 nanotubes as electron transfer accelerator, alcohol dehydrogenase as biocatalyst and polydiallyldime

150 e P450 2A6, glutathione S transferase P, and alcohol dehydrogenases as specialized indicators of hepa

151 The involvement of two primary alcohol dehydrogenases, BDH and BOH, in butane utilizati

152 s are the highest currently reported for the alcohol dehydrogenase bioanodes operating utilizing a di

153 centration is elevated and there is adequate alcohol dehydrogenase blockade, extracorporeal treatment

154 500 mg/L or 15.6 mmol/L in the absence of an alcohol dehydrogenase blocker; in the absence of a metha

155 distinct NAD(+)-independent, PQQ-containing alcohol dehydrogenases, BOH (a quinoprotein) and BDH (a

156 s cinnamoyl-CoA reductase (CCR) and cinnamyl alcohol dehydrogenase (CAD) catalyze the two key reducti

157 Cinnamyl alcohol dehydrogenase (CAD) catalyzes the conversion of

158 Cinnamyl alcohol dehydrogenase (CAD) catalyzes the final step in

159 oacidolysis degradative method, for cinnamyl alcohol dehydrogenase (CAD) deficiency in angiosperms ha

160 Silencing two CINNAMYL ALCOHOL DEHYDROGENASE (CAD) genes in Nicotiana attenuata

161 the Arabidopsis genome database as cinnamyl alcohol dehydrogenase (CAD) homologues, an in silico ana

162 recursors synthesized by the enzyme cinnamyl alcohol dehydrogenase (CAD).

163 Although SAD and classical cinnamyl alcohol dehydrogenases (CADs) catalyze the same reaction

164 cation and characterization of four cinnamyl alcohol dehydrogenases (CADs) from cucumber (Cucumis sat

165 nal dynamics in the proton transfer steps of alcohol dehydrogenase catalysis.

166 yme-linked immunosorbent assay (ELISA) using alcohol dehydrogenase-catalyzed gold nanoparticle seed-m

167 efficient and inexpensive biocatalysts (i.e. alcohol dehydrogenases, cellulases and esterases) that a

168 olution, the beta(1)beta(1) isoform of human alcohol dehydrogenase complexed with N-benzylformamide a

169 structure of the alphaalpha isoform of human alcohol dehydrogenase complexed with N-cyclopentyl-N-cyc

170 Structures of horse liver alcohol dehydrogenase complexed with NAD(+) and unreacti

171 le, periplasmic (37-residue leader sequence) alcohol dehydrogenase containing PQQ and heme c as cofac

172 amino acid sequence of BOH suggests a 67-kDa alcohol dehydrogenase containing pyrroloquinoline quinon

173 Inhibition of alcohol dehydrogenase, cytochrome P450 2E1, and catalase

174 The results show that in alcohol dehydrogenase, dynamic protein motion is in fact

175 thanol tolerant and that alcohol upregulates alcohol dehydrogenase E (AdhE) and potentiates pneumolys

176 oryzae (AspRedAm) was combined with a single alcohol dehydrogenase (either metagenomic ADH-150, an AD

177 Glucose 6-phospatase, alcohol dehydrogenase, elongation factor-TU, methylgluta

178 ells induce the expression of an alternative alcohol dehydrogenase encoded by the adh4 gene.

179 The study was performed using the alcohol dehydrogenase enzyme immobilised by covalent bin

180 of an ethanol biosensor based on the coupled alcohol dehydrogenase enzyme(ADH).

181 mong the structurally studied members of the alcohol dehydrogenase family in that it follows a random

182 affecting the seven AAD genes (putative aryl alcohol dehydrogenases), five ADH genes, and SFA1, showe

183 A tetrameric thermophilic alcohol dehydrogenase from Bacillus stearothermophilus (

184 The crystal structure of NAD(+)-dependent alcohol dehydrogenase from Bacillus stearothermophilus s

185 ilic enzyme (55% identity), NAD(+)-dependent alcohol dehydrogenase from Escherichia coli.

186 acid reductase from Nocardia iowensis and an alcohol dehydrogenase from Leifsonia sp. strain S749.

187 iopure (S)-alcohols in high yields using the alcohol dehydrogenase from Rhodococcus ruber (ADH-A), wh

188 ductase from Candida magnoliae ( CMCR) or an alcohol dehydrogenase from Saccharomyces cerevisiae ( Ym

189 y alcohols was achieved with W110A secondary alcohol dehydrogenase from Thermoanaerobacter ethanolicu

190 used to reduce NADP(+) to R-[4-3H]NADPH with alcohol dehydrogenase from Thermoanaerobium brockii at 4

191 d relies on a combination of two enzymes: an alcohol dehydrogenase (from Aromatoleum sp., Lactobacill

192 ivation involves increased expression of the alcohol dehydrogenase gene (ADH) and ethanolic fermentat

193 nd 10 unpreferred codons into the Drosophila alcohol dehydrogenase gene (Adh).

194 e to a mutated bifunctional acetaldehyde-CoA/alcohol dehydrogenase gene (adhE), hypothesize based on

195 dies examining this zinc-dependent switch in alcohol dehydrogenase gene expression, we isolated an ad

196 higher prevalence of ADH2*2, an allele of an alcohol dehydrogenase gene that protects against heavy d

197 ment containing the promoter of a Drosophila alcohol dehydrogenase gene, several translational positi

198 ADH (alcohol dehydrogenase) gene expression, enzyme activity,

199 Humans have seven alcohol dehydrogenase genes (ADH) falling into five clas

200 Two alcohol dehydrogenase genes (ADH2 and ADH3 on chromosome

201 the clinically significant enzymes including alcohol dehydrogenase, glucose 6-phosphate dehydrogenase

202 The logic network composed of three enzymes (alcohol dehydrogenase, glucose dehydrogenase, and glucos

203 lycinin, glycinin, Kunitz trypsin inhibitor, alcohol dehydrogenase, Gly m Bd 28K allergen, and sucros

204 yl-CoA dehydrogenase type II/amyloid binding alcohol dehydrogenase (HADH II/ABAD), a mitochondrial ox

205 al decades the hydride transfer catalyzed by alcohol dehydrogenase has been difficult to understand.

206 s into a gene annotated as encoding cinnamyl alcohol dehydrogenase, here designated M. truncatula CAD

207 , glucosidase, MYB transcription factor, and alcohol dehydrogenase, highly regulated due to insect in

208 ross-correlation analysis of the horse liver alcohol dehydrogenase HLADH.NAD(+).PhCH(2)O(-) complex h

209 of 10 ns with the dimeric enzyme horse liver alcohol dehydrogenase (HLADH) present as the reactive co

210 ely resembles that of mesophilic horse liver alcohol dehydrogenase (HLADH).

211 present computational studies of horse liver alcohol dehydrogenase (HLADH).

212 sted as inhibitors of purified Class I liver alcohol dehydrogenases: horse (EqADH E), human (HsADH1C*

213 nvestigated in two mutants of a thermophilic alcohol dehydrogenase (ht-ADH): Y25A (at the dimer inter

214 catalyzed by a series of mutant thermophilic alcohol dehydrogenases (ht-ADH), presenting evidence for

215 the thermophilic Bacillus stearothermophilus alcohol dehydrogenase (HtADH) closely resembles that of

216 s in relation to the homologous thermophilic alcohol dehydrogenase (htADH) from Bacillus stearothermo

217 deuterium (H/D) exchange of the thermophilic alcohol dehydrogenase (htADH) has been studied by using

218 binase A (RecA) and Saccharomyces cerevisiae alcohol dehydrogenase-I (YADH-I).

219 Bacteria were engineered such that alcohol dehydrogenase II (ADHII) was surface displayed.

220 nt distances from the NAD(+) binding site in alcohol dehydrogenase II was performed.

221 ia through a surface displayed redox enzyme, alcohol dehydrogenase II.

222 ith unfounded claims for a so-called sinapyl alcohol dehydrogenase in angiosperms.

223 ydride transfer reactions catalyzed by liver alcohol dehydrogenase in calculated energy profile and r

224 nthetic cinnamoyl CoA reductase and cinnamyl alcohol dehydrogenase in not only the lignifying TEs but

225 0 2E1 activity but increased the activity of alcohol dehydrogenase in the liver, without affecting th

226 ferase, cinnamoyl-CoA reductase and cinnamyl alcohol dehydrogenase in the presence of increasing conc

227 ult of low aldehyde reductase activity (i.e. alcohol dehydrogenase in the reverse reaction) of CsCAD

228 lization of horseradish peroxidase and yeast alcohol dehydrogenase in these glasses.

229 atocytes were incubated with antioxidants or alcohol dehydrogenase inhibitor prior to alcohol exposur

230 alone or in combination with ranitidine (an alcohol dehydrogenase inhibitor) while the biosensor sig

231 d efficiency in the chaperoning ability with alcohol dehydrogenase, insulin, and citrate synthase as

232 hable electrode concept by immobilisation of alcohol dehydrogenase into vapour-phase polymerised poly

233 S-Nitrosoglutathione reductase (GSNOR) is an alcohol dehydrogenase involved in the regulation of S-ni

234 at the D-2HG-producing mitochondrial enzyme, alcohol dehydrogenase, iron-containing protein 1 (ADHFE1

235 Horse liver alcohol dehydrogenase is a homodimer, the protomer havin

236 Binding of NAD+ to wild-type horse liver alcohol dehydrogenase is strongly pH-dependent and is li

237 We found that ADH3, the major mitochondrial alcohol dehydrogenase, is regulated in a manner similar

238 ted potent and selective inhibition of human alcohol dehydrogenase isoenzymes.

239 Oxidation processes with three of them, alcohol dehydrogenases isolated from horse liver (HLADH)

240 n system for Sulfolobus solfataricus ADH-10 (Alcohol Dehydrogenase isozyme 10) and its use in the dyn

241 ADH2, encoding the alcohol dehydrogenase isozyme required for ethanol oxida

242 For horse liver alcohol dehydrogenase, it was confirmed that the functio

243 e diversity are analyzed for three duplicate alcohol dehydrogenase loci (adh1-adh3) within a species-

244 is of associations between haplotypes at the Alcohol Dehydrogenase locus in Drosophila melanogaster t

245 mechanism of the zinc-dependent medium chain alcohol dehydrogenase (MDR) superfamily remain contentio

246 Here, we report an alcohol dehydrogenase-mediated cyclization step in the b

247 ith the incorporation of glucose oxidase and alcohol dehydrogenase/NAD(+) within the three-dimensiona

248 The cognate cDNA, with similarity to alcohol dehydrogenases (NtADH2) was expressed in E. coli

249 mall but important class of radical-mediated alcohol dehydrogenases operate.

250 r fumarate concentrations are measured using alcohol dehydrogenase or fumarase plus malic dehydrogena

251 ecombinant from Escherichia coli and primary alcohol dehydrogenase (PADH I), were characterized by th

252 ion of alcohol metabolism through either the alcohol dehydrogenase pathway or the cytochrome P450 sys

253 The psychrophilic alcohol dehydrogenase (psADH) cloned from Antarctic Mora

254 Highly abundant short-chain alcohol dehydrogenases (RDHs) in the retina were assumed

255 ding stabilization effect on the T.S. of the alcohol dehydrogenase reactions.

256 rad NSYK motif in the C-terminal short-chain alcohol dehydrogenase/reductase (SDR) domain, which may

257 ified was Hep27, a member of the short-chain alcohol dehydrogenase/reductase (SDR) family of enzymes.

258 er of a vast protein family, the short-chain alcohol dehydrogenase/reductase (SDR) family.

259 Together WOX1 binds Tau via its short-chain alcohol dehydrogenase/reductase domain and is likely to

260 bound Tau via its COOH-terminal short-chain alcohol dehydrogenase/reductase domain.

261 6), a conserved component of the short chain alcohol dehydrogenase/reductase superfamily active site

262 Members of the short chain alcohol dehydrogenase/reductase superfamily catalyze the

263 a highly conserved member of the short chain alcohol dehydrogenase/reductase superfamily with a repor

264 In this study, a short chain alcohol dehydrogenase/reductase that co-expresses with t

265 ) from Candida parapsilosis is a short-chain alcohol dehydrogenase/reductase.

266 Only one short-chain alcohol dehydrogenase/reductases (SDRs), which has been

267 nd product yields of eight other short-chain alcohol dehydrogenases/reductases.

268 regions of the Alcohol dehydrogenase (Adh), Alcohol dehydrogenase related (Adhr), Glucose dehydrogen

269 ilum PM1 (mdh2) predicted to encode a type I alcohol dehydrogenase related to the characterized metha

270 aliana) CAD5 and Populus tremuloides sinapyl alcohol dehydrogenase, respectively.

271 e the three-dimensional structure of sinapyl alcohol dehydrogenase (SAD) from Populus tremuloides (as

272 (Triticum aestivum) germin, maize (Zea mays) alcohol dehydrogenase, satellite tobacco necrosis virus

273 t requires CsgA, a member of the short-chain alcohol dehydrogenase (SCAD) family of proteins.

274 Short-chain alcohol dehydrogenases (SCADHs) synthesize a variety of

275 Expression of alcohol dehydrogenase sensitized Caco-2 cells to ethanol

276 to be metabolized, which requires functional alcohol dehydrogenase sodh-1.

277 sis, support the inclusion of SAD in a plant alcohol dehydrogenase subfamily that includes cinnamalde

278 ADH1 encodes the major zinc-dependent alcohol dehydrogenase that is utilized during fermentati

279 -chain mannitol dehydrogenases are secondary alcohol dehydrogenases that are of wide interest because

280 Five of these (phosphoglycerate mutase, alcohol dehydrogenase, thioredoxin peroxidase, catalase,

281 The use of purified and overexpressed alcohol dehydrogenases to synthesize enantiopure fluorin

282 protein of S. enterica is an iron-dependent alcohol dehydrogenase used for 1,2-PD catabolism.

283 Mutants of Lactobacillus kefir short-chain alcohol dehydrogenase, used here as ketoreductases (KRED

284 genes (HRG) PYRUVATE DECARBOXYLASE (VvPDC), ALCOHOL DEHYDROGENASE (VvADH2), SUCROSE SYNTHASE (VvSUSY

285 emperature in two variants of a thermophilic alcohol dehydrogenase: W87F and W87F:H43A.

286 erase, cinnamoyl-CoA reductase, and cinnamyl alcohol dehydrogenase were coordinately up-regulated.

287 tic activities of pyruvate decarboxylase and alcohol dehydrogenase were increased significantly compa

288 of serum albumin, streptavidin, avidin, and alcohol dehydrogenase were probed using cation-to-anion

289 lphaB crystallin when beta(L) crystallin and alcohol dehydrogenase were the chaperone substrates and

290 ol and its substituted analogues mediated by alcohol dehydrogenases were compared to the oxidations b

291 In the first method, eight alcohol dehydrogenases were investigated as biocatalysts

292 as AtCAD7 and 8 (highest homology to sinapyl alcohol dehydrogenase) were catalytically less active ov

293 a gene that codes for a putative short chain alcohol dehydrogenase, were distributed non-randomly bet

294 d alcohols (up to 99% ee) was achieved using alcohol dehydrogenases, whereas chiral transition-metal

295 The first was Thermoanaerobium brockii alcohol dehydrogenase, which stereospecifically catalyze

296 ation is similar to that of ADH that encodes alcohol dehydrogenase, which we have reported previously

297 biotransformation of the aldol adduct by an alcohol dehydrogenase without the need for intermediate

298 Results suggest that in the alcohol dehydrogenases without a Zn(II) cofactor in the

299 y large isotope effect associated with yeast alcohol dehydrogenase (YADH) catalyzed oxidation of etha

300 yde dehydrogenase (Bldh) and NADPH-dependent alcohol dehydrogenase (YqhD) increased 1-butanol product