1.1.1.311: (S)-1-phenylethanol dehydrogenase
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For detailed information about (S)-1-phenylethanol dehydrogenase, go to the full flat file.
Word Map on EC 1.1.1.311
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1.1.1.311
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s-1-phenylethanol
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acetophenone
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denitrifying
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racemic
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1-phenyl-1,2-ethanediol
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2-hydroxyacetophenone
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ethylbenzene
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enantioselective
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enantiomeric
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parapsilosis
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molybdenum
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gibsonii
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aromatoleum
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synthesis
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s-enantiomer
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kurthia
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isopropanol
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azoarcus
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gluconobacter
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cosubstrate
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aromaticum
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cctcc
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stereoinversion
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oxydans
- 1.1.1.311
-
s-1-phenylethanol
- acetophenone
-
denitrifying
-
racemic
- 1-phenyl-1,2-ethanediol
- 2-hydroxyacetophenone
- ethylbenzene
-
enantioselective
-
enantiomeric
-
parapsilosis
- molybdenum
-
gibsonii
-
aromatoleum
- synthesis
-
s-enantiomer
-
kurthia
- isopropanol
- azoarcus
-
gluconobacter
-
cosubstrate
- aromaticum
-
cctcc
-
stereoinversion
-
oxydans
Reaction
Synonyms
(S)-PED, PED, PedH, prelog-specific NADH-dependent (S)-1-phenylethanol dehydrogenase
ECTree
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Application
Application on EC 1.1.1.311 - (S)-1-phenylethanol dehydrogenase
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synthesis
application of (S)-1-phenylethanol dehydrogenase for asymmetric reduction of 42 prochiral ketones and 11 beta-keto esters to enantiopure secondary alcohols. The conversions are carried out in a batch reactor using recombinant Escherichia coli as whole-cell catalysts and isopropanol as reaction solvent and cosubstrate for NADH recovery. Ketones are converted to the respective secondary alcohols with excellent enantiomeric excesses and high productivities
synthesis
the enzyme recombinantly expressed in Escherichia coli is used for chemoenzymatic synthesis of enantiomerically enriched (S)- and (R)-gamma-aryl-gamma-butyrolactones, whereby the key step is an enzyme-catalyzed stereoselective reduction of methyl 4-oxo-4-arylbutanoates, (S)-PED-catalyzed bioreduction in preparative scale
synthesis
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application of (S)-1-phenylethanol dehydrogenase for asymmetric reduction of 42 prochiral ketones and 11 beta-keto esters to enantiopure secondary alcohols. The conversions are carried out in a batch reactor using recombinant Escherichia coli as whole-cell catalysts and isopropanol as reaction solvent and cosubstrate for NADH recovery. Ketones are converted to the respective secondary alcohols with excellent enantiomeric excesses and high productivities
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synthesis
-
the enzyme recombinantly expressed in Escherichia coli is used for chemoenzymatic synthesis of enantiomerically enriched (S)- and (R)-gamma-aryl-gamma-butyrolactones, whereby the key step is an enzyme-catalyzed stereoselective reduction of methyl 4-oxo-4-arylbutanoates, (S)-PED-catalyzed bioreduction in preparative scale
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