1.14.14.11: styrene monooxygenase
This is an abbreviated version!
For detailed information about styrene monooxygenase, go to the full flat file.
Word Map on EC 1.14.14.11
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1.14.14.11
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epoxidation
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enantioselective
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two-component
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s-styrene
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synthesis
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phenylacetic
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solvent-tolerant
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enantiopure
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phenylacetaldehyde
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two-liquid
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opacus
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s-epoxides
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taiwanensis
- 1.14.14.11
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epoxidation
-
enantioselective
-
two-component
-
s-styrene
- synthesis
-
phenylacetic
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solvent-tolerant
-
enantiopure
- phenylacetaldehyde
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two-liquid
- opacus
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s-epoxides
- taiwanensis
Reaction
Synonyms
FAD-specific styrene epoxidase, NSMOA, SMO, SmoA, StyA, StyA1, StyA1/StyA2B, StyA2B, StyAB
ECTree
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Application
Application on EC 1.14.14.11 - styrene monooxygenase
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synthesis
development of a highly diastereo- and enantio-selective enzymatic synthesis of glycidol derivatives with contiguous stereogenic centers
synthesis
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engineering of a stable whole-cell biocatalyst capable of (S)-2-phenyloxirane formation for continuous two-liquid-phase applications
synthesis
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production of enantiopure styrene oxide by recombinant Escherichia coli. Two-liquid phase fed-batch process is established for the production of (S)-styrene oxide with hexadecane as an apolar carrier solvent and a nutrient feed consisting of glucose, magnesium sulfate, and yeast extract. Production of 11 g of enantiopure (S)-styrene oxide per liter liquid volume in 10 h
synthesis
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production of optically pure (S)-styrene oxide, an important building block in organic synthesis. Recombinant Escherichia coli producing styrene monooxygenase catalyzes the formation of (S)-2-phenyloxirane from inexpensive styrene with an excellent enantiomeric excess of more than 99% at rates up to 180 U/g (dry weight) of cells
synthesis
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synthesis of (S)-styrene oxide. Investigation of factors influencing biocatalytic efficiency of oxygenase-based whole-cell biocatalysts under process conditions
synthesis
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synthesis of various chiral aryloxides, pilot-scale production of (S)-2-phenyloxirane
synthesis
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the enzyme converts aryl ethenyl compounds to the corresponding epoxides in optically pure forms and with good yields
synthesis
construcution of fusion proteins that join the C-terminus of the epoxidase StyA to the N-terminus of FAD reductase StyB through a linker peptide and application in the synthesis of of a broad range of substituted indoles to indigoid chromophores. The fusion proteins are self-regulated and couple efficiently NADH oxidation to styrene epoxidation
synthesis
in an organic solvent-water biphasic reaction system, recombinant enzyme enantioselectively converts linear terminal alkenes to their corresponding (S)-epoxyalkanes using glucose and molecular oxygen. When 1-heptene and 6-chloro-1-hexene are used as substrates (400 mM) under optimized conditions, 88.3mM (S)-1,2-epoxyheptane and 246.5mM (S)-1,2-epoxy-6-chlorohexane, respectively, accumulate in the organic phase with good enantiomeric excess (84.2% and 95.5%, respectively)
synthesis
Q0H7E8; Q0H7E7
overexpression of StyA and StyB significantly enhances the indigo production, reaching 52.13 mg/L after 24 h. Overexpression of oxide isomerase gene styC does not increase indigo yield
synthesis
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the enzyme converts aryl ethenyl compounds to the corresponding epoxides in optically pure forms and with good yields
-
synthesis
-
engineering of a stable whole-cell biocatalyst capable of (S)-2-phenyloxirane formation for continuous two-liquid-phase applications
-
synthesis
-
production of optically pure (S)-styrene oxide, an important building block in organic synthesis. Recombinant Escherichia coli producing styrene monooxygenase catalyzes the formation of (S)-2-phenyloxirane from inexpensive styrene with an excellent enantiomeric excess of more than 99% at rates up to 180 U/g (dry weight) of cells
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synthesis
-
production of enantiopure styrene oxide by recombinant Escherichia coli. Two-liquid phase fed-batch process is established for the production of (S)-styrene oxide with hexadecane as an apolar carrier solvent and a nutrient feed consisting of glucose, magnesium sulfate, and yeast extract. Production of 11 g of enantiopure (S)-styrene oxide per liter liquid volume in 10 h
-
synthesis
-
synthesis of various chiral aryloxides, pilot-scale production of (S)-2-phenyloxirane
-
synthesis
-
synthesis of (S)-styrene oxide. Investigation of factors influencing biocatalytic efficiency of oxygenase-based whole-cell biocatalysts under process conditions
-