EC Number   |
Application |
Reference |
|---|
   1.14.13.92 | synthesis |
phenylacetone monooxygenase (PAMO) catalyzes oxidation of ketones with molecular oxygen and NADPH with the formation of esters. PAMO demonstrates high catalytic constants in the oxidation of benzylacetone and other structurally similar aromatic ketones and can be used in the synthesis of flavoring substances, since the ester formed by benzylacetone oxidation has a pronounced fruity smell |
764116 |
| 1.14.13.92 | synthesis |
phenylacetone monooxygenase (PAMO) is an exceptionally robust Baeyer-Villiger monooxygenase, which makes it ideal for potential industrial applications, usage as an active catalyst for the Baeyer-Villiger conversion of cyclohexanone to caprolactone, which is important as monomer in polymer science |
744548 |
| 1.14.13.92 | synthesis |
phenylacetone monooxygenase (PAMO) is the most stable and thermo-tolerant member of the Baeyer-Villiger monooxygenase family, and the engineered enzyme is useful for the synthesis of industrially relevant compounds, in particular, in the biotransformation of long-chain aliphatic oils into potential biodiesels |
745991 |
| 1.14.13.92 | synthesis |
the enzyme has catalytic potential as a biocatalyst |
677171 |
| 1.14.13.92 | synthesis |
the enzyme is an ideal candidate for the synthesis of industrially relevant ester or lactone compounds. But its limited substrate scope has largely limited its industrial applications. The engineered mutant quadruple enzyme variant P253F/G254A/R258M/L443F exhibits significantly improved activity towards 2-octanone |
765535 |
| 1.14.13.92 | synthesis |
the enzyme is useful for kinetic resolution of a set of racemic substituted 3-phenylbutan-2-ones and synthesis of enantiopure compounds, overview |
690110 |
| 1.14.13.92 | synthesis |
the H2O2-resistant enzyme variants are robust biocatalysts for synthetic applications |
763862 |
| 1.14.13.92 | synthesis |
the thermally stable phenylacetone monooxygenase and engineered mutants can be used as a practical catalysts for enantioselective Baeyer-Villiger oxidations of several ketones on a preparative scale under in vitro conditions, overview |
671682 |
| 1.14.13.92 | synthesis |
usage of the enzyme for asymmetric sulfooxidation of thioanisole and of racemic 2-phenylpropionaldehyde in a Baeyer-Villiger oxidation reaction |
684245 |
