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• W2514977310 abstract "A transaminase from Halomonas elongata and four mutants generated by an in silico-based design were recombinantly produced in E. coli, purified and applied to the amination of mono-substituted aromatic carbonyl-derivatives. While benzaldehyde derivatives were excellent substrates, only NO2-acetophenones were transformed into the (S)-amine with a high enantioselectivity. The different behaviour of wild-type and mutated transaminases was assessed by in silico substrate binding mode studies." @default.
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• W2514977310 date "2016-01-01" @default.
• W2514977310 modified "2023-09-27" @default.
• W2514977310 title "Stereoelectronic effects in the reaction of aromatic substrates catalysed by Halomonas elongata transaminase and its mutants" @default.
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• W2514977310 doi "https://doi.org/10.1039/c6ob01629d" @default.
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