Cargando…
From Natural Methylation to Versatile Alkylations Using Halide Methyltransferases
Halide methyltransferases (HMTs) enable the enzymatic synthesis of S‐adenosyl‐l‐methionine (SAM) from S‐adenosyl‐l‐homocysteine (SAH) and methyl iodide. Characterisation of a range of naturally occurring HMTs and subsequent protein engineering led to HMT variants capable of synthesising ethyl, propy...
Autores principales: | Tang, Qingyun, Pavlidis, Ioannis V., Badenhorst, Christoffel P. S., Bornscheuer, Uwe T. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8453949/ https://www.ncbi.nlm.nih.gov/pubmed/33890381 http://dx.doi.org/10.1002/cbic.202100153 |
Ejemplares similares
-
Directed Evolution of a Halide Methyltransferase Enables Biocatalytic Synthesis of Diverse SAM Analogs
por: Tang, Qingyun, et al.
Publicado: (2020) -
Lights and Shadows of DMSO as Solvent for Tin Halide Perovskites
por: Pascual, Jorge, et al.
Publicado: (2022) -
An Ultrasensitive Fluorescence Assay for the Detection of Halides and Enzymatic Dehalogenation
por: Aslan‐Üzel, Aşkın S., et al.
Publicado: (2020) -
Carbon Monoxide Coupling Reactions: A New Concept for the Formation of Hexahydroxybenzene
por: Rosenthal, Uwe
Publicado: (2020) -
Recent trends in biocatalysis
por: Yi, Dong, et al.
Publicado: (2021)