Oxidation of 5‐hydroxymethylfurfural with a novel aryl alcohol oxidase from Mycobacterium sp. MS1601
Summary Bio‐based 5‐hydroxymethylfurfural (HMF) serves as an important platform for several chemicals, among which 2,5‐furan dicarboxylic acid (FDCA) has attracted considerable interest as a monomer for the production of polyethylene furanoate (PEF), a potential alternative for fossil‐based polyethy...
Main Authors: | Mahmoud Sayed, Yasser Gaber, Fredrik Junghus, Eric Valdés Martín, Sang‐Hyun Pyo, Rajni Hatti‐Kaul |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2022-08-01
|
Series: | Microbial Biotechnology |
Online Access: | https://doi.org/10.1111/1751-7915.14052 |
Similar Items
-
Complete oxidation of hydroxymethylfurfural to furandicarboxylic acid by aryl-alcohol oxidase
by: Ana Serrano, et al.
Published: (2019-09-01) -
Green conversion of 5‐hydroxymethylfurfural to furan‐2,5‐dicarboxylic acid by heterogeneous expression of 5‐hydroxymethylfurfural oxidase in Pseudomonas putida S12
by: Chih‐Ting Hsu, et al.
Published: (2020-07-01) -
Simultaneous Determination of Acrylamide and Hydroxymethylfurfural in Extruded Products by LC-MS/MS Method
by: Antun Jozinović, et al.
Published: (2019-05-01) -
Exploring Lactobacillus reuteri DSM20016 as a biocatalyst for transformation of longer chain 1,2-diols: Limits with microcompartment.
by: Lu Chen, et al.
Published: (2017-01-01) -
Directed evolution of the aryl-alcohol oxidase: Beyond the lab bench
by: Javier Viña-Gonzalez, et al.
Published: (2020-01-01)