2017
DOI: 10.1039/c7gc01696d
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The continuous oxidation of HMF to FDCA and the immobilisation and stabilisation of periplasmic aldehyde oxidase (PaoABC)

Abstract: One-pot multienzyme continuous cascade for the conversion of HMF to FDCA using HRP to activate GOaseM3-5 in situ.

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Cited by 90 publications
(97 citation statements)
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References 34 publications
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“…HMF and LA are regarded as top value-added chemicals obtained from carbohydrates;t hey are considered as "platform chemicals" for the synthesis of various polymers, pharmaceuticals, solvents, and fuels. [5,10,11] FDCA and FDME are used as monomers for polyethylene furanoate( PEF) and polypropylene furanoate (PPF)-bio-based polyesters that are planned to replace petro-based polyethylene terephthalate. [9] Last year,s everali ndustrial companies announced the building of plants for the production of HMF and its important derivatives-furan-2,5-dicarboxylic acid( FDCA) and dimethyl furan-2,5-dicarboxylate (FDME).…”
Section: Introductionmentioning
confidence: 99%
“…HMF and LA are regarded as top value-added chemicals obtained from carbohydrates;t hey are considered as "platform chemicals" for the synthesis of various polymers, pharmaceuticals, solvents, and fuels. [5,10,11] FDCA and FDME are used as monomers for polyethylene furanoate( PEF) and polypropylene furanoate (PPF)-bio-based polyesters that are planned to replace petro-based polyethylene terephthalate. [9] Last year,s everali ndustrial companies announced the building of plants for the production of HMF and its important derivatives-furan-2,5-dicarboxylic acid( FDCA) and dimethyl furan-2,5-dicarboxylate (FDME).…”
Section: Introductionmentioning
confidence: 99%
“…[120] In more recent studies on the preparation of isocyanate-free thermoplastics, 4b was prepared by couplingo fG Cand TC. FDCA can be produced by catalytic [124] or enzymatic strategies [125] from the oxidationo fn on-food-sourced, renewable, hydroxymethyl furfural (HMF) [126] and is regarded as a potentially renewablea lternative to TA. [118,122] These monomersw ere synthesized from the corresponding glycidyl bisepoxide by using TBAI as catalyst at 80 8C.…”
Section: Terminal Biscarbonatesmentioning
confidence: 99%
“…To develop more sustainable alternatives to carbonates 4a-d as rigid aromatic buildingb locks for the synthesis of PHUs, Li and coworkers [123] prepared 4e from 2,5-furandicarboxylic acid (FDCA). FDCA can be produced by catalytic [124] or enzymatic strategies [125] from the oxidationo fn on-food-sourced, renewable, hydroxymethyl furfural (HMF) [126] and is regarded as a potentially renewablea lternative to TA. [127] 4e was prepared by coupling FDCA with allyl bromide, followed by epoxidation of the resulting allyl ester with m-CPBA.…”
Section: Terminal Biscarbonatesmentioning
confidence: 99%
“…In addition to the oxidation of alcohols, AldO from S. coelicolor, can catalyse the oxidation of thiol groups (133). For example, L-dithiothreitol, which is identical to the sugar alcohol Lthreitol except for the presence of thiol groups instead of hydroxyl groups at the terminal carbon atoms, is oxidised to the corresponding thioaldehyde, which subsequently cyclises to a dithiohemiacetal (Scheme 10B).…”
Section: Subfamily 10: Alditol Oxidasesmentioning
confidence: 99%
“…Various other racemic secondary aromatic alcohols were also succesfully resolved in this manner. One of these variants was also used in combination with an aldehyde oxidase to achieve the conversion of 5-(hydroxymethyl)furfural to 2,5-furandicarboxylic acid (132,133).…”
Section: Galactose Oxidasementioning
confidence: 99%