Loading…

Selective Oxidation of 5‐Hydroxymethylfurfural to 2,5‐Diformylfuran in Biphasic Media using Immobilized Galactose Oxidase: Proof of Concept and Limitations

The oxidation of 5‐hydroxymethylfurfural (HMF) to 2,5‐diformylfuran (DFF) is a key reaction in valorizing biomass. DFF is hardly soluble in water, while HMF is often obtained from biorefineries in crude wet organic fractions. Thus, the reaction is challenging for both biocatalysis performed in aqueo...

Full description

Saved in:
Bibliographic Details
Published in:ChemCatChem 2024-02, Vol.16 (4), p.n/a
Main Authors: Milić, Milica, Byström, Emil, Domínguez de María, Pablo, Kara, Selin
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites cdi_FETCH-LOGICAL-c3124-35090404976657d2846d4e0ac4ee5ec9dede26c9c616bf8bec6c1eaa54d95b333
container_end_page n/a
container_issue 4
container_start_page
container_title ChemCatChem
container_volume 16
creator Milić, Milica
Byström, Emil
Domínguez de María, Pablo
Kara, Selin
description The oxidation of 5‐hydroxymethylfurfural (HMF) to 2,5‐diformylfuran (DFF) is a key reaction in valorizing biomass. DFF is hardly soluble in water, while HMF is often obtained from biorefineries in crude wet organic fractions. Thus, the reaction is challenging for both biocatalysis performed in aqueous media, and for chemocatalysis where the presence of water often results in catalyst poisoning. Galactose oxidase (GalOx) can selectively oxidize HMF to DFF and displays promising activity in aqueous‐organic media. In this study, GalOx was immobilized on ten carriers, assessing the immobilization yield, activity, and stability. Covalently immobilized GalOx catalyzed the oxidation of HMF to DFF in neat and water‐saturated EtOAc, and in biphasic systems of various water contents. At 50 % v/v H2O, the reaction was conducted at a semi‐preparative scale (50 mL) with no adverse effect on DFF yield. Some limitations arise, such as enzyme deactivation, and adsorption of DFF to the support, particularly in the aqueous fraction. Future options to upgrade the route may include designed stable enzymes under the presence of HMF/DFF, and the setup of microaqueous systems where DFF adsorption is minimized. The use of wet EtOAc media would be a promising approach in future biorefineries employing inexpensive crude wet organic fractions. Galactose oxidase (GalOx) immobilized on Purolite® LifetechTM ECR8215F catalyzed the oxidation of 5‐hydroxymethylfurfural (HMF) to 2,5‐diformylfuran (DFF) in ethyl acetate (EtOAc)‐based biphasic media, as well as neat and water‐saturated organic solvent. The results showcase a scalable system with an efficient catalyst with reusability potential.
doi_str_mv 10.1002/cctc.202301384
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2930345706</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2930345706</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3124-35090404976657d2846d4e0ac4ee5ec9dede26c9c616bf8bec6c1eaa54d95b333</originalsourceid><addsrcrecordid>eNqFUU1LxDAULKKgrl49B7y6a9qkaeNN69fCioJ6LmnyqpG2qUmqW0_-BP-B_81fYndX9CgMvAcz8-bBBMFeiCchxtGhlF5OIhwRHJKUrgVbYcqSMUk5X__dU7wZbDv3hDHjJIm3gs9bqEB6_QLoeq6V8No0yJQo_nr_uOyVNfO-Bv_YV2VnB4gKeYOigwV9qktj6yUjGqQbdKLbR-G0RFegtECd080Dmta1KXSl30ChC1EJ6Y37yXJwhG6sGdIGZKaR0HokGoVmutZ--YrbCTZKUTnY_Zmj4P787C67HM-uL6bZ8WwsSRjRMYkxxxRTnjAWJypKKVMUsJAUIAbJFSiImOSShawo0wIkkyEIEVPF44IQMgr2V3dba547cD5_Mp1thsg84gQTGieYDarJSiWtcc5CmbdW18L2eYjzRQn5ooT8t4TBwFeGV11B_486z7K77M_7DaVqkEg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2930345706</pqid></control><display><type>article</type><title>Selective Oxidation of 5‐Hydroxymethylfurfural to 2,5‐Diformylfuran in Biphasic Media using Immobilized Galactose Oxidase: Proof of Concept and Limitations</title><source>Wiley:Jisc Collections:Wiley Read and Publish Open Access 2024-2025 (reading list)</source><creator>Milić, Milica ; Byström, Emil ; Domínguez de María, Pablo ; Kara, Selin</creator><creatorcontrib>Milić, Milica ; Byström, Emil ; Domínguez de María, Pablo ; Kara, Selin</creatorcontrib><description>The oxidation of 5‐hydroxymethylfurfural (HMF) to 2,5‐diformylfuran (DFF) is a key reaction in valorizing biomass. DFF is hardly soluble in water, while HMF is often obtained from biorefineries in crude wet organic fractions. Thus, the reaction is challenging for both biocatalysis performed in aqueous media, and for chemocatalysis where the presence of water often results in catalyst poisoning. Galactose oxidase (GalOx) can selectively oxidize HMF to DFF and displays promising activity in aqueous‐organic media. In this study, GalOx was immobilized on ten carriers, assessing the immobilization yield, activity, and stability. Covalently immobilized GalOx catalyzed the oxidation of HMF to DFF in neat and water‐saturated EtOAc, and in biphasic systems of various water contents. At 50 % v/v H2O, the reaction was conducted at a semi‐preparative scale (50 mL) with no adverse effect on DFF yield. Some limitations arise, such as enzyme deactivation, and adsorption of DFF to the support, particularly in the aqueous fraction. Future options to upgrade the route may include designed stable enzymes under the presence of HMF/DFF, and the setup of microaqueous systems where DFF adsorption is minimized. The use of wet EtOAc media would be a promising approach in future biorefineries employing inexpensive crude wet organic fractions. Galactose oxidase (GalOx) immobilized on Purolite® LifetechTM ECR8215F catalyzed the oxidation of 5‐hydroxymethylfurfural (HMF) to 2,5‐diformylfuran (DFF) in ethyl acetate (EtOAc)‐based biphasic media, as well as neat and water‐saturated organic solvent. The results showcase a scalable system with an efficient catalyst with reusability potential.</description><identifier>ISSN: 1867-3880</identifier><identifier>EISSN: 1867-3899</identifier><identifier>DOI: 10.1002/cctc.202301384</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>5-hydroxymethylfurfural (HMF) ; Adsorption ; Aqueous solutions ; biocatalysis ; biphasic systems ; enzyme immobilization ; Galactose ; galactose oxidase ; Hydroxymethylfurfural ; Oxidase ; Oxidation ; Poisoning (reaction inhibition) ; Refining ; Stability analysis</subject><ispartof>ChemCatChem, 2024-02, Vol.16 (4), p.n/a</ispartof><rights>2023 The Authors. ChemCatChem published by Wiley-VCH GmbH</rights><rights>2023. This article is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3124-35090404976657d2846d4e0ac4ee5ec9dede26c9c616bf8bec6c1eaa54d95b333</cites><orcidid>0000-0001-6754-2814 ; 0000-0002-7322-4158</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Milić, Milica</creatorcontrib><creatorcontrib>Byström, Emil</creatorcontrib><creatorcontrib>Domínguez de María, Pablo</creatorcontrib><creatorcontrib>Kara, Selin</creatorcontrib><title>Selective Oxidation of 5‐Hydroxymethylfurfural to 2,5‐Diformylfuran in Biphasic Media using Immobilized Galactose Oxidase: Proof of Concept and Limitations</title><title>ChemCatChem</title><description>The oxidation of 5‐hydroxymethylfurfural (HMF) to 2,5‐diformylfuran (DFF) is a key reaction in valorizing biomass. DFF is hardly soluble in water, while HMF is often obtained from biorefineries in crude wet organic fractions. Thus, the reaction is challenging for both biocatalysis performed in aqueous media, and for chemocatalysis where the presence of water often results in catalyst poisoning. Galactose oxidase (GalOx) can selectively oxidize HMF to DFF and displays promising activity in aqueous‐organic media. In this study, GalOx was immobilized on ten carriers, assessing the immobilization yield, activity, and stability. Covalently immobilized GalOx catalyzed the oxidation of HMF to DFF in neat and water‐saturated EtOAc, and in biphasic systems of various water contents. At 50 % v/v H2O, the reaction was conducted at a semi‐preparative scale (50 mL) with no adverse effect on DFF yield. Some limitations arise, such as enzyme deactivation, and adsorption of DFF to the support, particularly in the aqueous fraction. Future options to upgrade the route may include designed stable enzymes under the presence of HMF/DFF, and the setup of microaqueous systems where DFF adsorption is minimized. The use of wet EtOAc media would be a promising approach in future biorefineries employing inexpensive crude wet organic fractions. Galactose oxidase (GalOx) immobilized on Purolite® LifetechTM ECR8215F catalyzed the oxidation of 5‐hydroxymethylfurfural (HMF) to 2,5‐diformylfuran (DFF) in ethyl acetate (EtOAc)‐based biphasic media, as well as neat and water‐saturated organic solvent. The results showcase a scalable system with an efficient catalyst with reusability potential.</description><subject>5-hydroxymethylfurfural (HMF)</subject><subject>Adsorption</subject><subject>Aqueous solutions</subject><subject>biocatalysis</subject><subject>biphasic systems</subject><subject>enzyme immobilization</subject><subject>Galactose</subject><subject>galactose oxidase</subject><subject>Hydroxymethylfurfural</subject><subject>Oxidase</subject><subject>Oxidation</subject><subject>Poisoning (reaction inhibition)</subject><subject>Refining</subject><subject>Stability analysis</subject><issn>1867-3880</issn><issn>1867-3899</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><recordid>eNqFUU1LxDAULKKgrl49B7y6a9qkaeNN69fCioJ6LmnyqpG2qUmqW0_-BP-B_81fYndX9CgMvAcz8-bBBMFeiCchxtGhlF5OIhwRHJKUrgVbYcqSMUk5X__dU7wZbDv3hDHjJIm3gs9bqEB6_QLoeq6V8No0yJQo_nr_uOyVNfO-Bv_YV2VnB4gKeYOigwV9qktj6yUjGqQbdKLbR-G0RFegtECd080Dmta1KXSl30ChC1EJ6Y37yXJwhG6sGdIGZKaR0HokGoVmutZ--YrbCTZKUTnY_Zmj4P787C67HM-uL6bZ8WwsSRjRMYkxxxRTnjAWJypKKVMUsJAUIAbJFSiImOSShawo0wIkkyEIEVPF44IQMgr2V3dba547cD5_Mp1thsg84gQTGieYDarJSiWtcc5CmbdW18L2eYjzRQn5ooT8t4TBwFeGV11B_486z7K77M_7DaVqkEg</recordid><startdate>20240222</startdate><enddate>20240222</enddate><creator>Milić, Milica</creator><creator>Byström, Emil</creator><creator>Domínguez de María, Pablo</creator><creator>Kara, Selin</creator><general>Wiley Subscription Services, Inc</general><scope>24P</scope><scope>WIN</scope><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0001-6754-2814</orcidid><orcidid>https://orcid.org/0000-0002-7322-4158</orcidid></search><sort><creationdate>20240222</creationdate><title>Selective Oxidation of 5‐Hydroxymethylfurfural to 2,5‐Diformylfuran in Biphasic Media using Immobilized Galactose Oxidase: Proof of Concept and Limitations</title><author>Milić, Milica ; Byström, Emil ; Domínguez de María, Pablo ; Kara, Selin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3124-35090404976657d2846d4e0ac4ee5ec9dede26c9c616bf8bec6c1eaa54d95b333</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>5-hydroxymethylfurfural (HMF)</topic><topic>Adsorption</topic><topic>Aqueous solutions</topic><topic>biocatalysis</topic><topic>biphasic systems</topic><topic>enzyme immobilization</topic><topic>Galactose</topic><topic>galactose oxidase</topic><topic>Hydroxymethylfurfural</topic><topic>Oxidase</topic><topic>Oxidation</topic><topic>Poisoning (reaction inhibition)</topic><topic>Refining</topic><topic>Stability analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Milić, Milica</creatorcontrib><creatorcontrib>Byström, Emil</creatorcontrib><creatorcontrib>Domínguez de María, Pablo</creatorcontrib><creatorcontrib>Kara, Selin</creatorcontrib><collection>Wiley Online Library (Open Access Collection)</collection><collection>Wiley Online Library Free Content</collection><collection>CrossRef</collection><jtitle>ChemCatChem</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Milić, Milica</au><au>Byström, Emil</au><au>Domínguez de María, Pablo</au><au>Kara, Selin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Selective Oxidation of 5‐Hydroxymethylfurfural to 2,5‐Diformylfuran in Biphasic Media using Immobilized Galactose Oxidase: Proof of Concept and Limitations</atitle><jtitle>ChemCatChem</jtitle><date>2024-02-22</date><risdate>2024</risdate><volume>16</volume><issue>4</issue><epage>n/a</epage><issn>1867-3880</issn><eissn>1867-3899</eissn><abstract>The oxidation of 5‐hydroxymethylfurfural (HMF) to 2,5‐diformylfuran (DFF) is a key reaction in valorizing biomass. DFF is hardly soluble in water, while HMF is often obtained from biorefineries in crude wet organic fractions. Thus, the reaction is challenging for both biocatalysis performed in aqueous media, and for chemocatalysis where the presence of water often results in catalyst poisoning. Galactose oxidase (GalOx) can selectively oxidize HMF to DFF and displays promising activity in aqueous‐organic media. In this study, GalOx was immobilized on ten carriers, assessing the immobilization yield, activity, and stability. Covalently immobilized GalOx catalyzed the oxidation of HMF to DFF in neat and water‐saturated EtOAc, and in biphasic systems of various water contents. At 50 % v/v H2O, the reaction was conducted at a semi‐preparative scale (50 mL) with no adverse effect on DFF yield. Some limitations arise, such as enzyme deactivation, and adsorption of DFF to the support, particularly in the aqueous fraction. Future options to upgrade the route may include designed stable enzymes under the presence of HMF/DFF, and the setup of microaqueous systems where DFF adsorption is minimized. The use of wet EtOAc media would be a promising approach in future biorefineries employing inexpensive crude wet organic fractions. Galactose oxidase (GalOx) immobilized on Purolite® LifetechTM ECR8215F catalyzed the oxidation of 5‐hydroxymethylfurfural (HMF) to 2,5‐diformylfuran (DFF) in ethyl acetate (EtOAc)‐based biphasic media, as well as neat and water‐saturated organic solvent. The results showcase a scalable system with an efficient catalyst with reusability potential.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/cctc.202301384</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-6754-2814</orcidid><orcidid>https://orcid.org/0000-0002-7322-4158</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1867-3880
ispartof ChemCatChem, 2024-02, Vol.16 (4), p.n/a
issn 1867-3880
1867-3899
language eng
recordid cdi_proquest_journals_2930345706
source Wiley:Jisc Collections:Wiley Read and Publish Open Access 2024-2025 (reading list)
subjects 5-hydroxymethylfurfural (HMF)
Adsorption
Aqueous solutions
biocatalysis
biphasic systems
enzyme immobilization
Galactose
galactose oxidase
Hydroxymethylfurfural
Oxidase
Oxidation
Poisoning (reaction inhibition)
Refining
Stability analysis
title Selective Oxidation of 5‐Hydroxymethylfurfural to 2,5‐Diformylfuran in Biphasic Media using Immobilized Galactose Oxidase: Proof of Concept and Limitations
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-24T22%3A48%3A11IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Selective%20Oxidation%20of%205%E2%80%90Hydroxymethylfurfural%20to%202,5%E2%80%90Diformylfuran%20in%20Biphasic%20Media%20using%20Immobilized%20Galactose%20Oxidase:%20Proof%20of%20Concept%20and%20Limitations&rft.jtitle=ChemCatChem&rft.au=Mili%C4%87,%20Milica&rft.date=2024-02-22&rft.volume=16&rft.issue=4&rft.epage=n/a&rft.issn=1867-3880&rft.eissn=1867-3899&rft_id=info:doi/10.1002/cctc.202301384&rft_dat=%3Cproquest_cross%3E2930345706%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3124-35090404976657d2846d4e0ac4ee5ec9dede26c9c616bf8bec6c1eaa54d95b333%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2930345706&rft_id=info:pmid/&rfr_iscdi=true