Biosynthesis of diisooctyl 2,5‐furandicarboxylate by Candida antarctica lipase B (CALB) immobilized on a macroporous epoxy resin

Abstract Diisooctyl 2,5‐furandicarboxylate (DEF), an ester derivative of 2,5‐furandicarboxylic acid (FDCA, a bio‐based platform chemical), resembles the physical and chemical properties of phthalates. Due to its excellent biodegradability, DEF is considered a safer alternative to the hazardous phtha...

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Published in:Biotechnology and Applied Biochemistry
Main Authors: Mang, Rongchen, Zhou, Yuyang, Du, Xuefei, Zhou, Hua, Zhu, Mingxin
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 2023
Subjects:
Online Access:http://dx.doi.org/10.1002/bab.2474
https://iubmb.onlinelibrary.wiley.com/doi/pdf/10.1002/bab.2474
id crwiley:10.1002/bab.2474
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spelling crwiley:10.1002/bab.2474 2024-06-02T07:55:59+00:00 Biosynthesis of diisooctyl 2,5‐furandicarboxylate by Candida antarctica lipase B (CALB) immobilized on a macroporous epoxy resin Mang, Rongchen Zhou, Yuyang Du, Xuefei Zhou, Hua Zhu, Mingxin 2023 http://dx.doi.org/10.1002/bab.2474 https://iubmb.onlinelibrary.wiley.com/doi/pdf/10.1002/bab.2474 en eng Wiley http://onlinelibrary.wiley.com/termsAndConditions#vor Biotechnology and Applied Biochemistry volume 70, issue 5, page 1772-1780 ISSN 0885-4513 1470-8744 journal-article 2023 crwiley https://doi.org/10.1002/bab.2474 2024-05-03T11:50:27Z Abstract Diisooctyl 2,5‐furandicarboxylate (DEF), an ester derivative of 2,5‐furandicarboxylic acid (FDCA, a bio‐based platform chemical), resembles the physical and chemical properties of phthalates. Due to its excellent biodegradability, DEF is considered a safer alternative to the hazardous phthalate plasticizers. Although FDCA esters are currently mainly produced by chemical synthesis, the enzymatic synthesis of DEF is a green, promising alternative. The current study investigated the biosynthesis of DEF by Candida antarctica lipase B (CALB) immobilized on macroporous resins. Out of five macroporous resins (NKA‐9, LX‐1000EP, LX‐1000HA, XAD‐7HP, and XAD‐8) evaluated, the LX‐1000EP epoxy resin was identified as the best carrier for CALB, and the XAD‐7HP weakly polar resin was identified as the second best. The optimal immobilization conditions were as follows: CALB (500 μL) and LX‐1000EP (0.1 g) were incubated in phosphate butter (20 mM, pH 6.0) for 10 h at 35°C. The resulting immobilized CALB (EP‐CALB) showed an activity of 639 U/g in the hydrolysis of p ‐nitrophenyl acetate, with an immobilization efficiency of 87.8% and an activity recovery rate of 56.4%. Using 0.02 g EP‐CALB as the catalyst in 10 mL toluene, and the molar ratio of 2,5‐dimethyl furanediformate (1 mmol/mL) and isooctyl alcohol (4 mmol/mL) that was 1:4, a DEF conversion rate of 91.3% was achieved after a 24‐h incubation at 50°C. EP‐CALB had similar thermal stability and organic solvent tolerance compared to Novozym 435, and both were superior to CALB immobilized on the XAD‐7HP resin. EP‐CALB also exhibited excellent operational stability, with a conversion rate of 52.6% after 10 repeated uses. EP‐CALB could be a promising alternative to Novozym 435 in the biomanufacturing of green and safe plasticizers such as DEF. Article in Journal/Newspaper Antarc* Antarctica Wiley Online Library Biotechnology and Applied Biochemistry 70 5 1772 1780
institution Open Polar
collection Wiley Online Library
op_collection_id crwiley
language English
description Abstract Diisooctyl 2,5‐furandicarboxylate (DEF), an ester derivative of 2,5‐furandicarboxylic acid (FDCA, a bio‐based platform chemical), resembles the physical and chemical properties of phthalates. Due to its excellent biodegradability, DEF is considered a safer alternative to the hazardous phthalate plasticizers. Although FDCA esters are currently mainly produced by chemical synthesis, the enzymatic synthesis of DEF is a green, promising alternative. The current study investigated the biosynthesis of DEF by Candida antarctica lipase B (CALB) immobilized on macroporous resins. Out of five macroporous resins (NKA‐9, LX‐1000EP, LX‐1000HA, XAD‐7HP, and XAD‐8) evaluated, the LX‐1000EP epoxy resin was identified as the best carrier for CALB, and the XAD‐7HP weakly polar resin was identified as the second best. The optimal immobilization conditions were as follows: CALB (500 μL) and LX‐1000EP (0.1 g) were incubated in phosphate butter (20 mM, pH 6.0) for 10 h at 35°C. The resulting immobilized CALB (EP‐CALB) showed an activity of 639 U/g in the hydrolysis of p ‐nitrophenyl acetate, with an immobilization efficiency of 87.8% and an activity recovery rate of 56.4%. Using 0.02 g EP‐CALB as the catalyst in 10 mL toluene, and the molar ratio of 2,5‐dimethyl furanediformate (1 mmol/mL) and isooctyl alcohol (4 mmol/mL) that was 1:4, a DEF conversion rate of 91.3% was achieved after a 24‐h incubation at 50°C. EP‐CALB had similar thermal stability and organic solvent tolerance compared to Novozym 435, and both were superior to CALB immobilized on the XAD‐7HP resin. EP‐CALB also exhibited excellent operational stability, with a conversion rate of 52.6% after 10 repeated uses. EP‐CALB could be a promising alternative to Novozym 435 in the biomanufacturing of green and safe plasticizers such as DEF.
format Article in Journal/Newspaper
author Mang, Rongchen
Zhou, Yuyang
Du, Xuefei
Zhou, Hua
Zhu, Mingxin
spellingShingle Mang, Rongchen
Zhou, Yuyang
Du, Xuefei
Zhou, Hua
Zhu, Mingxin
Biosynthesis of diisooctyl 2,5‐furandicarboxylate by Candida antarctica lipase B (CALB) immobilized on a macroporous epoxy resin
author_facet Mang, Rongchen
Zhou, Yuyang
Du, Xuefei
Zhou, Hua
Zhu, Mingxin
author_sort Mang, Rongchen
title Biosynthesis of diisooctyl 2,5‐furandicarboxylate by Candida antarctica lipase B (CALB) immobilized on a macroporous epoxy resin
title_short Biosynthesis of diisooctyl 2,5‐furandicarboxylate by Candida antarctica lipase B (CALB) immobilized on a macroporous epoxy resin
title_full Biosynthesis of diisooctyl 2,5‐furandicarboxylate by Candida antarctica lipase B (CALB) immobilized on a macroporous epoxy resin
title_fullStr Biosynthesis of diisooctyl 2,5‐furandicarboxylate by Candida antarctica lipase B (CALB) immobilized on a macroporous epoxy resin
title_full_unstemmed Biosynthesis of diisooctyl 2,5‐furandicarboxylate by Candida antarctica lipase B (CALB) immobilized on a macroporous epoxy resin
title_sort biosynthesis of diisooctyl 2,5‐furandicarboxylate by candida antarctica lipase b (calb) immobilized on a macroporous epoxy resin
publisher Wiley
publishDate 2023
url http://dx.doi.org/10.1002/bab.2474
https://iubmb.onlinelibrary.wiley.com/doi/pdf/10.1002/bab.2474
genre Antarc*
Antarctica
genre_facet Antarc*
Antarctica
op_source Biotechnology and Applied Biochemistry
volume 70, issue 5, page 1772-1780
ISSN 0885-4513 1470-8744
op_rights http://onlinelibrary.wiley.com/termsAndConditions#vor
op_doi https://doi.org/10.1002/bab.2474
container_title Biotechnology and Applied Biochemistry
container_volume 70
container_issue 5
container_start_page 1772
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