Reversible immobilization of enzyme on the “deck” for high-efficiency heterogeneous catalysis

IF 4.9 2区 工程技术 Q1 MATERIALS SCIENCE, PAPER & WOOD
Xing Zhu, Zuoyuan Lv, Longfang Ren, Mingliang Fan, Chenxi Du, Yuanyuan Qiang, Bin He
{"title":"Reversible immobilization of enzyme on the “deck” for high-efficiency heterogeneous catalysis","authors":"Xing Zhu,&nbsp;Zuoyuan Lv,&nbsp;Longfang Ren,&nbsp;Mingliang Fan,&nbsp;Chenxi Du,&nbsp;Yuanyuan Qiang,&nbsp;Bin He","doi":"10.1007/s10570-024-06165-4","DOIUrl":null,"url":null,"abstract":"<div><p>Enzyme immobilization has emerged as one of the pivotal technologies in enzyme engineering, offering substantial cost reductions associated with enzyme isolation and utilization. However, efficient catalysis of solid substrates with solid immobilized enzymes remains a challenge, typically exemplified by the hydrolysis of cellulose using immobilized cellulase. In this study, a novel system of reversible release and recycling of cellulase on the surface of low-density polyethylene (LDPE) \"hull\" was developed, inspired by the operational dynamics of carrier-based aircraft. The reversible formation and disruption of multiple hydrogen bonds between the grafted gelatin molecular chain on the LDPE surface and the modification arm of cellulase (poly (methacrylic acid-propenoic acid; PAA-PMAA) can be achieved through temperature control, thus enabling the reversible release and recycling of modified cellulase molecules on the LDPE surface. Results demonstrated that the release of modified cellulase (PLANE) from the LDPE surface overcame the mass transfer barrier inherent in traditional immobilized enzyme systems for catalyzing insoluble substrates. This was attributed to the dissolution of PLANE in the developed system, rendering its hydrolysis of the insoluble cellulose substrate comparable to that of the free enzyme. Upon completion of the reaction, the PLANE could be reversibly recycled on the surface of the macroscopic LDPE membrane, facilitated by the regeneration of multiple hydrogen bonds. Furthermore, the facile removal of the membrane aided in the convenient recycling of cellulase. Notably, the cellulase molecules in the system retained more than 50% of their biological activity even after 8 batches of reuse, making the process cost-effective. This method addressed the limitations of traditional immobilized enzymes, allowing the catalysis of solid substrates with elevated mass transfer and simultaneous easy recovery, thus standing out as a universal immobilization method.</p></div>","PeriodicalId":511,"journal":{"name":"Cellulose","volume":"31 15","pages":"9075 - 9086"},"PeriodicalIF":4.9000,"publicationDate":"2024-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cellulose","FirstCategoryId":"88","ListUrlMain":"https://link.springer.com/article/10.1007/s10570-024-06165-4","RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, PAPER & WOOD","Score":null,"Total":0}
引用次数: 0

Abstract

Enzyme immobilization has emerged as one of the pivotal technologies in enzyme engineering, offering substantial cost reductions associated with enzyme isolation and utilization. However, efficient catalysis of solid substrates with solid immobilized enzymes remains a challenge, typically exemplified by the hydrolysis of cellulose using immobilized cellulase. In this study, a novel system of reversible release and recycling of cellulase on the surface of low-density polyethylene (LDPE) "hull" was developed, inspired by the operational dynamics of carrier-based aircraft. The reversible formation and disruption of multiple hydrogen bonds between the grafted gelatin molecular chain on the LDPE surface and the modification arm of cellulase (poly (methacrylic acid-propenoic acid; PAA-PMAA) can be achieved through temperature control, thus enabling the reversible release and recycling of modified cellulase molecules on the LDPE surface. Results demonstrated that the release of modified cellulase (PLANE) from the LDPE surface overcame the mass transfer barrier inherent in traditional immobilized enzyme systems for catalyzing insoluble substrates. This was attributed to the dissolution of PLANE in the developed system, rendering its hydrolysis of the insoluble cellulose substrate comparable to that of the free enzyme. Upon completion of the reaction, the PLANE could be reversibly recycled on the surface of the macroscopic LDPE membrane, facilitated by the regeneration of multiple hydrogen bonds. Furthermore, the facile removal of the membrane aided in the convenient recycling of cellulase. Notably, the cellulase molecules in the system retained more than 50% of their biological activity even after 8 batches of reuse, making the process cost-effective. This method addressed the limitations of traditional immobilized enzymes, allowing the catalysis of solid substrates with elevated mass transfer and simultaneous easy recovery, thus standing out as a universal immobilization method.

Abstract Image

在 "甲板 "上可逆固定酶,实现高效异相催化
酶固定化技术已成为酶工程的关键技术之一,可大幅降低与酶分离和利用相关的成本。然而,使用固体固定化酶对固体底物进行高效催化仍然是一项挑战,使用固定化纤维素酶水解纤维素就是典型的例子。在这项研究中,受航母舰载机运行动力学的启发,开发了一种在低密度聚乙烯(LDPE)"船体 "表面可逆释放和回收纤维素酶的新型系统。通过温度控制,可以实现低密度聚乙烯表面接枝明胶分子链与纤维素酶修饰臂(聚甲基丙烯酸-丙烯酸;PAA-PMAA)之间多个氢键的可逆形成和破坏,从而实现低密度聚乙烯表面修饰纤维素酶分子的可逆释放和循环利用。研究结果表明,改性纤维素酶(PLANE)从低密度聚乙烯表面的释放克服了传统固定化酶系统在催化不溶性底物时固有的传质障碍。这要归功于 PLANE 在开发的系统中的溶解,使其对不溶性纤维素底物的水解作用与游离酶的水解作用相当。反应完成后,PLANE 可在宏观 LDPE 膜表面进行可逆循环,多重氢键的再生为其提供了便利。此外,膜的方便移除也有助于纤维素酶的方便回收。值得注意的是,该系统中的纤维素酶分子在经过 8 次重复使用后仍能保持 50% 以上的生物活性,使该工艺具有成本效益。这种方法解决了传统固定化酶的局限性,可以催化固体底物,传质能力强,同时易于回收,因此是一种通用的固定化方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Cellulose
Cellulose 工程技术-材料科学:纺织
CiteScore
10.10
自引率
10.50%
发文量
580
审稿时长
3-8 weeks
期刊介绍: Cellulose is an international journal devoted to the dissemination of research and scientific and technological progress in the field of cellulose and related naturally occurring polymers. The journal is concerned with the pure and applied science of cellulose and related materials, and also with the development of relevant new technologies. This includes the chemistry, biochemistry, physics and materials science of cellulose and its sources, including wood and other biomass resources, and their derivatives. Coverage extends to the conversion of these polymers and resources into manufactured goods, such as pulp, paper, textiles, and manufactured as well natural fibers, and to the chemistry of materials used in their processing. Cellulose publishes review articles, research papers, and technical notes.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信