Surface modification of HKUST-1 for enhanced activity of immobilized formate dehydrogenase used in CO2 hydrogenation

IF 6.4 3区 环境科学与生态学 Q2 ENERGY & FUELS Carbon Resources Conversion Pub Date : 2023-09-20 DOI:10.1016/j.crcon.2023.09.003
Shadeera Rouf , Yaser E. Greish , Bart Van der Bruggen , Sulaiman Al-Zuhair
{"title":"Surface modification of HKUST-1 for enhanced activity of immobilized formate dehydrogenase used in CO2 hydrogenation","authors":"Shadeera Rouf ,&nbsp;Yaser E. Greish ,&nbsp;Bart Van der Bruggen ,&nbsp;Sulaiman Al-Zuhair","doi":"10.1016/j.crcon.2023.09.003","DOIUrl":null,"url":null,"abstract":"<div><p>Post synthetic modification of a hydrophilic metal–organic framework (MOF), HKUST-1, with stearic acid (SA) was carried out to enhance the stability of HKUST-1 in aqueous solution to be used as a support for formate dehydrogenase (FDH) used for CO<sub>2</sub> conversion to formate. SA modification improved the hydrophobicity without affecting the morphology and crystal structure of MOF. Adsorption of FDH on the modified MOF (SA@HKUST-1) was compared to that of the native HKUST-1 and ZIF-L. The adsorption kinetics on all MOFs was found to follow pseudo-second order kinetics and the isotherm was best described by Freundlich model. The high stability of SA@HKUST-1 and enhanced hydrophobic interaction between support and CO<sub>2</sub> resulted in high catalytic efficiency and stability of FDH@SA@HKUST-1. The immobilized enzyme retained 95.1% of its initial activity after 4 cycles of repeated use. It was also shown that FDH@SA@HKUST-1 retained morphology and crystal structure after repeated use. Results of the present work provide novel insight into the influence of hydrophobic MOFs on the activity and stability of immobilized FDH. These findings are expected to assist in developing highly active and stable biocatalysts for CO<sub>2</sub> hydrogenation at commercial level.</p></div>","PeriodicalId":52958,"journal":{"name":"Carbon Resources Conversion","volume":"7 1","pages":"Article 100199"},"PeriodicalIF":6.4000,"publicationDate":"2023-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2588913323000704/pdfft?md5=bea436ffa4d2d11afdb4af0191399007&pid=1-s2.0-S2588913323000704-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Carbon Resources Conversion","FirstCategoryId":"1089","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2588913323000704","RegionNum":3,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENERGY & FUELS","Score":null,"Total":0}
引用次数: 0

Abstract

Post synthetic modification of a hydrophilic metal–organic framework (MOF), HKUST-1, with stearic acid (SA) was carried out to enhance the stability of HKUST-1 in aqueous solution to be used as a support for formate dehydrogenase (FDH) used for CO2 conversion to formate. SA modification improved the hydrophobicity without affecting the morphology and crystal structure of MOF. Adsorption of FDH on the modified MOF (SA@HKUST-1) was compared to that of the native HKUST-1 and ZIF-L. The adsorption kinetics on all MOFs was found to follow pseudo-second order kinetics and the isotherm was best described by Freundlich model. The high stability of SA@HKUST-1 and enhanced hydrophobic interaction between support and CO2 resulted in high catalytic efficiency and stability of FDH@SA@HKUST-1. The immobilized enzyme retained 95.1% of its initial activity after 4 cycles of repeated use. It was also shown that FDH@SA@HKUST-1 retained morphology and crystal structure after repeated use. Results of the present work provide novel insight into the influence of hydrophobic MOFs on the activity and stability of immobilized FDH. These findings are expected to assist in developing highly active and stable biocatalysts for CO2 hydrogenation at commercial level.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
提高固定化甲酸脱氢酶在CO2加氢中的活性
采用硬脂酸(SA)对亲水金属-有机骨架(MOF) hust -1进行了合成后改性,以提高hust -1在水溶液中的稳定性,作为甲酸脱氢酶(FDH)的载体,用于将CO2转化为甲酸。SA改性提高了MOF的疏水性,但不影响MOF的形貌和晶体结构。将改性MOF (SA@HKUST-1)对FDH的吸附效果与天然hust -1和ZIF-L进行比较。所有mof上的吸附动力学都符合准二级动力学,等温线最适合用Freundlich模型描述。SA@HKUST-1的高稳定性和载体与CO2之间增强的疏水相互作用使得FDH@SA@HKUST-1具有较高的催化效率和稳定性。经4次重复使用后,固定化酶仍保持95.1%的初始活性。结果表明,FDH@SA@HKUST-1在重复使用后仍能保留其形貌和晶体结构。本研究结果对疏水mof对固定化FDH活性和稳定性的影响提供了新的见解。这些发现将有助于开发高活性和稳定的生物催化剂,用于商业水平的二氧化碳加氢。
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 去求助
来源期刊
Carbon Resources Conversion
Carbon Resources Conversion Materials Science-Materials Science (miscellaneous)
CiteScore
9.90
自引率
11.70%
发文量
36
审稿时长
10 weeks
期刊介绍: Carbon Resources Conversion (CRC) publishes fundamental studies and industrial developments regarding relevant technologies aiming for the clean, efficient, value-added, and low-carbon utilization of carbon-containing resources as fuel for energy and as feedstock for materials or chemicals from, for example, fossil fuels, biomass, syngas, CO2, hydrocarbons, and organic wastes via physical, thermal, chemical, biological, and other technical methods. CRC also publishes scientific and engineering studies on resource characterization and pretreatment, carbon material innovation and production, clean technologies related to carbon resource conversion and utilization, and various process-supporting technologies, including on-line or off-line measurement and monitoring, modeling, simulations focused on safe and efficient process operation and control, and process and equipment optimization.
期刊最新文献
Outside Front Cover Outside Back Cover Developments and challenges on enhancement of photocatalytic CO2 reduction through photocatalysis Outside Front Cover Outside Back Cover
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1