Multiple effects driven by pulsed electric field to enhance the catalytic efficiency of the mussel-inspired proteolytic membrane in protein hydrolysis

贻贝 电场 水解 化学 催化作用 化学工程 色谱法 材料科学 生物化学 生物 工程类 生态学 物理 量子力学
作者
Zhe Chen,Shiyu Zhu,Haoran Zhang,Sheng Wang,Krystian Marszałek,Zhenzhou Zhu
出处
期刊:Chemical Engineering Journal [Elsevier BV]
卷期号:453: 139792-139792 被引量:3
标识
DOI:10.1016/j.cej.2022.139792
摘要

Although the immobilization of enzymes on the membrane is an effective method to improve enzyme stability and reusability, the immobilized enzyme also causes low activity and reduces substrate accessibility. In order to overcome these shortcomings and provide a viable proteolytic membrane with increasing enzyme activity and substrate accessibility, a pulsed electric field (PEF)-assisted proteolytic membrane (PAPM) was constructed by immobilizing PEF-treated pepsin on PDA and PEI co-deposited ultrafiltration membrane. The PEF-treated pepsin endowed high activity (165.33 ± 2.31 %) and charge amount (−3.95 mV), with stable and uniform particle size (39 nm). These phenomena were attributed to the multiple effects driven by PEF, including the diffusion effect, electrolysis reactions, and microstructural regulation. Specifically, PAPM retained 80 % of original pepsin activity and enhanced 25 % pepsin activity compared to the conventional proteolytic membrane (PM). Such improvement can be ascribed to two factors: Firstly, PEF regulated pepsin microstructure to an optimal structure (4.6 % increase of the α-helix and 4.0 % reduction of the random coil) for pepsin immobilization. Secondly, PEF changed pepsin charge properties from positive (+1.62 mV) to negative (−3.95 mV), while substrate charges were positive. Heterogeneous charge interactions between pepsin and substrates increased the accessibility of the substrate to immobilized pepsin, effectively promoting enzymatic reactions. This study offers a feasible method to prepare the proteolytic membrane in protein hydrolysis.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
清脆的天空完成签到,获得积分10
1秒前
1秒前
翎淮川完成签到,获得积分10
1秒前
1秒前
痴情的萃发布了新的文献求助20
2秒前
彭于晏应助小蝶采纳,获得10
2秒前
2秒前
小小小雅关注了科研通微信公众号
3秒前
ccc完成签到,获得积分10
3秒前
乐乐应助ALAI采纳,获得10
3秒前
迷人曼柔发布了新的文献求助10
4秒前
4秒前
搜集达人应助xx_2000采纳,获得10
4秒前
5秒前
qqq发布了新的文献求助10
6秒前
科研通AI6.2应助TSW采纳,获得10
7秒前
FashionBoy应助wmz采纳,获得10
7秒前
看书发布了新的文献求助10
8秒前
雪雪发布了新的文献求助10
9秒前
酱紫酱紫完成签到,获得积分10
9秒前
Catalparine_Haw完成签到,获得积分10
9秒前
9秒前
春夏爱科研完成签到,获得积分10
11秒前
云淡风轻完成签到,获得积分10
11秒前
英俊的铭应助看书采纳,获得10
12秒前
超级映安完成签到,获得积分10
12秒前
乐空思应助Magali采纳,获得30
13秒前
谨慎的向南完成签到,获得积分10
13秒前
科研通AI2S应助Ruby采纳,获得10
13秒前
mumu发布了新的文献求助10
14秒前
在水一方应助科研通管家采纳,获得10
15秒前
15秒前
tiptip应助科研通管家采纳,获得10
15秒前
完美世界应助科研通管家采纳,获得10
15秒前
Hello应助科研通管家采纳,获得30
15秒前
PUHAHA应助科研通管家采纳,获得10
15秒前
搜集达人应助科研通管家采纳,获得10
15秒前
Ava应助科研通管家采纳,获得10
15秒前
tiptip应助科研通管家采纳,获得20
15秒前
顾矜应助科研通管家采纳,获得30
15秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
PowerCascade: A Synthetic Dataset for Cascading Failure Analysis in Power Systems 2000
The Composition and Relative Chronology of Dynasties 16 and 17 in Egypt 1500
Picture this! Including first nations fiction picture books in school library collections 1500
Signals, Systems, and Signal Processing 610
Unlocking Chemical Thinking: Reimagining Chemistry Teaching and Learning 555
Scientific Writing and Communication: Papers, Proposals, and Presentations 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6370356
求助须知:如何正确求助?哪些是违规求助? 8184276
关于积分的说明 17266643
捐赠科研通 5424944
什么是DOI,文献DOI怎么找? 2870073
邀请新用户注册赠送积分活动 1847081
关于科研通互助平台的介绍 1693826