Recent innovations in immobilization of β-galactosidases for industrial and therapeutic applications

固定化酶 化学 水解 组合化学 有机化学
作者
Feiyu Duan,Tong Sun,Jingwen Zhang,Ke Wang,Yan Wen,Lili Lu
出处
期刊:Biotechnology Advances [Elsevier BV]
卷期号:61: 108053-108053 被引量:43
标识
DOI:10.1016/j.biotechadv.2022.108053
摘要

Immobilized enzymes are better suited for industrial applications than free enzymes due to their favorable properties such as ease of separation and reuse, and enhanced stability and storage life. β-Galactosidases are an important class of glycosidases with hydrolysis and transglycosylation activities, which are applied in industries for lactose hydrolysis and prebiotics synthesis worldwide. The recent innovations in immobilized β-galactosidases have improved the performance of the immobilized enzymes and broadened their applications in the fields of food, energy, and medicine. Innovations in β-galactosidase immobilization methods include rational adsorption based on enzyme features, layer by layer adsorption for strengthened ionic bonding, 3-D printing for rapid and elaborate entrapment, modifications of either materials or enzymes for ingenious covalent binding, nontoxic crosslinking, carrier-free immobilization, and oriented immobilization either through protein engineering or enzyme display on cells, membranes, and phages, along with innovations in carrier materials involving the introduction of graphene derivatives, polyaniline nanomaterials, nanofibers, nucleotide molecules, Langmuir-Blodgett films, and so on. These innovations have partially solved the problems associated with traditional methods, resulting in enzymes with highly retained activity, excellent stability, reduced microbial contamination, enzyme leakage, and reagent toxicity. The immobilized β-galactosidases with potential economic and environmental benefits have been extendedly used for hydrolysis of prodrugs for disease treatment, assembly of biosensors for lactose detection, synthesis of bioactive carbohydrates, and even production of food additives and industrial products, such as tagatose and bioethanol. This review describes the innovations in β-galactosidases immobilization and the applications of these immobilized enzymes. It not only enables the fully understanding of β-galactosidases, but also provides a valuable reference for the immobilization of other industrially-important enzymes.
最长约 10秒,即可获得该文献文件

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
刚刚
1秒前
1秒前
琪凯定理发布了新的文献求助10
1秒前
1秒前
乐乐应助巧蕊采纳,获得10
2秒前
csd完成签到,获得积分10
2秒前
2秒前
3秒前
4秒前
糖炒板栗完成签到,获得积分10
4秒前
4秒前
5秒前
SciGPT应助Lawfy采纳,获得10
5秒前
霍霍发布了新的文献求助10
6秒前
微笑艳一完成签到,获得积分10
6秒前
hahahaa完成签到,获得积分10
6秒前
6秒前
hutian发布了新的文献求助10
6秒前
有点礼貌但不多完成签到 ,获得积分20
6秒前
6秒前
Summer发布了新的文献求助10
7秒前
烟花应助minyun采纳,获得10
8秒前
上官若男应助天才大肥猫采纳,获得10
10秒前
11秒前
maffei发布了新的文献求助10
11秒前
琪凯定理完成签到,获得积分10
11秒前
李想完成签到,获得积分10
12秒前
小马甲应助clyhg采纳,获得10
12秒前
秋末发布了新的文献求助10
12秒前
12秒前
漱石发布了新的文献求助10
12秒前
cdercder应助无风风采纳,获得10
13秒前
大个应助阿航采纳,获得10
13秒前
着急的莹完成签到 ,获得积分10
15秒前
嘻嘻完成签到,获得积分10
15秒前
麦克雷发布了新的文献求助10
16秒前
李霞客完成签到,获得积分10
17秒前
18秒前
Jaelyn完成签到,获得积分10
19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
内視鏡的に摘除しえた十二指腸乳頭部腫瘍の2例 660
On nonlinear stability of contact discontinuities. In: Hyperbolic problems: theory, numerics, applications (Stony Brook, NY, 1994) 510
Management and the Arts 510
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
微电子器件实验教程 400
The Neuroscience of Language 400
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 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7680399
求助须知:如何正确求助?哪些是违规求助? 9244907
关于积分的说明 19931924
捐赠科研通 7251023
什么是DOI,文献DOI怎么找? 3287665
关于科研通互助平台的介绍 2445313
邀请新用户注册赠送积分活动 2290986