• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Immobilization of Multi-biocatalysts in Alginate Beads for Cofactor Regeneration and Improved Reusability.多生物催化剂固定于海藻酸钠珠粒用于辅因子再生及提高可重复使用性
J Vis Exp. 2016 Apr 22(110):53944. doi: 10.3791/53944.
2
Immobilization of L-arabinitol dehydrogenase on aldehyde-functionalized silicon oxide nanoparticles for L-xylulose production.将L-阿拉伯糖醇脱氢酶固定在醛功能化氧化硅纳米颗粒上用于生产L-木酮糖。
Appl Microbiol Biotechnol. 2014 Feb;98(3):1095-104. doi: 10.1007/s00253-013-5209-y. Epub 2013 Nov 6.
3
Enhanced stability of Bacillus licheniformis L-arabinose isomerase by immobilization with alginate.用海藻酸钠固定化提高地衣芽孢杆菌 L-阿拉伯糖异构酶的稳定性。
Prep Biochem Biotechnol. 2010;40(1):65-75. doi: 10.1080/10826060903400567.
4
Expression of chitinase gene in BL21 pET system and investigating the biocatalystic performance of chitinase-loaded AlgSep nanocomposite beads.在 BL21 pET 系统中表达几丁质酶基因,并研究负载几丁质酶的 AlgSep 纳米复合珠的生物催化性能。
Int J Biol Macromol. 2017 Nov;104(Pt B):1664-1671. doi: 10.1016/j.ijbiomac.2017.03.119. Epub 2017 Mar 24.
5
Combined of ultrasound irradiation with high hydrostatic pressure (US/HHP) as a new method to improve immobilization of dextranase onto alginate gel.超声辐照联合高静压(US/HHP)作为一种提高葡聚糖酶固定到海藻酸钠凝胶的新方法。
Ultrason Sonochem. 2014 Jul;21(4):1325-34. doi: 10.1016/j.ultsonch.2014.02.004. Epub 2014 Feb 15.
6
Immobilization of naringinase in PVA-alginate matrix using an innovative technique.采用创新技术将柚皮苷酶固定在 PVA-海藻酸钠基质中。
Appl Biochem Biotechnol. 2010 Apr;160(7):2129-47. doi: 10.1007/s12010-009-8733-6. Epub 2009 Aug 20.
7
Affinity covalent immobilization of glucoamylase onto ρ-benzoquinone-activated alginate beads: II. Enzyme immobilization and characterization.葡糖淀粉酶在 ρ-苯醌活化的海藻酸钠珠上的亲和共价固定化:Ⅱ.酶的固定化和特性。
Appl Biochem Biotechnol. 2011 May;164(1):45-57. doi: 10.1007/s12010-010-9113-y. Epub 2010 Nov 10.
8
Thermostable α-amylase immobilization: Enhanced stability and performance for starch biocatalysis.耐热α-淀粉酶的固定化:增强淀粉生物催化的稳定性和性能。
Biotechnol Appl Biochem. 2016 Jan-Feb;63(1):57-66. doi: 10.1002/bab.1350. Epub 2015 Apr 28.
9
Stabilization of Aspergillus parasiticus cytosine deaminase by immobilization on calcium alginate beads improved enzyme operational stability.通过固定在海藻酸钙珠上稳定寄生曲霉胞嘧啶脱氨酶,提高了酶的操作稳定性。
J Enzyme Inhib Med Chem. 2013 Dec;28(6):1217-20. doi: 10.3109/14756366.2012.724406. Epub 2012 Oct 3.
10
Combined cross-linked enzyme aggregates of glycerol dehydrogenase and NADH oxidase for high efficiency in situ NAD regeneration.甘油脱氢酶和烟酰胺腺嘌呤二核苷酸氧化酶的交联酶聚集体用于高效原位烟酰胺腺嘌呤二核苷酸再生。
Int J Biol Macromol. 2020 Feb 1;144:1013-1021. doi: 10.1016/j.ijbiomac.2019.09.178. Epub 2019 Oct 25.

引用本文的文献

1
Optimization of Glucose Dehydrogenase Immobilization Strategies in a 3D-Printed Millireactor.3D打印微反应器中葡萄糖脱氢酶固定化策略的优化
Micromachines (Basel). 2024 Dec 20;15(12):1514. doi: 10.3390/mi15121514.
2
Cloning, Expression and Characterization of a Highly Active Alcohol Dehydrogenase for Production of Ethyl (S)-4-Chloro-3-Hydroxybutyrate.用于生产(S)-4-氯-3-羟基丁酸乙酯的高活性乙醇脱氢酶的克隆、表达及特性研究
Indian J Microbiol. 2019 Jun;59(2):225-233. doi: 10.1007/s12088-019-00795-0. Epub 2019 Mar 18.

本文引用的文献

1
Engineering Novel and Improved Biocatalysts by Cell Surface Display.通过细胞表面展示工程化新型和改良的生物催化剂。
Ind Eng Chem Res. 2015 Apr 29;54(16):4021-4032. doi: 10.1021/ie504071f. Epub 2015 Jan 20.
2
Improved Enzyme Catalytic Characteristics upon Glutaraldehyde Cross-Linking of Alginate Entrapped Xylanase Isolated from Aspergillus flavus MTCC 9390.戊二醛交联从黄曲霉MTCC 9390分离的海藻酸钠包埋木聚糖酶后酶催化特性的改善
Enzyme Res. 2015;2015:210784. doi: 10.1155/2015/210784. Epub 2015 Aug 12.
3
One-step biosynthesis of α-keto-γ-methylthiobutyric acid from L-methionine by an Escherichia coli whole-cell biocatalyst expressing an engineered L-amino acid deaminase from Proteus vulgaris.通过表达来自普通变形杆菌的工程化L-氨基酸脱氨酶的大肠杆菌全细胞生物催化剂,由L-甲硫氨酸一步生物合成α-酮-γ-甲硫基丁酸。
PLoS One. 2014 Dec 22;9(12):e114291. doi: 10.1371/journal.pone.0114291. eCollection 2014.
4
Engineered whole-cell biocatalyst-based detoxification and detection of neurotoxic organophosphate compounds.基于工程化全细胞生物催化剂的神经毒剂有机磷化合物解毒和检测。
Biotechnol Adv. 2014 May-Jun;32(3):652-62. doi: 10.1016/j.biotechadv.2014.04.010. Epub 2014 Apr 26.
5
Role of surface residue 184 in the catalytic activity of NADH oxidase from Streptococcus pyogenes.化脓性链球菌NADH氧化酶催化活性中表面残基184的作用。
Appl Microbiol Biotechnol. 2014 Aug;98(16):7081-8. doi: 10.1007/s00253-014-5666-y. Epub 2014 Apr 1.
6
pH-rate profiles of L-arabinitol 4-dehydrogenase from Hypocrea jecorina and its application in L-xylulose production.棘孢木霉 L-阿拉伯糖醇 4-脱氢酶的 pH 值速率曲线及其在 L-木酮糖生产中的应用。
Bioorg Med Chem Lett. 2014 Jan 1;24(1):173-6. doi: 10.1016/j.bmcl.2013.11.047. Epub 2013 Nov 27.
7
Engineering of cofactor regeneration enhances (2S,3S)-2,3-butanediol production from diacetyl.辅因子再生工程增强了由双乙酰生产(2S,3S)-2,3-丁二醇的能力。
Sci Rep. 2013;3:2643. doi: 10.1038/srep02643.
8
Recent trends and applications of encapsulating materials for probiotic stability.最近用于益生菌稳定性的包封材料的趋势和应用。
Crit Rev Food Sci Nutr. 2013;53(3):231-44. doi: 10.1080/10408398.2010.524953.
9
Biocatalytic anti-Prelog stereoselective reduction of ethyl acetoacetate catalyzed by whole cells of Acetobacter sp. CCTCC M209061.醋酸杆菌 CCTCC M209061 全细胞催化的乙酰乙酸乙酯的生物催化反-Prelog 立体选择性还原。
J Biotechnol. 2013 Feb 10;163(3):292-300. doi: 10.1016/j.jbiotec.2012.10.023. Epub 2012 Nov 8.
10
A modular cell-based biosensor using engineered genetic logic circuits to detect and integrate multiple environmental signals.一种基于模块化细胞的生物传感器,使用工程遗传逻辑电路来检测和整合多种环境信号。
Biosens Bioelectron. 2013 Feb 15;40(1):368-76. doi: 10.1016/j.bios.2012.08.011. Epub 2012 Aug 23.

多生物催化剂固定于海藻酸钠珠粒用于辅因子再生及提高可重复使用性

Immobilization of Multi-biocatalysts in Alginate Beads for Cofactor Regeneration and Improved Reusability.

作者信息

Gao Hui, Khera Eshita, Lee Jung-Kul, Wen Fei

机构信息

Department of Chemical Engineering, Konkuk University.

Department of Chemical Engineering, University of Michigan.

出版信息

J Vis Exp. 2016 Apr 22(110):53944. doi: 10.3791/53944.

DOI:10.3791/53944
PMID:27166648
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4941993/
Abstract

We have recently developed a simple, reusable and coupled whole-cell biocatalytic system with the capability of cofactor regeneration and biocatalyst immobilization for improved production yield and sustained synthesis. Described herewith is the experimental procedure for the development of such a system consisting of two E. coli strains that express functionally complementary enzymes. Together, these two enzymes can function co-operatively to mediate the regeneration of expensive cofactors for improving the product yield of the bioreaction. In addition, the method of synthesizing an immobilized form of the coupled biocatalytic system by encapsulation of whole cells in calcium alginate beads is reported. As an example, we present the improved biosynthesis of L-xylulose from L-arabinitol by coupling E. coli cells expressing the enzymes L-arabinitol dehydrogenase or NADH oxidase. Under optimal conditions and using an initial concentration of 150 mM L-arabinitol, the maximal L-xylulose yield reached 96%, which is higher than those reported in the literature. The immobilized form of the coupled whole-cell biocatalysts demonstrated good operational stability, maintaining 65% of the yield obtained in the first cycle after 7 cycles of successive re-use, while the free cell system almost completely lost the catalytic activity. Therefore, the methods reported here provides two strategies that could help improve the industrial production of L-xylulose, as well as other value-added compounds requiring the use of cofactors in general.

摘要

我们最近开发了一种简单、可重复使用且耦合的全细胞生物催化系统,该系统具有辅因子再生和生物催化剂固定化的能力,可提高产量并实现持续合成。本文描述了开发这种系统的实验程序,该系统由表达功能互补酶的两种大肠杆菌菌株组成。这两种酶共同作用,可协同介导昂贵辅因子的再生,以提高生物反应的产物产量。此外,还报道了通过将全细胞封装在海藻酸钙珠中合成固定化耦合生物催化系统的方法。作为一个例子,我们展示了通过耦合表达L-阿拉伯糖醇脱氢酶或NADH氧化酶的大肠杆菌细胞,从L-阿拉伯糖醇改进生物合成L-木酮糖的过程。在最佳条件下,使用150 mM的L-阿拉伯糖醇初始浓度,L-木酮糖的最大产量达到96%,高于文献报道的产量。固定化耦合全细胞生物催化剂表现出良好的操作稳定性,在连续重复使用7个循环后,仍保持第一个循环产量的65%,而游离细胞系统几乎完全失去了催化活性。因此,本文报道的方法提供了两种策略,可有助于提高L-木酮糖以及一般需要使用辅因子的其他增值化合物的工业生产。