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β-葡萄糖苷酶在负载银离子和银纳米颗粒的丙烯酸织物上的可持续固定化,具有增强的稳定性和可重复使用性。

Sustainable Immobilization of β-Glucosidase onto Silver Ions and AgNPs-Loaded Acrylic Fabric with Enhanced Stability and Reusability.

作者信息

Almulaiky Yaaser Q, Alkabli J, El-Shishtawy Reda M

机构信息

Department of Chemistry, College of Science and Arts at Khulis, University of Jeddah, Jeddah 21921, Saudi Arabia.

Department of Chemistry, College of Science and Arts at Alkamil, University of Jeddah, Jeddah 23218, Saudi Arabia.

出版信息

Polymers (Basel). 2023 Nov 9;15(22):4361. doi: 10.3390/polym15224361.

Abstract

Modified polymer design has attracted significant attention for enzyme immobilization, offering promising applications. In this study, amine-terminated polymers were synthesized by incorporating functional groups into polyacrylonitrile using hexamethylenediamine. This work highlights the successful enzyme immobilization strategy using modified polymers, offering improved stability and expanded operational conditions for potential biotechnological applications. The resulting amino groups were utilized to capture silver ions, which were subsequently converted to silver nanoparticles (AgNPs). The obtained materials, AgNPs@TA-HMDA (acrylic textiles coated silver nanoparticles AgNPs) and Ag(I)@TA-HMDA (acrylic textiles coated with Ag ion) were employed as supports for β-glucosidase enzyme immobilization. The highest immobilization yields (IY%) were achieved with AgNPs@TA-HMDA at 92%, followed by Ag(I)@TA-HMDA at 79.8%, resulting in activity yields (AY%) of 81% and 73%, respectively. Characterization techniques such as FTIR, FE-SEM, EDX, TG/DTG, DSC, and zeta potential were employed to investigate the structural composition, surface morphologies, elemental composition, thermal properties, and surface charge of the support materials. After 15 reuses, the preservation percentages decreased to 76% for AgNPs@TA-HMDA/β-Glu and 65% for Ag(I)@TA-HMDA/β-Glu. Storage stability revealed that the decrease in activity for the immobilized enzymes was smaller than the free enzyme. The optimal pH for the immobilized enzymes was broader (pH 5.5 to 6.5) compared to the free enzyme (pH 5.0), and the optimal temperature for the immobilized enzymes was 60 °C, slightly higher than the free enzyme's optimal temperature of 50 °C. The kinetic analysis showed a slight increase in Michaelis constant (Km) values for the immobilized enzymes and a decrease in maximum velocity (Vmax), turnover number (Kcat), and specificity constant (Kcat/Km) values compared to the free enzyme. Through extensive characterization, we gained valuable insights into the structural composition and properties of the modified polymer supports. This research significantly contributes to the development of efficient biotechnological processes by advancing the field of enzyme immobilization and offering valuable knowledge for its potential applications.

摘要

改性聚合物设计在酶固定化方面引起了广泛关注,具有广阔的应用前景。在本研究中,通过使用六亚甲基二胺将官能团引入聚丙烯腈中来合成胺端基聚合物。这项工作突出了使用改性聚合物成功的酶固定化策略,为潜在的生物技术应用提供了更高的稳定性和更宽泛的操作条件。所得的氨基用于捕获银离子,随后将其转化为银纳米颗粒(AgNPs)。所获得的材料,AgNPs@TA-HMDA(涂覆有银纳米颗粒的丙烯酸纺织品)和Ag(I)@TA-HMDA(涂覆有银离子的丙烯酸纺织品)被用作β-葡萄糖苷酶固定化的载体。AgNPs@TA-HMDA的固定化产率(IY%)最高,为92%,其次是Ag(I)@TA-HMDA,为79.8%,相应的活性产率(AY%)分别为81%和73%。采用FTIR、FE-SEM、EDX、TG/DTG、DSC和zeta电位等表征技术来研究载体材料的结构组成、表面形貌、元素组成、热性能和表面电荷。经过15次重复使用后,AgNPs@TA-HMDA/β-Glu的保留率降至76%,Ag(I)@TA-HMDA/β-Glu的保留率降至65%。储存稳定性表明,固定化酶的活性下降幅度小于游离酶。与游离酶(pH 5.0)相比,固定化酶的最佳pH范围更宽(pH 5.5至6.5),固定化酶的最佳温度为60°C,略高于游离酶的最佳温度50°C。动力学分析表明,与游离酶相比,固定化酶的米氏常数(Km)值略有增加,最大速度(Vmax)、周转数(Kcat)和特异性常数(Kcat/Km)值降低。通过广泛的表征,我们对改性聚合物载体的结构组成和性能有了宝贵的认识。这项研究通过推动酶固定化领域的发展并为其潜在应用提供有价值的知识,对高效生物技术工艺的开发做出了重大贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2f2c/10674166/a8897174326c/polymers-15-04361-g001.jpg

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