Suhag Shashi, Jain Utkarsh, Chauhan Nidhi, Hooda Vinita
Department of Botany, Maharshi Dayanand University, Rohtak, India.
School of Health Sciences & Technology (SoHST), UPES, Dehradun, India.
Prep Biochem Biotechnol. 2025 Apr;55(4):470-490. doi: 10.1080/10826068.2024.2425970. Epub 2024 Nov 14.
In the current work, cellulase from was successfully immobilized on a novel epoxy-affixed chromium metal-organic framework/chitosan (Cr@-MIL-101/CS) support via covalent method using glutaraldehyde as a crosslinker. The bare and cellulase-bound support was characterized by using various microscopic and spectroscopic techniques. Immobilized cellulase exhibited a high immobilization yield of 0.7 ± 0.01 mg/cm, retaining 87.5 ± 0.04% of its specific activity and displaying enhanced catalytic performance. The immobilized enzyme was maximally active at pH 5.0, temperature 65 °C and 0.9 × 10-2 mg/ml saturating substrate concentration and the half-lives of free and immobilized cellulases were approximately 9 and 19 days, respectively. The decrease in activation energy, enthalpy change, and Gibbs free energy change, coupled with an increase in entropy change upon immobilization, indicated that the enzyme's efficiency, stability, and spontaneity in catalyzing the reaction were enhanced by immobilization. Additionally, the immobilized cellulase efficiently converted rice husk cellulose to glucose, with a quantification limit of 0.05%, linear measurement ranging from 0.1 to 0.9%, and 8.5% conversion efficiency. The present method exhibited a strong correlation (R = 0.998) with the DNS method, validating its reliability. Notably, the epoxy/Cr@-MIL-101/CS-bound cellulase demonstrated impressive thermal and pH stabilities, retaining 50% of its activity at 75 °C and over 96% at pH levels of 4.5 and 5.0 after 12 h. Furthermore, it showed excellent reusability, preserving 80% of its activity after 15 cycles and maintaining 50% of its activity even after 20 days of storage. These results suggest that epoxy/Cr@-MIL-101/CS/cellulase composites could be very effective for large-scale cellulose hydrolysis applications.
在当前工作中,通过使用戊二醛作为交联剂的共价方法,成功地将来源于[具体来源未给出]的纤维素酶固定在一种新型的环氧固定铬金属有机框架/壳聚糖(Cr@-MIL-101/CS)载体上。通过使用各种显微镜和光谱技术对裸露的载体以及结合了纤维素酶的载体进行了表征。固定化纤维素酶表现出较高的固定化产率,为0.7±0.01 mg/cm,保留了其比活性的87.5±0.04%,并显示出增强的催化性能。固定化酶在pH 5.0、温度65°C和0.9×10-2 mg/ml的饱和底物浓度下具有最大活性,游离纤维素酶和固定化纤维素酶的半衰期分别约为9天和19天。固定化后活化能、焓变和吉布斯自由能变化的降低,以及熵变的增加,表明固定化增强了酶催化反应的效率、稳定性和自发性。此外,固定化纤维素酶能有效地将稻壳纤维素转化为葡萄糖,定量限为0.05%,线性测量范围为0.1%至0.9%,转化效率为8.5%。本方法与DNS法具有很强的相关性(R = 0.998),验证了其可靠性。值得注意的是,环氧/Cr@-MIL-101/CS结合的纤维素酶表现出令人印象深刻的热稳定性和pH稳定性,在75°C下12小时后仍保留其活性的50%,在pH 4.5和5.0的水平下12小时后仍保留超过96%的活性。此外,它还表现出优异的可重复使用性,在15个循环后保留其活性的80%,即使在储存20天后仍保留其活性的50%。这些结果表明,环氧/Cr@-MIL-101/CS/纤维素酶复合材料对于大规模纤维素水解应用可能非常有效。