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Low-Temperature Water-Based De novo Synthesis of Composites Based on Nanosized ZIF-8 Polymorph and Embedded Candida rugosa Lipase


Citation

Hamidon, Noor Fazrieyana and Mohamed Tahir, Mohamed Ibrahim and Yaakob, Yazid and Mohammad Latif, Muhammad Alif and Abdulmalek, Emilia and Abdul Rahman, Mohd Basyaruddin (2026) Low-Temperature Water-Based De novo Synthesis of Composites Based on Nanosized ZIF-8 Polymorph and Embedded Candida rugosa Lipase. Journal of Cluster Science, 37. art. no. 112. pp. 1-18. ISSN 1040-7278; eISSN: 1572-8862

Abstract

In this study, Candida rugosa lipase (CRL) was embedded within nano-zeolitic imidazolate framework-8, nZIF-8 (1:35), synthesized with a zinc(II) ion to 2-methylimidazole (Zn2+: HmeIM) ratio of 1:35 using a water-based, de novo synthesis method at ambient temperature without any modulating agents. The optimization of the embedding process focused on three parameters: the molar ratio of zinc(II) ion to 2-methylimidazole (Zn2+: HmeIM), the concentration of partially purified lipase, and the duration of embedding process. Various physicochemical characterization techniques were employed to confirm and analyze the embedded lipase, including powder X-ray diffraction (PXRD), transmission electron microscopy (TEM), and energy dispersive X-ray (EDX) analysis. Additional characterization methods such as thermogravimetric analysis (TGA), N2 adsorption-desorption measurements, and Fourier transform infrared spectroscopy (FTIR) were also conducted for comprehensive analysis. The amount of lipase successfully embedded was quantified using the standard Bradford assay, with CRL3@nZIF-8(1:35) (Candida rugosa lipase (3.0 mg) immobilized on nano ZIF-8 synthesized with a Zn²⁺:HmeIM ratio of 1:35) achieving the highest immobilization of 89% with loading capacity of 17.7 mg/g. To evaluate the functional performance of the immobilized enzyme, a p-nitrophenyl palmitate (p-NPPal) hydrolysis assay was performed. The results showed a six-fold increase in enzymatic activity compared to the soluble lipase. These findings highlight the potential of nZIF-8(1:35) as a promising support material for lipase immobilization, functioning as a robust protective nanocomposite and as an enhancer of enzymatic performance, with the added capability of reusability in the CRL3@nZIF-8(1:35) system.


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Additional Metadata

Item Type: Article
Subject: Chemistry (all)
Subject: Biochemistry
Subject: Materials Science (all)
Divisions: Faculty of Science
Foundation Studies for Agricultural Science Program
Institute of Nanoscience and Nanotechnology
DOI Number: https://doi.org/10.1007/s10876-026-03065-4
Publisher: Springer
Keywords: Candida rugosa lipase; Embedment into ZIF-8; Hydrolytic activity; Nanosized ZIF-8
Sustainable Development Goals (SDGs): SDG 9: Industry, Innovation and Infrastructure
Depositing User: Ms. Siti Radziah Mohamed@mahmod
Date Deposited: 21 Jul 2026 01:22
Last Modified: 21 Jul 2026 01:22
Altmetrics: http://www.altmetric.com/details.php?domain=psasir.upm.edu.my&doi=10.1007/s10876-026-03065-4
URI: http://psasir.upm.edu.my/id/eprint/127149
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