Sequential Optimization of Multivariate Metal–Organic Framework Based Biocatalysis
Efficient biocascades require integrated optimization of both biocatalysts and reaction conditions. In the present study, we employ a Latin hypercube sampling-coupled Bayesian optimization (LHS-BO) workflow to sequentially optimizes multivariate Zr-based E-MOF (E-MOF = enzyme@metal-organic framework biocomposite) design and the downstream glucose oxidase-horseradish peroxidase (GOx-HRP) biocascade. Enzymatic assays, attenuated total reflectance Fourier transform infrared spectroscopic (ATR-FTIR) and ultraviolet-visible (UV-Vis) spectroscopic analyses confirm that the optimized multivariate E-MOFs, ZG67, and ZH16, stabilize GOx and HRP in bioactive conformations. ZG67 and ZH16 achieve high encapsulation efficiency (92.2% ± 0.7% and 90.2% ± 1.3%), retained activity (87.1% ± 2.2% and 102.9% ± 14.9%), and enhanced stability under thermal (51.3% ± 1.4% and 45.9% ± 8.7%) and solvent treatments (>80% and ≈60% residual activity, respectively, in ethanol or acetonitrile). The optimal GOx-HRP cascade condition identified by LHS-BO (R49) achieves over 95% of the theoretical maximum 2,3-diaminophenazine (DAP) production rate predicted by the microkinetic model. The strong agreement amongst the experimental data, machine learning modeling, and kinetic modeling validates the robustness of this sequential E-MOF optimization framework. This generalized LHS-BO strategy provides a powerful tool for rational E-MOF and multi-enzyme cascade design, advancing biocatalysis and reaction engineering.
Authors
- Ross Andrew Shalliker (ORCID: https://orcid.org/0000-0003-1443-2632)
- Christian J. Doonan (ORCID: https://orcid.org/0000-0003-2822-0956)
- Sisi Zheng
- Feng Li
- Weibin Liang
Institutions
- Information and Communication Technologies Centre (AU)
- The University of Adelaide (AU)
- Western Sydney University (AU)
Publication Details
- Journal
- Small
- Published
- 2026-02-17
- DOI
- https://doi.org/10.1002/smll.202512430
- Primary Topic
- Advanced Nanomaterials in Catalysis
- Type
- article
- Field-Weighted Citation Impact
- 0.00