Immobilization of Phospholipase D on Fe3O4@SiO2-Graphene Oxide Nanocomposites: A Strategy to Improve Catalytic Stability and Reusability in the Efficient Production of Phosphatidylserine
Phospholipase D (PLD) plays a pivotal role in the biosynthesis of phosphatidylserine (PS), but its practical application is constrained by limitations in stability and reusability. In this study, we successfully fabricated the Fe<sub>3</sub>O<sub>4</sub>@SiO<sub>2</sub>-graphene oxide (GO) nanocomposite by chemical binding of Fe<sub>3</sub>O<sub>4</sub>@SiO<sub>2</sub> and GO. Subsequently, PLD was immobilized onto the nanocomposite via physical adsorption, with the aim of enhancing catalytic stability, reducing mass transfer resistance, and improving reusability. Under optimal conditions, the immobilization efficiency reached 84.4%, with a PLD loading capacity of 111.4 mg/g<sub>support</sub>. The optimal pH for PS production by immobilized PLD shifted from 6.0 to 6.5, while the optimal temperature increased from 45 °C to 50 °C. Notably, the immobilized PLD demonstrated a shorter reaction time and a higher PS yield, achieving a 95.4% yield within 90 min, compared to the free PLD (78.1% yield within 150 min), representing a 1.04-fold improvement in production efficiency. Furthermore, the immobilized PLD exhibited outstanding storage stability and thermal stability, along with remarkable reusability. Even after being reused for 10 cycles, the PS yield still stays as high as 78.3%. These findings strongly suggest that the Fe<sub>3</sub>O<sub>4</sub>@SiO<sub>2</sub>-GO immobilized PLD has the potential for the efficient production of PS.
Authors
- Bishan Guo
- Juntan Wang
- Huiyi Shang (ORCID: https://orcid.org/0000-0002-3649-3607)
- Huijuan Li (ORCID: https://orcid.org/0000-0002-5135-5608)
- Haihua Zhu
Institutions
- Henan University (CN)
- Henan Academy of Sciences (CN)
- Institute of Chemistry (CN)
- Henan Agricultural University (CN)
Publication Details
- Journal
- Molecules
- Published
- 2025-02-16
- DOI
- https://doi.org/10.3390/molecules30040912
- Citations
- 3
- Primary Topic
- Enzyme Catalysis and Immobilization
- Type
- article
- Field-Weighted Citation Impact
- 2.42