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Engineering Saccharomyces boulardii for enhanced surface display capacity.
Luping Xu1,2, Xingjian Bai3, Deokyeol Jeong1,2
1Department of Food Science, Purdue University, West Lafayette, IN, 47907, USA.
Microbial Cell Factories
|April 1, 2025
Summary
Researchers optimized Saccharomyces boulardii (Sb) for enhanced protein display. A new engineered strain, LIP02, significantly improves surface display efficiency and stability for therapeutic applications.
Area of Science:
- Microbiology
- Biotechnology
- Molecular Biology
Background:
- Saccharomyces boulardii (Sb) is a probiotic yeast with therapeutic potential.
- Current applications utilize Sb's secretion and display for delivering therapeutic agents.
- Optimizing Sb's surface display efficiency is crucial for enhanced therapeutic delivery.
Purpose of the Study:
- To evaluate and enhance surface display systems in Saccharomyces boulardii.
- To engineer a modified Sb strain for improved protein display capacity and stability.
Main Methods:
- Systematic modification of Aga2- and Sed1-based display cassettes in Saccharomyces cerevisiae and Sb.
- Engineering of a novel Sb strain (LIP02) via AGA1 overexpression and deletion of cell wall-related genes.
- Genome integration of display cassettes in the engineered strain.
Main Results:
- Engineered LIP02 strain showed significantly enhanced display capacity compared to wild-type Sb.
- Genome integration improved display stability and expression over plasmid-based systems.
- Functionality of displayed β-glucosidase was confirmed with improved enzymatic activity.
Conclusions:
- The engineered LIP02 strain is a superior host for surface display in Sb.
- This optimized platform offers enhanced stability and efficiency for expressing therapeutic proteins and biomolecules.
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