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Updated: Apr 10, 2026

Immobilization of Multi-biocatalysts in Alginate Beads for Cofactor Regeneration and Improved Reusability
Published on: April 22, 2016
Collaborative self-assembled enzymes and self-immobilised biofilms for enhanced biocatalytic processes
Peifang Ren1, Wenjun Sun1, Chaowei Zhou1
1National Engineering Research Center for Biotechnology, College of Biotechnology and Pharmaceutical Engineering, Nanjing Tech University, Nanjing 211816, China; State Key Laboratory of Materials-Oriented Chemical Engineering, College of Biotechnology and Pharmaceutical Engineering, Nanjing Tech University, Nanjing 211816, China.
This study introduces a novel biocatalytic platform for continuous bio-based product manufacturing. The method uses co-immobilization to maintain high enzyme efficiency over multiple batches, overcoming key challenges in biocatalysis.
Area of Science:
- Biocatalysis
- Biotechnology
- Enzyme Engineering
Background:
- Continuous production of bio-based products is a major hurdle in biocatalysis.
- Existing methods face challenges in maintaining enzyme efficiency over extended periods.
Purpose of the Study:
- To develop a novel one-step biocatalytic platform for continuous production.
- To address the challenge of enzyme deactivation and loss in multi-batch processes.
Main Methods:
- Co-immobilization of enzymes on cell surfaces and carrier-bound biofilms.
- Utilizing surface-displayed enzymes for continuous catalytic conversion.
- Testing the platform with pullulanase for substrate hydrolysis and resistant starch production.
Main Results:
- Achieved over 99% conversion rate for pullulan in 16 batches with pullulanase.
- Demonstrated a space-time hydrolysis rate of 20 fg/L/d.
- Successfully produced resistant starch type 3 from natural starch.
Conclusions:
- The novel co-immobilization platform enables efficient, continuous biocatalysis.
- This strategy offers a promising solution for overcoming multi-batch catalysis challenges.
- The platform is highly suitable for controlled environment biological catalysis.
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