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May 15, 2026Bioresources and Bioprocessing1 citationsOpen Access

Proximity-enhanced co-immobilized enzyme cascade for efficient bioconversion of nicotine to 3-succinoylpyridine

YWY Q WangJZJiandong ZhangHYHongjing Yang

Key Points

  • The study aims to enhance the conversion of nicotine into 3-succinoylpyridine using a co-immobilized enzyme system.
  • Utilized a SpyCatcher/SpyTag enzyme scaffold for cofactor regeneration and enzyme co-immobilization.
  • Implemented AviTag-BirA-mediated biotinylation on streptavidin-coated supports.
  • Evaluated the conversion efficiency and stability of the enzyme system over multiple reuse cycles.
  • Achieved a nicotine-to-SP conversion rate of approximately 63%, significantly higher than the 42.7% from free enzymes.
  • Demonstrated over 60% retention of initial activity after eight reuse cycles.
  • Showed improved pH and thermal stability in the co-immobilized enzyme system.

Abstract

regeneration. To improve nicotine-to-SP conversion and facilitate multi-enzyme recycling, a SpyCatcher/SpyTag self-assembled cofactor regeneration enzyme scaffold was adopted, in conjunction with AviTag-BirA-mediated biotinylation for cascade enzyme site-specific co-immobilization on streptavidin-coated supports. This proximity-enhanced design promoted efficient cofactor cycling and boosted the nicotine-to-SP conversion to approximately 63%, much higher than the 42.7% achieved by free enzymes. The co-immobilized system also showed improved pH and thermal stability, retaining over 60% of its initial activity after eight reuse cycles. This modular biocatalytic strategy provides a green and promising route for the valorization of nicotine-rich tobacco waste.

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Cite This Study

Wang et al. (2026) studied this question.

synapsesocial.com/papers/6a06b998e7dec685947ac5cahttps://doi.org/10.1186/s40643-026-01066-9
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