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BODIPY-Glucosinolates for Rapid, High-throughput Screening Compatible Assays of Myrosinase

  • Yong Tang
  • , Yan Li
  • , Lingge Hu
  • , Fei Wang
  • , Li Qing Yu
  • , Hong Jiang*
  • , Xiaoyan Cui*
  • , Jingjing Wang*
  • , Ting Wang*
  • *Corresponding author for this work
  • East China Normal University
  • Ocean University of China
  • Hebei University
  • Tongji University
  • Shanghai Engineering Research Center of Topical Chinese Medicine

Research output: Contribution to journalArticlepeer-review

Abstract

The pursuit of high-performance myrosinase (MYR) systems for efficient production of bioactive isothiocyanates (ITCs) requires advanced enzymatic activity assays. Herein, we developed two dipyrromethene boron difluoride (BODIPY)-based fluorogenic probes for rapid and reliable monitoring of MYR activity. Upon hydrolysis by MYR, the probe BDP-GSL2 undergoes a specific cascade reaction involving glucosinolate (GSL) cleavage, Lossen rearrangement, and intermolecular cyclization, leading to a 110-fold fluorescence enhancement within 10 min at 37 °C or within 90 s at 50 °C. By BDP-GSL2, we demonstrated that Rmyr exhibited the highest catalytic efficiency among all tested microbial MYRs, both in vitro and in vivo. Furthermore, we established a high-throughput screening (HTS)-compatible, fluorescence-based method for rapid profiling of Pichia pastoris libraries expressing recombinant Rmyr. The ranking of top-performing clones from the HTS-compatible approach correlated well with results from glucose-based assays, validating the reliability of our method for identifying high-expressing clones.

Original languageEnglish
Pages (from-to)12504-12513
Number of pages10
JournalJournal of Agricultural and Food Chemistry
Volume74
Issue number15
DOIs
StatePublished - 22 Apr 2026

Keywords

  • enzyme assay
  • fluorescent probes
  • glucosinolate
  • HTS-compatible method
  • myrosinase

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