芥子酶
化学
硫代葡萄糖苷
生物化学
重组DNA
体外
酶
体外毒理学
水解
组合化学
色谱法
高通量筛选
突变
荧光
水解酶
黄蛋白
丝氨酸
活动站点
生物测定
催化作用
酶水解
作者
Yong Tang,Yong Li,Lingge Hu,Fei Wang,Li-Qing Yu,Hong Jiang,Xiaoyan Cui,Jianjun Wang,Ting Wang
标识
DOI:10.1021/acs.jafc.6c00088
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI