Glucosinolates
(GSLs), secondary metabolites synthesized by cruciferous
plants, can be hydrolyzed by myrosinase into compounds, such as isothiocyanates
(ITCs), with various bioactivities. Thus, myrosinase plays an important
role in the utilization of GSLs. We isolated a bacterial strain, which
was identified as Leclercia adecarboxylata, from
the rhizosphere soil of rape seedlings and identified two myrosinase
genes and an ITC hydrolase gene. Both myrosinases are intracellular
and have 658 amino acid residues. Via molecular docking and chemical
modification assays investigating the active sites of the myrosinases,
arginine was found to be essential for their catalytic activity. Transcriptomic
analysis of the response to sinigrin revealed significant up-regulation
of some genes involved in allyl-ITC detoxification, with metallo-β-lactamase
3836 having the highest fold change. Thus, we discovered two myrosinases
from L. adecarboxylata and demonstrated that the
mechanism of tolerance of the bacterium to allyl-ITC likely involved
metallo-β-lactamase activity.