Old Enzyme, New Role: The β-Glucosidase BglC of <i>Streptomyces scabiei</i> Interferes with the Plant Defense Mechanism by Hydrolyzing Scopolin
2021
Benoit Deflandre | Sébastien Rigali
The beta-glucosidase BglC fulfills multiple functions in both primary metabolism and induction of pathogenicity of <i>Streptomyces scabiei</i>, the causative agent of common scab in root and tuber crops. Indeed, this enzyme hydrolyzes cellobiose and cellotriose to feed glycolysis with glucose directly and modifies the intracellular concentration of these cello-oligosaccharides, which are the virulence elicitors. The inactivation of <i>bglC</i> led to unexpected phenotypes such as the constitutive overproduction of thaxtomin A, the main virulence determinant of <i>S</i>. <i>scabiei</i>. In this work, we reveal a new target substrate of BglC, the phytoalexin scopolin. Removal of the glucose moiety of scopolin generates scopoletin, a potent inhibitor of thaxtomin A production. The hydrolysis of scopolin by BglC displayed substrate inhibition kinetics, which contrasts with the typical Michaelis–Menten saturation curve previously observed for the degradation of its natural substrate cellobiose. Our work, therefore, reveals that BglC targets both cello-oligosaccharide elicitors emanating from the hosts of <i>S. scabiei</i>, and the scopolin phytoalexin generated by the host defense mechanisms, thereby occupying a key position to fine-tune the production of the main virulence determinant thaxtomin A.
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