A Lyt at the End of the Tunnel? Unraveling the complex interactions of the N-acetylglucosaminidase LytG in cell wall metabolism

Abstract

The growth and division of the Gram-positive cell requires the coordinated action of enzymes involved in the synthesis and degradation of the heteropolymer peptidoglycan. Herein, we present the use of the diamide masarimycin, an inhibitor of the exo-N-acetylglucosaminidase (GlcNAcase) LytG, as a chemical biology probe to elucidate biological role of this cell wall degrading enzyme. Using a combination of chemical biology and genetic approaches we provide the first evidence that LytG activity influences the elongation and division complexes in Bacillus subtilis. Chemical inhibition of LytG results in dysregulated cell elongation and localization of division plane and the induction of the cell wall stress response. In the presence of masarimycin, cells show asymmetrical thickening of the cell wall and dysregulation of division plane localization. The use of genetic and synergy/antagonism screens establishes connections to late-stage peptidoglycan synthesis, particularly related to cross-linking function. These results stand in stark contrast to those observed for the ΔlytG knockout, which does not exhibit these phenotypes. Cell wall labelling with a fluorescent D-amino acid and muropeptide analysis has highlighted a functional connection between LytG, the carboxypeptidase DacA, and D,D-endopeptidases. These results highlight the use of chemical probes such as masarimycin to inform on the biological function of autolysins through providing insight into the role LytG plays in cell growth and division.