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. Author manuscript; available in PMC: 2022 Jul 21.
Published in final edited form as: Dev Comp Immunol. 2014 Feb 6;45(1):1–9. doi: 10.1016/j.dci.2014.01.017

Fig. 5.

Fig. 5.

Hydrolysis of PGs by BmPGRP-S5 or lysozyme. Insoluble PGs from B. megaterium, B. subtilis, E. coli, S. aureus, and M. luteus were separately incubated with buffer (i.e., control), BmPGRP-S5 (with or without Zn2+), or lysozyme. Light scattering at 405 nm was monitored for 8 h. Asterisks indicate significant differences: *p < 0.05; **p < 0.01; ***p < 0.001 for pairwise comparisons by Student’s t-tests. ns, not significant.