Products/Services Used | Details | Operation |
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Codon Optimization | The cd11 gene was synthesized with codons optimized for Escherichia coli expression, and was cloned into the plasmid pGS21a between Nde I and Xho I restr iction sites with a C-terminal His-tag sequence (Genscript, NJ). | Get A Quote |
Bacterial lysins are potent antibacterial enzymes with potential applications in the treatment of bacterial infections. Some lysins lose activity in the growth media of target bacteria, and the underlying mechanism remains unclear. Here we use CD11, an autolysin of Clostridium difficile, as a model lysin to demonstrate that the inability of this enzyme to kill C. difficile in growth medium is not associated with inhibition of the enzyme activity by medium, or the modification of the cell wall peptidoglycan. Rather, wall teichoic acids (WTAs) appear to prevent the enzyme from binding to the cells and cleaving the cell wall peptidoglycan. By partially blocking the biosynthetic pathway of WTAs with tunicamycin, ce... More