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. 2005 Sep;187(17):6238–6241. doi: 10.1128/JB.187.17.6238-6241.2005

FIG. 2.

FIG. 2.

Immunodetection of the LytC lysozyme in the cell envelope of the TIGR4 strain. (A) Western blot analysis of cell extracts prepared from the following strains (indicated at the top): M31 (ΔlytA), M31C (ΔlytA lytC::ermC), R6 (wild type), R6C (R6 but lytC::ermC), TIGR4 (capsular serotype 4 strain), and P036 (TIGR4 but lytC::tet). The Mrs of the size standards (S) are indicated on the left. (B) The double-immunodiffusion experiment was performed on an agarose-coated microscope slide with anti-LytC antiserum in the center well (7) and cell envelope preparations from M31, P026 (TIGR4 but lytA::kan), P031 (TIGR4 but lytA::kan lytC::tet), and M31C in wells 1, 2, 3, and 6, respectively. In wells 4 and 5, phosphate-buffered saline and 1 μg of pure LytC, respectively, were used.