Skip to main content
. 2004 Sep;186(18):6050–6058. doi: 10.1128/JB.186.18.6050-6058.2004

FIG. 2.

FIG. 2.

Schematic representation of the mca inactivation in M. smegmatis and Southern analysis of mutants versus the parent strain, mc2155. (A) Site of disruption of the Ami37 mca mutant. (B) Southern analysis of BglII-digested genomic DNA from mc2155 (lane 3) and the mutants Ami37 (lane 2) and Ami40 (lane 1). Ten micrograms of DNA was loaded on the gel. The gel was hybridized with a probe for M. smegmatis mca that was PCR DIG-labeled using primers Pgint1082I-5′ and Pgint1082I-3′. The probe hybridized to a 6-kb BglII fragment in the parent strain. The disruption of mca in the mutants introduced a BglII site into the fragment which resulted in the probe hybridizing to two bands of 2 and 5 kb.