PCR master mix used in this study contains containing 2.5 μl of 10X Taq DNA polymerase (containing 100mM Tris
with pH 9.0, 500mM KCl, 15mM MgCl2 and 1% Triton X-100), 2.0 μl of 25mM of MgCl2, 1 μl of 10mM dNTP mix,
2 μl of each forward and reverse primer (4pmol/ μl) and 0.9 U/ μl of Taq DNA polymerase which was made up to 20
μl using molecular grade water. Then, this master mix was distributed to the PCR tubes and finally 5 μl of bacterial
lysate was added as template. Amplification was done following the conditions shown in Table.2.