“…Liquid nitrogen is most commonly used for homogenization (Wu et al, 2001). Some researchers used dry ice (Griffin et al, 2002), SDS lysis (Syn and Swarup, 2000), high-speed cell disruption (Muller et al, 1998) and glass bead/magnetic bead-vortexing/SDS lysis (Sambrook and Russel, 2001;Faggi et al, 2005), lysozyme lysis/enzyme digestion (Flamm et al, 1984a,b;Li et al, 2002), benzyl chloride lysis (Xue et al, 2006), sonication (Sharma et al, 2007), microwave exposure (Goodwin and Lee, 1993) and combinations of different methods (Zhang et al, 2008). In each method, the major objective lies with elimination of PCR inhibitors (metallic cations, polysaccharide, polyphenols, and other secondary metabolites) in DNA samples which would otherwise prevent DNA amplification.…”