A Comparison of Genomic DNA Extraction Protocols in Artemisia annuaL. for Large Scale Genetic Analyses Studies

Artemisia anuuaL. is an important economic medicinal plant well known for its bioactive compound artemisinin that is used as an antimalarial drug. Extraction of high-quality genomic DNA suitable for restriction enzyme reactions and PCR amplifications is very difficult due to the presence of high amounts of secondary metabolites in A. anuua. This study compared efficiency of Fermentas genomic DNA purification kit (FGDK), phenol–Chloroform, cetyltrimethyl ammonium bromide (CTAB), sodium dodecyl sulfate and Sarkosyl nitrogen methods for extraction of DNA. The quality and quantity DNA samples were determined by physical appearance, agarose gel electrophoresis, spectrophotometer and PCR amplifications. The study used Inter retrotransposon amplified polymorphism (IRAP), retrotransposon-microsatellite amplified polymorphism (REMAP) and start codon targeted-based primers. The results revealed that genomic DNA isolated by CTAB method was comparatively pure and produced clear polymorphic bands compared to the polymorphic bands noted on DNA extractions using other protocols.