Author/Authors :
Wangsomnuk, Preeya P. Department of Biology - Faculty of Science - Khon Kaen University, Khon Kaen, Thailand , Rittithum, Wipavadee Department of Biology - Faculty of Science - Khon Kaen University, Khon Kaen, Thailand , Ruttawat, Benjawan Department of Biology - Faculty of Science - Khon Kaen University, Khon Kaen, Thailand , Wangsomnuk, Pinich Department of Biology - Faculty of Science - Khon Kaen University, Khon Kaen, Thailand
Abstract :
Rubber tree is the main source of natural rubber and is the most important economic member
of the Hevea genus. Polysaccharides and polyphenols in mature leaf can reduce the success of DNA
extraction and downstream applications. This makes the isolation of high quality and molecular weight
DNA from mature leaves of rubber tree challenging. The DNA yield and purity obtained using eight
methods involving use of cetyltrimethylammonium bromide, SDS, and two commercial kits were
compared. The modified procedure from Moreira & Oliveira (2011) consistently yields approximately 34 μg
of high-quality amplifiable DNA with as little as 0.05 g fresh weight of mature leaf tissue of rubber tree.
The key changes in the procedure were (1) a short grinding of leaf powder in mortar with extraction
buffer after blending the leaf tissue in the presence of liquid nitrogen; (2) the optimization of the ratio of
tissue (weight) to buffer (volume); (3) CTAB was added only once and (4) reduction in the incubation
time of the macerated tissue in an extraction buffer including RNase A at 65 °C for 15 minutes. The
procedure was also applicable to seventeen other tropical plant species. This helped to avoid the
limitation of plant materials and could provide total DNA for further molecular studies.
Keywords :
DNA extraction , mature leaf , Hevea genus , 18S rRNA , trnL-F , ISSR , RAPD