Abstract

Polymerase chain reaction (PCR)-based applications in plant molecular biology and molecular diagnostics for plant pathogens require good quality DNA for reliable and reproducible results. Leaf tissue is often the choice for DNA extraction, but the use of other sources such as tubers, stems, or seeds, is not uncommon. The extraction of DNA from different tissue sources often requires different protocols. In this study, a simple protocol was established for the extraction of DNA from leaves, tubers, stems, seeds and even fungal mycelia. The protocol is simple and suitable for high-throughput DNA extraction using automated tissue grinders. It yielded large quantities of DNA (0.4 µg to 2 mg DNA from 100 mg tissue) of high quality from seeds of maize, soybean, and cowpea, tubers of yam, tuberous roots of cassava, and leaf tissues of banana and plantain, yam, cassava, maize, okra, mango, and other species. DNA was successfully used for the detection of fungal and viral pathogens and the genotyping of yam and cassava by PCR. 

Key words: DNA isolation, plant tissues, PCR amplification, pathogen detection, high throughput DNA extraction.

Abbreviation

 LTP, Low throughput; HTP, high throughput; DEB, DNA extraction buffer; PCR, polymerase chain reaction; ITS, internal transcribed spacer; BSV,Banana streak virus; ACMV, African cassava mosaic virus; EACMCV, East Africa cassava mosaic Cameroon virus; MSV, Maize streak virus; SSR, simple sequence repeat; PEG, polyethylene glycol.