Rapid isolation of DNA from dry and fresh samples of plants producing large amounts of secondary metabolites and essential oils

Khanuja, Suman P. S. ; Shasany, Ajit K. ; Darokar, M. P. ; Sushil Kumar, (1999) Rapid isolation of DNA from dry and fresh samples of plants producing large amounts of secondary metabolites and essential oils Plant Molecular Biology Reporter, 17 (1). 74_1-74_7. ISSN 0735-9640

Full text not available from this repository.

Official URL: http://www.springerlink.com/content/rl306335590uh2...

Related URL: http://dx.doi.org/10.1023/A:1007528101452

Abstract

The presence of certain metabolites has been observed to interfere with DNA isolation procedures and downstream reactions such as DNA restriction, amplification and cloning. The chemotypic heterogeneity among species may not permit optimal DNA yields with a single protocol, and thus, even closely related species may require different isolation protocols. Here we describe the essential steps of a rapid DNA isolation protocol that can be used for diverse medicinal and aromatic plants, which produce essential oils and secondary metabolites such as alkaloids, flavanoids, phenols, gummy polysaccharides, terpenes and quinones. The procedure is applicable to dry as well as fresh plant tissues. This protocol, in our experiments, permitted isolation of DNA from tissues of diverse plant species and produced fairly good yields. The isolated DNA proved amenable to PCR amplification and restriction digestion.

Item Type:Article
Source:Copyright of this article belongs to Springer.
Keywords:DNA Isolation; Dry Samples; Essential Oil; PCR Amplification; Secondary Metabolites
ID Code:52119
Deposited On:02 Aug 2011 07:48
Last Modified:02 Aug 2011 07:48

Repository Staff Only: item control page