| Literature DB >> 27033829 |
Mete Yilmaz1, Edward J Phlips1, Daniel Tillett1.
Abstract
DNA isolated from environmental samples often contains enzyme inhibitors disruptive to downstream molecular applications. Most of the existing methods of cyanobacterial DNA isolation do not effectively eliminate these inhibitors from sediment samples or cells collected from freshwater ecosystems. We describe improved methods based on the xanthogenate-SDS nucleic acid isolation (XS) method of Tillett and Neilan (2000). Our improved methods provided high-quality cyanobacterial DNA that could be amplified in PCR and digested with a restriction enzyme. Results were superior to several commercial kits. The DNA yield was also similar to that obtained via the standard XS method. These methods should provide valuable new tools for the expanded application of molecular genetics to limnological and oceanographic research.Entities:
Keywords: DNA; PEG; PVPP; cyanobacteria; fluorometry; humics; lake water; microcystin; sediment; xanthogenate
Year: 2009 PMID: 27033829 DOI: 10.1111/j.1529-8817.2009.00651.x
Source DB: PubMed Journal: J Phycol ISSN: 0022-3646 Impact factor: 2.923