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Direct detection of Kitasatospora species with a chaperone oligonucleotide microarray method lacking PCR amplification
Authors:Guenther Sebastian  Groth Ingrid  Schierack Peter  Grabley Susanne  Munder Thomas
Affiliation:1. Leibniz Institute for Natural Product Research and Infection Biology – Hans‐Kn?ll‐Institute, Jena, Germany;2. Fachhochschule Lausitz, Fachbereich Bio‐, Chemie‐ und Verfahrenstechnik, Senftenberg, Germany;3. CLONDIAG, Jena, Germany
Abstract:Identification of members of the genus Kitasatospora from soil samples has been introduced to evaluate occurrence of potential natural compound producers in different habitats. The microarray hybridization usually involves PCR amplification of the target DNA. Since PCR might lead to biased amplification, a diagnostic Kitasatospora microarray technique was improved by a protocol lacking PCR amplification prior to hybridization. The described advanced hybridization method used chaperone oligonucleotides for direct co-hybridization with genomic DNA on an oligonuclotide microarray with optical readout. ((c) 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim).
Keywords:Chaperone oligonucleotide microarray  16S−23S internal transcribed spacer  Kitasatospora
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