| Dokumentenart: | Artikel | ||||
|---|---|---|---|---|---|
| Titel eines Journals oder einer Zeitschrift: | FEMS Microbiology Ecology | ||||
| Verlag: | ELSEVIER SCIENCE BV | ||||
| Ort der Veröffentlichung: | AMSTERDAM | ||||
| Band: | 36 | ||||
| Nummer des Zeitschriftenheftes oder des Kapitels: | 2-3 | ||||
| Seitenbereich: | S. 139-151 | ||||
| Datum: | 2001 | ||||
| Institutionen: | Biologie und Vorklinische Medizin > Institut für Biophysik und physikalische Biochemie | ||||
| Identifikationsnummer: |
| ||||
| Stichwörter / Keywords: | STRAND-CONFORMATION POLYMORPHISM; RIBOSOMAL-RNA GENES; GRADIENT GEL-ELECTROPHORESIS; MICROBIAL DIVERSITY; COMMUNITY ANALYSIS; EXTRACTION; POLYMERASE; BACTERIA; MICROORGANISMS; SEDIMENT; community analysis; diversity; soil; DNA; polymerase chain reaction-restriction fragment length polymorphism-single strand conformation; polymorphism | ||||
| Dewey-Dezimal-Klassifikation: | 500 Naturwissenschaften und Mathematik > 570 Biowissenschaften, Biologie | ||||
| Status: | Veröffentlicht | ||||
| Begutachtet: | Ja, diese Version wurde begutachtet | ||||
| An der Universität Regensburg entstanden: | Ja | ||||
| Dokumenten-ID: | 73566 |
Web of ScienceZusammenfassung
This study compared different methods of direct DNA extraction and purification Ft om a silt loam soil and investigated the relationship between DNA quantity and sequence diversity. Five extraction methods and four purification techniques were investigated. Quantities of DNA extracted were between 3.4 +/- 0.55 and 54.3 +/- 8.18 mug g(-1) (dry wt) of soil with OD260/OD230 purity ratios between ...
Zusammenfassung
This study compared different methods of direct DNA extraction and purification Ft om a silt loam soil and investigated the relationship between DNA quantity and sequence diversity. Five extraction methods and four purification techniques were investigated. Quantities of DNA extracted were between 3.4 +/- 0.55 and 54.3 +/- 8.18 mug g(-1) (dry wt) of soil with OD260/OD230 purity ratios between 0.80 and 1.15. Analysis of sequence diversity in all extracts was conducted using PCR-single strand conformation polymorphism (SSCP). Profiles generated using universal 16S rDNA primers (Com1/Com2) were found to be identical when used to amplify 16S rDNA extracted directly from soil. The genus Pseudomonas was targeted in order to reduce profile complexity. which was apparent when using universal 16S rDNA primers. and which hindered direct comparison of sequence diversity, A Pseudomonas culture library and non-cultured Pseudomonas 16S rDNA genes were used to provide a background count of Pseudomonas operational taxonomic units present in the soil. Cloning and sequencing of amplicons generated using a Pseudomonas-specific: (Ps-Tor) and a universal 16S rDNA (Com2) primer, coupled with nested amplification (Com1/Com2 amplification from Ps-for/Ps-rev amplicons), used in conjunction with SSCP. revealed that environmental contaminants co-extracted with DNA, such as humic acid, significantly reduced primer specificity. SSCP uas sensitive enough to reveal template bias in different primer sets. PCR-restriction Fragment length-SSCP of Pseudomonas 16S rDNA amplified from soil-extracted DNA revealed distinct differences in sequence representation between extraction methods and showed that greater DNA yield is not synonymous with higher sequence diversity. We, therefore, suggest that DNA extractions from soil should be evaluated not only in terms of quantity and purity, but also in terms of the sequence diversity present. SSCP proved to be a valuable tool for the assessment of the methodologies commonly used in PCR-mediated microbial ecology studies. (C) 2001 Federation of European Microbiological Societies, Published by Elsevier Science B.V. All rights reserved.
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