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An effective method to extract DNA from environmental samples for polymerase chain reaction amplification and DNA fingerprint analysis

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Abstract

A rapid direct-extraction method was used to obtain DNA from environmental soil samples. Heat, enzymes, and guanidine isothiocyanate were utilized to lyse cells. The DNA was purified by agarose gel electrophoresis, amplified with 16S rRNA-based primers by use of the polymerase chain reaction, and then digested with the restriction endonucleasePalI. The extraction method was used to obtain DNA from a variety of plants, bacteria, and fungi includingGossypium hirsucum (cotton),Pseudomonas, Bacillus, Streptomyces, andColletotrichum. Up to 100 μg DNA/g (wet weight) of soil and 400 μg DNA/g of plant material were recovered. Restriction endonuclease analysis patterns of amplified rDNA from pure microbial cultures and plant species contained three to five different DNA fragments. Amplified rDNA of mixed population DNA extracts from soil samples, digested with the restriction endonucleasePalI, contained 12–20 DNA fragments, appearing as sample “fingerprints.” Results from eight environmental soil samples that were analyzed suggest that the amplified rDNA fingerprints can be used to help characterize the genetic and biological diversity of the microbial populations in these samples.

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Authors and Affiliations

  1. Biotechnology Program, United States Environmental Protection Agency, Environmental Research Laboratory, 200 S.W. 35th Street, 97333, Corvallis, OR, USA

    L. Arlene Porteous, John L. Armstrong, Ramon J. Seidler & Lidia S. Watrud

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  1. L. Arlene Porteous
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  2. John L. Armstrong
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  3. Ramon J. Seidler
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  4. Lidia S. Watrud
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Porteous, L.A., Armstrong, J.L., Seidler, R.J. et al. An effective method to extract DNA from environmental samples for polymerase chain reaction amplification and DNA fingerprint analysis. Current Microbiology 29, 301–307 (1994). https://doi.org/10.1007/BF01577445

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