Potential risks of gene amplification by PCR as determined by 16S rDNA analysis of a mixed-culture of strict barophilic bacteria

Microbial Ecology

Volumn 21, Issue 1, 1991, Pages 191-198

  Liesack, W ^a   Weyland, H ^b   Stackebrandt, E ^a  

^a UNIVERSITY OF QUEENSLAND   (Australia)

^b ALFRED WEGENER INSTITUTE FOR POLAR AND MARINE RESEARCH   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 51249171800     PISSN: 00953628     EISSN: 1432184X     Source Type: Journal    
DOI: 10.1007/BF02539153     Document Type: Article

References (23)

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4. Genetic diversity in Sargasso Sea bacterioplankton
5. Conservation of primary structure at 3′ end of 18S rRNA from eucaryotic cells
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8. Approaches for the molecular identification of streptomycetes in marine environment
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11. DNA recombination during PCR
12. Compilation of small ribosomal subunit RNA sequences
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14. Development and application of oligonucleotide probes for molecular identification of Xenorhabdus species
15. Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase
16. Additive similarity trees
17. Recovery of DNA from soils and sediments
18. Nucleotide sequence of the 16S rRNA from Vibrio anguillarum
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21. Barophilic and psychrophilic bacteria in the Antarctic Ocean