Sample processing effect on polymerase chain reaction used for identification of Campylobacter jejuni
Model samples of Campylobacter jejuni for polymerase chain reaction (PCR) were prepared by rapid and simple procedures consisting of centrifugation, proteinase K treatment, Chelex 100 treatment, and boiling lyses. A PCR based on specific amplification of the variable sequence of 16S rRNA gene was pe...
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Published in: | Folia microbiologica Vol. 49; no. 6; pp. 693 - 697 |
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Main Authors: | , , |
Format: | Journal Article |
Language: | English |
Published: |
United States
2004
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Subjects: | |
Online Access: | Get full text |
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Summary: | Model samples of Campylobacter jejuni for polymerase chain reaction (PCR) were prepared by rapid and simple procedures consisting of centrifugation, proteinase K treatment, Chelex 100 treatment, and boiling lyses. A PCR based on specific amplification of the variable sequence of 16S rRNA gene was performed using Tth DNA polymerase and the PCR products were visualized by agarose gel electrophoresis. The assay allowed the detection of 10 CFU/mL C. jejuni in the physiological saline and 100 CFU/mL in the basic Park and Sanders broth. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0015-5632 |
DOI: | 10.1007/BF02931551 |