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A general method for cloning recA genes of gram-positive bacteria by polymerase chain reaction.
An internal fragment of the recA gene from eight gram-positive organisms has been amplified by using degenerate primers in a polymerase chain reaction. The internal 348- or 360-bp recA DNA segments from Bacillus subtilis, Clostridium acetobutylicum, Lactobacillus bulgaricus, Lactobacillus helveticus...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | en |
| Publicado: |
1992
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC206342/ https://ncbi.nlm.nih.gov/pubmed/1629178 |
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