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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Bibliografiske detaljer

Udgivet i:	J Bacteriol
Principais autores:	Duwat, P, Ehrlich, S D, Gruss, A
Format:	Artigo
Sprog:	Inglês
Udgivet:	American Society for Microbiology (ASM) 1992
Fag:	Research Article
Online adgang:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC206342/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1629178/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/jb.174.15.5171-5175.1992
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