Nucleotide sequence of the Porphyromonas gingivalis W83 recA homolog and construction of a recA-deficient mutant.

Degenerate oligonucleotide primers were used in PCR to amplify a region of the recA homolog from Porphyromonas gingivalis W83. The resulting PCR fragment was used as a probe to identify a recombinant lambda DASH phage (L10) carrying the P. gingivalis recA homolog. The recA homolog was localized to a...

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Библиографические подробности

Опубликовано в::	Infect Immun
Главные авторы:	Fletcher, H M, Morgan, R M, Macrina, F L
Формат:	Artigo
Язык:	Inglês
Опубликовано:	American Society for Microbiology (ASM) 1997
Предметы:	Research Article
Online-ссылка:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC175659/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9353038/ https://ncbi.nlm.nih.govhttps://doi.org/10.1128/iai.65.11.4592-4597.1997
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