| Literature DB >> 6752128 |
Abstract
Salmonella phage P22 was utilized as a vector for phage Mu cts d1(Apr lac) mutagenesis in Salmonella typhimurium. Efficient transposition of phage Mu d1 and the construction of gene fusions were readily accomplished with this procedure. Mutants blocked in the biosynthesis of NAD+ and in pyridine nucleotide cycle metabolism were isolated by this method, resulting in nadB-lac, nadC-lac, and pncB-lac gene fusions.Entities:
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Year: 1982 PMID: 6752128 PMCID: PMC221562 DOI: 10.1128/jb.152.2.959-962.1982
Source DB: PubMed Journal: J Bacteriol ISSN: 0021-9193 Impact factor: 3.490