Abstract
A quantitative assay for the N protein of bacteriophage lambda has been used to study the in vivo regulation of N gene expression. The assay makes use of the observation that in a cell-free protein-synthesizing system from Escherichia coli programmed with lambdaN(-) DNA the lambda endolysin is made only if N protein is added to the reaction. The rate of synthesis of N protein in vivo is negatively controlled by the products of the CI and tof genes of the phage. Furthermore, N protein activity is extremely unstable in vivo. During normal cell growth at 35 degrees , the half-life of N protein is about 2 min.
MeSH Terms
Cell-Free System
Chromosome Mapping
Coliphages/enzymology,metabolism
Endopeptidases/analysis,biosynthesis
Escherichia coli
Genes
Genes, Regulator
Kinetics
Lysogeny
Temperature
Transcription, Genetic
Viral Proteins/analysis,biosynthesis,metabolism
Chemicals
Viral Proteins
Endopeptidases
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Greenblatt J
References (25)
25 references, click to expand
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