A DNA-damaging agent, mitomycin C, derepresses the site-specific excision of two integrative and potentially conjugative elements from Streptococcus thermophilus, ICESt1 and ICESt3. The regulation pathway involves a repressor related to phage lambda cI repressor. It could also involve a putative regulator related to another type of phage repressors, the "cI-like" repressors.

Correction After the publication of this work [1], we became aware that the legends for Figures 2, 3 and 4 were not in the correct order. The legends should be as follows: Figure 2: Escherichia coli lambda lysogen DNA and average transcript levels after treatment with 10 J/m2 UV light. The x-axis is the position of genes on the E. coli chromosome. The E. coli origin is at the 0 position on the ...

Defects in the bacterial recB or recC or phage red or int gene did not impair ultraviolet light-induced clear mutations of lambda phage. Clear mutants of cI and cII genes were not enriched among RecA-promoted UV-induced recombinants between the N and O genes which closely encompass the c genes. No correlation was observed between UV-induced mutation and genetic recombination.

The temperate bacteriophages lambda and P22 share similarities in their site-specific recombination reactions. Both require phage-encoded integrase (Int) proteins for integrative recombination and excisionase (Xis) proteins for excision. These proteins bind to core-type, arm-type, and Xis binding sites to facilitate the reaction. lambda and P22 Xis proteins are both small proteins (lambda Xis, ...

In a thermosensitive dnaZ mutant lysogenic for lambda, induction of the prophage development was provoked at the restrictive temperature. In dnaD strain, spontaneous release of lambda proceeded even at 43 degrees C, but distinct induction of the prophage development was not caused by a heat treatment. Similarly, shift up of growth temperature did not lead to induction of lambda in lysogens carr...

Bacteriophage lambda is one of the most extensively studied organisms and has been a primary model for understanding basic modes of genetic regulation. Here, we examine the progress of lambda gene expression during phage development by ribosome profiling and, thereby, provide a very-high-resolution view of lambda gene expression. The known genes are expressed in a predictable fashion, authentic...

Tn5-tagged invasion plasmid DNA (pWR110) from Shigella flexneri serotype 5 (strain M90T) was cloned into the expression vector lambda gt11. Recombinant phage (lambda gt11Sfl) expressing pWR110-encoded polypeptide antigens were identified by using rabbit antisera directed against S. flexneri M90T invasion plasmid antigens. Antigens encoded by lambda gt11Sfl recombinant phage were characterized b...