A temperate bacteriophage, designated rlt, was inducible from the group N lactic streptococcus, Streptococcus cremoris R,, by ultraviolet irradiation or mitomycin C treatment. Induced lysates produced plaques on lawns of three closely related S. cremoris strains, AM1, SK11, and US3. Strain SK11 was readily lysogenized. S. cremoris AM1 was the most reliable indicator strain, although the age of the culture used for seeding plates was critical. Zones of lysis but no plaque formation were observed on lawns of nine additional S. cremoris strains. Phage r1t could not be detected in filtrates of stationary-phase R, cultures and was near the limits of detection in logarithmically growing cultures. Phage levels were still very low (1 plaque-forming unit on AM1 per 10 induced cells) in induced lysates of R1 cultures. These low levels of detectable phage may be attributable to an inadequate indicator, lysogenization of the indicator, adsorption of induced phage to cellular debris, concurrent induction of other undetectable phages, or the production of high proportions of defective phages. Electron micrographs of induced R, lysates revealed a high incidence of incomplete phage particles, fragments, and ghosts. MATERIALS AND METHODS Streptococcal strains. All of the cultures used in this study were cheese starter strains of S. lactis and S. cremoris from the collection of the New Zealand Dairy Research Institute. Bacteriophages. Temperate bacteriophage, designated rlt, was isolated from UV-induced lysates of S. cremoris R1. The virulent bacteriophages, rlv (NZDRI 652), am, (NZDRI 601), and sk,, (NZDRI 690), were drawn from the New Zealand Dairy Research Institute collection. Media and growth of cultures. M16 broth and M16 agar were prepared as previously described (8). Streptococci were grown routinely at 22 or 30 C, without shaking, in M16 broth from a 2% inoculum of an overnight (22 C, 16 h) broth culture. Optical density. Optical density (OD) of cultures was measured in a Bausch and Lomb Spectronic 20 colorimeter. An OD value of 0.2 at 580 nm represented approximately 108 colony-forming units (CFU)/ml. Colony counts. Samples were first diluted with 210