. In this communication we provide evidence that the recombination event is favored by phage infection. The entire nucleotide sequence of plasmid pAH90 was determined and found to contain 24 open reading frames (ORFs) responsible for phenotypes which include restriction-modification, phage adsorption inhibition, plasmid replication, cadmium resistance, cobalt transport, and conjugative mobilization. The cadmium resistance property, encoded by the cadA gene, which has an associated regulatory gene (cadC), is of particular interest, as it facilitated the selection of pAH90 in other phage-sensitive lactococci after electroporation. In addition, we report the identification of a group II selfsplicing intron bounded by two exons which have the capacity to encode a relaxase implicated in conjugation in gram-positive bacteria. The functionality of this intron was evident by demonstrating splicing in vivo. Given that pAH90 encodes potent phage defense systems which act at different stages in the phage lytic cycle, the linkage of these with a food-grade selectable marker on a replicon that can be mobilized among lactococci has significant potential for natural strain improvement for industrial dairy fermentations which are susceptible to phage inhibition.Lactococcus lactis is widely used as a starter bacterium for the manufacture of Cheddar cheese and other fermented products by the dairy industry (9) and for that reason has attracted intensive research over the last 20 years (1, 4, 27, 70). Lactococci normally contain a rich diversity of plasmids, many of which are responsible for key industrial traits including lactose catabolism, proteinase production, polysaccharide production, bacteriocin production and immunity, and bacteriophage resistance (11,19,20,21,28,39). Consequently, plasmid mobilization has formed the backbone of numerous strain enhancement regimens to facilitate the transfer of desirable properties into specific bacterial strains that can be employed in fermentations as starter cultures. The conjugal transfer of phage resistance plasmids to phage-sensitive dairy starters has been the focus of considerable research attention (7,23,33,47,51,56). These strategies are aimed at protecting lactococcal strains from the ever-present threat of phage infection during industrial dairy fermentations (16,33,44).Natural phage defense mechanisms such as adsorption inhibition (Ads), injection blocking, restriction/modification (R/ M), and abortive infection (Abi) systems are widespread in lactococci and can coexist and complement each other in cheese-making strains, helping prevent the infection and proliferation of phage (13, 47). However, there are limits to the extent to which natural (food-grade) strategies can be used to introduce and artificially stack phage resistance mechanisms within strains. This is principally because of the paucity of readily selectable markers for phage resistance plasmids, leading to difficulties in recognizing those genuine phage-resistant transconjugants which may arise (47). Antibiotic r...