The genetic manipulation of marine double-stranded DNA (dsDNA) bacteriophage PM2 (Corticoviridae) has been limited so far. The isolation of an autonomously replicating DNA element of Pseudoalteromonas haloplanktis TAC125 and construction of a shuttle vector replicating in both Escherichia coli and Pseudoalteromonas enabled us to design a set of conjugative shuttle plasmids encoding tRNA suppressors for amber mutations. Using a host strain carrying a suppressor plasmid allows the introduction and analysis of nonsense mutations in PM2. Here, we describe the isolation and characterization of a suppressor-sensitive PM2 sus2 mutant deficient in the structural protein P10. To infect and replicate, PM2 delivers its 10-kbp genome across the cell envelopes of two gram-negative Pseudoalteromonas species. The events leading to the internalization of the circular supercoiled dsDNA are puzzling. In a poorly understood process that follows receptor recognition, the virion capsid disassembles and the internal membrane fuses with the host outer membrane. While beginning to unravel the mechanism of this process, we found that protein P10 plays an essential role in the host cell penetration.The study of membrane-containing bacteriophages has produced notable knowledge of the assembly and structure of biological membranes and virus structures (18, 32). The availability of genetic tools has been valuable in the study of many bacterial viruses with a membrane (36, 37). The understanding of these sophisticated virus systems has relied on the isolation and analysis of phage mutants. A recent example of this is the X-ray crystallography structure of the membrane-containing phage PRD1, which was solved using a nonsense mutant particle, Sus539, lacking the receptor binding protein P2 (1, 8). Moreover, suppressor-sensitive mutants of PRD1 have been valuable in assigning functions to viral proteins. Recently, we initiated the structural characterization of bacteriophage PM2 as a new model system (2, 19;