In plasmolyzed Escherichia coli, wall and membrane adhered to one another at 200 to 400 localized areas. This number of specialized wall areas per cell was of the same order of magnitude as the total number of bacteriophage receptors. When bacteriophages TI to T7 were adsorbed to the bacteria, they were seen to attach almost exclusively to these areas. Comparisons of the number of adsorbed phage particles observed in ultrathin sections and the expected number of phages per cell were in agreement. These results suggest a sharing of receptive areas by the various phages. Adsorption to the wall-membrane associations would permit the virus to release its nucleic acid at an area closest to the cell's protoplasmic contents. After the electron microscopic description of bacteriophage particles by Ruska (23), Luria and Anderson (17), and Luria, Delbruck, and Anderson (19), the mode of virus adsorption to surfaces of susceptible cells could be studied successfully: Anderson (2) clearly demonstrated that bacteriophages Ti and T5 adsorbed to their host cells with the tips of their tails. T-even bacteriophage adsorption involves the specific attachment of tail fibers to the bacterial receptor (13, 26, 32, 33), followed by changes in their contractile tail sheaths and baseplates (3, 14, 26, 27). However, the mode of attachment of other phage types, like T3 and T7, is still unknown (18). Extracts from bacterial envelopes contain receptor activity and function as competitive inhibitors for virus attachment to bacterial host cells (6, 16, 31). Frank, Zarnitz, and Weidel (8) showed that the deoxyribonucleic acid (DNA) of bacteriophage T5 is ejected through the tip of the tail when the particles react with receptor prepara