Abstract
Colicin E-resistant mutants were isolated in E. coli K-12 which, although still apparently possessing the E receptor and adsorbing colicin, were nevertheless insensitive (refractory) to its effect. Eight phenotypic groups were obtained, but some mutants from three of these groups were all shown to map at gal, whereas a second refractory locus, giving resistance to El alone, mapped close to thy. It is suggested that the successful fixation of any of the three distinct colicins of group-E may involve a dual role for the cell surface "receptor," the first for the binding of the protein and the second for the correct orientation of the bound molecule relative to the cytoplasmic membrane. The majority of the refractory mutants isolated may derive from changes in components concerned with the second of these receptor functions. Two groups of mutants, however, refractory to only El or E2, probably reflect changes in the intra-cellular transmission systems which specifically mediate the effects of these two colicins, the changes not allowing transmission through the cytoplasmic membrane to the respective targets of the colicins. The El adsorption site was shown to be distinct from that for E2 and E3, indicating an early separation of the colicin E transmission systems.

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