A genetic analysis of Escherichia coli P6, a large-cell, radiation-resistant strain of E. coli, established that it originated as the result of a mutational event. The gene responsible for the complex P6 phenotype was located at 61 i 0.5 min on the E. coli linkage map. The close resemblance of conjugal and transductional recombinants to one or the other parent without indication of an intermediate class suggests that only a single gene may be involved. Escherichia coli P6 was isolated by Ogg and Zelle (16) after camphor treatment of E. coli 82/r, an adenine-dependent derivative of E. coli B/r. P6 cells were larger, weighed about three times more, contained approximately three times more deoxyribonucleic acid (DNA) and ribonucleic acid (RNA), and were more resistant to X-rays than the parent (16, 21). Preliminary genetic experiments (F+ X F-crosses) showed that colonial morphology, cell size, radiation resistance, and an unselected property, Ti resistance, segregated as a unit (21). These results suggested that a pleiotrophic mutation was responsible for the complex phenotype of P6. The results of experiments designed to establisht the genetic constitution of E. coli P6 are reported here. Using both conjugation and transduction techniques, we mapped the P6 gene, lar-J, at 61 + 0.5 min on the E. coli linkage map. Recombinants characterized in terms of the properties originally used to describe the two parental strains resembled either one or the other parent. There were no indications of intermediate-type recombinants. Thus, the complex phenotype of E. coli P6 appears to be due to the mutation of a single gene. MATERIALS AND METHODS Symbols. The recommendations of Demerec et al. (6) with regard to genotypic and phenotypic designa-I Part of a thesis submitted by the senior author in partial fulfillment of the requirements for the Ph.D. degree,