Drug-resistance(r) determinants, r21(tet), r1(cml), and r11(str.sul), were obtained from R factors, and were capable of conferring resistance to tetracycline, chloramphenicol, and to both streptomycin and sulfanilamide, respectively. They were integrated into the chromosome ofEscherichia coli K12 and nontransmissible by conjugation.As described previously, the recombinant T-tet factor was formed and conjugally transmissible when E. coli K12 r(tet) + was infected with T95 one of the transfer factors. Similarly, the recombinants T-tet.cml and T-tet.str.sul factors were formed by the interaction between T-tet factor and resistance determinants r1(cml) and r11(str.snl), respectively. Subsequently, T-tet.cml.str.sul factor was formed by the recombination between T-tet.cml factor and r11(str.sul) determinant, and T-tet.str.sul.cml factor was produced by the infection of E. coli K12 r1(cml)+ with T-tet.str.sul factor. These recombinants were conjugally transmissible and transduced by phage P1 as one unit. These results strongly suggested the origin of R factors which were capable of conferring multiple resistance and transmissible by conjugation. According to the segregational patterns of resistance determinants by transduction and by conjugal transmission, the genetic structure of T-tet.cml.str.sul factors was established as being circular and the linkage order of the determinants of these factors was described.The resistance determinants in transductants were consistently segregated between a determinant governing tetracycline (TC) resistance and those responsible for resistance to chloramphenicol(CM), streptomycin(SM) and sulfanilamide(SA) in the transduction of R(TC.CM.SM.SA) factor in E group Salmonella with either bacteriophage epsilon [3] or P22 [25]. It was found that the TC resistance determinants, (tet) in transductants were all nontransferable by conjugation and not cured by treatment with acridine dyes [3]. The (tet) determinant in Salmonella was transferred to Escherichia coli K12 strain in cooperation with the F factor. The F+ (tet) conjugants were capable of transmitting their (tet) determinant by conjugation but the F-(tet) conjugants were not [4]. When E. coli strain carrying the nontransmissible (tet) determinant was infected with F, F', R or T factors, the recombinants F-tet, F'-tet, R-tet and T-tet factors were formed [5,7,11,12,18]. These results strongly suggested. that R factors originated from the formation of recombinants between otherwise nontransmissible resistance(r) determinants and sex factors. This paper deals with the formation of recombinant T-r factors resulting in the formation of multiple resistance factors.