Recombineering is a highly e cient DNA cloning and modi cation technique by using the recombinasemediated homologous recombination. Selection/counterselection cassette is often used in chromosomal DNA or large episomal DNA manipulation, in which the selection marker is used for the rst step cassette selection, while the counterselection marker is used for the second step replacement of the cassette by the target gene. A variety of selection/counterselection cassettes are reported, however, they suffer from the shortcomings of the requirement of pre-engineered strain or speci c culture medium. Herein, we report a novel S-tetR-ptetA-ccdB-aacC1-S selection/counterselection cassette that sidesteps the shortcomings. As a proof-of-concept, one-step gene cloning (0.7 kb, 1.7 kb, and 4.2 kb) and two-step Escherichia coli chromosomal gene knock-in (0.7 kb and 4.2 kb) were performed. The gene cloning and gene knock-in e ciencies are high up to 90%. The cassette adds a powerful tool to the recombineering repertoire.