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Previous attempts to introduce transposon Tn4001 intoMycoplasma pulmonis andMycoplasma arthritidis have not been successful, possibly due to functional failure of the transposon's gentamicin resistance determinant. Tn4001C and Tn4001T were constructed, respectively, by insertion of a chloramphenicol acetyltransferase gene and thetetM tetracycline resistance determinant into Tn4001 . Both Tn4001C and Tn4001T transposed inM. pulmonis , and Tn4001T transposed inM. arthritidis . The incorporation of a Tn4001T derivative that containedlacZ into eitherMycoplasma species resulted in transformants with readily detectable LacZ activity. Tn4001T may be of general utility for use as a mycoplasma cloning vehicle becausetetM functions in all species ofMycoplasma examined thus far.

Construction and Use of Derivatives of Transposon Tn 4001 That Function in Mycoplasma pulmonis and Mycoplasma arthritidis