Abstract
Previous attempts to introduce transposon Tn4001 into Mycoplasma pulmonis and Mycoplasma 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 the tetM tetracycline resistance determinant into Tn4001. Both Tn4001C and Tn4001T transposed in M. pulmonis, and Tn4001T transposed in M. arthritidis. The incorporation of a Tn4001T derivative that contained lacZ into either Mycoplasma species resulted in transformants with readily detectable LacZ activity. Tn4001T may be of general utility for use as a mycoplasma cloning vehicle because tetM functions in all species of Mycoplasma examined thus far.
MeSH Terms
Chloramphenicol O-Acetyltransferase/genetics
Cloning, Molecular
DNA Transposable Elements/genetics
Drug Resistance, Microbial/genetics
Electrophoresis, Polyacrylamide Gel
Genetic Vectors
Gentamicins
Lac Operon
Molecular Sequence Data
Mycoplasma/genetics
Tetracycline
Chemicals
DNA Transposable Elements
Gentamicins
Chloramphenicol O-Acetyltransferase
Tetracycline
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Dybvig K
Department of Comparative Medicine, University of Alabama at Birmingham, Birmingham, Alabama 35294, USA.
[email protected]
French C T
Voelker L L
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