The condition of an electroporation method was re-evaluated for the introduction of foreign plasmid DNA into Rhodococcus equi. The method is based on an electroporation of the bacteria made competent by culturing in a broth containing glycine and by heat shock at 50 degrees C. Transformation of R. equi could be achieved with a chloramphenicol-resistant shuttle vector originating from Rhodococcus fascians at an efficiency of about 10(4) transformants/mu g DNA. The bacteria were also shown to become competent when they were incubated with a chemical transformation buffer prior to washing with an electroporation buffer.
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Texas A&M Univ, Coll Vet Med, Dept Vet Pathobiol, College Stn, TX 77843 USATexas A&M Univ, Coll Vet Med, Dept Vet Pathobiol, College Stn, TX 77843 USA
Bryan, L. K.
Clark, S. D.
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Texas A&M Univ, Coll Vet Med, Dept Vet Pathobiol, College Stn, TX 77843 USATexas A&M Univ, Coll Vet Med, Dept Vet Pathobiol, College Stn, TX 77843 USA
Clark, S. D.
Diaz-Delgado, J.
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Texas A&M Univ, Coll Vet Med, Dept Vet Pathobiol, College Stn, TX 77843 USATexas A&M Univ, Coll Vet Med, Dept Vet Pathobiol, College Stn, TX 77843 USA
Diaz-Delgado, J.
Lawhon, S. D.
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Texas A&M Univ, Coll Vet Med, Dept Vet Pathobiol, College Stn, TX 77843 USATexas A&M Univ, Coll Vet Med, Dept Vet Pathobiol, College Stn, TX 77843 USA
Lawhon, S. D.
Edwards, J. F.
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Texas A&M Univ, Coll Vet Med, Dept Vet Pathobiol, College Stn, TX 77843 USATexas A&M Univ, Coll Vet Med, Dept Vet Pathobiol, College Stn, TX 77843 USA