Transposon Tn916 mutagenesis in Clostridium botulinum.
AUTOR(ES)
Lin, W J
RESUMO
The study of toxinogenesis and other properties in Clostridium botulinum is limited by the absence of genetic methods that enable construction of defined mutants. In this study, tetracycline-resistant transposon Tn916 in Enterococcus faecalis was conjugatively transferred in filter matings to group I Clostridium botulinum strains Hall A and 113B. The Tn916 transfer frequencies to C. botulinum ranged from 10(-8) to 10(-5) Tcr transconjugant per recipient depending on the donor strain. Southern blot analyses of EcoRI or HindIII chromosomal digests extracted from randomly selected Tcr transconjugants showed that the transposon inserted at different sites in the recipient chromosome, and the copy number of Tn916 varied from one to three. Tn916 insertion gave several different auxotrophic mutants. This approach should be useful for the study of genes important in growth, survival, and toxinogenesis in C. botulinum.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=183902Documentos Relacionados
- Transposon Tn916 mutagenesis in Bacillus anthracis.
- Excision of the Conjugative Transposon Tn916 in Lactococcus lactis
- Location of sites of transposon Tn916 insertion in the Mycoplasma mycoides genome.
- Conjugal transfer of transposon Tn916 from Streptococcus faecalis to Mycoplasma hominis.
- Introduction of transposon Tn916 DNA into Haemophilus influenzae and Haemophilus parainfluenzae.