Streptococcus mutans GS-5 was transformed with the Escherichia coli plasmid pAM150 containing the cloned streptococcal transposon Tn916. Southern blot analyses with the tetracycline-resistant determinant of Tn916 showed that Tn916 was inserted into the chromosome of S. mutans at a variety of different sites. Tn916 insertions resulted in the inactivation of genes that code for various steps in the biosynthesis of several different amino acids. Two auxotrophs which contained a single copy of Tn916 were shown to revert to prototrophy at frequencies of about 10(-8). All of the revertant prototrophs were susceptible to tetracycline, indicating regeneration of the functional gene by excision of Tn916
Procino, J.K., Marri, L., Shockman, G.D., DANEO-MOORE, L. (1988). Tn916 insertional inactivation of multiple genes on the chromosome of Streptococcus mutans. INFECTION AND IMMUNITY, 56(11), 2866-2870 [10.1128/iai.56.11.2866-2870.1988].
Tn916 insertional inactivation of multiple genes on the chromosome of Streptococcus mutans
MARRI L.;
1988-01-01
Abstract
Streptococcus mutans GS-5 was transformed with the Escherichia coli plasmid pAM150 containing the cloned streptococcal transposon Tn916. Southern blot analyses with the tetracycline-resistant determinant of Tn916 showed that Tn916 was inserted into the chromosome of S. mutans at a variety of different sites. Tn916 insertions resulted in the inactivation of genes that code for various steps in the biosynthesis of several different amino acids. Two auxotrophs which contained a single copy of Tn916 were shown to revert to prototrophy at frequencies of about 10(-8). All of the revertant prototrophs were susceptible to tetracycline, indicating regeneration of the functional gene by excision of Tn916| File | Dimensione | Formato | |
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https://hdl.handle.net/11365/8416
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