Affiliation:
1. Departments of Crop Sciences1 and
2. Microbiology,2 University of Illinois at Urbana-Champaign, Urbana, Illinois 61801
Abstract
ABSTRACT
Agrobacterium tumefaciens
C58 and its derivatives give rise to spontaneous mutants resistant to tetracycline at a high frequency. We observed that a mutation affecting a tRNA processing function significantly affected the emergence of such mutants, suggesting that C58 contained a positively acting gene conferring resistance to tetracycline. A cosmid clone conferring resistance to tetracycline in
Escherichia coli
and
Agrobacterium
was isolated from a genomic bank of one such mutant. Subcloning, transposon mutagenesis, and DNA sequence analysis revealed that this DNA fragment contained two divergently transcribed genes,
tetA
and
tetR
, encoding products that were very similar to proteins of the Tet(A) class of tetracycline resistance systems. In the clone from this mutant,
tetR
was disrupted by an IS
426
. The homologous region from wild-type NT1 contained an intact
tetR
gene and did not confer resistance to tetracycline. Hybridization analysis showed that of 22 members of the genus
Agrobacterium
surveyed, only strains C58 and T37 contained the
tet
determinant. Moreover, only these two strains mutated to resistance to this antibiotic. Unlike other Tet(A) systems, neither tetracycline nor a series of its derivatives induced the expression of this
tet
gene unit. Other polycyclic compounds, including many of plant origin, also did not induce this
tet
gene system. The divergent promoter region of this
tet
system contained a single inverted repeat element identical to one such operator repeat in the promoter region of the
tet
determinant from the IncP1α R plasmid RP4. TetR repressor proteins from the
Agrobacterium tet
system and from RP4 interacted with the heterologous operators. While the repressive effect of the TetR protein from strain C58 (TetR
C58
) on the
tetA
gene from strain RP4 (
tetA
RP4
) was not relieved by tetracycline, repression of
tetA
C58
by TetR
RP4
was lifted by this antibiotic.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
46 articles.
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