Literature DB >> 2156799

A cryptic 65-kilobase-pair transposonlike element isolated from Bacteroides uniformis has homology with Bacteroides conjugal tetracycline resistance elements.

N B Shoemaker1, A A Salyers.   

Abstract

A 65-kilobase-pair element, XBU4422, which has some transposonlike characteristics but carries no known antibiotic resistance genes, has been isolated from Bacteroides uniformis 0061. XBU4422 was trapped on Bacteroides-Escherichia coli shuttle vectors during experiments in which one of the conjugal Bacteroides tetracycline resistance (Tcr) elements was being used to mobilize the shuttle vectors to Bacteroides recipients. Results of Southern hybridization experiments showed that XBU4422 is normally integrated in the B. uniformis 0061 chromosome and is found only in some strains. Insertion of XBU4422 in the shuttle vectors was site specific and orientation specific. Nonmobilizable vectors that had acquired XBU4422 became transmissible and could be transferred to Bacteroides or E. coli recipients. In B. uniformis transconjugants, the XBU4422 insertion in the vectors was usually intact, but XBU4422 was always lost in matings with E. coli, Bacteroides thetaiotaomicron, or B. ovatus. The loss of XBU4422 did not visibly alter the vector; in the case of E. coli, the loss of the insertion appeared to be RecA dependent. Although XBU4422 carried no antibiotic resistances, it shared regions of homology with six conjugal Bacteroides Tcr elements; this homology was strongest with the ends of XBU4422. Using a strain of B. thetaiotaomicron that contains no XBU4422-hybridizing sequences, we showed that the ends of XBU4422 were probably reacting with the ends of the Tcr elements. These results provide the first direct evidence that the Tcr elements, like XBU4422, are integrated in the chromosome and that insertion of the least some Tcr elements, such as TcrEmr DOT, is relatively site specific.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 2156799      PMCID: PMC208658          DOI: 10.1128/jb.172.4.1694-1702.1990

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  20 in total

1.  PREPARATION OF TRANSFORMING DEOXYRIBONUCLEIC ACID BY PHENOL TREATMENT.

Authors:  H SAITO; K I MIURA
Journal:  Biochim Biophys Acta       Date:  1963-08-20

2.  A complementation analysis of the restriction and modification of DNA in Escherichia coli.

Authors:  H W Boyer; D Roulland-Dussoix
Journal:  J Mol Biol       Date:  1969-05-14       Impact factor: 5.469

3.  Mechanism of F factor-enhanced excision of transposon Tn5.

Authors:  D E Berg; C Egner; J B Lowe
Journal:  Gene       Date:  1983-04       Impact factor: 3.688

4.  Evidence that the clindamycin-erythromycin resistance gene of Bacteroides plasmid pBF4 is on a transposable element.

Authors:  N B Shoemaker; E P Guthrie; A A Salyers; J F Gardner
Journal:  J Bacteriol       Date:  1985-05       Impact factor: 3.490

5.  Comparison of the transposon-like structures encoding clindamycin resistance in Bacteroides R-plasmids.

Authors:  C J Smith; M A Gonda
Journal:  Plasmid       Date:  1985-05       Impact factor: 3.466

6.  Tn4399, a conjugal mobilizing transposon of Bacteroides fragilis.

Authors:  D W Hecht; M H Malamy
Journal:  J Bacteriol       Date:  1989-07       Impact factor: 3.490

7.  Expression in Escherichia coli of cryptic tetracycline resistance genes from bacteroides R plasmids.

Authors:  D G Guiney; P Hasegawa; C E Davis
Journal:  Plasmid       Date:  1984-05       Impact factor: 3.466

8.  Plasmid transfer from Escherichia coli to Bacteroides fragilis: differential expression of antibiotic resistance phenotypes.

Authors:  D G Guiney; P Hasegawa; C E Davis
Journal:  Proc Natl Acad Sci U S A       Date:  1984-11       Impact factor: 11.205

9.  Tetracycline-dependent appearance of plasmidlike forms in Bacteroides uniformis 0061 mediated by conjugal Bacteroides tetracycline resistance elements.

Authors:  N B Shoemaker; A A Salyers
Journal:  J Bacteriol       Date:  1988-04       Impact factor: 3.490

10.  Characterization of a novel tetracycline resistance that functions only in aerobically grown Escherichia coli.

Authors:  B S Speer; A A Salyers
Journal:  J Bacteriol       Date:  1988-04       Impact factor: 3.490

View more
  27 in total

1.  Integration and excision of a Bacteroides conjugative transposon, CTnDOT.

Authors:  Q Cheng; B J Paszkiet; N B Shoemaker; J F Gardner; A A Salyers
Journal:  J Bacteriol       Date:  2000-07       Impact factor: 3.490

2.  Genes involved in production of plasmidlike forms by a Bacteroides conjugal chromosomal element share amino acid homology with two-component regulatory systems.

Authors:  A M Stevens; J M Sanders; N B Shoemaker; A A Salyers
Journal:  J Bacteriol       Date:  1992-05       Impact factor: 3.490

3.  NBU1, a mobilizable site-specific integrated element from Bacteroides spp., can integrate nonspecifically in Escherichia coli.

Authors:  N B Shoemaker; G R Wang; A A Salyers
Journal:  J Bacteriol       Date:  1996-06       Impact factor: 3.490

4.  The Bacteroides mobilizable insertion element, NBU1, integrates into the 3' end of a Leu-tRNA gene and has an integrase that is a member of the lambda integrase family.

Authors:  N B Shoemaker; G R Wang; A A Salyers
Journal:  J Bacteriol       Date:  1996-06       Impact factor: 3.490

5.  Insertion and excision of Bacteroides conjugative chromosomal elements.

Authors:  L A Bedzyk; N B Shoemaker; K E Young; A A Salyers
Journal:  J Bacteriol       Date:  1992-01       Impact factor: 3.490

6.  Activities of the Porphyromonas gingivalis PrtP proteinase determined by construction of prtP-deficient mutants and expression of the gene in Bacteroides species.

Authors:  G A Barkocy-Gallagher; J W Foley; M S Lantz
Journal:  J Bacteriol       Date:  1999-01       Impact factor: 3.490

7.  Characterization of a new type of Bacteroides conjugative transposon, Tcr Emr 7853.

Authors:  M P Nikolich; N B Shoemaker; G R Wang; A A Salyers
Journal:  J Bacteriol       Date:  1994-11       Impact factor: 3.490

8.  Characterization of the mobilization region of a Bacteroides insertion element (NBU1) that is excised and transferred by Bacteroides conjugative transposons.

Authors:  L Y Li; N B Shoemaker; A A Salyers
Journal:  J Bacteriol       Date:  1993-10       Impact factor: 3.490

9.  Excision, transfer, and integration of NBU1, a mobilizable site-selective insertion element.

Authors:  N B Shoemaker; G R Wang; A M Stevens; A A Salyers
Journal:  J Bacteriol       Date:  1993-10       Impact factor: 3.490

10.  Tetracycline regulation of genes on Bacteroides conjugative transposons.

Authors:  A M Stevens; N B Shoemaker; L Y Li; A A Salyers
Journal:  J Bacteriol       Date:  1993-10       Impact factor: 3.490

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.