Literature DB >> 390404

Primary structure of a chloramphenicol acetyltransferase specified by R plasmids.

W V Shaw, L C Packman, B D Burleigh, A Dell, H R Morris, B S Hartley.   

Abstract

Naturally occurring isolates of chloramphenicol-resistant bacteria commonly synthesise chloramphenicol acetyltransferase (EC 2.3.28; CAT) in amounts which are sufficient to account for the resistance phenotype and often harbour plasmids which carry the structural gene for CAT. The findings of CAT in such diverse prokaryotes as Proteus mirabilis, Agrobacterium tumefaciens, Streptomyces sp., and a soil Flavobacterium has led to speculation concerning the origin and evolution of the more commonly observed CAT variants specified by plasmids in clinically important bacteria. To provide a more solid basis for studying the evolution and spread of CAT within prokaryotes we chose to determine the complete amino acid sequence of a type I variant of CAT, the variant known to be associated with most F-like plasmids conferring chloramphenicol resistance. The sequence has been determined by combining the results obtained from manual and automated sequential degradation with those obtained by mass spectrometry of peptides generated by enzymatic digestion. The directly determined primary structure is identical with that predicted by the DNA sequence analysis of the chloramphenicol resistance transponson Tn9 known to specify a type I variant of chloramphenicol acetyltransferase.

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Year:  1979        PMID: 390404     DOI: 10.1038/282870a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  49 in total

1.  Comparative sequence analysis of the catB gene from Clostridium butyricum.

Authors:  A S Huggins; T L Bannam; J I Rood
Journal:  Antimicrob Agents Chemother       Date:  1992-11       Impact factor: 5.191

2.  A transcriptional regulator and ABC transporters link stress tolerance, (p)ppGpp, and genetic competence in Streptococcus mutans.

Authors:  Kinda Seaton; Sang-Joon Ahn; Ann M Sagstetter; Robert A Burne
Journal:  J Bacteriol       Date:  2010-12-10       Impact factor: 3.490

3.  Relationship between the Clostridium perfringens catQ gene product and chloramphenicol acetyltransferases from other bacteria.

Authors:  T L Bannam; J I Rood
Journal:  Antimicrob Agents Chemother       Date:  1991-03       Impact factor: 5.191

4.  Nucleotide sequences of genes encoding the type II chloramphenicol acetyltransferases of Escherichia coli and Haemophilus influenzae, which are sensitive to inhibition by thiol-reactive reagents.

Authors:  I A Murray; J V Martinez-Suarez; T J Close; W V Shaw
Journal:  Biochem J       Date:  1990-12-01       Impact factor: 3.857

5.  Transcription of the HS2 enhancer toward a cis-linked gene is independent of the orientation, position, and distance of the enhancer relative to the gene.

Authors:  S Kong; D Bohl; C Li; D Tuan
Journal:  Mol Cell Biol       Date:  1997-07       Impact factor: 4.272

6.  Determination of gene products and coding regions from the murE-murF region of Escherichia coli.

Authors:  I N Maruyama; A H Yamamoto; Y Hirota
Journal:  J Bacteriol       Date:  1988-08       Impact factor: 3.490

7.  Characterization of the genome of Pseudomonas aeruginosa bacteriophage phi PLS27 with particular reference to the ends of the DNA.

Authors:  B J Allan; P Davies; E B Carstens; A M Kropinski
Journal:  J Virol       Date:  1989-04       Impact factor: 5.103

8.  Nucleotide sequence and functional map of pC194, a plasmid that specifies inducible chloramphenicol resistance.

Authors:  S Horinouchi; B Weisblum
Journal:  J Bacteriol       Date:  1982-05       Impact factor: 3.490

9.  Expression of plant tumor-specific proteins in minicells of Escherichia coli: a fusion protein of lysopine dehydrogenase with chloramphenicol acetyltransferase.

Authors:  J Schröder; A Hillebrand; W Klipp; A Pühler
Journal:  Nucleic Acids Res       Date:  1981-10-24       Impact factor: 16.971

10.  Nucleotide sequence and phylogeny of a chloramphenicol acetyltransferase encoded by the plasmid pSCS7 from Staphylococcus aureus.

Authors:  S Schwarz; M Cardoso
Journal:  Antimicrob Agents Chemother       Date:  1991-08       Impact factor: 5.191

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