Literature DB >> 1874395

Localisation of the aminoglycoside-(3)-N-acetyltransferase isoenzyme II in Escherichia coli.

J S Vliegenthart1, P A Ketelaar-van Gaalen, J Eelhart, J A van de Klundert.   

Abstract

For the location of the aminoglycoside-(3)-N-acetyltransferase isoenzyme II (AAC(3)-II) in the bacterial cell, two strains were studied: Escherichia coli HB101(pJV03), producing the 31-kDa AAC (3)-II enzyme, and E. coli HB101, which served as a control. From each strain five protein fractions were prepared: culture supernatant, and proteins occurring in the periplasm, cytoplasm, inner membrane and outer membrane. All fractions were tested for enzymatic activity of AAC(3)-II. Most of the acetylating activity was found in the cytoplasmic fraction. The distribution of marker enzymes showed a good separation between the periplasmic and the cytoplasmic fraction.

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Year:  1991        PMID: 1874395     DOI: 10.1016/0378-1097(91)90479-t

Source DB:  PubMed          Journal:  FEMS Microbiol Lett        ISSN: 0378-1097            Impact factor:   2.742


  2 in total

Review 1.  Aminoglycoside modifying enzymes.

Authors:  Maria S Ramirez; Marcelo E Tolmasky
Journal:  Drug Resist Updat       Date:  2010-09-15       Impact factor: 18.500

2.  The aminoglycoside 6'-N-acetyltransferase type Ib encoded by Tn1331 is evenly distributed within the cell's cytoplasm.

Authors:  Ken J Dery; Britta Søballe; Mavee S L Witherspoon; Duyen Bui; Robert Koch; David J Sherratt; Marcelo E Tolmasky
Journal:  Antimicrob Agents Chemother       Date:  2003-09       Impact factor: 5.191

  2 in total

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