Literature DB >> 9158759

Effects of penicillin-binding protein 4 overproduction in Staphylococcus aureus.

U U Henze1, M Roos, B Berger-Bächi.   

Abstract

The pbp4 gene of a Staphylococcus aureus strain selected stepwise in vitro for growth on increasing concentrations of penicillin and of its susceptible parent strain showed overall identity except in the promoter region. In the mutant a deletion upstream of the pbp4 structural gene removed 90 nucleotides (nt) that were framed by a 12 nt inverted repeat. This deletion occurred in step 4 of the in vitro selection procedure and was paralleled by a significant increase in the penicillin-binding protein 4 (PBP4) production. The in vitro step selected mutant showed a remarkable increase in the cross-linking of the peptidoglycan compared to its parent. This was linked to morphological changes in the appearance of the cells, which were surrounded by a very thick and fuzzy cell wall.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 9158759     DOI: 10.1089/mdr.1996.2.193

Source DB:  PubMed          Journal:  Microb Drug Resist        ISSN: 1076-6294            Impact factor:   3.431


  13 in total

1.  The AbcA transporter of Staphylococcus aureus affects cell autolysis.

Authors:  G Schrader-Fischer; B Berger-Bächi
Journal:  Antimicrob Agents Chemother       Date:  2001-02       Impact factor: 5.191

Review 2.  FemABX peptidyl transferases: a link between branched-chain cell wall peptide formation and beta-lactam resistance in gram-positive cocci.

Authors:  S Rohrer; B Berger-Bächi
Journal:  Antimicrob Agents Chemother       Date:  2003-03       Impact factor: 5.191

3.  Transcription analysis of the Staphylococcus aureus gene encoding penicillin-binding protein 4.

Authors:  T L Domanski; B L de Jonge; K W Bayles
Journal:  J Bacteriol       Date:  1997-04       Impact factor: 3.490

4.  PBP4 activity and its overexpression are necessary for PBP4-mediated high-level β-lactam resistance.

Authors:  Li Basuino; Ambre Jousselin; J Andrew N Alexander; Natalie C J Strynadka; Mariana G Pinho; Henry F Chambers; Som S Chatterjee
Journal:  J Antimicrob Chemother       Date:  2018-05-01       Impact factor: 5.790

5.  High-Level Resistance of Staphylococcus aureus to β-Lactam Antibiotics Mediated by Penicillin-Binding Protein 4 (PBP4).

Authors:  Stephanie M Hamilton; J Andrew N Alexander; Eun Ju Choo; Li Basuino; Thaina M da Costa; Anatoly Severin; Marilyn Chung; Sandra Aedo; Natalie C J Strynadka; Alexander Tomasz; Som S Chatterjee; Henry F Chambers
Journal:  Antimicrob Agents Chemother       Date:  2017-05-24       Impact factor: 5.191

6.  Endopeptidase penicillin-binding proteins 4 and 7 play auxiliary roles in determining uniform morphology of Escherichia coli.

Authors:  Bernadette M Meberg; Avery L Paulson; Richa Priyadarshini; Kevin D Young
Journal:  J Bacteriol       Date:  2004-12       Impact factor: 3.490

7.  Role of penicillin-binding protein 4 in expression of vancomycin resistance among clinical isolates of oxacillin-resistant Staphylococcus aureus.

Authors:  J E Finan; G L Archer; M J Pucci; M W Climo
Journal:  Antimicrob Agents Chemother       Date:  2001-11       Impact factor: 5.191

8.  Morphological and genetic differences in two isogenic Staphylococcus aureus strains with decreased susceptibilities to vancomycin.

Authors:  Andrea Reipert; Kerstin Ehlert; Thomas Kast; Gabriele Bierbaum
Journal:  Antimicrob Agents Chemother       Date:  2003-02       Impact factor: 5.191

9.  Staphylococcus aureus PBP4 is essential for beta-lactam resistance in community-acquired methicillin-resistant strains.

Authors:  Guido Memmi; Sergio R Filipe; Mariana G Pinho; Zhibiao Fu; Ambrose Cheung
Journal:  Antimicrob Agents Chemother       Date:  2008-08-25       Impact factor: 5.191

10.  Neisseria gonorrhoeae penicillin-binding protein 3 demonstrates a pronounced preference for N(epsilon)-acylated substrates.

Authors:  Sridhar Peddi; Robert A Nicholas; William G Gutheil
Journal:  Biochemistry       Date:  2009-06-23       Impact factor: 3.162

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.