Increased overall antibiotic susceptibility in Staphylococcus aureus femAB null mutants. - Wikidata - wikimedia - TriplyDB

Increased overall antibiotic susceptibility in Staphylococcus aureus femAB null mutants.

Increased overall antibiotic susceptibility in Staphylococcus aureus femAB null mutants.

http://www.wikidata.org/entity/Q33692894

about

Structure and Functional Diversity of GCN5-Related N-Acetyltransferases (GNAT)Living with an imperfect cell wall: compensation of femAB inactivation in Staphylococcus aureus.Peptidoglycan crosslinking relaxation plays an important role in Staphylococcus aureus WalKR-dependent cell viability.Relaxed substrate specificity leads to extensive tRNA mischarging by Streptococcus pneumoniae class I and class II aminoacyl-tRNA synthetases FemABX peptidyl transferases: a link between branched-chain cell wall peptide formation and beta-lactam resistance in gram-positive cocci.Mutation in the C-di-AMP cyclase dacA affects fitness and resistance of methicillin resistant Staphylococcus aureus.The essential Staphylococcus aureus gene fmhB is involved in the first step of peptidoglycan pentaglycine interpeptide formation Lysostaphin-resistant variants of Staphylococcus aureus demonstrate reduced fitness in vitro and in vivo.Discovery of novel S. aureus autolysins and molecular engineering to enhance bacteriolytic activity.Bacterial transfer RNAs.Uniformity of glycyl bridge lengths in the mature cell walls of fem mutants of methicillin-resistant Staphylococcus aureus Lipid II-independent trans editing of mischarged tRNAs by the penicillin resistance factor MurM Direction of aminoacylated transfer RNAs into antibiotic synthesis and peptidoglycan-mediated antibiotic resistance Characterization of peptidoglycan in fem-deletion mutants of methicillin-resistant Staphylococcus aureus by solid-state NMR The Staphylococcus aureus Membrane Protein SA2056 Interacts with Peptidoglycan Synthesis Enzymes.Role in cell permeability of an essential two-component system in Staphylococcus aureus

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P2860

Increased overall antibiotic susceptibility in Staphylococcus aureus femAB null mutants.

http://www.wikidata.org/entity/Q33692894

description

1998 nî lūn-bûn

@nan

1998 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

1998 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

1998年の論文

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1998年論文

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1998年論文

@zh-hant

1998年論文

@zh-hk

1998年論文

@zh-mo

1998年論文

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1998年论文

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name

Increased overall antibiotic susceptibility in Staphylococcus aureus femAB null mutants.

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Increased overall antibiotic susceptibility in Staphylococcus aureus femAB null mutants.

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type

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Increased overall antibiotic susceptibility in Staphylococcus aureus femAB null mutants.

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Increased overall antibiotic susceptibility in Staphylococcus aureus femAB null mutants.

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prefLabel

Increased overall antibiotic susceptibility in Staphylococcus aureus femAB null mutants.

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Increased overall antibiotic susceptibility in Staphylococcus aureus femAB null mutants.

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Antimicrobial Agents and Chemotherapy

P1476

Increased overall antibiotic susceptibility in Staphylococcus aureus femAB null mutants.

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Berger-Bächi B

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Ling B

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P2860

Specificities of FemA and FemB for different glycine residues: FemB cannot substitute for FemA in staphylococcal peptidoglycan pentaglycine side chain formation

Cell wall monoglycine cross-bridges and methicillin hypersusceptibility in a femAB null mutant of methicillin-resistant Staphylococcus aureus.

Consequences of the interaction of beta-lactam antibiotics with penicillin binding proteins from sensitive and resistant Staphylococcus aureus strains.

Influence of femB on methicillin resistance and peptidoglycan metabolism in Staphylococcus aureus.

femA, which encodes a factor essential for expression of methicillin resistance, affects glycine content of peptidoglycan in methicillin-resistant and methicillin-susceptible Staphylococcus aureus strains.

Increase in transduction efficiency of Tn551 mediated by the methicillin resistance marker.

Comparison of the E Test to agar dilution, broth microdilution, and agar diffusion susceptibility testing techniques by using a special challenge set of bacteria.

Membrane topology of the metal-tetracycline/H+ antiporter TetA(K) from Staphylococcus aureus.

Cloning and characterization of femA and femB from Staphylococcus epidermidis.

Distribution of genes encoding erythromycin ribosomal methylases and an erythromycin efflux pump in epidemiologically distinct groups of staphylococci.

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