2022
DOI: 10.1128/cmr.00150-21
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Class C β-Lactamases: Molecular Characteristics

Abstract: Class C β-lactamases or cephalosporinases can be classified into two functional groups (1, 1e) with considerable molecular variability (≤20% sequence identity). These enzymes are mostly encoded by chromosomal and inducible genes and are widespread among bacteria, including Proteobacteria in particular.

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Cited by 24 publications
(28 citation statements)
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“…Those encoding the cephalosporinase AmpC (and all of their regulatory proteins AmpR, AmpD, AmpE, AmpG) were present in all the genomes; however, mutations in AmpC, AmpR, and AmpD were specific to the different subclades as observed for other species of Enterobacterales 13 ( Table S3 ). In addition to the highly conserved AmpC motifs (64SXSK, 150YXN, and 315KTG) and other conserved residues linked to the reference AmpC β-lactamase of Serratia SRT/SST, we observed amino acid variations at positions N86K and R91H in the “lineage Sn” linked to subclade 2B, apparently located in the middle of an alpha-helix (H) and a bend or turn 29,30 . A number of mutations (GC>AT) in the intergenic region between the ampC and ampR genes in these 2B isolates could have increased the number of stop codons affecting the half-life of AmpC and decreased the ability to degrade the antibiotic as suggested 31 .…”
Section: Resultsmentioning
confidence: 90%
“…Those encoding the cephalosporinase AmpC (and all of their regulatory proteins AmpR, AmpD, AmpE, AmpG) were present in all the genomes; however, mutations in AmpC, AmpR, and AmpD were specific to the different subclades as observed for other species of Enterobacterales 13 ( Table S3 ). In addition to the highly conserved AmpC motifs (64SXSK, 150YXN, and 315KTG) and other conserved residues linked to the reference AmpC β-lactamase of Serratia SRT/SST, we observed amino acid variations at positions N86K and R91H in the “lineage Sn” linked to subclade 2B, apparently located in the middle of an alpha-helix (H) and a bend or turn 29,30 . A number of mutations (GC>AT) in the intergenic region between the ampC and ampR genes in these 2B isolates could have increased the number of stop codons affecting the half-life of AmpC and decreased the ability to degrade the antibiotic as suggested 31 .…”
Section: Resultsmentioning
confidence: 90%
“…Subsequently, energy minimization was performed using GROMOS96 implemented in Swiss PDB Viewer 4.1.0 [ 28 ]. Based on prior reports [ 29 , 30 , 31 , 32 ], three active sites of PDC were identified as follows: Ser62, Val63, Ser64, and Lys65 (here, motif 1), Tyr149, Ser150, and Asn151 (here, motif 2), Lys314, Thr315, and Gly316 (here, motif 3).…”
Section: Methodsmentioning
confidence: 99%
“…Furthermore, since A. baumannii has strong invasive virulence factors, such as outer membrane proteins, lipopolysaccharides and phospholipases, the treatment of A. baumannii infection has been regarded as a great threat to clinical practice [ 3 ]. Antibiotics such as carbapenems, β-lactam antibiotics and polymyxins, are commonly used clinically to treat A. baumannii infections [ 4 , 5 , 6 ]. However, the treatment of multi-drug resistant (MDR) A. baumannii is further aggravated by the abuse of antibiotics and the evolution of bacteria.…”
Section: Introductionmentioning
confidence: 99%