2016
DOI: 10.1007/s00216-015-9270-5
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Comparative study between macrolide regulatory proteins MphR(A) and MphR(E) in ligand identification and DNA binding based on the rapid in vitro detection system

Abstract: The macrolide regulatory protein MphR(A) has been widely studied and used in various aspects such as metabolism monitoring, exogenous gene expression, and in vivo and in vitro macrolide antibiotic screening. Another macrolide regulatory protein, MphR(E), has rarely been reported. In this study, in vitro ELISA-type systems were established for MphR(A) and MphR(E) to study their correlation. The reactivity of 14 macrolide antibiotics and pseudo-macrolide antibiotics was tested in the systems. The results indicat… Show more

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Cited by 11 publications
(13 citation statements)
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“…The first two classes lead to resistance by modification of the target site, while the third class results in macrolide inactivation. In particular, Mph(A) and Mph(E) seem to confer resistance to erythromycin, clarithromycin, azithromycin, and oleandomycin, but only in the presence of specific regulatory proteins [137].…”
Section: Resistance To Macrolides-lincosamides-streptogramin Antibioticsmentioning
confidence: 99%
“…The first two classes lead to resistance by modification of the target site, while the third class results in macrolide inactivation. In particular, Mph(A) and Mph(E) seem to confer resistance to erythromycin, clarithromycin, azithromycin, and oleandomycin, but only in the presence of specific regulatory proteins [137].…”
Section: Resistance To Macrolides-lincosamides-streptogramin Antibioticsmentioning
confidence: 99%
“…Pathogenic E. coli strains characteristically harbor antibiotic resistance genes. MphA is responsible for production of macrolide 2′-phosphotransferase I that inactivates 14-ring macrolides, such as erythromycin and oleandomycin [12]. Another drug resistance gene, AmpC, encodes AmpC β-lactamase that degrades penicillins [13].…”
Section: Introductionmentioning
confidence: 99%
“…In contrast, mphJ expression increases only three-fold when B. brevis VM4 is challenged with ¼ MIC tylosin. The inducible expression of macrolide resistance genes is known to be dependent on substrate structure [30][31][32], particularly the presence or absence of sugars on the C3 position, and ring size. Therefore, we also compared mphI and mphJ expression in response to pikromycin, a natural ketolide similar to erythromycin but without a cladinose on the C3 position ( Fig.…”
Section: B Brevis Vm4 Is Sensitive To Macrolide Antibiotics Despite mentioning
confidence: 99%