Kanamycin Uptake into E. Coli Is Facilitated by OmpF and OmpC Porin Channels Located in the Outer Membrane

Author(s):  
Jayesh Arun Bafna ◽  
Eulàlia Sans-Serramitjana ◽  
Silvia Acosta-Gutiérrez ◽  
Igor Bodrenko ◽  
Daniel Hörömpöli ◽  
...  

<p>Despite decades of therapeutic application of aminoglycosides, it is still a matter of debate if porins contribute to the translocation of the antibiotics across the bacterial outer membrane. Here, we quantified the uptake of kanamycin across the major porin channels OmpF and OmpC present in the outer membrane of <i>E. coli.</i> Our analysis revealed that, despite its relatively large size, about 10 - 20 kanamycin molecules per second permeate through OmpF and OmpC under a 10 mM concentration gradient, whereas OmpN does not allow the passage. Molecular simulations elucidate the uptake mechanism of kanamycin through these porins. Whole-cell studies with a decisive set of <i>E. coli</i> porin mutants provide evidence that translocation of kanamycin <i>via</i> porins is relevant for antibiotic potency.</p>

2020 ◽  
Author(s):  
Jayesh Arun Bafna ◽  
Eulàlia Sans-Serramitjana ◽  
Silvia Acosta-Gutiérrez ◽  
Igor Bodrenko ◽  
Daniel Hörömpöli ◽  
...  

<p>Despite decades of therapeutic application of aminoglycosides, it is still a matter of debate if porins contribute to the translocation of the antibiotics across the bacterial outer membrane. Here, we quantified the uptake of kanamycin across the major porin channels OmpF and OmpC present in the outer membrane of <i>E. coli.</i> Our analysis revealed that, despite its relatively large size, about 10 - 20 kanamycin molecules per second permeate through OmpF and OmpC under a 10 mM concentration gradient, whereas OmpN does not allow the passage. Molecular simulations elucidate the uptake mechanism of kanamycin through these porins. Whole-cell studies with a decisive set of <i>E. coli</i> porin mutants provide evidence that translocation of kanamycin <i>via</i> porins is relevant for antibiotic potency.</p>


2016 ◽  
Vol 63 (3) ◽  
Author(s):  
Iwona Komaniecka ◽  
Katarzyna Zamłyńska ◽  
Radosław Zan ◽  
Magdalena Staszczak ◽  
Jarosław Pawelec ◽  
...  

Six rhizobium (Rhizobium leguminosarum bv. Trifolii TA1, Sinorhizobium meliloti 1021, Mesorhizobium huakuii IFO 15243T, Ochrobactrum lupini LUP 21T, Bradyrhizobium japonicum USDA110 and B. elkaniiUSDA 76) and two Escherichia coli strains (E. coli ATCC 25922 and E. coli HB 101) were compared in respect to polymyxin B and EDTA resistance, as well as bacterial outer membrane (OM) permeability to a fluorescent hydrophobic agent (N-phenyl-1-naphthylamine - NPN). TEM (Transmission Electron Microscopy) and a microbial test demonstrated that all the rhizobia were much more resistant to polymyxin B in comparison with E. coli strains. EDTA and polymyxin B enhance permeability of B. japonicum and O. lupini OM. Other rhizobia incorporated NPN independently of the presence of membrane-deteriorating agents; however, the level of fluorescence (measured as NPN absorption) was strain dependent.


Author(s):  
Dipak Kathayat ◽  
Yosra A. Helmy ◽  
Loic Deblais ◽  
Vishal Srivastava ◽  
Gary Closs ◽  
...  

APEC is a subgroup of ExPEC, and genetic similarities of APEC with human ExPECs, including uropathogenic E. coli (UPEC) and neonatal meningitis E. coli (NMEC), have been reported. Our study identified a novel small molecule growth inhibitor, GI-7, as reducing APEC infection in chickens with an efficacy similar to that of the currently used antibiotic sulfadimethoxine, notably with an 8-times-lower dose.


ChemCatChem ◽  
2021 ◽  
Vol 13 (19) ◽  
pp. 4080-4086
Author(s):  
Ji‐Won Song ◽  
Yoonjin Baeg ◽  
Ha‐Yeon Jeong ◽  
Jinwon Lee ◽  
Deok‐Kun Oh ◽  
...  

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