Kanamycin Uptake into Escherichia coli Is Facilitated by OmpF and OmpC Porin Channels Located in the Outer Membrane

被引:42
作者
Bafna, Jayesh Arun [1 ]
Sans-Serramitjana, Eulalia [1 ]
Acosta-Gutierrez, Silvia [2 ]
Bodrenko, Igor, V [3 ]
Hoeroempoeli, Daniel [4 ,5 ]
Berscheid, Anne [4 ,5 ]
Broetz-Oesterhelt, Heike [4 ,5 ]
Winterhalter, Mathias [1 ]
Ceccarelli, Matteo [3 ,6 ,7 ]
机构
[1] Jacobs Univ Bremen, Dept Life Sci & Chem, D-28719 Bremen, Germany
[2] UCL, Dept Chem, London WC1E 6BT, England
[3] Cittadella Univ Monserrato, Sez Cagliari, IOM CNR, I-09042 Monserrato, Italy
[4] Univ Tubingen, Interfac Inst Microbiol & Infect Med, Dept Microbial Bioact Cpds, D-72076 Tubingen, Germany
[5] German Ctr Infect Res DZIF, Partner Site, D-72076 Tubingen, Germany
[6] Univ Cagliari, Dept Phys, I-09042 Monserrato, Italy
[7] Cittadella Univ Monserrato, CNR IOM, I-09042 Monserrato, Italy
来源
ACS INFECTIOUS DISEASES | 2020年 / 6卷 / 07期
关键词
E; coli; OmpF; OmpC; OmpN; bacterial porins; optimal transport;
D O I
10.1021/acsinfecdis.0c00102
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
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 Escherichia coli. Our analysis revealed that, despite its relatively large size, about 10-20 kanamycin molecules per second permeate through OmpF and OmpC under a 10 mu M 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 defined set of E. coli porin mutants provide evidence that translocation of kanamycin via porins is relevant for antibiotic potency. The values are discussed with respect to other antibiotics.
引用
收藏
页码:1855 / 1865
页数:11
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