Review
- Membrane Proteins as a Regulator for Antibiotic Persistence in Gram‑Negative Bacteria
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Jia Xin Yee , Juhyun Kim , Jinki Yeom
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J. Microbiol. 2023;61(3):331-341. Published online February 17, 2023
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DOI: https://doi.org/10.1007/s12275-023-00024-w
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Abstract
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Antibiotic treatment failure threatens our ability to control bacterial infections that can cause chronic diseases. Persister bacteria
are a subpopulation of physiological variants that becomes highly tolerant to antibiotics. Membrane proteins play crucial
roles in all living organisms to regulate cellular physiology. Although a diverse membrane component involved in persistence
can result in antibiotic treatment failure, the regulations of antibiotic persistence by membrane proteins has not been fully
understood. In this review, we summarize the recent advances in our understanding with regards to membrane proteins in
Gram-negative bacteria as a regulator for antibiotic persistence, highlighting various physiological mechanisms in bacteria.
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Citations
Citations to this article as recorded by

- Amino Acid and Au(III) Self-Assembled Supramolecular Nanozymes for Antimicrobial Applications
Yunzhu Xu, Dahai Hou, Min Zhao, Tong Zhao, Yong Ma, Yafeng Zhang, Yang Guo, Weiwei Tao, Hui Wang
ACS Applied Nano Materials.2024; 7(19): 22505. CrossRef -
PhoPQ-mediated lipopolysaccharide modification governs intrinsic resistance to tetracycline and glycylcycline antibiotics in
Escherichia coli
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mSystems.2024;[Epub] CrossRef - Bacterial Regulatory Mechanisms for the Control of Cellular Processes: Simple Organisms’ Complex Regulation
Jin-Won Lee
Journal of Microbiology.2023; 61(3): 273. CrossRef
Journal Article
- Photodynamic antimicrobial activity of new porphyrin derivatives against methicillin resistant Staphylococcus aureus
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Hüseyin Ta , Ay , Nermin Topalo , Vildan Alptüzün
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J. Microbiol. 2018;56(11):828-837. Published online October 24, 2018
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DOI: https://doi.org/10.1007/s12275-018-8244-7
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Abstract
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Methicillin resistant Staphylococcus aureus (MRSA) with
multiple drug resistance patterns is frequently isolated from
skin and soft tissue infections that are involved in chronic
wounds. Today, difficulties in the treatment of MRSA associated
infections have led to the development of alternative
approaches such as antimicrobial photodynamic therapy. This
study aimed to investigate photoinactivation with cationic
porphyrin derivative compounds against MRSA in in-vitro
conditions. In the study, MRSA clinical isolates with different
antibiotic resistance profiles were used. The newly synthesized
cationic porphyrin derivatives (PM, PE, PPN, and PPL) were used
as photosensitizer, and 655 nm diode laser was used as light
source. Photoinactivation experiments were performed by
optimizing energy doses and photosensitizer concentrations.
In photoinactivation experiments with different energy densities
and photosensitizer concentrations, more than 99% reduction
was achieved in bacterial cell viability. No decrease
in bacterial survival was observed in control groups. It was
determined that there was an increase in photoinactivation
efficiency by increasing the energy dose. At the energy dose
of 150 J/cm2 a survival reduction of over 6.33 log10 was observed
in each photosensitizer type. While 200 μM PM concentration
was required for this photoinactivation, 12.50 μM
was sufficient for PE, PPN, and PPL. In our study, antimicrobial
photodynamic therapy performed with cationic porphyrin
derivatives was found to have potent antimicrobial efficacy
against multidrug resistant S. aureus which is frequently
isolated from wound infections.
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Citations
Citations to this article as recorded by

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RSC Advances.2024; 14(5): 3122. CrossRef - Photo-Inactivation of Staphylococcus aureus by Diaryl-Porphyrins
Viviana Teresa Orlandi, Eleonora Martegani, Nicola Trivellin, Fabrizio Bolognese, Enrico Caruso
Antibiotics.2023; 12(2): 228. CrossRef - Enhancement of the mechanical and antibacterial properties of Bis-GMA/TEGDMA dental composite incorporated with ZnO/CS and Si/PMMA core–shell nanostructures
Izel Ok, Ahmet Aykac
Chemical Papers.2023; 77(11): 6959. CrossRef - Antimicrobial photodynamic in vitro inactivation of Enterococcus spp. and Staphylococcus spp. strains using tetra-cationic platinum(II) porphyrins
Ticiane da Rosa Pinheiro, Carolina Gonzalez Urquhart, Thiago Vargas Acunha, Roberto Christ Vianna Santos, Bernardo Almeida Iglesias
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M. G. Seeger, C. S. Machado, B. A. Iglesias, F. S. F. Vogel, J. F. Cargnelutti
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Ayşe Akbiyik, Hüseyin Taşli, Nermin Topaloğlu, Vildan Alptüzün, Sülünay Parlar, Selçuk Kaya
Photodiagnosis and Photodynamic Therapy.2022; 40: 103066. CrossRef - Efficacy of chemical and photoactivated disinfectants against Candida Albicans and assessment of hardness, roughness, and mass loss of acrylic denture base resin
Fahad Alkhtani
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Jianhua Huang, Shutian Wu, Minfeng Wu, Qingyu Zeng, Xiuli Wang, Hongwei Wang
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Samar Al-Saleh, Ahmed Heji Albaqawi, Feras Alrawi, Huda I. Tulbah, Amal S Al-Qahtani, Emal Heer, Sidra Sadaf Nisar, Fahim Vohra, Tariq Abduljabbar
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Ece Polat, Kyungsu Kang
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Research Support, Non-U.S. Gov't
- Copper as an Antimicrobial Agent against Opportunistic Pathogenic and Multidrug Resistant Enterobacter Bacteria
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Wen-Xiao Tian , Shi Yu , Muhammad Ibrahim , Abdul Wareth Almonaofy , Liu He , Qiu Hui , Zhu Bo , Bin Li , Guan-lin Xie
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J. Microbiol. 2012;50(4):586-593. Published online July 21, 2012
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DOI: https://doi.org/10.1007/s12275-012-2067-8
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44
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Abstract
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Infections by Enterobacter species are common and are multidrug resistant. The use of bactericidal surface materials such as copper has lately gained attention as an effective antimicrobial agent due to its deadly effects on bacteria, yeast, and viruses. The aim of the current study was to assess the antibacterial activity of copper surfaces against Enterobacter species. The antibacterial activity of copper surfaces was tested by overlying 5×106 CFU/ml suspensions of representative Enterobacter strains and comparing bacterial survival counts on copper surfaces at room temperature. Iron, stainless steel, and polyvinylchloride (PVC) were used as controls. The mechanisms responsible for bacterial killing on copper surfaces were investigated by a mutagenicity assay of the D-cycloserin (cyclA gene), single cell gel electrophoresis, a staining technique, and inductively coupled plasma mass spectroscopy. Copper yielded a significant decrease in the viable bacterial counts at 2 h exposure and a highly significant decrease at 4 h. Loss of cell integrity and a significantly higher influx of copper into bacterial cells exposed to copper surfaces, as compared to those exposed to the controls, were documented. There was no increase in mutation rate and DNA damage indicating that copper contributes to bacterial killing by adversely affecting cellular structure without directly targeting the genomic DNA. These findings suggest that copper’s antibacterial activity against Enterobacter species could be utilized in health care facilities and in food processing plants to reduce the bioburden, which would increase protection for susceptible members of the community.