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The mechanisms of Cu import across the bacterial outer membrane have been investigated only in a few cases. One such mechanism involves the outer membrane OprC transporter with a unique CxxxM-HxM metal-binding site, discovered recently. This newly identified site in OprC is located outside the cell and is, therefore, most likely to bind Cu(II) through this domain. Since OprC may interact with azurin to facilitate the removal of copper, our study investigated the potential role of CopM metallophore. We selected two putative metal-binding sites in CopM, characterized by MxxHH and MHxxH motifs, which can bind Cu(II) and may interact with the extracellular CxxxM-HxM motif of OprC. At pH 7, the MxxHH motif in CopM was the most effective ligand for Cu(II) ions compared to the MHxxH domain and the novel CxxxM-HxM site in OprC. Furthermore, the CxxxM-HxM site in OprC, where a cysteine residue also binds Cu(II) ions alongside histidine, does not effectively compete with the MxxHH metal-binding site in CopM. This comparison suggests that the CopM MxxHH domain binds Cu(II) ions very strongly and is unable to give them back to the OprC; therefore, it is perhaps transported together with copper ions through OprC into the bacterial cell.
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http://dx.doi.org/10.1021/acs.inorgchem.4c05101 | DOI Listing |
ACS Biomater Sci Eng
September 2025
Departamento de Genética, Evolução, Microbiologia e Immunologia, Instituto de Biologia, Universidade Estadual de Campinas - UNICAMP, Campinas, São Paulo 13083-862, Brazil.
Violacein exhibits antitumor activity, indicating potential for future clinical application. However, an efficient delivery system is required for the clinical use of this hydrophobic compound. Effective delivery systems can enhance the solubility and bioavailability of hydrophobic compounds like violacein, facilitating its clinical application for antitumor therapy.
View Article and Find Full Text PDFNat Aging
September 2025
State Key Laboratory of Conservation and Utilization of Bio-resources in Yunnan and Center for Life Sciences, School of Life Sciences, Yunnan University, Kunming, China.
Membraneless organelles assembled by liquid-liquid phase separation interact with diverse membranous organelles to regulate distinct cellular processes. It remains unknown how membraneless organelles are engaged in mitochondrial homeostasis. Here we demonstrate that mitochondria-associated translation organelles (MATOs) mediate local synthesis of proteins required for structural and functional maintenance of mitochondria.
View Article and Find Full Text PDFInt J Food Microbiol
September 2025
Department of Food and Nutrition, College of Human Ecology, Seoul National University, Seoul, 08826, Republic of Korea; Research Institute of Human Ecology, Seoul National University, Seoul, 08826, Republic of Korea. Electronic address:
This study explored the antimicrobial efficacy and mechanism of a combined treatment using chlorogenic acid (CGA) and UV-A (365 nm) irradiation against four major foodborne pathogens-Escherichia coli O157:H7, Salmonella Typhimurium, Listeria monocytogenes, and Staphylococcus aureus-in both buffer and acidic beverage matrices. The CGA + UVA treatment showed strong bactericidal effects, particularly in green plum juice, where complete inactivation of L. monocytogenes was achieved (> 8-log reduction).
View Article and Find Full Text PDFBiomed Pharmacother
September 2025
Department of Nursing, Guangxi Medical University Nursing College, Nanning, Guangxi 530021, China. Electronic address:
The voltage-dependent anion channel (VDAC) family proteins can be subdivided into three isoforms: VDAC1, VDAC2, and VDAC3. As core channels of the mitochondrial outer membrane, these proteins exhibit paradoxical regulatory roles in cancer development. This review systematically summarizes their structural and functional characteristics, as well as the contradictory mechanisms in tumorigenesis and progression.
View Article and Find Full Text PDFBiotechnol Lett
September 2025
Department of Chemical Engineering, Hongik University, Sangsu-dong, Mapo-gu, Seoul, 04066, Republic of Korea.
The cell surface display system employs carrier proteins to present target proteins on the outer membrane of cells. This system enables functional proteins to be exposed on the exterior of living cells without cell lysis, allowing direct interaction with the surrounding environment. A major limitation of conventional approaches is the difficulty in displaying large-sized enzymes or antibodies, despite their critical roles in applications requiring functional domains that must remain intact, such as catalytic or antigen-binding sites.
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