Diana Olimpo, Caterina D'Angelo, Paola Imbimbo, Marco Morelli, Maria Luisa Tutino, Andrea Carpentieri, Daria Maria Monti, Eugenio Notomista, Ermenegilda Parrilli
{"title":"与生物膜斗争的新见解:来自南极海洋细菌Psychrobacter sp. TAE2020的PsyOmp38蛋白。","authors":"Diana Olimpo, Caterina D'Angelo, Paola Imbimbo, Marco Morelli, Maria Luisa Tutino, Andrea Carpentieri, Daria Maria Monti, Eugenio Notomista, Ermenegilda Parrilli","doi":"10.1111/1751-7915.70249","DOIUrl":null,"url":null,"abstract":"<p>Antibiofilm molecules can enhance the effectiveness of antibiotics and prevent biofilm formation. Antarctic marine bacteria have been found to secrete antibiofilm molecules, likely as part of a strategy for competitive survival. The protein-polysaccharide complex CATASAN, produced by the Antarctic bacterium <i>Psychrobacter</i> sp. TAE2020, has been shown to interfere with all stages of <i>Staphylococcus epidermidis</i> biofilm development. This study investigates the contribution of <i>Psy</i>Omp38, the protein component of CATASAN, to the complex's antibiofilm activity. The protein was heterologously expressed in <i>Escherichia coli</i>, purified, and characterised, revealing its ability to inhibit <i>Staphylococcus epidermidis</i> adhesion to surfaces, interfere with biofilm formation, and disrupt mature biofilms. Following biocompatibility assessment, <i>Psy</i>Omp38 was tested in combination with vancomycin as a potential treatment for established infections, revealing a reduction in the minimum biofilm eradication concentration (MBEC) of vancomycin. The potential of <i>Psy</i>Omp38 for material functionalisation was also explored. The protein was deposited onto silicone-based surfaces, and the coated materials were tested in a continuous-flow system that simulated real-life conditions. Additionally, the three-dimensional structure of <i>Psy</i>Omp38 was predicted and compared with homologous proteins. The structural analysis not only revealed the unique features of <i>Psy</i>Omp38 but also provided important insights into the molecular mechanisms underlying its antibiofilm activity.</p>","PeriodicalId":209,"journal":{"name":"Microbial Biotechnology","volume":"18 10","pages":""},"PeriodicalIF":5.2000,"publicationDate":"2025-10-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12504631/pdf/","citationCount":"0","resultStr":"{\"title\":\"Novel Insights Into the Struggle Against Biofilm: The PsyOmp38 Protein From the Antarctic Marine Bacterium Psychrobacter sp. 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The protein was heterologously expressed in <i>Escherichia coli</i>, purified, and characterised, revealing its ability to inhibit <i>Staphylococcus epidermidis</i> adhesion to surfaces, interfere with biofilm formation, and disrupt mature biofilms. Following biocompatibility assessment, <i>Psy</i>Omp38 was tested in combination with vancomycin as a potential treatment for established infections, revealing a reduction in the minimum biofilm eradication concentration (MBEC) of vancomycin. The potential of <i>Psy</i>Omp38 for material functionalisation was also explored. The protein was deposited onto silicone-based surfaces, and the coated materials were tested in a continuous-flow system that simulated real-life conditions. Additionally, the three-dimensional structure of <i>Psy</i>Omp38 was predicted and compared with homologous proteins. 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Novel Insights Into the Struggle Against Biofilm: The PsyOmp38 Protein From the Antarctic Marine Bacterium Psychrobacter sp. TAE2020
Antibiofilm molecules can enhance the effectiveness of antibiotics and prevent biofilm formation. Antarctic marine bacteria have been found to secrete antibiofilm molecules, likely as part of a strategy for competitive survival. The protein-polysaccharide complex CATASAN, produced by the Antarctic bacterium Psychrobacter sp. TAE2020, has been shown to interfere with all stages of Staphylococcus epidermidis biofilm development. This study investigates the contribution of PsyOmp38, the protein component of CATASAN, to the complex's antibiofilm activity. The protein was heterologously expressed in Escherichia coli, purified, and characterised, revealing its ability to inhibit Staphylococcus epidermidis adhesion to surfaces, interfere with biofilm formation, and disrupt mature biofilms. Following biocompatibility assessment, PsyOmp38 was tested in combination with vancomycin as a potential treatment for established infections, revealing a reduction in the minimum biofilm eradication concentration (MBEC) of vancomycin. The potential of PsyOmp38 for material functionalisation was also explored. The protein was deposited onto silicone-based surfaces, and the coated materials were tested in a continuous-flow system that simulated real-life conditions. Additionally, the three-dimensional structure of PsyOmp38 was predicted and compared with homologous proteins. The structural analysis not only revealed the unique features of PsyOmp38 but also provided important insights into the molecular mechanisms underlying its antibiofilm activity.
期刊介绍:
Microbial Biotechnology publishes papers of original research reporting significant advances in any aspect of microbial applications, including, but not limited to biotechnologies related to: Green chemistry; Primary metabolites; Food, beverages and supplements; Secondary metabolites and natural products; Pharmaceuticals; Diagnostics; Agriculture; Bioenergy; Biomining, including oil recovery and processing; Bioremediation; Biopolymers, biomaterials; Bionanotechnology; Biosurfactants and bioemulsifiers; Compatible solutes and bioprotectants; Biosensors, monitoring systems, quantitative microbial risk assessment; Technology development; Protein engineering; Functional genomics; Metabolic engineering; Metabolic design; Systems analysis, modelling; Process engineering; Biologically-based analytical methods; Microbially-based strategies in public health; Microbially-based strategies to influence global processes