98%
921
2 minutes
20
Staphylococcus aureus is a common food-borne pathogenic microorganism that poses a serious threat to food quality and safety, and can do harm to human health. In the past, researchers relied on antibiotics to control Staphylococcus aureus, though very effective, yet it was also worrying in the aspect of bio-safety. In fact, anti-idiotypic antibody (Anti-Id) shows its potential to mimic some of the structural and biological functions of antigens. Therefore, in this study, based on Anti-Id theory and technology, we expect to obtain the vancomycin Anti-Id which can mimic vancomycin against Staphylococcus aureus from a human phage display domain antibody library. After four rounds of bio-panning, a total of 18 positive Anti-Ids were obtained. Among them, two Anti-Ids named Anti-Id-2C12 and Anti-Id-1F5 were identified as "β" type Anti-Ids, and afterwards they were selected for gene cloning and protein expression in prokaryotic expression system. As a result, a concentration of purified proteins with 568.6 μg/mL (Anti-Id-2C12) and 602.3 μg/mL (Anti-Id-1F5) were successfully obtained, and their minimum inhibitory concentration (MIC) values for Staphylococcus aureus were 125 and 200 μg/mL, respectively. As they are human heavy-chain domain antibodies, which were theoretically harmless to humans, they have the potential application value as preservatives in food and edible agricultural products.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.imlet.2022.04.005 | DOI Listing |
Int J Biol Macromol
September 2025
School of Ethnic Medicine, Chengdu University of Traditional Chinese Medicine, China. Electronic address:
Wound healing is often hindered by bacterial infection, oxidative stress, and bleeding. Traditional dressings cannot simultaneously regulate multiple microenvironments. To address the shortcomings of traditional dressings, this study constructed a dual-network photothermal responsive multifunctional hydrogel OBCTCu based on four natural ingredients, including Bletilla striata polysaccharide (BSP), chitosan (CS), tannic acid (TA), and Cu.
View Article and Find Full Text PDFInt J Biol Macromol
September 2025
School of textile science and Engineering, Wuhan Textile University, Wuhan, Hubei, 430000, China.
As living standards continue to rise, the demand for advanced cotton textiles that fulfill enhanced functional requirements has grown significantly. Therefore, the development of multifunctional antibacterial/hydrophobic cotton fabrics holds considerable practical value. In this study, a zeolitic imidazolate framework (ZIF-8) based hybrid material, ZIF/SiO-LDS (Long-chain derivative of silane), was synthesized via a co-precipitation method using silica, zinc nitrate hexahydrate, 3-aminopropyltriethoxysilane (KH-550), 2-methylimidazole and hexadecyltrimethylsilane (HDTMS).
View Article and Find Full Text PDFJ Ethnopharmacol
September 2025
Center for Biosciences, Federal University of Pernambuco - UFPE, 50670-901, Recife, Brazil.
Ethnopharmacological Relevance: Myrciaria pilosa is a medicinal species traditionally used to treat inflammation, pain and infectious diseases. Essential oils extracted from medicinal plants have recently gained prominence as adjuvants in combating microbial resistance due to their antimicrobial properties and synergistic potential when combined with conventional antibiotics.
Aim Of The Study: Investigated the chemical composition, antibacterial activity, antibiofilm effects, and antibiotic-enhancing properties of Myrciaria pilosa essential oil.
Toxicon
September 2025
Departamento de Bioquímica, Centro de Biociências, Universidade Federal de Pernambuco, Recife, Pernambuco, Brazil. Electronic address:
Lithobates palmipes is a frog species whose skin secretions contain peptides belonging to the ranatuerin, brevinin, and temporin families. In this study, the peptide ranatuerin-2PMe was isolated and evaluated for its antimicrobial, hemolytic, antiproliferative, and chemotactic activities. Ranatuerin-2PMe (2933.
View Article and Find Full Text PDFBioorg Med Chem
September 2025
Pharmaceutical Chemistry Department, Faculty of Pharmacy, Ain Shams University, Abbassia, Cairo 11566, Egypt. Electronic address:
With the continued upsurge of antibiotic resistance and reduced susceptibility to almost all frontline antibiotics, there is a pressing need for the development of new, effective, and safe alternatives. In this study, a scaffold-hopping strategy was utilized to develop a novel class of penicillin-binding protein 2a (PBP2a) inhibitors, centered around a 4H-chromen-4-one core structure. These newly designed compounds demonstrated strong antibacterial efficacy against methicillin-resistant Staphylococcus aureus (MRSA) and other drug-resistant gram-positive pathogens.
View Article and Find Full Text PDF