RESUMO
The aim of this study is to assess the antibacterial and anti-biofilm properties of the lipid extract from Mantidis ootheca against the gentamycin resistant Pseudomonas aeruginosa. The chemical composition of the lipid extract and its relative proportion were determined using the technique of gas chromatography coupled with mass spectrometry (GC-MS). Antibacterial susceptibility tests were performed using a disc diffusion assay and the minimum inhibition concentration (MIC) was determined by way of the agar dilution method. The anti-biofilm test was carried out with crystal violet staining and scanning electron microscopy (SEM). There were 16 compounds detected, and the most abundant components were sesquiterpenoids, monoterpenes, and trace aromatic compounds. The MIC for P. aeruginosa was 4 mg/ml and the eradication effect on preformed biofilms was established and compared with a ciprofloxacin control. The results of our study indicated that a lipid extract from M. ootheca could be used as a topical and antibacterial agent with anti-biofilm activity in the future.
Assuntos
Antibacterianos/farmacologia , Biofilmes/efeitos dos fármacos , Mantódeos , Pseudomonas aeruginosa/efeitos dos fármacos , Animais , Cromatografia Gasosa-Espectrometria de Massas , Mantódeos/química , Testes de Sensibilidade MicrobianaRESUMO
Microorganisms provide both beneficial and harmful effects to human beings. Beneficial effects come from the symbiotic relationship that exists between humans and microbiota, but then several human illnesses have turned some friendly microbes into opportunistic pathogens, causing several microbial-related diseases. Various efforts have been made to create and utilize antimicrobial agents in the treatment and prevention of these infections, but such efforts have been hampered by the emergence of antimicrobial resistance. Despite extensive studies on drug discovery to alleviate this problem, issues with the toxicity and tolerance of certain compounds and continuous microbial evolution have forced researchers to focus on screening various phytochemical dietary compounds for antimicrobial activity. Linolenic acid and its derivatives (eicosapentaenoic acid and docosahexaenoic acid) are omega-3 fatty acids that have been studied due to their role in human health, being important for the brain, the eye, the cardiovascular system, and general human growth. However, their utilization as antimicrobial agents has not been widely appreciated, perhaps due to a lack of understanding of antimicrobial mechanisms, toxicity, and route of administration. Therefore, this review focuses on the efficacy, mechanism, and toxicity of omega-3 fatty acids as alternative therapeutic agents for treating and preventing diseases associated with pathogenic microorganisms.
Assuntos
Anti-Infecciosos/química , Infecções Bacterianas/tratamento farmacológico , Infecções Bacterianas/microbiologia , Ácidos Graxos Ômega-3/química , Animais , Animais Geneticamente Modificados , Antioxidantes/química , Membrana Celular/efeitos dos fármacos , Ensaios Clínicos como Assunto , Ácidos Docosa-Hexaenoicos/química , Farmacorresistência Bacteriana , Ácido Eicosapentaenoico/química , Peixes , Humanos , Lipídeos/química , Camundongos , Microbiota , Ratos , Ácido alfa-Linolênico/químicaRESUMO
In this study, an anti-oxidant and anti-tumor protein Latcripin-3 of Lentinula edodes C91-3 was expressed in Escherichia coli. for the first time. According to the cDNA library, the full-length gene of Latcripin-3 was cloned by the methods of 3'-full rapid amplification of cDNA Ends (RACE) and 5'-full RACE. The structural domain gene of Latcripin-3 was inserted into the pET32 a(+). The functional protein of Latcripin-3 was expressed in Rosetta-gami (DE3) E. coli, evaluated by Western blotting and mass spectrometry. DPPH testing showed that the protein Latcripin-3 can scavenge free radicals remarkably well. The activity of functional protein Latcripin-3 on A549 cells was studied with flow cytometry and the MTT method. The MTT assay results showed that there was a decreases in cell viability in a dose-dependent and time-dependent manner in protein Latcripin-3 treated groups. Flow cytometry demonstrated that Latcripin-3 can induce apoptosis and block S phase dramatically in human A549 lung cancer cells as compared to the control group. At the same time, the cell ultrastructure observed by transmission electron microscopy supported the results of flow cytometry. This research offers new insights and advantages for identifying anti-oxidant and anti-tumor proteins.
Assuntos
Antineoplásicos/metabolismo , Antioxidantes/metabolismo , Apoptose , Proliferação de Células , Proteínas Fúngicas/metabolismo , Neoplasias Pulmonares/metabolismo , Cogumelos Shiitake/química , Adenocarcinoma/metabolismo , Adenocarcinoma/patologia , Western Blotting , Ciclo Celular , Citometria de Fluxo , Proteínas Fúngicas/genética , Proteínas Fúngicas/isolamento & purificação , Humanos , Neoplasias Pulmonares/patologia , Células Tumorais CultivadasRESUMO
In the title compound, C(14)H(11)BrN(2)O(3)·H(2)O, the dihedral angle between the two benzene rings of the Schiff base is 22.7â (2)° and an intra-molecular O-Hâ¯O hydrogen bond is observed. In the crystal, mol-ecules are linked into layers parallel to the ab plane by O-Hâ¯O and N-Hâ¯O hydrogen bonds.