نمایش مختصر رکورد

dc.contributor.authorHassani, Soniaen_US
dc.contributor.authorSotoodehnejadnematalahi, Fattahen_US
dc.contributor.authorFateh, Abolfazlen_US
dc.contributor.authorSiadat, Seyed Davaren_US
dc.date.accessioned1401-06-20T06:39:07Zfa_IR
dc.date.accessioned2022-09-11T06:39:27Z
dc.date.available1401-06-20T06:39:07Zfa_IR
dc.date.available2022-09-11T06:39:27Z
dc.date.issued2021-05-01en_US
dc.date.issued1400-02-11fa_IR
dc.identifier.citation(1400). مجله مطالعات علوم پزشکی, 32(3), 225-233.fa_IR
dc.identifier.issn2717-008X
dc.identifier.urihttp://umj.umsu.ac.ir/article-1-5197-en.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/928092
dc.description.abstractBackground & Aims: Bacteria naturally secret nano-scale vesicles containing a wide range of biomolecules, such as proteins, DNA, and RNA. These vesicles are called extracellular vesicles (EVs). EVs play important roles in host-microbiota interactions. For isolating EVs, different methods have been proposed and each method has its advantages and also limitations. Therefore, in the current study, efficacy of two methods used for extraction of EVs was investigated. Materials & Methods: For this purpose, Bifidobacterium bifidum was cultured in MRS broth under anaerobic conditions. In the first isolation protocol, ultra-centrifugation was used (Ultra-method) and in the second protocol, ultra-centrifugation (Non-Ultra method) was not used. After isolation, protein content was measured by the NanoDrop system. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) technique was utilized to compare protein pattern of the EVs. Scanning electron microscopy (SEM) images of the EVs҆ samples were taken and size of the EVs was evaluated by Digimizer software. Results: The results showed that the EVs isolated by the Ultra-method had significantly higher vesicle-associated protein content compared to those isolated by the Non-Ultra method (3.42 and 0.26 mg/ml, respectively). More and larger EVs (up to 235 nm and with frequent size ranging between 100 – 125 nm) were isolated by the Ultra-method compared to the Non-Ultra method (up to 117 nm and with frequent size ranging between 50–75 nm). Also, protein patterns of the EVs were similar in both methods and protein bands were observed at 25 to 250 KDa in both methods. Conclusion: Our results showed that ultra-centrifugation method is a more proper method for isolation of B. bifidum-derived EVs and produces a higher amount of EVs with higher protein content and proper sizes. However, further studies are required to confirm our results.en_US
dc.languageEnglish
dc.language.isoen_US
dc.publisherدانشگاه علوم پزشکی ارومیهfa_IR
dc.relation.ispartofمجله مطالعات علوم پزشکیfa_IR
dc.relation.ispartofStudies in Medical Sciencesen_US
dc.subjectBifidobacterium bifidumen_US
dc.subjectExtracellular Vesiclesen_US
dc.subjectUltra-Centrifugationen_US
dc.subjectIsolation Methodsen_US
dc.subjectمیکروبیولوژیen_US
dc.titleEvaluation of efficiency of Methods used for extraction of Bifidobacterium bifidum-Derived Extracellular Vesicles: An experimental studyen_US
dc.typeTexten_US
dc.typeResearchen_US
dc.contributor.departmentPh.D, Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iranen_US
dc.contributor.departmentPh.D, Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iranen_US
dc.contributor.departmentPh.D, Department of Mycobacteriology and Pulmonary Research, Pasteur Institute of Iran, Tehran, Iranen_US
dc.contributor.departmentPh.D, Microbiology Research Center (MRC), Pasteur Institute of Iran, Tehran, Iran (Corresponding Author)en_US
dc.citation.volume32
dc.citation.issue3
dc.citation.spage225
dc.citation.epage233


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