نمایش مختصر رکورد

dc.contributor.authorBiglari, Saraen_US
dc.contributor.authorShahidi, Gholam Hoseinen_US
dc.contributor.authorSharifi, Gholam Rezaen_US
dc.date.accessioned1399-07-08T23:36:37Zfa_IR
dc.date.accessioned2020-09-29T23:36:37Z
dc.date.available1399-07-08T23:36:37Zfa_IR
dc.date.available2020-09-29T23:36:37Z
dc.date.issued2014-09-01en_US
dc.date.issued1393-06-10fa_IR
dc.date.submitted2014-05-08en_US
dc.date.submitted1393-02-18fa_IR
dc.identifier.citationBiglari, Sara, Shahidi, Gholam Hosein, Sharifi, Gholam Reza. (2014). Production of gold nanoparticles by Streptomyces djakartensis isolate B-5. Nanomedicine Journal, 1(4), 229-237. doi: 10.7508/nmj.2015.04.003en_US
dc.identifier.issn2322-3049
dc.identifier.issn2322-5904
dc.identifier.urihttps://dx.doi.org/10.7508/nmj.2015.04.003
dc.identifier.urihttp://nmj.mums.ac.ir/article_2713.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/158533
dc.description.abstractObjective(s):  <br/>Biosynthesis of gold nanoparticles (NGPs) is environmentally safer than chemical and physical procedures. This method requires no use of toxic solvents and synthesis of dangerous products and is environmentally safe. In this study, we report the biosynthesis of NGPs using Streptomyces djakartensis <br/>isolate B-5.   <br/>Materials and Methods: <br/>NGPs were biosynthesized by reducing aqueous gold chloride solution via a Streptomyces isolate without the need for any additive for protecting nanoparticles from aggregation. We characterized the responsible Streptomycete<span><span>; its genome DNA was isolated, purified and 16S rRNA was amplified by PCR. The amplified isolate was sequenced; using the BLAST search tool from NCBI, the microorganism was identified to species level.   <br/></span></span><br/>Results: <br/>Treating chloroauric acid solutions with this bacterium resulted in reduction of gold ions and formation of stable NGPs. TEM and SEM electro micrographs of NGPs indicated size range from 2- 25 nm with average of 9.09 nm produced intracellular by the bacterium. SEM electro micrographs revealed morphology of spores and mycelia. The amplified PCR fragment of 16S rRNA gene was cloned and sequenced from both sides; it consisted of 741 nucleotides. According to NCBI GenBank, the bacterium had 97.1% homology with Streptomyces djakartensis <span><span>strain RT-49. The GenBank accession number for partial 16S rRNA gene was recorded as JX162550.   <br/></span></span><br/>Conclusion: <br/>Optimized application of such findings may create applications of Streptomycetes for use as bio-factories in eco-friendly production of NGPs to serve in demanding industries and related biomedical areas. Research in this area should also focus on the unlocking the full mechanism of NGPs biosynthesis by Streptomycetes<span><span>. </span></span>en_US
dc.format.extent610
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherMashhad University of Medical Sciencesen_US
dc.relation.ispartofNanomedicine Journalen_US
dc.relation.isversionofhttps://dx.doi.org/10.7508/nmj.2015.04.003
dc.subjectBio-factoryen_US
dc.subjectGreen synthesisen_US
dc.subjectNanogolden_US
dc.subjectBiosynthesisen_US
dc.subjectrRNAen_US
dc.subjectStreptomycesen_US
dc.titleProduction of gold nanoparticles by Streptomyces djakartensis isolate B-5en_US
dc.typeTexten_US
dc.typeResearch Paperen_US
dc.contributor.departmentDepartment of Agricultural Biotechnology, College of Agriculture, Shahid Bahonar University of Kerman, Iranen_US
dc.contributor.departmentDepartment of Plant pathology, College of Agriculture, Shahid Bahonar University of Kerman, Iranen_US
dc.contributor.departmentDepartment of Agricultural Biotechnology, College of Agriculture, Hormozgan University, Iranen_US
dc.citation.volume1
dc.citation.issue4
dc.citation.spage229
dc.citation.epage237


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