Bioproduction, structure elucidation and in vitro antiproliferative effect of eumelanin pigment from Streptomyces parvus BSB49

MakaleAçık ErişimScopus SJRQ2
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Özet

In this study, the structure of the purified extracellular eumelanin pigment isolated from Streptomyces spp. was elucidated by detailed analysis via two different spectroscopic techniques (FT-IR and NMR). In vitro antiproliferative effects of eumelanin were evaluated on HeLa cell line. These experiments were carried out with the evaluation of the parameters including cell viability, cell index, and mitotic index. With the cell viability and cell index, IC50 concentration of eumelanin was determined as 10 μM. This result showed that the IC50 concentration of eumelanin decreased the values of cell viability, cell index and mitotic index. These changes are statistically significant (p ' 0.01). The ability of the dissolved eumelanin (250 μg mL−1) to scavenge free radicals was determined via DPPH and ABTS and was shown to be about 87.73% and 75.2%, respectively, compared with standard antioxidants. It was observed that dry weights of eumelanin yield among the selected strains ranged from 160 to 240 mg L−1. The strain with the highest production potential was selected for 16S rDNA sequence analysis and, accordingly, the selected strain BSB49 was identified as Streptomyces parvus and the sequence analysis results were deposited in NCBI under accession number MK894155.

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https://rdlopen.rawdatalibrary.net/r/bayburt/13256Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1007/s00203-020-01956-2Yayıncı resmi DOI adresi
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Scopus
47
WoS
40
OpenAlex
48
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Tam Kayıt
AlanDeğerDil
dc.contributor.authorBayram, Sinan
dc.contributor.authorDengiz, Cagatay
dc.contributor.authorGerçek, Yusuf Can
dc.contributor.authorCetin, Idil
dc.contributor.authorTopcul, Mehmet R.
dc.date.accessioned2026-10-29T19:10:42.418180651Z
dc.date.available2026-10-29T19:10:42.418180651Z
dc.date.issued2020
dc.description.abstractIn this study, the structure of the purified extracellular eumelanin pigment isolated from Streptomyces spp. was elucidated by detailed analysis via two different spectroscopic techniques (FT-IR and NMR). In vitro antiproliferative effects of eumelanin were evaluated on HeLa cell line. These experiments were carried out with the evaluation of the parameters including cell viability, cell index, and mitotic index. With the cell viability and cell index, IC50 concentration of eumelanin was determined as 10 μM. This result showed that the IC50 concentration of eumelanin decreased the values of cell viability, cell index and mitotic index. These changes are statistically significant (p ' 0.01). The ability of the dissolved eumelanin (250 μg mL−1) to scavenge free radicals was determined via DPPH and ABTS and was shown to be about 87.73% and 75.2%, respectively, compared with standard antioxidants. It was observed that dry weights of eumelanin yield among the selected strains ranged from 160 to 240 mg L−1. The strain with the highest production potential was selected for 16S rDNA sequence analysis and, accordingly, the selected strain BSB49 was identified as Streptomyces parvus and the sequence analysis results were deposited in NCBI under accession number MK894155.
dc.description.sponsorshipBayburt University
dc.description.sponsorshipBayburt Üniversitesi, BÜ, (2019/01-69001-04)
dc.identifier.doi10.1007/s00203-020-01956-2
dc.identifier.eissn1432-072X
dc.identifier.endpage2409
dc.identifier.issn0302-8933
dc.identifier.issue9
dc.identifier.pmid32591909
dc.identifier.scopus2-s2.0-85086841102
dc.identifier.startpage2401
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/bayburt/13256
dc.identifier.volume202
dc.identifier.wosWOS:000543620700002
dc.language.isoen
dc.publisherSpringer Science and Business Media Deutschland GmbH
dc.relation.ispartofArchives of Microbiology
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAntioxidant effect
dc.subjectAntiproliferative effect
dc.subjectBioproduction
dc.subjectEumelanin
dc.subjectStructure elucidation
dc.subject.classificationMicrobiology
dc.subject.otherCell Survival
dc.subject.otherHeLa Cells
dc.subject.otherHumans
dc.subject.otherInhibitory Concentration 50
dc.subject.otherMagnetic Resonance Spectroscopy
dc.subject.otherMelanins
dc.subject.otherRNA, Ribosomal, 16S
dc.subject.otherSpectroscopy, Fourier Transform Infrared
dc.subject.otherStreptomyces
dc.subject.otherDNA 16S
dc.subject.othereumelanin
dc.subject.othermelanin
dc.subject.otherRNA 16S
dc.subject.otherABTS radical scavenging assay
dc.subject.otherantioxidant activity
dc.subject.otherantiproliferative activity
dc.subject.otherArticle
dc.subject.otherbacterial strain
dc.subject.otherbiotechnological production
dc.subject.othercell viability
dc.subject.otherchemical structure
dc.subject.othercontrolled study
dc.subject.otherDPPH radical scavenging assay
dc.subject.otherdry weight
dc.subject.otherFourier transform infrared spectroscopy
dc.subject.otherHeLa cell line
dc.subject.otherhuman
dc.subject.otherhuman cell
dc.subject.otherIC50
dc.subject.otherin vitro study
dc.subject.othermitosis index
dc.subject.othernonhuman
dc.subject.othernuclear magnetic resonance spectroscopy
dc.subject.othernucleotide sequence
dc.subject.otherpriority journal
dc.subject.othersequence analysis
dc.subject.otherStreptomyces parvus
dc.subject.otherultraviolet visible spectroscopy
dc.subject.otherchemistry
dc.subject.otherdrug effect
dc.subject.othergenetics
dc.subject.otherinfrared spectroscopy
dc.titleBioproduction, structure elucidation and in vitro antiproliferative effect of eumelanin pigment from Streptomyces parvus BSB49
dc.typeArticle
rdl.citation.openalex48
rdl.citation.scopus47
rdl.citation.wos40
rdl.departmentDepartment of Medical Services and Techniques, Vocational School of Health Services, Bayburt University, 69000, Bayburt, Turkey
rdl.departmentDepartment of Chemistry, Faculty of Sciences, Middle East Technical University, 06800, Ankara, Turkey
rdl.departmentDepartment of Biology, Faculty of Science, İstanbul University, 34116, Istanbul, Turkey
rdl.departmentCenter for Research and Practice in Biotechnologies of Genetically Modified Organisms, İstanbul University, Beyazit, 34126, Istanbul, Turkey
rdl.oa.statusgreen
rdl.oa.statuspreprint
rdl.oa.urlhttps://hdl.handle.net/11511/40653
rdl.scopus.quartileQ2
rdl.sdgSDG03
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)