Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/2181
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dc.contributor.authorStanković, Slavišaen_US
dc.contributor.authorMihajlović, Sanjaen_US
dc.contributor.authorDraganić, V.en_US
dc.contributor.authorDimkić, Ivicaen_US
dc.contributor.authorVukotić, Goranen_US
dc.contributor.authorBerić, Tanjaen_US
dc.contributor.authorFira, Djordjeen_US
dc.date.accessioned2019-10-23T08:52:29Z-
dc.date.available2019-10-23T08:52:29Z-
dc.date.issued2012-10-29-
dc.identifier.issn0354-4664-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/2181-
dc.description.abstractA collection of 205 natural isolates of Bacillus was tested for the presence of genes for biosynthesis of antimicrobial lipopeptides, iturin, surfactin, fengycin and bacillomycin D. For the detection of iturin producers by PCR screening, we used forward ITUP1-F and reverse ITUP2-R primers which are capable of detecting a 2-kb region that includes the intergenic sequence between the ituA and ituB genes. A 675-bp fragment from the gene sfp from B. subtilis encoding 4'-phosphopantetheinyl transferase involved in the biosynthesis of surfactin was targeted for amplification by using primers P17 and P18. Other two pairs of primers were BACC1F and BACC1R for bacillomycin D and FEND1F and FEND1R for potential fengycin producers, respectively. The results of the screening showed that the majority of tested strains had more than one biosynthetic operon, since 81% possessed the genes for bacillomycin D production, 54% for surfactin, 38% for iturin and 25% for fengycin production.en_US
dc.publisherSrpsko biološko društvo i grupa naučnih institutaen_US
dc.relation.ispartofArchives of Biological Sciencesen_US
dc.subjectBacillomycinen_US
dc.subjectBacillusen_US
dc.subjectFengycinen_US
dc.subjectIturinen_US
dc.subjectSurfactinen_US
dc.titleScreening for the presence of biosynthetic genes for antimicrobial lipopeptides in natural isolates of Bacillus spen_US
dc.typeArticleen_US
dc.identifier.doi10.2298/ABS1204425S-
dc.identifier.scopus2-s2.0-84867804543-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/84867804543-
dc.description.rankM23en_US
dc.description.impact0.791en_US
dc.description.startpage1425en_US
dc.description.endpage1432en_US
dc.relation.issn0354-4664en_US
dc.description.volume64en_US
dc.description.issue4en_US
item.cerifentitytypePublications-
item.openairetypeArticle-
item.fulltextWith Fulltext-
item.grantfulltextrestricted-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptChair of Microbiology-
crisitem.author.deptChair of Biochemistry and Molecular Biology-
crisitem.author.deptChair of Biochemistry and Molecular Biology-
crisitem.author.deptChair of Microbiology-
crisitem.author.deptChair of Biochemistry and Molecular Biology-
crisitem.author.orcid0000-0003-0527-8741-
crisitem.author.orcid0000-0002-0425-5938-
crisitem.author.orcid0000-0001-9343-6214-
crisitem.author.orcid0000-0002-4860-2225-
crisitem.author.orcid0000-0002-8773-8213-
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