EpsA is an essential gene in exopolysaccharide production in Lactobacillus johnsonii FI9785

MakaleAçık ErişimScopus SJRQ1

Özet

Lactobacillus johnsonii FI9785 has an eps gene cluster which is required for the biosynthesis of homopolymeric exopolysaccharides (EPS)-1 and heteropolymeric EPS-2 as a capsular layer. The first gene of the cluster, epsA, is the putative transcriptional regulator. In this study we showed the crucial role of epsA in EPS biosynthesis by demonstrating that deletion of epsA resulted in complete loss of both EPS-1 and EPS-2 on the cell surface. Plasmid complementation of the epsA gene fully restored EPS production, as confirmed by transmission electron microscopy and nuclear magnetic resonance (NMR) analysis. Furthermore, this complementation resulted in a twofold increase in the expression levels of this gene, which almost doubled amounts of EPS production in comparison with the wild-type strain. Analysis of EPS by NMR showed an increased ratio of the heteropolysaccharide to homopolysaccharide in the complemented strain and allowed identification of the acetylated residue in EPS-2 as the (1,4)-linked βGlcp unit, with the acetyl group located at O-6. These findings indicate that epsA is a positive regulator of EPS production and that EPS production can be manipulated by altering its expression.

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https://rdlopen.rawdatalibrary.net/r/bayburt/13877Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1111/1751-7915.12314Yayıncı resmi DOI adresi
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Scopus
43
WoS
38
OpenAlex
39
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Tam Kayıt
AlanDeğerDil
dc.contributor.authorDertli, Enes
dc.contributor.authorMayer, Melinda J.
dc.contributor.authorColquhoun, Ian J.
dc.contributor.authorNarbad, Arjan
dc.date.accessioned2026-10-29T19:11:34.965480762Z
dc.date.available2026-10-29T19:11:34.965480762Z
dc.date.issued2016
dc.description.abstractLactobacillus johnsonii FI9785 has an eps gene cluster which is required for the biosynthesis of homopolymeric exopolysaccharides (EPS)-1 and heteropolymeric EPS-2 as a capsular layer. The first gene of the cluster, epsA, is the putative transcriptional regulator. In this study we showed the crucial role of epsA in EPS biosynthesis by demonstrating that deletion of epsA resulted in complete loss of both EPS-1 and EPS-2 on the cell surface. Plasmid complementation of the epsA gene fully restored EPS production, as confirmed by transmission electron microscopy and nuclear magnetic resonance (NMR) analysis. Furthermore, this complementation resulted in a twofold increase in the expression levels of this gene, which almost doubled amounts of EPS production in comparison with the wild-type strain. Analysis of EPS by NMR showed an increased ratio of the heteropolysaccharide to homopolysaccharide in the complemented strain and allowed identification of the acetylated residue in EPS-2 as the (1,4)-linked βGlcp unit, with the acetyl group located at O-6. These findings indicate that epsA is a positive regulator of EPS production and that EPS production can be manipulated by altering its expression.
dc.description.sponsorshipBiotechnology and Biological Sciences Research Council, BBSRC, (BBS/E/F/00044453)
dc.description.sponsorshipBiotechnology and Biological Sciences Research Council, BBSRC
dc.identifier.doi10.1111/1751-7915.12314
dc.identifier.eissn1751-7915
dc.identifier.endpage501
dc.identifier.issn1751-7907
dc.identifier.issue4
dc.identifier.pmcidPMC4919991
dc.identifier.pmid26401596
dc.identifier.scopus2-s2.0-84976557103
dc.identifier.startpage496
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/bayburt/13877
dc.identifier.volume9
dc.identifier.wosWOS:000379689900008
dc.language.isoen
dc.publisherJohn Wiley and Sons Ltd
dc.relation.ispartofMicrobial Biotechnology
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subject.classificationBiotechnology & Applied Microbiology
dc.subject.classificationMicrobiology
dc.subject.otherexopolysaccharide
dc.subject.otherArticle
dc.subject.otherbacterial gene
dc.subject.otherbacterial strain
dc.subject.otherbiosynthesis
dc.subject.othercell surface
dc.subject.othercontrolled study
dc.subject.otherEpsA gene
dc.subject.othergene deletion
dc.subject.othergene expression
dc.subject.othergene function
dc.subject.otherLactobacillus johnsonii
dc.subject.othernonhuman
dc.subject.othernuclear magnetic resonance
dc.subject.otherplasmid
dc.subject.othertransmission electron microscopy
dc.titleEpsA is an essential gene in exopolysaccharide production in Lactobacillus johnsonii FI9785
dc.typeArticle
rdl.citation.openalex39
rdl.citation.scopus43
rdl.citation.wos38
rdl.departmentDepartment of Gut Health and Food Safety, Institute of Food Research, Norwich, Colney, NR4 7UA, UK
rdl.departmentDepartment of Food Engineering, Faculty of Engineering, Bayburt University, Bayburt, 69000, Turkey
rdl.departmentAnalytical Sciences Unit, Institute of Food Research, Norwich, Colney, NR4 7UA, UK
rdl.oa.statusgold
rdl.oa.statusgreen
rdl.oa.urlhttps://sfamjournals.onlinelibrary.wiley.com/doi/pdfdirect/10.1111/1751-7915.12314
rdl.scopus.quartileQ1
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)