EpsA is an essential gene in exopolysaccharide production in Lactobacillus johnsonii FI9785
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.
- Scopus
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- WoS
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- OpenAlex
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Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Dertli, Enes | |
| dc.contributor.author | Mayer, Melinda J. | |
| dc.contributor.author | Colquhoun, Ian J. | |
| dc.contributor.author | Narbad, Arjan | |
| dc.date.accessioned | 2026-10-29T19:11:34.965480762Z | |
| dc.date.available | 2026-10-29T19:11:34.965480762Z | |
| dc.date.issued | 2016 | |
| dc.description.abstract | 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. | |
| dc.description.sponsorship | Biotechnology and Biological Sciences Research Council, BBSRC, (BBS/E/F/00044453) | |
| dc.description.sponsorship | Biotechnology and Biological Sciences Research Council, BBSRC | |
| dc.identifier.doi | 10.1111/1751-7915.12314 | |
| dc.identifier.eissn | 1751-7915 | |
| dc.identifier.endpage | 501 | |
| dc.identifier.issn | 1751-7907 | |
| dc.identifier.issue | 4 | |
| dc.identifier.pmcid | PMC4919991 | |
| dc.identifier.pmid | 26401596 | |
| dc.identifier.scopus | 2-s2.0-84976557103 | |
| dc.identifier.startpage | 496 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/bayburt/13877 | |
| dc.identifier.volume | 9 | |
| dc.identifier.wos | WOS:000379689900008 | |
| dc.language.iso | en | |
| dc.publisher | John Wiley and Sons Ltd | |
| dc.relation.ispartof | Microbial Biotechnology | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject.classification | Biotechnology & Applied Microbiology | |
| dc.subject.classification | Microbiology | |
| dc.subject.other | exopolysaccharide | |
| dc.subject.other | Article | |
| dc.subject.other | bacterial gene | |
| dc.subject.other | bacterial strain | |
| dc.subject.other | biosynthesis | |
| dc.subject.other | cell surface | |
| dc.subject.other | controlled study | |
| dc.subject.other | EpsA gene | |
| dc.subject.other | gene deletion | |
| dc.subject.other | gene expression | |
| dc.subject.other | gene function | |
| dc.subject.other | Lactobacillus johnsonii | |
| dc.subject.other | nonhuman | |
| dc.subject.other | nuclear magnetic resonance | |
| dc.subject.other | plasmid | |
| dc.subject.other | transmission electron microscopy | |
| dc.title | EpsA is an essential gene in exopolysaccharide production in Lactobacillus johnsonii FI9785 | |
| dc.type | Article | |
| rdl.citation.openalex | 39 | |
| rdl.citation.scopus | 43 | |
| rdl.citation.wos | 38 | |
| rdl.department | Department of Gut Health and Food Safety, Institute of Food Research, Norwich, Colney, NR4 7UA, UK | |
| rdl.department | Department of Food Engineering, Faculty of Engineering, Bayburt University, Bayburt, 69000, Turkey | |
| rdl.department | Analytical Sciences Unit, Institute of Food Research, Norwich, Colney, NR4 7UA, UK | |
| rdl.oa.status | gold | |
| rdl.oa.status | green | |
| rdl.oa.url | https://sfamjournals.onlinelibrary.wiley.com/doi/pdfdirect/10.1111/1751-7915.12314 | |
| rdl.scopus.quartile | Q1 | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.source.index | PUBMED | |
| rdl.wos.index | Science Citation Index Expanded (SCI-EXPANDED) |
