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Ellagitannin-Lipid Interaction by HR-MAS NMR Spectroscopy

Puljula Elina; Karonen Maarit; Virtanen Valtteri; Räikkönen Susanna

dc.contributor.authorPuljula Elina
dc.contributor.authorKaronen Maarit
dc.contributor.authorVirtanen Valtteri
dc.contributor.authorRäikkönen Susanna
dc.date.accessioned2022-10-28T12:33:24Z
dc.date.available2022-10-28T12:33:24Z
dc.identifier.urihttps://www.utupub.fi/handle/10024/160374
dc.description.abstractEllagitannins have antimicrobial activity, which might be related to their interactions with membrane lipids. We studied the interactions of 12 different ellagitannins and pentagalloylglucose with a lipid extract of Escherichia coli by high-resolution magic angle spinning NMR spectroscopy. The nuclear Overhauser effect was utilized to measure the cross relaxation rates between ellagitannin and lipid protons. The shifting of lipid signals in 1H NMR spectra of ellagitannin-lipid mixture due to ring current effect was also observed. The ellagitannins that showed interaction with lipids had clear structural similarities. All ellagitannins that had interactions with lipids had glucopyranose cores. In addition to the central polyol, the most important structural feature affecting the interaction seemed to be the structural flexibility of the ellagitannin. Even dimeric and trimeric ellagitannins could penetrate to the lipid bilayers if their structures were flexible with free galloyl and hexahydroxydiphenoyl groups.
dc.language.isoen
dc.publisherMDPI
dc.titleEllagitannin-Lipid Interaction by HR-MAS NMR Spectroscopy
dc.identifier.urnURN:NBN:fi-fe2021042825176
dc.relation.volume26
dc.contributor.organizationfi=orgaaninen kemia ja kemiallinen biologia|en=Laboratory of Organic Chemistry and Chemical Biology|
dc.contributor.organization-code2606303
dc.converis.publication-id53389122
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/53389122
dc.identifier.eissn1420-3049
dc.identifier.jour-issn1420-3049
dc.okm.affiliatedauthorVirtanen, Valtteri
dc.okm.affiliatedauthorPuljula, Elina
dc.okm.affiliatedauthorKaronen, Maarit
dc.okm.discipline116 Kemiafi_FI
dc.okm.discipline116 Chemical sciencesen_GB
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeJournal article
dc.publisher.countrySwitzerlanden_GB
dc.publisher.countrySveitsifi_FI
dc.publisher.country-codeCH
dc.relation.articlenumberARTN 373
dc.relation.doi10.3390/molecules26020373
dc.relation.ispartofjournalMolecules
dc.relation.issue2
dc.year.issued2021


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