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Significative Inactivation of SARS-CoV-2 3CL- Protease by Camellia sinensis Galloylated theaflavins: Processing conditions to maximize TF-3,3 -DG content

dc.contributor.authorPaiva, Lisete
dc.contributor.authorRato, Catarina
dc.contributor.authorBaptista, José
dc.date.accessioned2024-03-05T12:34:11Z
dc.date.available2024-03-05T12:34:11Z
dc.date.issued2022-07-08
dc.date.updated2024-03-04T13:24:48Z
dc.description.abstractABSTRACT: Since the last decade of the 19th century, the Camellia sinensis tea plant is commercially produced in one unique place in Europe, the volcanic São Miguel Island of the Azores Archipelago (Portugal) [1,2]. The molecular constituents of C. sinensis, in particular the galloylated theaflavins, mainly theaflavin-3,3’-di-O-gallate (TF-3,3’-DG), have been reported to inhibit SARS-CoV-2 3-chymotrypsin-like protease (3CLpro), a crucial enzyme required for the cleavage of its polyproteins (1a and 1ab) to produce vital individual functional proteins for viral cell replication [3]. According to Ohgitani [4] the virus treated with galloylated theaflavins, particularly TF-3,3’-DG, at 100 µM showed less than 1/10.000 infectivity compared to untreated virus. The TF-3,3’-DG content increased 50.91% with increased fermentation time from 1 to 3 hrs at room temperature (RT) and increased 41.26% at 35 °C of fermentation temperature. Furthermore, TF-3,3’-DG increased 29.40% with increasing temperature from RT to 70 °C in short extraction time (1:30 hrs) and oppositely decreased 18.44% with increasing temperature from RT to 70 °C in long extraction time (16:00 hrs). Taking all of the in vitro reported studies by several research teams and the in vivo results comparing the COVID-19 infections (mortality per million of population) in high tea consumption (4.28%) as compared with low tea consumption countries [5], the aim of this study was to investigate the steps of tea manufacturing conditions which lead to maximum TF-3,3’-DG content and, given its potential impact as an inhibitor of the 3CLpro enzyme, to create a novel antiviral Azorean black tea.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationPaiva, L., Rato, C., & Baptista, J. (2022). Significative Inactivation of SARS-CoV-2 3CL- Protease by Camellia sinensis Galloylated theaflavins: Processing conditions to maximize TF-3,3’-DG contente. “Concepts of Dairy & Veterinary Sciences”, 5(1), 490-492. DOI: 10.32474/CDVS.2022.05.000202pt_PT
dc.identifier.doi10.32474/CDVS.2022.05.000202pt_PT
dc.identifier.issn2637-4649
dc.identifier.slugcv-prod-3958342
dc.identifier.urihttp://hdl.handle.net/10400.3/6967
dc.language.isoengpt_PT
dc.publisherLupine Publisherspt_PT
dc.subjectTea (C. sinensis) Flowerpt_PT
dc.subjectSão Miguel Island (Azores)pt_PT
dc.subjectCOVID-19pt_PT
dc.titleSignificative Inactivation of SARS-CoV-2 3CL- Protease by Camellia sinensis Galloylated theaflavins: Processing conditions to maximize TF-3,3 -DG contentpt_PT
dc.typeperiodical
dspace.entity.typePublication
oaire.citation.endPage492pt_PT
oaire.citation.issue1pt_PT
oaire.citation.startPage490pt_PT
oaire.citation.titleConcepts of Dairy & Veterinary Sciencespt_PT
oaire.citation.volume5pt_PT
person.familyNamePaiva
person.familyNameCastela dos Santos Rato
person.familyNameBaptista
person.givenNameLisete
person.givenNameCatarina
person.givenNameJosé
person.identifier417913
person.identifierF-5784-2012
person.identifier.ciencia-idF015-95D2-365B
person.identifier.ciencia-idE21A-1EBF-7FAB
person.identifier.orcid0000-0001-5281-2148
person.identifier.orcid0000-0002-8292-2433
person.identifier.orcid0000-0003-3035-7134
person.identifier.ridAGN-4771-2022
person.identifier.scopus-author-id37102328200
person.identifier.scopus-author-idhttps://www.scopus.com/authid/detail.uri?authorId=16319572200
rcaap.cv.cienciaidF015-95D2-365B | Lisete Sousa Paiva
rcaap.rightsopenAccesspt_PT
rcaap.typecontributionToPeriodicalpt_PT
relation.isAuthorOfPublicatione9a12d8f-9dc0-408c-a601-b83f56cd9831
relation.isAuthorOfPublicationd39c9858-6509-4635-a45b-1c8655b6fd26
relation.isAuthorOfPublicationb72fac75-b4a3-4f0c-bdff-9c2ac8bd4794
relation.isAuthorOfPublication.latestForDiscoverye9a12d8f-9dc0-408c-a601-b83f56cd9831

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