Cargando…

Metabolomic and Transcriptional Profiling of Oleuropein Bioconversion into Hydroxytyrosol during Table Olive Fermentation by Lactiplantibacillus plantarum

This study aims to elucidate the mechanisms responsible for the bioconversion of oleuropein into low-molecular-weight phenolic compounds in two selected Lactiplantibacillus plantarum strains, namely, C11C8 and F3.5, under stress brine conditions and at two different temperatures (16°C and 30°C). For...

Descripción completa

Detalles Bibliográficos
Autores principales: Vaccalluzzo, Amanda, Solieri, Lisa, Tagliazucchi, Davide, Cattivelli, Alice, Martini, Serena, Pino, Alessandra, Caggia, Cinzia, Randazzo, Cinzia L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8939334/
https://www.ncbi.nlm.nih.gov/pubmed/35170988
http://dx.doi.org/10.1128/aem.02019-21
_version_ 1784672711009632256
author Vaccalluzzo, Amanda
Solieri, Lisa
Tagliazucchi, Davide
Cattivelli, Alice
Martini, Serena
Pino, Alessandra
Caggia, Cinzia
Randazzo, Cinzia L.
author_facet Vaccalluzzo, Amanda
Solieri, Lisa
Tagliazucchi, Davide
Cattivelli, Alice
Martini, Serena
Pino, Alessandra
Caggia, Cinzia
Randazzo, Cinzia L.
author_sort Vaccalluzzo, Amanda
collection PubMed
description This study aims to elucidate the mechanisms responsible for the bioconversion of oleuropein into low-molecular-weight phenolic compounds in two selected Lactiplantibacillus plantarum strains, namely, C11C8 and F3.5, under stress brine conditions and at two different temperatures (16°C and 30°C). For this purpose, we adopted an experimental strategy that combined high-resolution mass spectrometry, in silico functional analysis of glycoside hydrolase family 1 (GH1)-encoding candidate genes, and gene expression studies. The oleuropein hydrolysis products and the underlying enzymatic steps were identified, and a novel putative bgl gene was detected, using seven strains belonging to the same species as controls. According to metabolomic analysis, a new intermediate compound (decarboxymethyl dialdehydic form of oleuropein aglycone) was revealed. In addition, strain C11C8 showed a decrease in the oleuropein content greater than that of the F3.5 strain (30% versus 15%) at a temperature of 16°C. The highest increase in hydroxytyrosol was depicted by strain C11C8 at a temperature of 30°C. PCR assays and sequencing analyses revealed that both strains possess bglH1, bglH2, and bglH3 genes. Furthermore, a reverse transcription-PCR (RT-PCR) assay showed that bglH3 is the only gene transcribed under all tested conditions, while bglH2 is switched off in strain C11C8 grown at cold temperatures, and no transcription was detected for the bglH1 gene. The bglH3 gene encodes a 6-phospho-β-glucosidase, suggesting how phospho-β-glucosidase activity could belong to the overall metabolic strategy undertaken by L. plantarum to survive in an environment poor in free sugars, like table olives. IMPORTANCE In the present study, a new candidate gene, bglH3, responsible for the β-glucosidase-positive phenotype in L. plantarum was detected, providing the basis for the future marker-assisted selection of L. plantarum starter strains with a β-glucosidase-positive phenotype. Furthermore, the ability of selected strains to hydrolyze oleuropein at low temperatures is important for application as starter cultures on an industrial scale.
format Online
Article
Text
id pubmed-8939334
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-89393342022-03-23 Metabolomic and Transcriptional Profiling of Oleuropein Bioconversion into Hydroxytyrosol during Table Olive Fermentation by Lactiplantibacillus plantarum Vaccalluzzo, Amanda Solieri, Lisa Tagliazucchi, Davide Cattivelli, Alice Martini, Serena Pino, Alessandra Caggia, Cinzia Randazzo, Cinzia L. Appl Environ Microbiol Food Microbiology This study aims to elucidate the mechanisms responsible for the bioconversion of oleuropein into low-molecular-weight phenolic compounds in two selected Lactiplantibacillus plantarum strains, namely, C11C8 and F3.5, under stress brine conditions and at two different temperatures (16°C and 30°C). For this purpose, we adopted an experimental strategy that combined high-resolution mass spectrometry, in silico functional analysis of glycoside hydrolase family 1 (GH1)-encoding candidate genes, and gene expression studies. The oleuropein hydrolysis products and the underlying enzymatic steps were identified, and a novel putative bgl gene was detected, using seven strains belonging to the same species as controls. According to metabolomic analysis, a new intermediate compound (decarboxymethyl dialdehydic form of oleuropein aglycone) was revealed. In addition, strain C11C8 showed a decrease in the oleuropein content greater than that of the F3.5 strain (30% versus 15%) at a temperature of 16°C. The highest increase in hydroxytyrosol was depicted by strain C11C8 at a temperature of 30°C. PCR assays and sequencing analyses revealed that both strains possess bglH1, bglH2, and bglH3 genes. Furthermore, a reverse transcription-PCR (RT-PCR) assay showed that bglH3 is the only gene transcribed under all tested conditions, while bglH2 is switched off in strain C11C8 grown at cold temperatures, and no transcription was detected for the bglH1 gene. The bglH3 gene encodes a 6-phospho-β-glucosidase, suggesting how phospho-β-glucosidase activity could belong to the overall metabolic strategy undertaken by L. plantarum to survive in an environment poor in free sugars, like table olives. IMPORTANCE In the present study, a new candidate gene, bglH3, responsible for the β-glucosidase-positive phenotype in L. plantarum was detected, providing the basis for the future marker-assisted selection of L. plantarum starter strains with a β-glucosidase-positive phenotype. Furthermore, the ability of selected strains to hydrolyze oleuropein at low temperatures is important for application as starter cultures on an industrial scale. American Society for Microbiology 2022-03-22 /pmc/articles/PMC8939334/ /pubmed/35170988 http://dx.doi.org/10.1128/aem.02019-21 Text en Copyright © 2022 Vaccalluzzo et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Food Microbiology
Vaccalluzzo, Amanda
Solieri, Lisa
Tagliazucchi, Davide
Cattivelli, Alice
Martini, Serena
Pino, Alessandra
Caggia, Cinzia
Randazzo, Cinzia L.
Metabolomic and Transcriptional Profiling of Oleuropein Bioconversion into Hydroxytyrosol during Table Olive Fermentation by Lactiplantibacillus plantarum
title Metabolomic and Transcriptional Profiling of Oleuropein Bioconversion into Hydroxytyrosol during Table Olive Fermentation by Lactiplantibacillus plantarum
title_full Metabolomic and Transcriptional Profiling of Oleuropein Bioconversion into Hydroxytyrosol during Table Olive Fermentation by Lactiplantibacillus plantarum
title_fullStr Metabolomic and Transcriptional Profiling of Oleuropein Bioconversion into Hydroxytyrosol during Table Olive Fermentation by Lactiplantibacillus plantarum
title_full_unstemmed Metabolomic and Transcriptional Profiling of Oleuropein Bioconversion into Hydroxytyrosol during Table Olive Fermentation by Lactiplantibacillus plantarum
title_short Metabolomic and Transcriptional Profiling of Oleuropein Bioconversion into Hydroxytyrosol during Table Olive Fermentation by Lactiplantibacillus plantarum
title_sort metabolomic and transcriptional profiling of oleuropein bioconversion into hydroxytyrosol during table olive fermentation by lactiplantibacillus plantarum
topic Food Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8939334/
https://www.ncbi.nlm.nih.gov/pubmed/35170988
http://dx.doi.org/10.1128/aem.02019-21
work_keys_str_mv AT vaccalluzzoamanda metabolomicandtranscriptionalprofilingofoleuropeinbioconversionintohydroxytyrosolduringtableolivefermentationbylactiplantibacillusplantarum
AT solierilisa metabolomicandtranscriptionalprofilingofoleuropeinbioconversionintohydroxytyrosolduringtableolivefermentationbylactiplantibacillusplantarum
AT tagliazucchidavide metabolomicandtranscriptionalprofilingofoleuropeinbioconversionintohydroxytyrosolduringtableolivefermentationbylactiplantibacillusplantarum
AT cattivellialice metabolomicandtranscriptionalprofilingofoleuropeinbioconversionintohydroxytyrosolduringtableolivefermentationbylactiplantibacillusplantarum
AT martiniserena metabolomicandtranscriptionalprofilingofoleuropeinbioconversionintohydroxytyrosolduringtableolivefermentationbylactiplantibacillusplantarum
AT pinoalessandra metabolomicandtranscriptionalprofilingofoleuropeinbioconversionintohydroxytyrosolduringtableolivefermentationbylactiplantibacillusplantarum
AT caggiacinzia metabolomicandtranscriptionalprofilingofoleuropeinbioconversionintohydroxytyrosolduringtableolivefermentationbylactiplantibacillusplantarum
AT randazzocinzial metabolomicandtranscriptionalprofilingofoleuropeinbioconversionintohydroxytyrosolduringtableolivefermentationbylactiplantibacillusplantarum