Proteomics disclose the effect of carbaon and nitrogen sources on GABA production by Levilactobacillus brevis CRL 2013

Autores
Cataldo, Pablo Gabriel; Ríos Colombo, Natalia Soledad; Savoy, Graciela; Saavedra, Maria Lucila; Hebert, Elvira Maria
Año de publicación
2022
Idioma
inglés
Tipo de recurso
documento de conferencia
Estado
versión publicada
Descripción
Gamma-aminobutyric acid (GABA) is a non-protein amino acid, which functions as the main inhibitory neurotransmitter in humans showing potential for improving several mental health conditions such as stress and anxiety. The microbiota-gut-brain axis is a bidirectional communication pathway between the central nervous system and the gut microbiota, which is mediated by several direct and indirect stimuli. Microbial GABA synthesis within the gut can affect host mental health outcomes. In bacteria, GABA is produced and released by the glutamate decarboxylase (GAD) system, which consists of three key elements: the positive transcriptional regulator (GadR), the glutamate/GABA antiporter (GadC) and the glutamate decarboxylase enzymes (GadA and/or GadB). Understanding the molecular characteristics of GABA production by the microbiota can provide insights into new therapies for mental health. Therefore, the aim of this study was to assess the effect of different nitrogen; yeast extract (YE) and casitone (C); and carbon (hexose and pentose) sources on the fermentation profile and GABA production by the efficient GABA producer, Levilactobacillus (L.) brevis CRL 2013 strain and explore the associated proteomic changes. GABA accumulated up to 72 h in glucose and fructose- CDM (CDMGF) supplemented with YE and C; this was related to a reduction in glutamate concentration and an increase in the extracellular pH. Lactic acid, acetic acid, and ethanol (2.5 g/L) could be detected in the fermented medium. In CDM-Xylose (CDMX), the cell density was markedly higher than in CDMGF, presenting the highest values of lactic (5.6 g/L) and acetic (3 g/L) acids while ethanol was not detected. Moreover, GABA production decreased about 13 times and the amount of residual glutamate was significantly higher (9 times) with respect to the CDMGF. The initial addition of ethanol to the CDMX increased both GABA production and the levels of organic acids. The proteomic data revealed that GadA was upregulated in CDMGF in the presence of YE and C (294 and 50 times, respectively). Under these conditions, GadB expression remained unchanged, whereas CcpA and HPr kinase were upregulated after YE and C supplementation (3.7 and 2-fold respectively). Furthermore, YE and C supplementation in the CDMGF induced the differential expression of proteases and peptidases. These expression trends were confirmed by transcriptional assays (RT-qPCR) with recA as the housekeeping gene. Additionally, ethanol supplementation increased gadA expression in the CDMX. Our results expand knowledge about the regulation of the GAD system in lactic acid bacteria, where carbon and nitrogen sources as well as some fermentation by-products may play a key role and support the use of L. brevis CRL2013 as a microbial cell factory for the efficient production of GABA using alternative energy sources.
Fil: Cataldo, Pablo Gabriel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Centro de Referencia para Lactobacilos; Argentina
Fil: Ríos Colombo, Natalia Soledad. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Centro de Referencia para Lactobacilos; Argentina
Fil: Savoy, Graciela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Centro de Referencia para Lactobacilos; Argentina
Fil: Saavedra, Maria Lucila. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Centro de Referencia para Lactobacilos; Argentina
Fil: Hebert, Elvira Maria. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Centro de Referencia para Lactobacilos; Argentina
LVII Annual Meeting of the Argentine Society for Biochemistry and Molecular Biology Research; XVI Annual Meeting of the Argentinean Society for General Microbiology
Ciudad Autónoma de Buenos Aires
Argentina
Sociedad Argentina de Microbiología General
Sociedad Argentina de Investigación Bioquímica y Biología Molecular
Materia
GABA
LACTIC ACID BACTERIA
PROTEOMICS
RT-qPCR
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/275714

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repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Proteomics disclose the effect of carbaon and nitrogen sources on GABA production by Levilactobacillus brevis CRL 2013Cataldo, Pablo GabrielRíos Colombo, Natalia SoledadSavoy, GracielaSaavedra, Maria LucilaHebert, Elvira MariaGABALACTIC ACID BACTERIAPROTEOMICSRT-qPCRhttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Gamma-aminobutyric acid (GABA) is a non-protein amino acid, which functions as the main inhibitory neurotransmitter in humans showing potential for improving several mental health conditions such as stress and anxiety. The microbiota-gut-brain axis is a bidirectional communication pathway between the central nervous system and the gut microbiota, which is mediated by several direct and indirect stimuli. Microbial GABA synthesis within the gut can affect host mental health outcomes. In bacteria, GABA is produced and released by the glutamate decarboxylase (GAD) system, which consists of three key elements: the positive transcriptional regulator (GadR), the glutamate/GABA antiporter (GadC) and the glutamate decarboxylase enzymes (GadA and/or GadB). Understanding the molecular characteristics of GABA production by the microbiota can provide insights into new therapies for mental health. Therefore, the aim of this study was to assess the effect of different nitrogen; yeast extract (YE) and casitone (C); and carbon (hexose and pentose) sources on the fermentation profile and GABA production by the efficient GABA producer, Levilactobacillus (L.) brevis CRL 2013 strain and explore the associated proteomic changes. GABA accumulated up to 72 h in glucose and fructose- CDM (CDMGF) supplemented with YE and C; this was related to a reduction in glutamate concentration and an increase in the extracellular pH. Lactic acid, acetic acid, and ethanol (2.5 g/L) could be detected in the fermented medium. In CDM-Xylose (CDMX), the cell density was markedly higher than in CDMGF, presenting the highest values of lactic (5.6 g/L) and acetic (3 g/L) acids while ethanol was not detected. Moreover, GABA production decreased about 13 times and the amount of residual glutamate was significantly higher (9 times) with respect to the CDMGF. The initial addition of ethanol to the CDMX increased both GABA production and the levels of organic acids. The proteomic data revealed that GadA was upregulated in CDMGF in the presence of YE and C (294 and 50 times, respectively). Under these conditions, GadB expression remained unchanged, whereas CcpA and HPr kinase were upregulated after YE and C supplementation (3.7 and 2-fold respectively). Furthermore, YE and C supplementation in the CDMGF induced the differential expression of proteases and peptidases. These expression trends were confirmed by transcriptional assays (RT-qPCR) with recA as the housekeeping gene. Additionally, ethanol supplementation increased gadA expression in the CDMX. Our results expand knowledge about the regulation of the GAD system in lactic acid bacteria, where carbon and nitrogen sources as well as some fermentation by-products may play a key role and support the use of L. brevis CRL2013 as a microbial cell factory for the efficient production of GABA using alternative energy sources.Fil: Cataldo, Pablo Gabriel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Centro de Referencia para Lactobacilos; ArgentinaFil: Ríos Colombo, Natalia Soledad. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Centro de Referencia para Lactobacilos; ArgentinaFil: Savoy, Graciela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Centro de Referencia para Lactobacilos; ArgentinaFil: Saavedra, Maria Lucila. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Centro de Referencia para Lactobacilos; ArgentinaFil: Hebert, Elvira Maria. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Centro de Referencia para Lactobacilos; ArgentinaLVII Annual Meeting of the Argentine Society for Biochemistry and Molecular Biology Research; XVI Annual Meeting of the Argentinean Society for General MicrobiologyCiudad Autónoma de Buenos AiresArgentinaSociedad Argentina de Microbiología GeneralSociedad Argentina de Investigación Bioquímica y Biología MolecularTech Science Press2022info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/conferenceObjectReuniónJournalhttp://purl.org/coar/resource_type/c_5794info:ar-repo/semantics/documentoDeConferenciaapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/275714Proteomics disclose the effect of carbaon and nitrogen sources on GABA production by Levilactobacillus brevis CRL 2013; LVII Annual Meeting of the Argentine Society for Biochemistry and Molecular Biology Research; XVI Annual Meeting of the Argentinean Society for General Microbiology; Ciudad Autónoma de Buenos Aires; Argentina; 2021; 144-1440327-95451667-5746CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://www.techscience.com/biocell/v46nSuppl.1/46213/pdfInternacionalinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-12-23T14:37:05Zoai:ri.conicet.gov.ar:11336/275714instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-12-23 14:37:06.235CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Proteomics disclose the effect of carbaon and nitrogen sources on GABA production by Levilactobacillus brevis CRL 2013
title Proteomics disclose the effect of carbaon and nitrogen sources on GABA production by Levilactobacillus brevis CRL 2013
spellingShingle Proteomics disclose the effect of carbaon and nitrogen sources on GABA production by Levilactobacillus brevis CRL 2013
Cataldo, Pablo Gabriel
GABA
LACTIC ACID BACTERIA
PROTEOMICS
RT-qPCR
title_short Proteomics disclose the effect of carbaon and nitrogen sources on GABA production by Levilactobacillus brevis CRL 2013
title_full Proteomics disclose the effect of carbaon and nitrogen sources on GABA production by Levilactobacillus brevis CRL 2013
title_fullStr Proteomics disclose the effect of carbaon and nitrogen sources on GABA production by Levilactobacillus brevis CRL 2013
title_full_unstemmed Proteomics disclose the effect of carbaon and nitrogen sources on GABA production by Levilactobacillus brevis CRL 2013
title_sort Proteomics disclose the effect of carbaon and nitrogen sources on GABA production by Levilactobacillus brevis CRL 2013
dc.creator.none.fl_str_mv Cataldo, Pablo Gabriel
Ríos Colombo, Natalia Soledad
Savoy, Graciela
Saavedra, Maria Lucila
Hebert, Elvira Maria
author Cataldo, Pablo Gabriel
author_facet Cataldo, Pablo Gabriel
Ríos Colombo, Natalia Soledad
Savoy, Graciela
Saavedra, Maria Lucila
Hebert, Elvira Maria
author_role author
author2 Ríos Colombo, Natalia Soledad
Savoy, Graciela
Saavedra, Maria Lucila
Hebert, Elvira Maria
author2_role author
author
author
author
dc.subject.none.fl_str_mv GABA
LACTIC ACID BACTERIA
PROTEOMICS
RT-qPCR
topic GABA
LACTIC ACID BACTERIA
PROTEOMICS
RT-qPCR
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv Gamma-aminobutyric acid (GABA) is a non-protein amino acid, which functions as the main inhibitory neurotransmitter in humans showing potential for improving several mental health conditions such as stress and anxiety. The microbiota-gut-brain axis is a bidirectional communication pathway between the central nervous system and the gut microbiota, which is mediated by several direct and indirect stimuli. Microbial GABA synthesis within the gut can affect host mental health outcomes. In bacteria, GABA is produced and released by the glutamate decarboxylase (GAD) system, which consists of three key elements: the positive transcriptional regulator (GadR), the glutamate/GABA antiporter (GadC) and the glutamate decarboxylase enzymes (GadA and/or GadB). Understanding the molecular characteristics of GABA production by the microbiota can provide insights into new therapies for mental health. Therefore, the aim of this study was to assess the effect of different nitrogen; yeast extract (YE) and casitone (C); and carbon (hexose and pentose) sources on the fermentation profile and GABA production by the efficient GABA producer, Levilactobacillus (L.) brevis CRL 2013 strain and explore the associated proteomic changes. GABA accumulated up to 72 h in glucose and fructose- CDM (CDMGF) supplemented with YE and C; this was related to a reduction in glutamate concentration and an increase in the extracellular pH. Lactic acid, acetic acid, and ethanol (2.5 g/L) could be detected in the fermented medium. In CDM-Xylose (CDMX), the cell density was markedly higher than in CDMGF, presenting the highest values of lactic (5.6 g/L) and acetic (3 g/L) acids while ethanol was not detected. Moreover, GABA production decreased about 13 times and the amount of residual glutamate was significantly higher (9 times) with respect to the CDMGF. The initial addition of ethanol to the CDMX increased both GABA production and the levels of organic acids. The proteomic data revealed that GadA was upregulated in CDMGF in the presence of YE and C (294 and 50 times, respectively). Under these conditions, GadB expression remained unchanged, whereas CcpA and HPr kinase were upregulated after YE and C supplementation (3.7 and 2-fold respectively). Furthermore, YE and C supplementation in the CDMGF induced the differential expression of proteases and peptidases. These expression trends were confirmed by transcriptional assays (RT-qPCR) with recA as the housekeeping gene. Additionally, ethanol supplementation increased gadA expression in the CDMX. Our results expand knowledge about the regulation of the GAD system in lactic acid bacteria, where carbon and nitrogen sources as well as some fermentation by-products may play a key role and support the use of L. brevis CRL2013 as a microbial cell factory for the efficient production of GABA using alternative energy sources.
Fil: Cataldo, Pablo Gabriel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Centro de Referencia para Lactobacilos; Argentina
Fil: Ríos Colombo, Natalia Soledad. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Centro de Referencia para Lactobacilos; Argentina
Fil: Savoy, Graciela. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Centro de Referencia para Lactobacilos; Argentina
Fil: Saavedra, Maria Lucila. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Centro de Referencia para Lactobacilos; Argentina
Fil: Hebert, Elvira Maria. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Centro de Referencia para Lactobacilos; Argentina
LVII Annual Meeting of the Argentine Society for Biochemistry and Molecular Biology Research; XVI Annual Meeting of the Argentinean Society for General Microbiology
Ciudad Autónoma de Buenos Aires
Argentina
Sociedad Argentina de Microbiología General
Sociedad Argentina de Investigación Bioquímica y Biología Molecular
description Gamma-aminobutyric acid (GABA) is a non-protein amino acid, which functions as the main inhibitory neurotransmitter in humans showing potential for improving several mental health conditions such as stress and anxiety. The microbiota-gut-brain axis is a bidirectional communication pathway between the central nervous system and the gut microbiota, which is mediated by several direct and indirect stimuli. Microbial GABA synthesis within the gut can affect host mental health outcomes. In bacteria, GABA is produced and released by the glutamate decarboxylase (GAD) system, which consists of three key elements: the positive transcriptional regulator (GadR), the glutamate/GABA antiporter (GadC) and the glutamate decarboxylase enzymes (GadA and/or GadB). Understanding the molecular characteristics of GABA production by the microbiota can provide insights into new therapies for mental health. Therefore, the aim of this study was to assess the effect of different nitrogen; yeast extract (YE) and casitone (C); and carbon (hexose and pentose) sources on the fermentation profile and GABA production by the efficient GABA producer, Levilactobacillus (L.) brevis CRL 2013 strain and explore the associated proteomic changes. GABA accumulated up to 72 h in glucose and fructose- CDM (CDMGF) supplemented with YE and C; this was related to a reduction in glutamate concentration and an increase in the extracellular pH. Lactic acid, acetic acid, and ethanol (2.5 g/L) could be detected in the fermented medium. In CDM-Xylose (CDMX), the cell density was markedly higher than in CDMGF, presenting the highest values of lactic (5.6 g/L) and acetic (3 g/L) acids while ethanol was not detected. Moreover, GABA production decreased about 13 times and the amount of residual glutamate was significantly higher (9 times) with respect to the CDMGF. The initial addition of ethanol to the CDMX increased both GABA production and the levels of organic acids. The proteomic data revealed that GadA was upregulated in CDMGF in the presence of YE and C (294 and 50 times, respectively). Under these conditions, GadB expression remained unchanged, whereas CcpA and HPr kinase were upregulated after YE and C supplementation (3.7 and 2-fold respectively). Furthermore, YE and C supplementation in the CDMGF induced the differential expression of proteases and peptidases. These expression trends were confirmed by transcriptional assays (RT-qPCR) with recA as the housekeeping gene. Additionally, ethanol supplementation increased gadA expression in the CDMX. Our results expand knowledge about the regulation of the GAD system in lactic acid bacteria, where carbon and nitrogen sources as well as some fermentation by-products may play a key role and support the use of L. brevis CRL2013 as a microbial cell factory for the efficient production of GABA using alternative energy sources.
publishDate 2022
dc.date.none.fl_str_mv 2022
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dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/275714
Proteomics disclose the effect of carbaon and nitrogen sources on GABA production by Levilactobacillus brevis CRL 2013; LVII Annual Meeting of the Argentine Society for Biochemistry and Molecular Biology Research; XVI Annual Meeting of the Argentinean Society for General Microbiology; Ciudad Autónoma de Buenos Aires; Argentina; 2021; 144-144
0327-9545
1667-5746
CONICET Digital
CONICET
url http://hdl.handle.net/11336/275714
identifier_str_mv Proteomics disclose the effect of carbaon and nitrogen sources on GABA production by Levilactobacillus brevis CRL 2013; LVII Annual Meeting of the Argentine Society for Biochemistry and Molecular Biology Research; XVI Annual Meeting of the Argentinean Society for General Microbiology; Ciudad Autónoma de Buenos Aires; Argentina; 2021; 144-144
0327-9545
1667-5746
CONICET Digital
CONICET
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