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
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/275714
Ver los metadatos del registro completo
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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. |
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2022 |
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2022 |
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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 |
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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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