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Understanding the response of Desulfovibrio desulfuricans ATCC 27774 to the electron acceptors nitrate and sulfate - biosynthetic costs modulate substrate selection.

Identifieur interne : 000A46 ( Main/Exploration ); précédent : 000A45; suivant : 000A47

Understanding the response of Desulfovibrio desulfuricans ATCC 27774 to the electron acceptors nitrate and sulfate - biosynthetic costs modulate substrate selection.

Auteurs : Joana R. Sousa [Portugal] ; Célia M. Silveira [Portugal] ; Pedro Fontes [Portugal] ; Catarina Roma-Rodrigues [Portugal] ; Alexandra R. Fernandes [Portugal] ; Gonzalez Van Driessche [Portugal] ; Bart Devreese [Belgique] ; Isabel Moura [Portugal] ; José J G. Moura [Portugal] ; M Gabriela Almeida [Portugal]

Source :

RBID : pubmed:28847524

Descripteurs français

English descriptors

Abstract

Sulfate-reducing bacteria (SRB) are a diverse group of anaerobic microorganisms that obtain their energy from dissimilatory sulfate reduction. Some SRB species have high respiratory versatility due to the possible use of alternative electron acceptors. A good example is Desulfovibrio desulfuricans ATCC 27774, which grows in the presence of nitrate (end product: ammonium) with higher rates and yields to those observed in sulfate containing medium (end product: sulfide). In this work, the mechanisms supporting the respiratory versatility of D. desulfuricans were unraveled through the analysis of the proteome of the bacterium under different experimental conditions. The most remarkable difference in the two-dimensional gel electrophoresis maps is the high number of spots exclusively represented in the nitrate medium. Most of the proteins with increase abundance are involved in the energy metabolism and the biosynthesis of amino acids (or proteins), especially those participating in ammonium assimilation processes. qPCR analysis performed during different stages of the bacterium's growth showed that the genes involved in nitrate and nitrite reduction (napA and nrfA, respectively) have different expressions profiles: while napA did not vary significantly, nrfA was highly expressed at a 6h time point. Nitrite levels measured along the growth curve revealed a peak at 3h. Thus, the initial consumption of nitrate and concomitant production of nitrite must induce nrfA expression. The activation of alternative mechanisms for energy production, aside several N-assimilation metabolisms and detoxification processes, solves potential survival problems in adapting to different environments and contributes to higher bacterial growth rates.

DOI: 10.1016/j.bbapap.2017.07.021
PubMed: 28847524


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<term>Bacterial Proteins (metabolism)</term>
<term>Culture Media (chemistry)</term>
<term>Culture Media (pharmacology)</term>
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<term>Desulfovibrio desulfuricans (genetics)</term>
<term>Desulfovibrio desulfuricans (growth & development)</term>
<term>Desulfovibrio desulfuricans (metabolism)</term>
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<term>Electrons (MeSH)</term>
<term>Electrophoresis, Gel, Two-Dimensional (MeSH)</term>
<term>Gene Expression Regulation, Bacterial (MeSH)</term>
<term>Gene Ontology (MeSH)</term>
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<term>Nitrate Reductase (metabolism)</term>
<term>Nitrates (metabolism)</term>
<term>Nitrates (pharmacology)</term>
<term>Nitrite Reductases (genetics)</term>
<term>Nitrite Reductases (metabolism)</term>
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<term>Proteome (genetics)</term>
<term>Proteome (metabolism)</term>
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<term>Anaérobiose (génétique)</term>
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<term>Desulfovibrio desulfuricans (effets des médicaments et des substances chimiques)</term>
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<term>Milieux de culture (pharmacologie)</term>
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<term>Nitrate reductase (métabolisme)</term>
<term>Nitrates (métabolisme)</term>
<term>Nitrates (pharmacologie)</term>
<term>Nitrite reductases (génétique)</term>
<term>Nitrite reductases (métabolisme)</term>
<term>Oxydoréduction (MeSH)</term>
<term>Protéines bactériennes (génétique)</term>
<term>Protéines bactériennes (métabolisme)</term>
<term>Protéome (génétique)</term>
<term>Protéome (métabolisme)</term>
<term>Régulation de l'expression des gènes bactériens (MeSH)</term>
<term>Sulfates (métabolisme)</term>
<term>Sulfates (pharmacologie)</term>
<term>Transport d'électrons (MeSH)</term>
<term>Voies et réseaux métaboliques (MeSH)</term>
<term>Électrons (MeSH)</term>
<term>Électrophorèse bidimensionnelle sur gel (MeSH)</term>
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<term>Culture Media</term>
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<term>Bacterial Proteins</term>
<term>Nitrate Reductase</term>
<term>Nitrite Reductases</term>
<term>Proteome</term>
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<term>Milieux de culture</term>
</keywords>
<keywords scheme="MESH" qualifier="croissance et développement" xml:lang="fr">
<term>Desulfovibrio desulfuricans</term>
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<term>Desulfovibrio desulfuricans</term>
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<term>Nitrite reductases</term>
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<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en">
<term>Bacterial Proteins</term>
<term>Desulfovibrio desulfuricans</term>
<term>Nitrate Reductase</term>
<term>Nitrates</term>
<term>Nitrite Reductases</term>
<term>Proteome</term>
<term>Sulfates</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr">
<term>Desulfovibrio desulfuricans</term>
<term>Nitrate reductase</term>
<term>Nitrates</term>
<term>Nitrite reductases</term>
<term>Protéines bactériennes</term>
<term>Protéome</term>
<term>Sulfates</term>
</keywords>
<keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr">
<term>Milieux de culture</term>
<term>Nitrates</term>
<term>Sulfates</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en">
<term>Culture Media</term>
<term>Nitrates</term>
<term>Sulfates</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Electron Transport</term>
<term>Electrons</term>
<term>Electrophoresis, Gel, Two-Dimensional</term>
<term>Gene Expression Regulation, Bacterial</term>
<term>Gene Ontology</term>
<term>Metabolic Networks and Pathways</term>
<term>Molecular Sequence Annotation</term>
<term>Oxidation-Reduction</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Annotation de séquence moléculaire</term>
<term>Gene Ontology</term>
<term>Oxydoréduction</term>
<term>Régulation de l'expression des gènes bactériens</term>
<term>Transport d'électrons</term>
<term>Voies et réseaux métaboliques</term>
<term>Électrons</term>
<term>Électrophorèse bidimensionnelle sur gel</term>
</keywords>
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<front>
<div type="abstract" xml:lang="en">Sulfate-reducing bacteria (SRB) are a diverse group of anaerobic microorganisms that obtain their energy from dissimilatory sulfate reduction. Some SRB species have high respiratory versatility due to the possible use of alternative electron acceptors. A good example is Desulfovibrio desulfuricans ATCC 27774, which grows in the presence of nitrate (end product: ammonium) with higher rates and yields to those observed in sulfate containing medium (end product: sulfide). In this work, the mechanisms supporting the respiratory versatility of D. desulfuricans were unraveled through the analysis of the proteome of the bacterium under different experimental conditions. The most remarkable difference in the two-dimensional gel electrophoresis maps is the high number of spots exclusively represented in the nitrate medium. Most of the proteins with increase abundance are involved in the energy metabolism and the biosynthesis of amino acids (or proteins), especially those participating in ammonium assimilation processes. qPCR analysis performed during different stages of the bacterium's growth showed that the genes involved in nitrate and nitrite reduction (napA and nrfA, respectively) have different expressions profiles: while napA did not vary significantly, nrfA was highly expressed at a 6h time point. Nitrite levels measured along the growth curve revealed a peak at 3h. Thus, the initial consumption of nitrate and concomitant production of nitrite must induce nrfA expression. The activation of alternative mechanisms for energy production, aside several N-assimilation metabolisms and detoxification processes, solves potential survival problems in adapting to different environments and contributes to higher bacterial growth rates.</div>
</front>
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<DateCompleted>
<Year>2018</Year>
<Month>02</Month>
<Day>08</Day>
</DateCompleted>
<DateRevised>
<Year>2018</Year>
<Month>09</Month>
<Day>17</Day>
</DateRevised>
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<Journal>
<ISSN IssnType="Print">1570-9639</ISSN>
<JournalIssue CitedMedium="Print">
<Volume>1865</Volume>
<Issue>11 Pt A</Issue>
<PubDate>
<Year>2017</Year>
<Month>Nov</Month>
</PubDate>
</JournalIssue>
<Title>Biochimica et biophysica acta. Proteins and proteomics</Title>
<ISOAbbreviation>Biochim Biophys Acta Proteins Proteom</ISOAbbreviation>
</Journal>
<ArticleTitle>Understanding the response of Desulfovibrio desulfuricans ATCC 27774 to the electron acceptors nitrate and sulfate - biosynthetic costs modulate substrate selection.</ArticleTitle>
<Pagination>
<MedlinePgn>1455-1469</MedlinePgn>
</Pagination>
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<ELocationID EIdType="doi" ValidYN="Y">10.1016/j.bbapap.2017.07.021</ELocationID>
<Abstract>
<AbstractText>Sulfate-reducing bacteria (SRB) are a diverse group of anaerobic microorganisms that obtain their energy from dissimilatory sulfate reduction. Some SRB species have high respiratory versatility due to the possible use of alternative electron acceptors. A good example is Desulfovibrio desulfuricans ATCC 27774, which grows in the presence of nitrate (end product: ammonium) with higher rates and yields to those observed in sulfate containing medium (end product: sulfide). In this work, the mechanisms supporting the respiratory versatility of D. desulfuricans were unraveled through the analysis of the proteome of the bacterium under different experimental conditions. The most remarkable difference in the two-dimensional gel electrophoresis maps is the high number of spots exclusively represented in the nitrate medium. Most of the proteins with increase abundance are involved in the energy metabolism and the biosynthesis of amino acids (or proteins), especially those participating in ammonium assimilation processes. qPCR analysis performed during different stages of the bacterium's growth showed that the genes involved in nitrate and nitrite reduction (napA and nrfA, respectively) have different expressions profiles: while napA did not vary significantly, nrfA was highly expressed at a 6h time point. Nitrite levels measured along the growth curve revealed a peak at 3h. Thus, the initial consumption of nitrate and concomitant production of nitrite must induce nrfA expression. The activation of alternative mechanisms for energy production, aside several N-assimilation metabolisms and detoxification processes, solves potential survival problems in adapting to different environments and contributes to higher bacterial growth rates.</AbstractText>
<CopyrightInformation>Copyright © 2017 Elsevier B.V. All rights reserved.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y">
<Author ValidYN="Y">
<LastName>Sousa</LastName>
<ForeName>Joana R</ForeName>
<Initials>JR</Initials>
<AffiliationInfo>
<Affiliation>UCIBIO-REQUIMTE, Departamento de Química, Faculdade de Ciências e Tecnologia, Universidade NOVA de Lisboa, 2829-516 Monte de Caparica, Portugal.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Silveira</LastName>
<ForeName>Célia M</ForeName>
<Initials>CM</Initials>
<AffiliationInfo>
<Affiliation>UCIBIO-REQUIMTE, Departamento de Química, Faculdade de Ciências e Tecnologia, Universidade NOVA de Lisboa, 2829-516 Monte de Caparica, Portugal; Instituto de Tecnologia Química e Biológica António Xavier, Universidade NOVA de Lisboa, Av. da República, 2780-157 Oeiras, Portugal.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Fontes</LastName>
<ForeName>Pedro</ForeName>
<Initials>P</Initials>
<AffiliationInfo>
<Affiliation>UCIBIO-REQUIMTE, Departamento de Química, Faculdade de Ciências e Tecnologia, Universidade NOVA de Lisboa, 2829-516 Monte de Caparica, Portugal.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Roma-Rodrigues</LastName>
<ForeName>Catarina</ForeName>
<Initials>C</Initials>
<AffiliationInfo>
<Affiliation>UCIBIO, Departamento Ciências da Vida, Faculdade de Ciências e Tecnologia, Universidade NOVA de Lisboa, 2829-516 Monte de Caparica, Portugal.</Affiliation>
</AffiliationInfo>
</Author>
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<LastName>Fernandes</LastName>
<ForeName>Alexandra R</ForeName>
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<AffiliationInfo>
<Affiliation>UCIBIO, Departamento Ciências da Vida, Faculdade de Ciências e Tecnologia, Universidade NOVA de Lisboa, 2829-516 Monte de Caparica, Portugal.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Van Driessche</LastName>
<ForeName>Gonzalez</ForeName>
<Initials>G</Initials>
<AffiliationInfo>
<Affiliation>UCIBIO, Departamento Ciências da Vida, Faculdade de Ciências e Tecnologia, Universidade NOVA de Lisboa, 2829-516 Monte de Caparica, Portugal.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Devreese</LastName>
<ForeName>Bart</ForeName>
<Initials>B</Initials>
<AffiliationInfo>
<Affiliation>Laboratory for Protein Biochemistry and Biomolecular Engineering, Department of Biochemistry and Microbiology, Gent University, 9000 Gent, Belgium.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Moura</LastName>
<ForeName>Isabel</ForeName>
<Initials>I</Initials>
<AffiliationInfo>
<Affiliation>UCIBIO-REQUIMTE, Departamento de Química, Faculdade de Ciências e Tecnologia, Universidade NOVA de Lisboa, 2829-516 Monte de Caparica, Portugal.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Moura</LastName>
<ForeName>José J G</ForeName>
<Initials>JJG</Initials>
<AffiliationInfo>
<Affiliation>UCIBIO-REQUIMTE, Departamento de Química, Faculdade de Ciências e Tecnologia, Universidade NOVA de Lisboa, 2829-516 Monte de Caparica, Portugal.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Almeida</LastName>
<ForeName>M Gabriela</ForeName>
<Initials>MG</Initials>
<AffiliationInfo>
<Affiliation>UCIBIO-REQUIMTE, Departamento de Química, Faculdade de Ciências e Tecnologia, Universidade NOVA de Lisboa, 2829-516 Monte de Caparica, Portugal; Centro de Investigação Interdisciplinar Egas Moniz (CiiEM), Instituto Superior de Ciências da Saúde Egas Moniz, Campus Universitário, Quinta da Granja, 2829-511 Caparica, Portugal. Electronic address: mg.almeida@fct.unl.pt.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
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<PublicationType UI="D016428">Journal Article</PublicationType>
<PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic">
<Year>2017</Year>
<Month>08</Month>
<Day>25</Day>
</ArticleDate>
</Article>
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<Country>Netherlands</Country>
<MedlineTA>Biochim Biophys Acta Proteins Proteom</MedlineTA>
<NlmUniqueID>101731734</NlmUniqueID>
<ISSNLinking>1570-9639</ISSNLinking>
</MedlineJournalInfo>
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<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D001426">Bacterial Proteins</NameOfSubstance>
</Chemical>
<Chemical>
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<NameOfSubstance UI="D003470">Culture Media</NameOfSubstance>
</Chemical>
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<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D020543">Proteome</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D013431">Sulfates</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>EC 1.7.-</RegistryNumber>
<NameOfSubstance UI="D009572">Nitrite Reductases</NameOfSubstance>
</Chemical>
<Chemical>
<RegistryNumber>EC 1.7.99.4</RegistryNumber>
<NameOfSubstance UI="D050901">Nitrate Reductase</NameOfSubstance>
</Chemical>
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<DescriptorName UI="D000693" MajorTopicYN="N">Anaerobiosis</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
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<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
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<Keyword MajorTopicYN="Y">Ammonium assimilation</Keyword>
<Keyword MajorTopicYN="Y">Desulfovibrio desulfuricans ATCC 27774</Keyword>
<Keyword MajorTopicYN="Y">Energy metabolism</Keyword>
<Keyword MajorTopicYN="Y">Nitrate reduction</Keyword>
<Keyword MajorTopicYN="Y">Proteomics</Keyword>
<Keyword MajorTopicYN="Y">Respiratory flexibility</Keyword>
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