Characterization and expression analysis of the cytochrome bd oxidase operon from Desulfovibrio gigas

Bibliographic Details
Main Author: Machado, Patrícia
Publication Date: 2006
Other Authors: Félix, Rute, Rodrigues, Rute, Oliveira, Solange, Rodrigues-Pousada, Claudina
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://hdl.handle.net/10174/1579
Summary: Abstract: Although classified as anaerobic, Desulfovibrio gigas contains a functional canonical membrane respiratory chain, including a cytochrome bd quinol oxidase as its terminal element. In the present study, we report the identification of the operon cydAB encoding the two subunits of cytochrome bd from this bacterium. Two hypothetical promoter regions and sequences resembling transcriptional regulators-binding sites have been identified. Amino acid sequence analysis revealed a high similarity to cytochrome bd from other organisms, presenting the conserved residues typical from these proteins. Reverse transcription polymerase chain reaction (RT-PCR) and Northern blot analysis confirmed the operon transcription. Gene expression was assessed by real-time RT-PCR in cells grown in different media and under exposure to oxygen and nitric oxide. mRNA levels were slightly enhanced in the presence of 150 mu M NO. However, in the presence of 10 mu M NO, a decrease was observed of the steady-state population of cydAB mRNA. No considerable effect was observed in the presence of fumarate/sulfate medium, 60 mu M O-2 or 10 mu M NO.
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spelling Characterization and expression analysis of the cytochrome bd oxidase operon from Desulfovibrio gigasDesulfovibrio gigascytochrome bd oxidaseAbstract: Although classified as anaerobic, Desulfovibrio gigas contains a functional canonical membrane respiratory chain, including a cytochrome bd quinol oxidase as its terminal element. In the present study, we report the identification of the operon cydAB encoding the two subunits of cytochrome bd from this bacterium. Two hypothetical promoter regions and sequences resembling transcriptional regulators-binding sites have been identified. Amino acid sequence analysis revealed a high similarity to cytochrome bd from other organisms, presenting the conserved residues typical from these proteins. Reverse transcription polymerase chain reaction (RT-PCR) and Northern blot analysis confirmed the operon transcription. Gene expression was assessed by real-time RT-PCR in cells grown in different media and under exposure to oxygen and nitric oxide. mRNA levels were slightly enhanced in the presence of 150 mu M NO. However, in the presence of 10 mu M NO, a decrease was observed of the steady-state population of cydAB mRNA. No considerable effect was observed in the presence of fumarate/sulfate medium, 60 mu M O-2 or 10 mu M NO.2009-04-15T15:43:40Z2009-04-152006-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article35775 bytesapplication/pdfhttp://hdl.handle.net/10174/1579http://hdl.handle.net/10174/1579engpag 274-281CURRENT MICROBIOLOGY452livrendndndndnd226Machado, PatríciaFélix, RuteRodrigues, RuteOliveira, SolangeRodrigues-Pousada, Claudinainfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2024-01-03T18:37:17Zoai:dspace.uevora.pt:10174/1579Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T11:50:07.651776Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Characterization and expression analysis of the cytochrome bd oxidase operon from Desulfovibrio gigas
title Characterization and expression analysis of the cytochrome bd oxidase operon from Desulfovibrio gigas
spellingShingle Characterization and expression analysis of the cytochrome bd oxidase operon from Desulfovibrio gigas
Machado, Patrícia
Desulfovibrio gigas
cytochrome bd oxidase
title_short Characterization and expression analysis of the cytochrome bd oxidase operon from Desulfovibrio gigas
title_full Characterization and expression analysis of the cytochrome bd oxidase operon from Desulfovibrio gigas
title_fullStr Characterization and expression analysis of the cytochrome bd oxidase operon from Desulfovibrio gigas
title_full_unstemmed Characterization and expression analysis of the cytochrome bd oxidase operon from Desulfovibrio gigas
title_sort Characterization and expression analysis of the cytochrome bd oxidase operon from Desulfovibrio gigas
author Machado, Patrícia
author_facet Machado, Patrícia
Félix, Rute
Rodrigues, Rute
Oliveira, Solange
Rodrigues-Pousada, Claudina
author_role author
author2 Félix, Rute
Rodrigues, Rute
Oliveira, Solange
Rodrigues-Pousada, Claudina
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Machado, Patrícia
Félix, Rute
Rodrigues, Rute
Oliveira, Solange
Rodrigues-Pousada, Claudina
dc.subject.por.fl_str_mv Desulfovibrio gigas
cytochrome bd oxidase
topic Desulfovibrio gigas
cytochrome bd oxidase
description Abstract: Although classified as anaerobic, Desulfovibrio gigas contains a functional canonical membrane respiratory chain, including a cytochrome bd quinol oxidase as its terminal element. In the present study, we report the identification of the operon cydAB encoding the two subunits of cytochrome bd from this bacterium. Two hypothetical promoter regions and sequences resembling transcriptional regulators-binding sites have been identified. Amino acid sequence analysis revealed a high similarity to cytochrome bd from other organisms, presenting the conserved residues typical from these proteins. Reverse transcription polymerase chain reaction (RT-PCR) and Northern blot analysis confirmed the operon transcription. Gene expression was assessed by real-time RT-PCR in cells grown in different media and under exposure to oxygen and nitric oxide. mRNA levels were slightly enhanced in the presence of 150 mu M NO. However, in the presence of 10 mu M NO, a decrease was observed of the steady-state population of cydAB mRNA. No considerable effect was observed in the presence of fumarate/sulfate medium, 60 mu M O-2 or 10 mu M NO.
publishDate 2006
dc.date.none.fl_str_mv 2006-01-01T00:00:00Z
2009-04-15T15:43:40Z
2009-04-15
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10174/1579
http://hdl.handle.net/10174/1579
url http://hdl.handle.net/10174/1579
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv pag 274-281
CURRENT MICROBIOLOGY
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