author_facet Kwon, Dong H.
Versalovic, James
Kwon, Dong H.
Versalovic, James
author Kwon, Dong H.
Versalovic, James
spellingShingle Kwon, Dong H.
Versalovic, James
Helicobacter
Fur‐Independent Induction of Helicobacter pylori Flavodoxin‐Encoding Gene (fldA) Under Iron Starvation
Infectious Diseases
Gastroenterology
General Medicine
author_sort kwon, dong h.
spelling Kwon, Dong H. Versalovic, James 1083-4389 1523-5378 Wiley Infectious Diseases Gastroenterology General Medicine http://dx.doi.org/10.1111/j.1523-5378.2009.00669.x <jats:title>Abstract</jats:title><jats:p><jats:bold>Background and Aims:</jats:bold> <jats:italic>Helicobacter pylori</jats:italic> infection is associated with a variety of diseases including gastric cancer. Flavodoxin is an electron transfer protein containing a flavin mononucleotide prosthetic group and substituted an iron‐containing electron transfer protein under iron‐limiting conditions. <jats:italic>H. pylori</jats:italic> flavodoxin has been reported but its pathogenic role is unclear. The aim of this study is to understand a pathogenic role of <jats:italic>H. pylori </jats:italic>flavodoxin under iron‐limiting condition.</jats:p><jats:p><jats:bold>Methods:</jats:bold> The flavodoxin‐encoding gene (<jats:italic>fldA</jats:italic>) was cloned from one of clinical <jats:italic>H. pylori</jats:italic> isolates (DU17) and its transcript was quantified by primer extension, Northern hybridization, and real‐time polymerase chain reaction in different concentrations of an iron chelator. The <jats:italic>fldA</jats:italic> transcript was also quantified in <jats:italic>H. pylori</jats:italic> ATCC 700392, lacking a ferric uptake regulatory (fur) protein.</jats:p><jats:p><jats:bold>Result:</jats:bold> Nucleotide sequence of the <jats:italic>fldA</jats:italic> from <jats:italic>H. pylori</jats:italic> DU17 revealed a 492‐bp (164 amino acids) open reading frame with a deduced amino acid sequence having 97% identity to that from the complete genomic sequence of <jats:italic>H. pylori </jats:italic>26695. The deduced promoter [–35, –10, and +1] of the <jats:italic>fldA</jats:italic> was 56‐bp upstream from the first codon of FldA. The <jats:italic>fldA </jats:italic>transcript (~0.55‐kb) was induced up to 14‐fold in both wild‐type and <jats:italic>fur</jats:italic>‐knocked‐out strains under iron‐limiting conditions, suggesting that the <jats:italic>fldA</jats:italic> induction is independent to the Fur protein.</jats:p><jats:p><jats:bold>Conclusion:</jats:bold> The <jats:italic>fldA</jats:italic> gene may play an important role in iron starvation conditions.</jats:p> Fur‐Independent Induction of <i>Helicobacter pylori</i> Flavodoxin‐Encoding Gene (<i>fldA</i>) Under Iron Starvation Helicobacter
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recordtype ai
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title Fur‐Independent Induction of Helicobacter pylori Flavodoxin‐Encoding Gene (fldA) Under Iron Starvation
title_unstemmed Fur‐Independent Induction of Helicobacter pylori Flavodoxin‐Encoding Gene (fldA) Under Iron Starvation
title_full Fur‐Independent Induction of Helicobacter pylori Flavodoxin‐Encoding Gene (fldA) Under Iron Starvation
title_fullStr Fur‐Independent Induction of Helicobacter pylori Flavodoxin‐Encoding Gene (fldA) Under Iron Starvation
title_full_unstemmed Fur‐Independent Induction of Helicobacter pylori Flavodoxin‐Encoding Gene (fldA) Under Iron Starvation
title_short Fur‐Independent Induction of Helicobacter pylori Flavodoxin‐Encoding Gene (fldA) Under Iron Starvation
title_sort fur‐independent induction of <i>helicobacter pylori</i> flavodoxin‐encoding gene (<i>flda</i>) under iron starvation
topic Infectious Diseases
Gastroenterology
General Medicine
url http://dx.doi.org/10.1111/j.1523-5378.2009.00669.x
publishDate 2009
physical 141-146
description <jats:title>Abstract</jats:title><jats:p><jats:bold>Background and Aims:</jats:bold> <jats:italic>Helicobacter pylori</jats:italic> infection is associated with a variety of diseases including gastric cancer. Flavodoxin is an electron transfer protein containing a flavin mononucleotide prosthetic group and substituted an iron‐containing electron transfer protein under iron‐limiting conditions. <jats:italic>H. pylori</jats:italic> flavodoxin has been reported but its pathogenic role is unclear. The aim of this study is to understand a pathogenic role of <jats:italic>H. pylori </jats:italic>flavodoxin under iron‐limiting condition.</jats:p><jats:p><jats:bold>Methods:</jats:bold> The flavodoxin‐encoding gene (<jats:italic>fldA</jats:italic>) was cloned from one of clinical <jats:italic>H. pylori</jats:italic> isolates (DU17) and its transcript was quantified by primer extension, Northern hybridization, and real‐time polymerase chain reaction in different concentrations of an iron chelator. The <jats:italic>fldA</jats:italic> transcript was also quantified in <jats:italic>H. pylori</jats:italic> ATCC 700392, lacking a ferric uptake regulatory (fur) protein.</jats:p><jats:p><jats:bold>Result:</jats:bold> Nucleotide sequence of the <jats:italic>fldA</jats:italic> from <jats:italic>H. pylori</jats:italic> DU17 revealed a 492‐bp (164 amino acids) open reading frame with a deduced amino acid sequence having 97% identity to that from the complete genomic sequence of <jats:italic>H. pylori </jats:italic>26695. The deduced promoter [–35, –10, and +1] of the <jats:italic>fldA</jats:italic> was 56‐bp upstream from the first codon of FldA. The <jats:italic>fldA </jats:italic>transcript (~0.55‐kb) was induced up to 14‐fold in both wild‐type and <jats:italic>fur</jats:italic>‐knocked‐out strains under iron‐limiting conditions, suggesting that the <jats:italic>fldA</jats:italic> induction is independent to the Fur protein.</jats:p><jats:p><jats:bold>Conclusion:</jats:bold> The <jats:italic>fldA</jats:italic> gene may play an important role in iron starvation conditions.</jats:p>
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author Kwon, Dong H., Versalovic, James
author_facet Kwon, Dong H., Versalovic, James, Kwon, Dong H., Versalovic, James
author_sort kwon, dong h.
container_issue 2
container_start_page 141
container_title Helicobacter
container_volume 14
description <jats:title>Abstract</jats:title><jats:p><jats:bold>Background and Aims:</jats:bold> <jats:italic>Helicobacter pylori</jats:italic> infection is associated with a variety of diseases including gastric cancer. Flavodoxin is an electron transfer protein containing a flavin mononucleotide prosthetic group and substituted an iron‐containing electron transfer protein under iron‐limiting conditions. <jats:italic>H. pylori</jats:italic> flavodoxin has been reported but its pathogenic role is unclear. The aim of this study is to understand a pathogenic role of <jats:italic>H. pylori </jats:italic>flavodoxin under iron‐limiting condition.</jats:p><jats:p><jats:bold>Methods:</jats:bold> The flavodoxin‐encoding gene (<jats:italic>fldA</jats:italic>) was cloned from one of clinical <jats:italic>H. pylori</jats:italic> isolates (DU17) and its transcript was quantified by primer extension, Northern hybridization, and real‐time polymerase chain reaction in different concentrations of an iron chelator. The <jats:italic>fldA</jats:italic> transcript was also quantified in <jats:italic>H. pylori</jats:italic> ATCC 700392, lacking a ferric uptake regulatory (fur) protein.</jats:p><jats:p><jats:bold>Result:</jats:bold> Nucleotide sequence of the <jats:italic>fldA</jats:italic> from <jats:italic>H. pylori</jats:italic> DU17 revealed a 492‐bp (164 amino acids) open reading frame with a deduced amino acid sequence having 97% identity to that from the complete genomic sequence of <jats:italic>H. pylori </jats:italic>26695. The deduced promoter [–35, –10, and +1] of the <jats:italic>fldA</jats:italic> was 56‐bp upstream from the first codon of FldA. The <jats:italic>fldA </jats:italic>transcript (~0.55‐kb) was induced up to 14‐fold in both wild‐type and <jats:italic>fur</jats:italic>‐knocked‐out strains under iron‐limiting conditions, suggesting that the <jats:italic>fldA</jats:italic> induction is independent to the Fur protein.</jats:p><jats:p><jats:bold>Conclusion:</jats:bold> The <jats:italic>fldA</jats:italic> gene may play an important role in iron starvation conditions.</jats:p>
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spelling Kwon, Dong H. Versalovic, James 1083-4389 1523-5378 Wiley Infectious Diseases Gastroenterology General Medicine http://dx.doi.org/10.1111/j.1523-5378.2009.00669.x <jats:title>Abstract</jats:title><jats:p><jats:bold>Background and Aims:</jats:bold> <jats:italic>Helicobacter pylori</jats:italic> infection is associated with a variety of diseases including gastric cancer. Flavodoxin is an electron transfer protein containing a flavin mononucleotide prosthetic group and substituted an iron‐containing electron transfer protein under iron‐limiting conditions. <jats:italic>H. pylori</jats:italic> flavodoxin has been reported but its pathogenic role is unclear. The aim of this study is to understand a pathogenic role of <jats:italic>H. pylori </jats:italic>flavodoxin under iron‐limiting condition.</jats:p><jats:p><jats:bold>Methods:</jats:bold> The flavodoxin‐encoding gene (<jats:italic>fldA</jats:italic>) was cloned from one of clinical <jats:italic>H. pylori</jats:italic> isolates (DU17) and its transcript was quantified by primer extension, Northern hybridization, and real‐time polymerase chain reaction in different concentrations of an iron chelator. The <jats:italic>fldA</jats:italic> transcript was also quantified in <jats:italic>H. pylori</jats:italic> ATCC 700392, lacking a ferric uptake regulatory (fur) protein.</jats:p><jats:p><jats:bold>Result:</jats:bold> Nucleotide sequence of the <jats:italic>fldA</jats:italic> from <jats:italic>H. pylori</jats:italic> DU17 revealed a 492‐bp (164 amino acids) open reading frame with a deduced amino acid sequence having 97% identity to that from the complete genomic sequence of <jats:italic>H. pylori </jats:italic>26695. The deduced promoter [–35, –10, and +1] of the <jats:italic>fldA</jats:italic> was 56‐bp upstream from the first codon of FldA. The <jats:italic>fldA </jats:italic>transcript (~0.55‐kb) was induced up to 14‐fold in both wild‐type and <jats:italic>fur</jats:italic>‐knocked‐out strains under iron‐limiting conditions, suggesting that the <jats:italic>fldA</jats:italic> induction is independent to the Fur protein.</jats:p><jats:p><jats:bold>Conclusion:</jats:bold> The <jats:italic>fldA</jats:italic> gene may play an important role in iron starvation conditions.</jats:p> Fur‐Independent Induction of <i>Helicobacter pylori</i> Flavodoxin‐Encoding Gene (<i>fldA</i>) Under Iron Starvation Helicobacter
spellingShingle Kwon, Dong H., Versalovic, James, Helicobacter, Fur‐Independent Induction of Helicobacter pylori Flavodoxin‐Encoding Gene (fldA) Under Iron Starvation, Infectious Diseases, Gastroenterology, General Medicine
title Fur‐Independent Induction of Helicobacter pylori Flavodoxin‐Encoding Gene (fldA) Under Iron Starvation
title_full Fur‐Independent Induction of Helicobacter pylori Flavodoxin‐Encoding Gene (fldA) Under Iron Starvation
title_fullStr Fur‐Independent Induction of Helicobacter pylori Flavodoxin‐Encoding Gene (fldA) Under Iron Starvation
title_full_unstemmed Fur‐Independent Induction of Helicobacter pylori Flavodoxin‐Encoding Gene (fldA) Under Iron Starvation
title_short Fur‐Independent Induction of Helicobacter pylori Flavodoxin‐Encoding Gene (fldA) Under Iron Starvation
title_sort fur‐independent induction of <i>helicobacter pylori</i> flavodoxin‐encoding gene (<i>flda</i>) under iron starvation
title_unstemmed Fur‐Independent Induction of Helicobacter pylori Flavodoxin‐Encoding Gene (fldA) Under Iron Starvation
topic Infectious Diseases, Gastroenterology, General Medicine
url http://dx.doi.org/10.1111/j.1523-5378.2009.00669.x