Literature DB >> 7496998

Aminoacid utilization by Helicobacter pylori.

G L Mendz1, S L Hazell.   

Abstract

Utilization of aminoacids during growth by laboratory adapted and wild type Helicobacter pylori strains was investigated employing nuclear magnetic resonance spectroscopy and aminoacid analysis. All H. pylori strains tested showed growth rates with doubling times of approx. 11.5 hr in liquid cultures with semi-defined media or with defined aminoacid broth without carbohydrates. Fast utilization of several aminoacids at rates between 80 and 250 microM/hr was observed in culture broths inoculated with approx. 10(7) cells/ml; and acetate, formate and succinate accumulated as catabolic products in the growth media. Suspensions of bacterial cells and lysates in isotonic solutions converted arginine, asparagine, aspartate, glutamine, and serine used as sole substrates at significant rates; and under these conditions the principal metabolic products observed were acetate, formate, succinate and lactate. The findings of the study indicated that H. pylori can survive employing aminoacids as the basic nutrients, and suggested some of these metabolites were utilized via fermentative pathways with common characteristics to those found in anaerobes.

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Year:  1995        PMID: 7496998     DOI: 10.1016/1357-2725(95)00069-2

Source DB:  PubMed          Journal:  Int J Biochem Cell Biol        ISSN: 1357-2725            Impact factor:   5.085


  27 in total

1.  Genome-scale metabolic model of Helicobacter pylori 26695.

Authors:  Christophe H Schilling; Markus W Covert; Iman Famili; George M Church; Jeremy S Edwards; Bernhard O Palsson
Journal:  J Bacteriol       Date:  2002-08       Impact factor: 3.490

2.  Helicobacter pylori arginase inhibits nitric oxide production by eukaryotic cells: a strategy for bacterial survival.

Authors:  A P Gobert; D J McGee; M Akhtar; G L Mendz; J C Newton; Y Cheng; H L Mobley; K T Wilson
Journal:  Proc Natl Acad Sci U S A       Date:  2001-11-20       Impact factor: 11.205

3.  Gastric Metabolomics Detects Helicobacter pylori Correlated Loss of Numerous Metabolites in Both the Corpus and Antrum.

Authors:  Daniela Keilberg; Nina Steele; Sili Fan; Christina Yang; Yana Zavros; Karen M Ottemann
Journal:  Infect Immun       Date:  2021-01-19       Impact factor: 3.441

4.  Coupled amino acid deamidase-transport systems essential for Helicobacter pylori colonization.

Authors:  Damien Leduc; Julien Gallaud; Kerstin Stingl; Hilde de Reuse
Journal:  Infect Immun       Date:  2010-04-05       Impact factor: 3.441

5.  A revised annotation and comparative analysis of Helicobacter pylori genomes.

Authors:  Ivo G Boneca; Hilde de Reuse; Jean-Charles Epinat; Maude Pupin; Agnès Labigne; Ivan Moszer
Journal:  Nucleic Acids Res       Date:  2003-03-15       Impact factor: 16.971

6.  Helicobacter pylori rocF is required for arginase activity and acid protection in vitro but is not essential for colonization of mice or for urease activity.

Authors:  D J McGee; F J Radcliff; G L Mendz; R L Ferrero; H L Mobley
Journal:  J Bacteriol       Date:  1999-12       Impact factor: 3.490

7.  N-methyl D-aspartate channels link ammonia and epithelial cell death mechanisms in Helicobacter pylori Infection.

Authors:  Ji Hye Seo; James G Fox; Richard M Peek; Susan J Hagen
Journal:  Gastroenterology       Date:  2011-09-16       Impact factor: 22.682

8.  Cometabolism of a nongrowth substrate: L-serine utilization by Corynebacterium glutamicum.

Authors:  Roman Netzer; Petra Peters-Wendisch; Lothar Eggeling; Hermann Sahm
Journal:  Appl Environ Microbiol       Date:  2004-12       Impact factor: 4.792

9.  Expanded metabolic reconstruction of Helicobacter pylori (iIT341 GSM/GPR): an in silico genome-scale characterization of single- and double-deletion mutants.

Authors:  Ines Thiele; Thuy D Vo; Nathan D Price; Bernhard Ø Palsson
Journal:  J Bacteriol       Date:  2005-08       Impact factor: 3.490

10.  A novel mechanism for resistance to the antimetabolite N-phosphonoacetyl-L-aspartate by Helicobacter pylori.

Authors:  B P Burns; G L Mendz; S L Hazell
Journal:  J Bacteriol       Date:  1998-11       Impact factor: 3.490

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