Literature DB >> 15507000

In silico exploration of the fructose-6-phosphate phosphorylation step in glycolysis: genomic evidence of the coexistence of an atypical ATP-dependent along with a PPi-dependent phosphofructokinase in Propionibacterium freudenreichii subsp. shermanii.

Guillaume Meurice1, Catherine Deborde, Daniel Jacob, Hélène Falentin, Patrick Boyaval, Diliana Dimova.   

Abstract

We performed a detailed bioinformatic study of the catalytic step of fructose-6-phosphate phosphorylation in glycolysis based on the raw genomic draft of Propionibacterium freudenreichii subsp. shermanii (P. shermanii) ATCC9614 [Meurice et al., 2004]. Our results provide the first in silico evidence of the coexistence of genes coding for an ATP-dependent phosphofructokinase (ATP-PFK) and a PPi-dependent phosphofructokinase (PPi-PFK), whereas the fructose-1,6-bisphosphatase (FBP) and ADP-dependent phosphofructokinase (ADP-PFK) are absent. The deduced amino acid sequence corresponding to the PPi-PFK (AJ508922) shares 100% similarity with the already characterised propionibacterial protein (P29495; Ladror et al., 1991]. The unexpected ATP-PFK gene (AJ509827) encodes a protein of 373 aa which is highly similar (50% positive residues) along at least 95% of its sequence length to different well-characterised ATP-PFKs. The characteristic PROSITE pattern important for the enzyme function of ATP-PFKs (PS00433) was conserved in the putative ATP-PFK sequence: 8 out of 9 amino acid residues. According to the recent evolutionary study of PFK proteins with different phosphate donors [Bapteste et al., 2003], the propionibacterial ATP-PFK harbours a G104-K124 residue combination, which strongly suggested that this enzyme belongs to the group of atypical ATP-PFKs. According to our phylogenetic analyses the amino acid sequence of the ATP-PFK is clustered with the atypical ATP-PFKs from group III of the Siebers classification [Siebers et al., 1998], whereas the expected PPi-PFK protein is closer to the PPi-PFKs from clade P [Müller et al., 2001]. The possible significance of the co-existence of these two PFKs and their importance for the regulation of glycolytic pathway flux in P. shermanii is discussed.

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Year:  2004        PMID: 15507000

Source DB:  PubMed          Journal:  In Silico Biol        ISSN: 1386-6338


  4 in total

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Authors:  Jilai Zhou; Daniel G Olson; D Aaron Argyros; Yu Deng; Walter M van Gulik; Johannes P van Dijken; Lee R Lynd
Journal:  Appl Environ Microbiol       Date:  2013-02-22       Impact factor: 4.792

2.  The complete genome of Propionibacterium freudenreichii CIRM-BIA1, a hardy actinobacterium with food and probiotic applications.

Authors:  Hélène Falentin; Stéphanie-Marie Deutsch; Gwenaël Jan; Valentin Loux; Anne Thierry; Sandrine Parayre; Marie-Bernadette Maillard; Julien Dherbécourt; Fabien J Cousin; Julien Jardin; Patricia Siguier; Arnaud Couloux; Valérie Barbe; Benoit Vacherie; Patrick Wincker; Jean-François Gibrat; Claude Gaillardin; Sylvie Lortal
Journal:  PLoS One       Date:  2010-07-23       Impact factor: 3.240

3.  Three rounds (1R/2R/3R) of genome duplications and the evolution of the glycolytic pathway in vertebrates.

Authors:  Dirk Steinke; Simone Hoegg; Henner Brinkmann; Axel Meyer
Journal:  BMC Biol       Date:  2006-06-06       Impact factor: 7.431

4.  Mutations and genomic islands can explain the strain dependency of sugar utilization in 21 strains of Propionibacterium freudenreichii.

Authors:  Valentin Loux; Mahendra Mariadassou; Sintia Almeida; Hélène Chiapello; Amal Hammani; Julien Buratti; Annie Gendrault; Valérie Barbe; Jean-Marc Aury; Stéphanie-Marie Deutsch; Sandrine Parayre; Marie-Noëlle Madec; Victoria Chuat; Gwenaël Jan; Pierre Peterlongo; Vasco Azevedo; Yves Le Loir; Hélène Falentin
Journal:  BMC Genomics       Date:  2015-04-15       Impact factor: 3.969

  4 in total

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