Literature DB >> 27836849

Identification of a New Phosphatase Enzyme Potentially Involved in the Sugar Phosphate Stress Response in Pseudomonas fluorescens.

Susan Maleki1,2, Radka Hrudikova1, Sergey B Zotchev1, Helga Ertesvåg3.   

Abstract

The alginate-producing bacterium Pseudomonas fluorescens utilizes the Entner-Doudoroff (ED) and pentose phosphate (PP) pathways to metabolize fructose, since the upper part of its Embden-Meyerhof-Parnas pathway is defective. Our previous study indicated that perturbation of the central carbon metabolism by diminishing glucose-6-phosphate dehydrogenase activity could lead to sugar phosphate stress when P. fluorescens was cultivated on fructose. In the present study, we demonstrate that PFLU2693, annotated as a haloacid dehalogenase-like enzyme, is a new sugar phosphate phosphatase, now designated Spp, which is able to dephosphorylate a range of phosphate substrates, including glucose 6-phosphate and fructose 6-phosphate, in vitro The effect of spp overexpression on growth and alginate production was investigated using both the wild type and several mutant strains. The results obtained suggested that sugar phosphate accumulation caused diminished growth in some of the mutant strains, since this was partially relieved by spp overexpression. On the other hand, overexpression of spp in fructose-grown alginate-producing strains negatively affected both growth and alginate production. The latter implies that Spp dephosphorylates the sugar phosphates, thus depleting the pool of these important metabolites. Deletion of the spp gene did not affect growth of the wild-type strain on fructose, but the gene could not be deleted in the alginate-producing strain. This indicates that Spp is essential for relieving the cells of sugar phosphate stress in P. fluorescens actively producing alginate. IMPORTANCE: In enteric bacteria, the sugar phosphate phosphatase YigL is known to play an important role in combating stress caused by sugar phosphate accumulation. In this study, we identified a sugar phosphate phosphatase, designated Spp, in Pseudomonas fluorescens Spp utilizes glucose 6-phosphate, fructose 6-phosphate, and ribose 5-phosphate as substrates, and overexpression of the gene had a positive effect on growth in P. fluorescens mutants experiencing sugar phosphate stress. The gene was localized downstream of gnd and zwf-2, which encode enzymes involved in the pentose phosphate and Entner-Doudoroff pathways. Genes encoding Spp homologues were identified in similar genetic contexts in some bacteria belonging to several phylogenetically diverse families, suggesting similar functions.
Copyright © 2016 American Society for Microbiology.

Entities:  

Keywords:  PFLU2693; Pseudomonas fluorescens; YigL; alginate biosynthesis; phosphatase; sugar phosphate phosphatase; sugar phosphate stress response

Mesh:

Substances:

Year:  2016        PMID: 27836849      PMCID: PMC5203634          DOI: 10.1128/AEM.02361-16

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  31 in total

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3.  Insights into the assembly of the alginate biosynthesis machinery in Pseudomonas aeruginosa.

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5.  Genome-wide analysis of substrate specificities of the Escherichia coli haloacid dehalogenase-like phosphatase family.

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6.  Random mutagenesis of the PM promoter as a powerful strategy for improvement of recombinant-gene expression.

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Journal:  Nat Chem Biol       Date:  2016-06-13       Impact factor: 15.040

Review 8.  Ins and outs of glucose transport systems in eubacteria.

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9.  The small RNA SgrS controls sugar-phosphate accumulation by regulating multiple PTS genes.

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Review 10.  Microbial alginate production, modification and its applications.

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  3 in total

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2.  129Xe NMR-Protein Sensor Reveals Cellular Ribose Concentration.

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3.  Identification of Regulatory Genes and Metabolic Processes Important for Alginate Biosynthesis in Azotobacter vinelandii by Screening of a Transposon Insertion Mutant Library.

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