Abstract

The 3-polyprenyl-4-hydroxybenzoate decarboxylase (UbiD) catalyzes the conversion of 3-polyprenyl-4-hydroxybenzoate to 2-polyprenylphenol in the biosynthesis of ubiquinone. Pseudomonas aeruginosa contains two genes (PA0254 and PA5237) that are related in sequence to putative UbiD enzymes. A bioinformatics analysis suggests that the UbiD sequence family can be divided into two subclasses, with PA5237 and PA0254 belonging to different branches of this family. The three-dimensional structure of PA0254 has been determined using single wavelength anomalous diffraction and molecular replacement in two different crystal forms to resolutions of 1.95 and 2.3 Å, respectively. The subunit of PA0254 consists of three domains, an N-terminal α/β domain, a split β-barrel with a similar fold of a family of flavin reductases and a C-terminal α/β domain with a topology characteristic for the UbiD protein family. The middle domain contains a metal binding site adjacent to a large open cleft that may represent the active site. The two protein ligands binding a magnesium ion, His188 and Glu229, invariant in the PA0254 subclass, are also conserved in a corresponding metal site found in one of the FMN binding proteins from the split β-barrel fold family. PA0254 forms, in contrast to the hexameric UbiD from E. coli and P. aeruginosa, a homo-dimer. Insertion of four residues in a loop region in the PA0254 type enzymes results in structural differences that are incompatible with hexamer assembly.

Highlights

  • Ubiquinone (Coenzyme Q) functions as an electron carrier in the respiratory chains located in the plasma membrane of prokaryotes and inner mitochondrial membrane of eukaryotes

  • Bacterial mutants with a disrupted ubiquinone biosynthesis display a variety of pleiotropic phenotypes, for instance inability to grow on non-fermenting substrates such as maltose and succinate, while retaining the ability to utilize glucose

  • The pathway starts with the elimination of pyruvate from chorismate, the first committed step in ubiquinone biosynthesis

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Summary

Introduction

Ubiquinone (Coenzyme Q) functions as an electron carrier in the respiratory chains located in the plasma membrane of prokaryotes and inner mitochondrial membrane of eukaryotes. Ubiquinone is composed of a benzoquinone ring and a hydrophobic polyprenyl chain of varying length [2]. The pathway starts with the elimination of pyruvate from chorismate, the first committed step in ubiquinone biosynthesis. The length of the prenyl side chain, while constant for each species, varies between organisms from 6–10 isoprene units, with typically nine units in P. aeruginosa [2]. Based on the results of genetic knock-out studies in E. coli, two genes, denoted ubiX and ubiD, have been assigned to encode decarboxylases that catalyze the conversion of 3-octaprenyl-4-hydroxybenzoate to 2-octaprenylphenol in bacteria and yeast [6]. It has been hypothesized that they may act together in the decarboxylation step of ubiquinone synthesis

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