Literature DB >> 15778500

Biosynthesis of UDP-N-acetyl-L-fucosamine, a precursor to the biosynthesis of lipopolysaccharide in Pseudomonas aeruginosa serotype O11.

Erin F Mulrooney1, Karen K H Poon, David J McNally, Jean-Robert Brisson, Joseph S Lam.   

Abstract

UDP-N-acetyl-L-fucosamine is a precursor to l-fucosamine in the lipopolysaccharide of Pseudomonas aeruginosa serotype O11 and the capsule of Staphylococcus aureus type 5. We have demonstrated previously the involvement of three enzymes, WbjB, WbjC, and WbjD, in the biosynthesis of UDP-2-acetamido-2,6-dideoxy-L-galactose or UDP-N-acetyl-L-fucosamine (UDP-l-FucNAc). An intermediate compound from the coupled-reaction of WbjB-WbjC with the initial substrate UDP-2-acetamido-2-deoxy-alpha-D-glucose or UDP-N-acetyl-D-glucosamine (UDP-GlcNAc) was purified, and the structure was determined by NMR spectroscopy to be UDP-2-acetamido-2,6-dideoxy-L-talose (UDP-L-PneNAc). WbjD could then convert this intermediate into a new product with the same mass, consistent with a C-2 epimerization reaction. Those results led us to propose a pathway for the biosynthesis of UDP-L-FucNAc; however, the exact enzymatic activity of each of these proteins has not been defined. Here, we describe a fast protein liquid chromatography (FPLC)-based anion-exchange procedure, which allowed the separation and purification of the products of C-2 epimerization due to WbjD. Also, the application of a cryogenically cooled probe in NMR spectrometry offers the greatest sensitivity for determining the structures of minute quantities of materials, allowing the identification of the final product of the pathway. Our results showed that WbjB is bifunctional, catalyzing firstly C-4, C-6 dehydration and secondly C-5 epimerization in the reaction with the substrate UDP-D-GlcNAc, producing two intermediates. WbjC is also bifunctional, catalyzing C-3 epimerization of the second intermediate followed by reduction at C-4. The FPLC-based procedure provided good resolution of the final product of WbjD reaction from its epimer/substrate UDP-l-PneNAc, and the use of the cryogenically cooled probe in NMR revealed unequivocally that the final product is UDP-L-FucNAc.

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Year:  2005        PMID: 15778500     DOI: 10.1074/jbc.M500612200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  15 in total

1.  Predicted functions and linkage specificities of the products of the Streptococcus pneumoniae capsular biosynthetic loci.

Authors:  David M Aanensen; Angeliki Mavroidi; Stephen D Bentley; Peter R Reeves; Brian G Spratt
Journal:  J Bacteriol       Date:  2007-08-31       Impact factor: 3.490

2.  Genetic relatedness of the Streptococcus pneumoniae capsular biosynthetic loci.

Authors:  Angeliki Mavroidi; David M Aanensen; Daniel Godoy; Ian C Skovsted; Margit S Kaltoft; Peter R Reeves; Stephen D Bentley; Brian G Spratt
Journal:  J Bacteriol       Date:  2007-08-31       Impact factor: 3.490

3.  lfnA from Pseudomonas aeruginosa O12 and wbuX from Escherichia coli O145 encode membrane-associated proteins and are required for expression of 2,6-dideoxy-2-acetamidino-L-galactose in lipopolysaccharide O antigen.

Authors:  Jerry D King; Erin F Mulrooney; Evgeny Vinogradov; Bernd Kneidinger; Kristen Mead; Joseph S Lam
Journal:  J Bacteriol       Date:  2007-12-21       Impact factor: 3.490

4.  The structural basis for catalytic function of GMD and RMD, two closely related enzymes from the GDP-D-rhamnose biosynthesis pathway.

Authors:  Jerry D King; Karen K H Poon; Nicole A Webb; Erin M Anderson; David J McNally; Jean-Robert Brisson; Paul Messner; R M Garavito; Joseph S Lam
Journal:  FEBS J       Date:  2009-05       Impact factor: 5.542

5.  Giant virus Megavirus chilensis encodes the biosynthetic pathway for uncommon acetamido sugars.

Authors:  Francesco Piacente; Cristina De Castro; Sandra Jeudy; Antonio Molinaro; Annalisa Salis; Gianluca Damonte; Cinzia Bernardi; Chantal Abergel; Michela G Tonetti
Journal:  J Biol Chem       Date:  2014-07-17       Impact factor: 5.157

Review 6.  Pseudomonas aeruginosa lipopolysaccharide: a major virulence factor, initiator of inflammation and target for effective immunity.

Authors:  Gerald B Pier
Journal:  Int J Med Microbiol       Date:  2007-04-27       Impact factor: 3.473

7.  Pseudomonas aeruginosa isolates from dental unit waterlines can be divided in two distinct groups, including one displaying phenotypes similar to isolates from cystic fibrosis patients.

Authors:  Myriam M Ouellet; Annie Leduc; Christine Nadeau; Jean Barbeau; Steve J Charette
Journal:  Front Microbiol       Date:  2015-01-21       Impact factor: 5.640

8.  Biosynthesis of three N-acetylaminosugar-conjugated flavonoids using engineered Escherichia coli.

Authors:  A Ra Cho; Su Jin Lee; Bong Gyu Kim; Joong-Hoon Ahn
Journal:  Microb Cell Fact       Date:  2016-10-24       Impact factor: 5.328

9.  Crystal structure of the capsular polysaccharide synthesizing protein CapE of Staphylococcus aureus.

Authors:  Takamitsu Miyafusa; Jose M M Caaveiro; Yoshikazu Tanaka; Martin E Tanner; Kouhei Tsumoto
Journal:  Biosci Rep       Date:  2013-06-11       Impact factor: 3.840

10.  Genetic analysis of the capsular biosynthetic locus from all 90 pneumococcal serotypes.

Authors:  Stephen D Bentley; David M Aanensen; Angeliki Mavroidi; David Saunders; Ester Rabbinowitsch; Matthew Collins; Kathy Donohoe; David Harris; Lee Murphy; Michael A Quail; Gabby Samuel; Ian C Skovsted; Margit Staum Kaltoft; Bart Barrell; Peter R Reeves; Julian Parkhill; Brian G Spratt
Journal:  PLoS Genet       Date:  2006-03-10       Impact factor: 5.917

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