Literature DB >> 18275154

Biosynthesis of CMP-N,N'-diacetyllegionaminic acid from UDP-N,N'-diacetylbacillosamine in Legionella pneumophila.

Pavel A Glaze1, David C Watson, N Martin Young, Martin E Tanner.   

Abstract

Legionaminic acid is a nine-carbon alpha-keto acid that is similar in structure to other members of the sialic acid family that includes neuraminic acid and pseudaminic acid. It is found as a component of the lipopolysaccharide in several bacterial species and is perhaps best known for its presence in the O-antigen of the causative agent of Legionnaires' disease, Legionella pneumophila. In this work, the enzymes responsible for the biosynthesis and activation of N, N'-diacetyllegionaminic acid are identified for the first time. A cluster of three L. pneumophila genes bearing homology to known sialic acid biosynthetic genes ( neuA,B,C) were cloned and overexpressed in Escherichia coli. The NeuC homologue was found to be a hydrolyzing UDP- N, N'-diacetylbacillosamine 2-epimerase that converts UDP- N, N'-diacetylbacillosamine into 2,4-diacetamido-2,4,6-trideoxymannose and UDP. Stereochemical and isotopic labeling studies showed that the enzyme utilizes a mechanism involving an initial anti elimination of UDP to form a glycal intermediate and a subsequent syn addition of water to generate product. This is similar to the hydrolyzing UDP- N-acetylglucosamine 2-epimerase (NeuC) of sialic acid biosynthesis, but the L. pneumophila enzyme would not accept UDP-GlcNAc as an alternate substrate. The NeuB homologue was found to be a N, N'-diacetyllegionaminic acid synthase that condenses 2,4-diacetamido-2,4,6-trideoxymannose with phosphoenolpyruvate (PEP), although the in vitro activity of the recombinant enzyme (isolated as a MalE fusion protein) was very low. The synthase activity was dependent on the presence of a divalent metal ion, and the reaction proceeded via a C-O bond cleavage process, similar to the reactions catalyzed by the sialic acid and pseudaminic acid synthases. Finally, the NeuA homologue was shown to possess the CMP- N, N'-diacetyllegionaminic acid synthetase activity that generates the activated form of legionaminic acid used in lipopolysaccharide biosynthesis. Together, the three enzymes constitute a pathway that converts a UDP-linked bacillosamine derivative into a CMP-linked legionaminic acid derivative.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18275154     DOI: 10.1021/bi702364s

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  19 in total

1.  The N-acylneuraminate cytidyltransferase gene, neuA, is heterogenous in Legionella pneumophila strains but can be used as a marker for epidemiological typing in the consensus sequence-based typing scheme.

Authors:  Claudia Farhat; Massimo Mentasti; Enno Jacobs; Norman K Fry; Christian Lück
Journal:  J Clin Microbiol       Date:  2011-09-28       Impact factor: 5.948

2.  Development of a multicomponent kinetic assay of the early enzymes in the Campylobacter jejuni N-linked glycosylation pathway.

Authors:  James P Morrison; Jerry M Troutman; Barbara Imperiali
Journal:  Bioorg Med Chem       Date:  2010-10-29       Impact factor: 3.641

3.  Human symbiont Bacteroides thetaiotaomicron synthesizes 2-keto-3-deoxy-D-glycero-D- galacto-nononic acid (KDN).

Authors:  Liangbing Wang; Zhibing Lu; Karen N Allen; Patrick S Mariano; Debra Dunaway-Mariano
Journal:  Chem Biol       Date:  2008-09-22

4.  Stereoselective Synthesis of the Equatorial Glycosides of Legionaminic Acid.

Authors:  Oskar Popik; Bibek Dhakal; David Crich
Journal:  J Org Chem       Date:  2017-06-02       Impact factor: 4.354

5.  Innovations in host and microbial sialic acid biosynthesis revealed by phylogenomic prediction of nonulosonic acid structure.

Authors:  Amanda L Lewis; Nolan Desa; Elizabeth E Hansen; Yuriy A Knirel; Jeffrey I Gordon; Pascal Gagneux; Victor Nizet; Ajit Varki
Journal:  Proc Natl Acad Sci U S A       Date:  2009-07-28       Impact factor: 11.205

6.  L. pneumophila CMP-5,7-di-N-acetyllegionaminic acid synthetase (LpCLS)-involved chemoenzymatic synthesis of sialosides and analogues.

Authors:  John B McArthur; Abhishek Santra; Wanqing Li; Anoopjit S Kooner; Ziqi Liu; Hai Yu; Xi Chen
Journal:  Org Biomol Chem       Date:  2020-01-08       Impact factor: 3.876

7.  Therapeutic CMP-Nonulosonates against Multidrug-Resistant Neisseria gonorrhoeae.

Authors:  Sunita Gulati; Ian C Schoenhofen; Theresa Lindhout-Djukic; Melissa J Schur; Corinna S Landig; Sudeshna Saha; Lingquan Deng; Lisa A Lewis; Bo Zheng; Ajit Varki; Sanjay Ram
Journal:  J Immunol       Date:  2020-05-20       Impact factor: 5.422

8.  Genomic Characterization of Candidate Division LCP-89 Reveals an Atypical Cell Wall Structure, Microcompartment Production, and Dual Respiratory and Fermentative Capacities.

Authors:  Noha H Youssef; Ibrahim F Farag; C Ryan Hahn; Jessica Jarett; Eric Becraft; Emiley Eloe-Fadrosh; Jorge Lightfoot; Austin Bourgeois; Tanner Cole; Stephanie Ferrante; Mandy Truelock; William Marsh; Michael Jamaleddine; Samantha Ricketts; Ronald Simpson; Allyson McFadden; Wouter Hoff; Nikolai V Ravin; Stefan Sievert; Ramunas Stepanauskas; Tanja Woyke; Mostafa Elshahed
Journal:  Appl Environ Microbiol       Date:  2019-05-02       Impact factor: 4.792

9.  Influence of side chain conformation and configuration on glycosyl donor reactivity and selectivity as illustrated by sialic acid donors epimeric at the 7-position.

Authors:  Pavan K Kancharla; David Crich
Journal:  J Am Chem Soc       Date:  2013-12-09       Impact factor: 15.419

10.  A Diazido Mannose Analogue as a Chemoenzymatic Synthon for Synthesizing Di-N-acetyllegionaminic Acid-Containing Glycosides.

Authors:  Abhishek Santra; An Xiao; Hai Yu; Wanqing Li; Yanhong Li; Linh Ngo; John B McArthur; Xi Chen
Journal:  Angew Chem Int Ed Engl       Date:  2018-02-14       Impact factor: 15.336

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.