Literature DB >> 17371506

Molecular dissection of the biosynthetic relationship between phthiocerol and phthiodiolone dimycocerosates and their critical role in the virulence and permeability of Mycobacterium tuberculosis.

Roxane Siméone1, Patricia Constant, Wladimir Malaga, Christophe Guilhot, Mamadou Daffé, Christian Chalut.   

Abstract

Phthiocerol dimycocerosates and related compounds are important molecules in the biology of Mycobacterium tuberculosis, playing a key role in the permeability barrier and in pathogenicity. Both phthiocerol dimycocerosates, the major compounds, and phthiodiolone dimycocerosates, the minor constituents, are found in the cell envelope of M. tuberculosis, but their specific roles in the biology of the tubercle bacillus have not been established yet. According to the current model of their biosynthesis, phthiocerol is produced from phthiodiolone through a two-step process in which the keto group is first reduced and then methylated. We have previously identified the methyltransferase enzyme that is involved in this process, encoded by the gene Rv2952 in M. tuberculosis. In this study, we report the construction and biochemical analyses of an M. tuberculosis strain mutated in gene Rv2951c. This mutation prevents the formation of phthiocerol and phenolphthiocerol derivatives, but leads to the accumulation of phthiodiolone dimycocerosates and glycosylated phenolphthiodiolone dimycocerosates. These results provide the formal evidence that Rv2951c encodes the ketoreductase catalyzing the reduction of phthiodiolone and phenolphthiodiolone to yield phthiotriol and phenolphthiotriol, which are the substrates of the methyltransferase encoded by gene Rv2952. We also compared the resistance to SDS and replication in mice of the Rv2951c mutant, deficient in synthesis of phthiocerol dimycocerosates but producing phthiodiolone dimycocerosates, with those of a wild-type strain and a mutant without phthiocerol and phthiodiolone dimycocerosates. The results established the functional redundancy between phthiocerol and phthiodiolone dimycocerosates in both the protection of the mycobacterial cell and the pathogenicity of M. tuberculosis in mice.

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Year:  2007        PMID: 17371506     DOI: 10.1111/j.1742-4658.2007.05740.x

Source DB:  PubMed          Journal:  FEBS J        ISSN: 1742-464X            Impact factor:   5.542


  19 in total

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Authors:  Jeremy D Selengut; Daniel H Haft
Journal:  J Bacteriol       Date:  2010-07-30       Impact factor: 3.490

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Journal:  Antimicrob Agents Chemother       Date:  2015-06-01       Impact factor: 5.191

3.  Defining mycobacteria: Shared and specific genome features for different lifestyles.

Authors:  Varalakshmi D Vissa; Rama Murthy Sakamuri; Wei Li; Patrick J Brennan
Journal:  Indian J Microbiol       Date:  2009-02-05       Impact factor: 2.461

4.  A monoacylglycerol lipase from Mycobacterium smegmatis Involved in bacterial cell interaction.

Authors:  Rabeb Dhouib; Françoise Laval; Frédéric Carrière; Mamadou Daffé; Stéphane Canaan
Journal:  J Bacteriol       Date:  2010-07-02       Impact factor: 3.490

5.  Genetics of Capsular Polysaccharides and Cell Envelope (Glyco)lipids.

Authors:  Mamadou Daffé; Dean C Crick; Mary Jackson
Journal:  Microbiol Spectr       Date:  2014

6.  Mycobacterial phenolic glycolipid virulence factor biosynthesis: mechanism and small-molecule inhibition of polyketide chain initiation.

Authors:  Julian A Ferreras; Karen L Stirrett; Xuequan Lu; Jae-Sang Ryu; Clifford E Soll; Derek S Tan; Luis E N Quadri
Journal:  Chem Biol       Date:  2007-12-27

7.  F420H2 Is Required for Phthiocerol Dimycocerosate Synthesis in Mycobacteria.

Authors:  Endang Purwantini; Lacy Daniels; Biswarup Mukhopadhyay
Journal:  J Bacteriol       Date:  2016-07-13       Impact factor: 3.490

8.  Identification of the missing trans-acting enoyl reductase required for phthiocerol dimycocerosate and phenolglycolipid biosynthesis in Mycobacterium tuberculosis.

Authors:  Roxane Siméone; Patricia Constant; Christophe Guilhot; Mamadou Daffé; Christian Chalut
Journal:  J Bacteriol       Date:  2007-04-27       Impact factor: 3.490

9.  A lipid profile typifies the Beijing strains of Mycobacterium tuberculosis: identification of a mutation responsible for a modification of the structures of phthiocerol dimycocerosates and phenolic glycolipids.

Authors:  Gaëlle Huet; Patricia Constant; Wladimir Malaga; Marie-Antoinette Lanéelle; Kristin Kremer; Dick van Soolingen; Mamadou Daffé; Christophe Guilhot
Journal:  J Biol Chem       Date:  2009-08-02       Impact factor: 5.157

10.  Cholesterol metabolism increases the metabolic pool of propionate in Mycobacterium tuberculosis.

Authors:  Xinxin Yang; Natasha M Nesbitt; Eugenie Dubnau; Issar Smith; Nicole S Sampson
Journal:  Biochemistry       Date:  2009-05-12       Impact factor: 3.162

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