The methyl-branched fortifications of Mycobacterium tuberculosis.

Mycobacterium tuberculosis continues to be the predominant global infectious agent, annually killing over three million people. Recommended drug regimens have the potential to control tuberculosis, but lack of adherence to such regimens has resulted in the emergence of resistant strains. Mycobacterium tuberculosis has an unusual cell envelope, rich in unique long-chain lipids, that provides a very hydrophobic barrier to antibiotic access. Such lipids, however, can be drug targets, as exemplified by the action of the front-line drug isoniazid on mycolic acid biosynthesis. A number of these lipids are potential key virulence factors and their structures are based on very characteristic methyl-branched long-chain acids and alcohols. This review details the history, structure, and genetic aspects of the biosynthesis of these methyl-branched components, good examples of which are the phthiocerols and the mycocerosic and mycolipenic acids.

[1]  B. Gicquel,et al.  Analysis of the phthiocerol dimycocerosate locus of Mycobacterium tuberculosis. Evidence that this lipid is involved in the cell wall permeability barrier. , 2001, The Journal of biological chemistry.

[2]  D. Minnikin,et al.  Studies relating to phthiocerol. Part V. Phthiocerol A and B , 1966 .

[3]  P. Kolattukudy,et al.  Synthesis of mycocerosic acids from methylmalonyl coenzyme A by cell-free extracts of Mycobacterium tuberculosis var. bovis BCG. , 1983, The Journal of biological chemistry.

[4]  E. Lederer,et al.  [ON THE CHEMICAL STRUCTURE OF MYCOSIDE B]. , 1963, Biochimica et biophysica acta.

[5]  S. Bron,et al.  SecDF of Bacillus subtilis, a Molecular Siamese Twin Required for the Efficient Secretion of Proteins* , 1998, The Journal of Biological Chemistry.

[6]  E. Lederer,et al.  Structure of Phthiocerol , 1959, Nature.

[7]  P. Kolattukudy,et al.  Methylmalonyl coenzyme A selectivity of cloned and expressed acyltransferase and beta-ketoacyl synthase domains of mycocerosic acid synthase from Mycobacterium bovis BCG , 1997, Journal of bacteriology.

[8]  M. Daffé,et al.  Polyphthienoyl trehalose, glycolipids specific for virulent strains of the tubercle bacillus. , 1988, European journal of biochemistry.

[9]  M. Saier,et al.  Two novel families of bacterial membrane proteins concerned with nodulation, cell division and transport , 1994, Molecular microbiology.

[10]  P. Brennan,et al.  Novel type-specific lipooligosaccharides from Mycobacterium tuberculosis. , 1991, Biochemistry.

[11]  M. Daffé,et al.  The envelope layers of mycobacteria with reference to their pathogenicity. , 1998, Advances in microbial physiology.

[12]  A. Azad,et al.  Targeted replacement of the mycocerosic acid synthase gene in Mycobacterium bovis BCG produces a mutant that lacks mycosides. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[13]  William R. Jacobs,et al.  Complex lipid determines tissue-specific replication of Mycobacterium tuberculosis in mice , 1999, Nature.

[14]  P. Kolattukudy,et al.  Molecular cloning and sequencing of the gene for mycocerosic acid synthase, a novel fatty acid elongating multifunctional enzyme, from Mycobacterium tuberculosis var. bovis Bacillus Calmette-Guerin. , 1992, The Journal of biological chemistry.

[15]  H. Sprecher,et al.  The Mycobacterium tuberculosis pks2 Gene Encodes the Synthase for the Hepta- and Octamethyl-branched Fatty Acids Required for Sulfolipid Synthesis* , 2001, The Journal of Biological Chemistry.

[16]  K. Bloch [10] Fatty acid synthases from Mycobacterium phlei , 1975 .

[17]  W. Jacobs,et al.  Molecular genetics of mycobacteria. , 2000 .

[18]  A. Azad,et al.  Biochemistry and molecular genetics of cell‐wall lipid biosynthesis in mycobacteria , 1997, Molecular microbiology.

[19]  D. Minnikin,et al.  Mycolipenates and mycolipanolates of trehalose from mycobacterium tuberculosis. , 1985, Journal of general microbiology.

[20]  P. Kolattukudy,et al.  A Newly Identified Methyl-branched Chain Fatty Acid Synthesizing Enzyme from Mycobacterium tuberculosis var.bovis BCG* , 1998, The Journal of Biological Chemistry.

[21]  D. Minnikin,et al.  Structural elucidation of a novel family of acyltrehaloses from Mycobacterium tuberculosis. , 1992, Biochemistry.

[22]  S T Cole,et al.  Analysis of the proteome of Mycobacterium tuberculosis in silico. , 1999, Tubercle and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease.

[23]  M. Goodfellow,et al.  Microbiological classification and identification. , 1980, Society for Applied Bacteriology symposium series.

[24]  P. Kolattukudy,et al.  An Acyl-CoA Synthase (acoas) Gene Adjacent to the Mycocerosic Acid Synthase (mas) Locus Is Necessary for Mycocerosyl Lipid Synthesis in Mycobacterium tuberculosisvar. bovis BCG* , 1998, The Journal of Biological Chemistry.

[25]  A. Azad,et al.  Gene Knockout Reveals a Novel Gene Cluster for the Synthesis of a Class of Cell Wall Lipids Unique to Pathogenic Mycobacteria* , 1997, The Journal of Biological Chemistry.

[26]  D. Minnikin,et al.  Structural elucidation of new phenolic glycolipids from Mycobacterium tuberculosis. , 1994, Biochimica et biophysica acta.

[27]  J. Asselineau The bacterial lipids , 1966 .

[28]  B. Barrell,et al.  Deciphering the biology of Mycobacterium tuberculosis from the complete genome sequence , 1998, Nature.

[29]  G. Besra,et al.  Lipids and Carbohydrates of Mycobacterium tuberculosis , 1994 .

[30]  W. Wood,et al.  Mycobacterium smegmatis fatty acid synthetase. A mechanism based on steady state rates and product distributions. , 1977, The Journal of biological chemistry.

[31]  R. Timpl,et al.  Role of the Cell Wall Phenolic Glycolipid-1 in the Peripheral Nerve Predilection of Mycobacterium leprae , 2000, Cell.

[32]  P. Kolattukudy,et al.  Cloning, sequencing and characterization of a fatty acid synthase-encoding gene from Mycobacterium tuberculosis var. bovis BCG. , 1996, Gene.

[33]  R. J. Anderson,et al.  THE CHEMISTRY OF THE LIPIDS OF TUBERCLE BACILLI LXXII. FATTY ACIDS OCCURRING IN THE WAX PREPARED FROM TUBERCULIN RESIDUES. CONCERNING MYCOCEROSIC ACID , 1945 .

[34]  C. Ratledge,et al.  The Biology of the mycobacteria , 1982 .

[35]  S. Ehlers,et al.  Molecular mechanics of the mycobacterial cell wall: from horizontal layers to vertical scaffolds. , 2000, International journal of medical microbiology : IJMM.

[36]  S. Donadio,et al.  Polyketide synthesis: prospects for hybrid antibiotics. , 1993, Annual review of microbiology.

[37]  R. J. Anderson Structural Peculiarities of Acid-fast Bacterial Lipids. , 1941 .

[38]  K. Bloch,et al.  Mycobacterium smegmatis fatty acid synthetase. Long chain transacylase chain length specificity. , 1977, The Journal of biological chemistry.

[39]  M R Barer,et al.  Lipid domains of mycobacteria studied with fluorescent molecular probes , 1999, Molecular microbiology.

[40]  M. Daffé,et al.  Structure of the major triglycosyl phenol-phthiocerol of Mycobacterium tuberculosis (strain Canetti). , 1987, European journal of biochemistry.

[41]  D. Minnikin,et al.  Lipid composition in the classification and identification of acid-fast bacteria. , 1980, Society for Applied Bacteriology symposium series.

[42]  G. L. Lange,et al.  Isolation of 2,4-dimethyldocosanoic acid from the lipids of tubercle bacillus , 1964 .

[43]  M. Goren Sulfolipid I of Mycobacterium tuberculosis, strain H37Rv. I. Purification and properties. , 1970, Biochimica et biophysica acta.

[44]  R. J. Anderson,et al.  THE CHEMISTRY OF THE LIPIDS OF TUBERCLE BACILLI XLVI. PHTHIOCEROL, A NEW ALCOHOL FROM THE WAX OF THE HUMAN TUBERCLE BACILLUS , 1936 .

[45]  P. Kolattukudy,et al.  Fatty acid biosynthesis in Mycobacterium tuberculosis var. bovis Bacillus Calmette-Guérin. Purification and characterization of a novel fatty acid synthase, mycocerosic acid synthase, which elongates n-fatty acyl-CoA with methylmalonyl-CoA. , 1985, The Journal of biological chemistry.

[46]  G. Sumrell,et al.  STRUCTURAL FEATURES OF AN ACID OF THE PHTHIOIC TYPE1 , 1950 .

[47]  P. Kolattukudy,et al.  Open reading frame 3, which is adjacent to the mycocerosic acid synthase gene, is expressed as an acyl coenzyme A synthase in Mycobacterium bovis BCG , 1997, Journal of bacteriology.

[48]  M. Casal Mycobacteria of clinical interest. , 1986 .

[49]  E. Lederer,et al.  Sur la structure chimique du mycoside B , 1963 .

[50]  J. Caballero,et al.  The act cluster contains regulatory and antibiotic export genes, direct targets for translational control by the bldA tRNA gene of streptomyces , 1991, Cell.

[51]  B. Barrell,et al.  Massive gene decay in the leprosy bacillus , 2001, Nature.

[52]  J. Chanley,et al.  Dextrorotatory Acids of Tubercle Bacilli Lipids , 1950, Nature.

[53]  D. W. Smith,et al.  DETECTION OF SPECIFIC LIPIDS IN MYCOBACTERIA BY INFRARED SPECTROSCOPY , 1960, Journal of bacteriology.

[54]  G. Besra,et al.  Role of the major antigen of Mycobacterium tuberculosis in cell wall biogenesis. , 1997, Science.

[55]  L L Iversen The chemistry of the brain. , 1979, Scientific American.

[56]  E. Julián,et al.  Occurrence of an antigenic triacyl trehalose in clinical isolates and reference strains of Mycobacterium tuberculosis. , 1997, FEMS microbiology letters.