Structure of the major triglycosyl phenol-phthiocerol of <em>Mycobacterium tuberculosis</em> (strain Canetti).

Phenol-phthiocerol glycolipids have been found previously in Mycobacterium leprae, M. kansasii, M. boris and M. marinum, but not in M. tuberculosis. A search for such glycolipids in this latter species showed that the Canetti strains of M. tuberculosis synthesize a major triglycosyl phenol-phthiocerol, accompanied by minor amounts of other glycolipids with a similar aglycone moiety. The triglycoside moiety has the following structure: 2,3,4-tri-O-methyl L-fucopyranosyl(α1 → 3)L-rhamnopyranosyl(α1 → 3)2-O-methyl L-rhamnopyranosyl(α1 -. The aglycone moiety consists in phenol-phthiocerol (two homologs). Its two secondary alcohol functions are esterified by mycocerosic acids (homologs with 26-32 carbon atoms and with 2-4 methyl branches). The proposed structure differs on several points from the M. leprae glycolipids, but presents some analogy with the major glycolipid of M. kansasii. A minor monoglycosyl phenol-phthiocerol was also studied. Its overall structure is very similar to that of M. bovis, with 2-O-methyl rhamnose as sugar moiety. [ABSTRACT FROM AUTHOR]