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Phosphatidylinositol Is an Essential Phospholipid of Mycobacteria
- Source :
- Journal of Biological Chemistry. 275:30092-30099
- Publication Year :
- 2000
- Publisher :
- Elsevier BV, 2000.
-
Abstract
- Phosphatidylinositol (PI) and metabolically derived products such as the phosphatidylinositol mannosides and linear and mature branched lipomannan and lipoarabinomannan are prominent phospholipids/lipoglycans of Mycobacterium sp. believed to play important roles in the structure and physiology of the bacterium as well as during host infection. To determine if PI is an essential phospholipid of mycobacteria, we identified the pgsA gene of Mycobacterium tuberculosis encoding the phosphatidylinositol synthase enzyme and constructed a pgsA conditional mutant of Mycobacterium smegmatis. The ability of this mutant to synthesize phosphatidylinositol synthase and subsequently PI was dependent on the presence of a functional copy of the pgsA gene carried on a thermosensitive plasmid. The mutant grew like the control strain under permissive conditions (30 degrees C), but ceased growing when placed at 42 degrees C, a temperature at which the rescue plasmid is lost. Loss of cell viability at 42 degrees C was observed when PI and phosphatidylinositol dimannoside contents dropped to approximately 30 and 50% of the wild-type levels, respectively. This work provides the first evidence of the essentiality of PI to the survival of mycobacteria. PI synthase is thus an essential enzyme of Mycobacterium that shows promise as a drug target for anti-tuberculosis therapy.
- Subjects :
- Molecular Sequence Data
Mycobacterium smegmatis
Mutant
Transferases (Other Substituted Phosphate Groups)
Phosphatidylinositols
Biochemistry
Mycobacterium
Microbiology
chemistry.chemical_compound
Plasmid
Amino Acid Sequence
Crossing Over, Genetic
Phosphatidylinositol
Molecular Biology
Phospholipids
Lipoarabinomannan
Lipomannan
Sequence Homology, Amino Acid
biology
ATP synthase
Mycobacterium tuberculosis
Cell Biology
CDP-Diacylglycerol-Inositol 3-Phosphatidyltransferase
biology.organism_classification
chemistry
Genes, Bacterial
Mutation
biology.protein
Genes, Lethal
Subjects
Details
- ISSN :
- 00219258
- Volume :
- 275
- Database :
- OpenAIRE
- Journal :
- Journal of Biological Chemistry
- Accession number :
- edsair.doi.dedup.....69a72492c161eab0256ebee140587a32
- Full Text :
- https://doi.org/10.1074/jbc.m004658200