The two chorismate mutases from both Mycobacterium tuberculosis and Mycobacterium smegmatis: biochemical analysis and limited regulation of promoter activity by aromatic amino acids.

Abstract

Chorismate mutase (CM) catalyzes the rearrangement of chorismate to prephenate in the biosynthetic pathway that forms phenylalanine and tyrosine in bacteria, fungi, plants, and apicomplexan parasites. Since this enzyme is absent from mammals, it represents a promising target for the development of new antimycobacterial drugs, which are needed to combat Mycobacterium tuberculosis, the causative agent of tuberculosis. Until recently, two putative open reading frames (ORFs), Rv0948c and Rv1885c, showing low sequence similarity to CMs have been described as "conserved hypothetical proteins" in the M. tuberculosis genome. However, we and others demonstrated that these ORFs are in fact monofunctional CMs of the AroQ structural class and that they are differentially localized in the mycobacterial cell. Since homologues to the M. tuberculosis enzymes are also present in Mycobacterium smegmatis, we cloned the coding sequences corresponding to ORFs MSMEG5513 and MSMEG2114 from the latter. The CM activities of both ORFs was determined, as well as their translational start sites. In addition, we analyzed the promoter activities of three M. tuberculosis loci related to phenylalanine and tyrosine biosynthesis under a variety of conditions using M. smegmatis as a surrogate host. Our results indicate that the aroQ (Rv0948c), *aroQ (Rv1885c), and fbpB (Rv1886c) genes from M. tuberculosis are constitutively expressed or subjected to minor regulation by aromatic amino acids levels, especially tryptophan.

• Authors: Cristopher Z Schneider, Tanya Parish, Luiz A Basso, Diógenes S Santos
• Journal: Journal of bacteriology (J Bacteriol) Vol. 190 Issue 1 Pg. 122-34 (Jan 2008) ISSN: 1098-5530 [Electronic] United States
• PMID: 17965159 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Amino Acids, Aromatic
• Antitubercular Agents
• Bacterial Proteins
• DNA Primers
• Chorismate Mutase

Topics

• Amino Acid Sequence
• Amino Acids, Aromatic (pharmacology)
• Antitubercular Agents (pharmacology)
• Bacterial Proteins (genetics, metabolism)
• Base Sequence
• Chorismate Mutase (genetics, metabolism)
• DNA Primers
• Gene Expression Regulation, Bacterial (drug effects)
• Gene Expression Regulation, Enzymologic (drug effects)
• Humans
• Kinetics
• Molecular Sequence Data
• Mycobacterium smegmatis (enzymology, genetics)
• Mycobacterium tuberculosis (enzymology, genetics)
• Plasmids
• Promoter Regions, Genetic
• Protein Biosynthesis