| Title | Cloning and expression of the trehalose-phosphate phosphatase of Mycobacterium tuberculosis: comparison to the enzyme from Mycobacterium smegmatis. | | Author(s) | Edavana VK, Pastuszak I, Carroll JD, Thampi P, Abraham EC, Elbein AD | | Institution | Department of Biochemistry and Molecular Biology, The University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA. | | Source | Arch Biochem Biophys 2004 Jun 15; 426(2):250-7. | | MeSH | Amino Acid Sequence
Cloning, Organism
Enzyme Activation
Escherichia coli
Gene Expression Regulation, Bacterial
Gene Expression Regulation, Enzymologic
Heat
Hydrogen-Ion Concentration
Magnesium
Molecular Sequence Data
Molecular Weight
Mycobacterium smegmatis
Mycobacterium tuberculosis
Oligosaccharides
Phospholipids
Phosphoric Monoester Hydrolases
Protein Conformation
Protein Structure, Secondary
Sequence Homology, Amino Acid
Species Specificity
Substrate Specificity
| | Abstract | Two open reading frames in the Mycobacterium tuberculosis genome, Rv3372 and Rv2006, have about 25% sequence identity at the amino acid level to the trehalose-phosphate phosphatase (TPP) purified from Mycobacterium smegmatis. However, the protein produced from the cloned Rv3372 gene has a molecular weight of about 45kDa whereas the trehalose-P phosphatase purified from M. smegmatis has a molecular weight of about 27kDa. We expressed the Rv3372 protein in Escherichia coli and show here that it is a trehalose-P phosphatase with very similar properties to the M. smegmatis TPP, i.e., complete specificity for trehalose-phosphate as the substrate, an almost absolute requirement for Mg(2+), and a pH optimum of 7-7.5. On the other hand, in contrast to the M. smegmatis enzyme, the Rv3372 protein was much less stable to heat and much less sensitive to inhibition by diumycin and moenomycin. In fact, both of these antibiotics stimulate enzyme activity at low concentrations and only inhibit the activity at higher antibiotic concentrations. Antibody prepared against the 27kDa TPP does not cross react with the 45kDa TPP nor does antibody against the 45kDa TPP cross react with the 27kDa TPP. Nevertheless, studies of secondary structure by circular dichroism indicate that the two enzymes are quite similar in structure. The product of the other gene, Rv2006, is a 159kDa protein with no detectable phosphatase activity. Thus, its function is currently unknown. | | Language | eng | | Pub Type(s) | Comparative Study
Journal Article
Research Support, U.S. Gov't, P.H.S.
| | PubMed ID | 15158675 |
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