Rv0989c encodes a novel (E)-geranyl diphosphate synthase facilitating decaprenyl diphosphate biosynthesis in Mycobacterium tuberculosis |
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Authors: | Mann Francis M Thomas Jill A Peters Reuben J |
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Affiliation: | Department of Biochemistry, Biophysics, and Molecular Biology, Iowa State University, Ames, IA, United States |
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Abstract: | Mycobacterium tuberculosis (Mtb) has a highly complex cell wall, which is required for both bacterial survival and infection. Cell wall biosynthesis is dependent on decaprenyl diphosphate as a glyco-carrier, which is hence an essential metabolite in this pathogen. Previous biochemical studies indicated (E)-geranyl diphosphate (GPP) is required for the synthesis of decaprenyl diphosphate. Here we demonstrate that Rv0989c encodes the “missing” GPP synthase, representing the first such enzyme to be characterized from bacteria, and which presumably is involved in decaprenyl diphosphate biosynthesis in Mtb. Our investigation also has revealed previously unrecognized substrate plasticity of the farnesyl diphosphate synthases from Mtb, resolving previous discrepancies between biochemical and genetic studies of cell wall biosynthesis. |
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Keywords: | Abbreviations: Mtb, Mycobacterium tuberculosis IPP, isopentenyl diphosphate DMAPP, dimethylallyl diphosphate GPP, geranyl diphosphate FPP, farnesyl diphosphate GGPP, geranylgeranyl diphosphate GC, gas chromatography Pol-P, polyprenyl phosphate FID, flame ionization detector MS, mass spectrometer FARM, first aspartate-rich motif SARM, second aspartate-rich motif |
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