Medical Journals

A Solanesyl-diphosphate Synthase Localizes in Glycosomes of Trypanosoma Cruzi.

Authors:
  • Ferella Marcela
  • Montalvetti Andrea
  • Rohloff Peter
  • Miranda Kildare
  • Fang Jianmin
  • Reina Silvia
  • Kawamukai Makoto
  • Búa Jacqueline
  • Nilsson Daniel
  • Pravia Carlos
  • Katzin Alejandro
  • Cassera Maria B
  • Aslund Lena
  • Andersson Björn
  • Docampo Roberto
  • Bontempi Esteban J

From: Instituto Nacional de Parasitología Dr. M. Fatala Chabén, Av. Paseo Colón 568, Administración Nacional de Laboratorios e Institutos de Salud, Ministerio de Salud, Buenos Aires 1063, Argentina.

The Journal of biological chemistry

  • Publish Date: Dec 2006
  • ISSN: 0021-9258
  • Volume: 281
  • Issue: 51
  • Pages: 39339-48
  • Medium: Print
  • Language: English
  • Citation (JAMA): Ferella Marcela, Montalvetti Andrea, Rohloff Peter, et al. A Solanesyl-diphosphate Synthase Localizes in Glycosomes of Trypanosoma Cruzi.. J. Biol. Chem. Dec 2006;281:39339-48

Abstract

We report the cloning of a Trypanosoma cruzi gene encoding a solanesyl-diphosphate synthase, TcSPPS. The amino acid sequence (molecular mass approximately 39 kDa) is homologous to polyprenyl-diphosphate synthases from different organisms, showing the seven conserved motifs and the typical hydrophobic profile. TcSPPS preferred geranylgeranyl diphosphate as the allylic substrate. The final product, as determined by TLC, had nine isoprene units. This suggests that the parasite synthesizes mainly ubiquinone-9 (UQ-9), as described for Trypanosoma brucei and Leishmania major. In fact, that was the length of the ubiquinone extracted from epimastigotes, as determined by high-performance liquid chromatography. Expression of TcSPPS was able to complement an Escherichia coli ispB mutant. A punctuated pattern in the cytoplasm of the parasite was detected by immunofluorescence analysis with a specific polyclonal antibody against TcSPPS. An overlapping fluorescence pattern was observed using an antibody directed against the glycosomal marker pyruvate phosphate dikinase, suggesting that this step of the isoprenoid biosynthetic pathway is located in the glycosomes. Co-localization in glycosomes was confirmed by immunogold electron microscopy and subcellular fractionation. Because UQ has a central role in energy production and in reoxidation of reduction equivalents, TcSPPS is promising as a new chemotherapeutic target.

Mesh Headings (Keywords): Alkyl and Aryl Transferases, Amino Acid Sequence, Animals, Chromatography, Thin Layer, Cloning, Molecular, Cosmids, Escherichia coli, Genetic Complementation Test, Microbodies, Mitochondria, Molecular Sequence Data, Sequence Homology, Amino Acid, Substrate Specificity, Trypanosoma cruzi, Ubiquinone


Check for Full Text / PubMed Unique Identifier (PMID): 17062572


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The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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