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Theor Biol Med Model. 2009 Sep 10;6:22. doi: 10.1186/1742-4682-6-22.

Comparative modeling of DNA and RNA polymerases from Moniliophthora perniciosa mitochondrial plasmid.

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1
Departamento de Ciências Biológicas, Universidade Estadual de Feira de Santana, Feira de Santana, Brazil. bandradefsa@yahoo.com.br

Abstract

BACKGROUND:

The filamentous fungus Moniliophthora perniciosa (Stahel) Aime & Phillips-Mora is a hemibiotrophic Basidiomycota that causes witches' broom disease of cocoa (Theobroma cacao L.). This disease has resulted in a severe decrease in Brazilian cocoa production, which changed the position of Brazil in the market from the second largest cocoa exporter to a cocoa importer. Fungal mitochondrial plasmids are usually invertrons encoding DNA and RNA polymerases. Plasmid insertions into host mitochondrial genomes are probably associated with modifications in host generation time, which can be involved in fungal aging. This association suggests activity of polymerases, and these can be used as new targets for drugs against mitochondrial activity of fungi, more specifically against witches' broom disease. Sequencing and modeling: DNA and RNA polymerases of M. perniciosa mitochondrial plasmid were completely sequenced and their models were carried out by Comparative Homology approach. The sequences of DNA and RNA polymerase showed 25% of identity to 1XHX and 1ARO (pdb code) using BLASTp, which were used as templates. The models were constructed using Swiss PDB-Viewer and refined with a set of Molecular Mechanics (MM) and Molecular Dynamics (MD) in water carried out with AMBER 8.0, both working under the ff99 force fields, respectively. Ramachandran plots were generated by Procheck 3.0 and exhibited models with 97% and 98% for DNA and RNA polymerases, respectively. MD simulations in water showed models with thermodynamic stability after 2000 ps and 300 K of simulation.

CONCLUSION:

This work contributes to the development of new alternatives for controlling the fungal agent of witches' broom disease.

PMID:
19744344
PMCID:
PMC2746187
DOI:
10.1186/1742-4682-6-22
[Indexed for MEDLINE]
Free PMC Article
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