
pmid: 22390826
The cDNA of a benzophenone synthase (BPS), a type III polyketide synthase (PKS), was cloned and the recombinant protein expressed from the fruit pericarps of Garcinia mangostana L., which contains mainly prenylated xanthones. The obtained GmBPS showed an amino acid sequence identity of 77-78% with other plant BPSs belonging to the same family (Clusiaceae). The recombinant enzyme produced 2,4,6-trihydroxybenzophenone as the predominant product with benzoyl CoA as substrate. It also accepted other substrates, such as other plant PKSs, and used 1-3 molecules of malonyl CoA to form various phloroglucinol-type and polyketide lactone-type compounds. Thus, providing GmBPS with various substrates in vivo might redirect the xanthone biosynthetic pathway.
DNA, Complementary, Molecular Sequence Data, Garcinia mangostana, Substrate Specificity, Kinetics, Carbon-Carbon Ligases, Sequence Analysis, Protein, Escherichia coli, Mutagenesis, Site-Directed, Amino Acid Sequence, Cloning, Molecular, Sequence Alignment, Chromatography, High Pressure Liquid, Phylogeny, Plant Proteins
DNA, Complementary, Molecular Sequence Data, Garcinia mangostana, Substrate Specificity, Kinetics, Carbon-Carbon Ligases, Sequence Analysis, Protein, Escherichia coli, Mutagenesis, Site-Directed, Amino Acid Sequence, Cloning, Molecular, Sequence Alignment, Chromatography, High Pressure Liquid, Phylogeny, Plant Proteins
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