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acridone/dental caries
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Probing the hydrogen bond involving Acridone trapped in a hydrophobic biological nanocavity: Integrated spectroscopic and docking analyses.
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Spectroscopic analysis reveal that Acridone (AD) penetrates through the structure and enters the hydrophobic cavity of β-Lactoglobulin (βLG), a protein containing two tryptophan (Trp) residues, and interacts with only with Trp residue (Trp 19). Interaction of AD with only one Trp is confirmed from
Cloning and structure-function analyses of quinolone- and acridone-producing novel type III polyketide synthases from Citrus microcarpa.
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Two novel type III polyketide synthases, quinolone synthase (QNS) and acridone synthase (ACS), were cloned from Citrus microcarpa (Rutaceae). The deduced amino acid sequence of C. microcarpa QNS is unique, and it shared only 56-60% identities with C. microcarpa ACS, Medicago sativa chalcone synthase
Transformation of acridone synthase to chalcone synthase.
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Acridone synthase (ACS) and chalcone synthase (CHS) catalyse the pivotal reactions in the formation of acridone alkaloids or flavonoids. While acridone alkaloids are confined almost exclusively to the Rutaceae, flavonoids occur abundantly in all seed-bearing plants. ACSs and CHSs had been cloned
Starter substrate specificities of wild-type and mutant polyketide synthases from Rutaceae.
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Chalcone synthases (CHSs) and acridone synthases (ACSs) belong to the superfamily of type III polyketide synthases (PKSs) and condense the starter substrate 4-coumaroyl-CoA or N-methylanthraniloyl-CoA with three malonyl-CoAs to produce flavonoids and acridone alkaloids, respectively. ACSs which have
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