Publications by authors named "Adam M Takos"

Article Synopsis
  • The lotus plant, Lotus japonicus, produces hydroxynitrile glucoside (HNG) compounds that can release toxic hydrogen cyanide when damaged, functioning as a defense against herbivores.
  • BGD2 is the main enzyme that activates these toxic compounds in leaves, while an alternative enzyme called BGD3 plays a crucial role in floral cyanogenesis, particularly in specific floral tissues.
  • The study also highlights that L. japonicus flowers contain HNGs and their diglycosides in nectar, suggesting a balance between attracting pollinators and defending against herbivores in the plant's reproductive structures.
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Article Synopsis
  • Lotus japonicus produces cyanogenic glucosides, lotaustralin and linamarin, which release hydrogen cyanide when tissue is disrupted through hydrolysis by β-glucosidase.
  • BGD2 is the primary enzyme for cyanogenesis in leaves, while BGD4 is crucial for breaking down non-cyanogenic rhodiocyanosides.
  • A single amino acid change in BGD4 allows it to specialize in these substrates, indicating an evolutionary adaptation from a common ancestor that possessed broader enzyme activity.
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The alkaloids characteristically produced by the subfamily Amaryllidoideae of the Amaryllidaceae, bulbous plant species that include well know genera such as Narcissus (daffodils) and Galanthus (snowdrops), are a source of new pharmaceutical compounds. Presently, only the Amaryllidaceae alkaloid galanthamine, an acetylcholinesterase inhibitor used to treat symptoms of Alzheimer's disease, is produced commercially as a drug from cultivated plants. However, several Amaryllidaceae alkaloids have shown great promise as anti-cancer drugs, but their further clinical development is restricted by their limited commercial availability.

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A complex of R2R3-MYB and bHLH transcription factors, stabilized by WD40 repeat proteins, regulates gene transcription for plant cell pigmentation and epidermal cell morphology. It is the MYB component of this complex which specifies promoter target activation. The Arabidopsis MYB TT2 regulates proanthocyanidin (PA) biosynthesis by activating the expression of ANR (anthocyanidin reductase), the gene product of which catalyzes the first committed step of this pathway.

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In plants, the genomic clustering of non-homologous genes for the biosynthesis of chemical defense compounds is an emerging theme. Gene clustering is also observed for polymorphic sexual traits under balancing selection, and examples in plants are self-incompatibility and floral dimorphy. The chemical defense pathways organized as gene clusters are self-contained biosynthetic modules under opposing selection pressures and adaptive polymorphisms, often the presence or absence of a functional pathway, are observed in nature.

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Cyanogenic glucosides are amino acid-derived defence compounds found in a large number of vascular plants. Their hydrolysis by specific β-glucosidases following tissue damage results in the release of hydrogen cyanide. The cyanogenesis deficient1 (cyd1) mutant of Lotus japonicus carries a partial deletion of the CYP79D3 gene, which encodes a cytochrome P450 enzyme that is responsible for the first step in cyanogenic glucoside biosynthesis.

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Proanthocyanidins (PAs; or condensed tannins) can protect plants against herbivores, contribute to the taste of many fruits, and act as dietary antioxidants beneficial for human health. We have previously shown that in grapevine (Vitis vinifera) PA synthesis involves both leucoanthocyanidin reductase (LAR) and anthocyanidin reductase (ANR). Here we report the characterization of a grapevine MYB transcription factor VvMYBPA1, which controls expression of PA pathway genes including both LAR and ANR.

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Anthocyanins are secondary metabolites found in higher plants that contribute to the colors of flowers and fruits. In apples (Malus domestica Borkh.), several steps of the anthocyanin pathway are coordinately regulated, suggesting control by common transcription factors.

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