11 research outputs found

    The scaffold-forming steps of plant alkaloid biosynthesis

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    Alkaloids from plants are characterised by structural diversity and bioactivity, and maintain a privileged position in both modern and traditional medicines. In recent years, there have been significant advances in elucidating the biosynthetic origins of plant alkaloids. In this review, I will describe the progress made in determining the metabolic origins of the so-called true alkaloids, specialised metabolites derived from amino acids containing a nitrogen heterocycle. By identifying key biosynthetic steps that feature in the majority of pathways, I highlight the key roles played by modifications to primary metabolism, iminium reactivity and spontaneous reactions in the molecular and evolutionary origins of these pathways

    Tropane alkaloids: chemistry, pharmacology, biosynthesis and production

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    Tropane alkaloids (TA) are valuable secondary plant metabolites which are mostly found in high concentrations in the Solanaceae and Erythroxylaceae families. The TAs, which are characterized by their unique bicyclic tropane ring system, can be divided into three major groups: hyoscyamine and scopolamine, cocaine and calystegines. Although all TAs have the same basic structure, they differ immensely in their biological, chemical and pharmacological properties. Scopolamine, also known as hyoscine, has the largest legitimate market as a pharmacological agent due to its treatment of nausea, vomiting, motion sickness, as well as smooth muscle spasms while cocaine is the 2nd most frequently consumed illicit drug globally. This review provides a comprehensive overview of TAs, highlighting their structural diversity, use in pharmaceutical therapy from both historical and modern perspectives, natural biosynthesis in planta and emerging production possibilities using tissue culture and microbial biosynthesis of these compounds

    Tropane Alkaloids: Chemistry, Pharmacology, Biosynthesis and Production

    No full text
    Tropane alkaloids (TA) are valuable secondary plant metabolites which are mostly found in high concentrations in the Solanaceae and Erythroxylaceae families. The TAs, which are characterized by their unique bicyclic tropane ring system, can be divided into three major groups: hyoscyamine and scopolamine, cocaine and calystegines. Although all TAs have the same basic structure, they differ immensely in their biological, chemical and pharmacological properties. Scopolamine, also known as hyoscine, has the largest legitimate market as a pharmacological agent due to its treatment of nausea, vomiting, motion sickness, as well as smooth muscle spasms while cocaine is the 2nd most frequently consumed illicit drug globally. This review provides a comprehensive overview of TAs, highlighting their structural diversity, use in pharmaceutical therapy from both historical and modern perspectives, natural biosynthesis in planta and emerging production possibilities using tissue culture and microbial biosynthesis of these compounds

    Structure and Function of Enzymes Involved in the Biosynthesis of Tropane Alkaloids

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    Tropane alkaloids are found in a scattered distribution among the angiosperm families including members within the Solanaceae, Erythroxylaceae, Convolvulaceae, and Brassicaceae. Recent studies regarding the origins of tropane production provide strong evidence for a polyphyletic origin, suggesting that novel enzymes from different gene families have been recruited during the course of flowering plant evolution. Tropane alkaloid biosynthesis is best documented on the molecular genetic and biochemical level from solanaceous species. Regardless of the system chosen, there are currently gaps in the knowledge of enzyme structure-function relationships and how they influence tropane alkaloid biosynthesis. Obtaining insights on structure-function relationships of tropane biosynthetic enzymes is critical to understanding regulation, turnover, and flux of metabolites through the pathway. In this review, we discuss the current state of knowledge regarding structure-function relationships of the known steps involved in tropane biosynthesis.This is a post-peer-review, pre-copyedit version of a chapter published as Kim, Neill, Benjamin Chavez, Charles Stewart, and John C. D’Auria. "Structure and Function of Enzymes Involved in the Biosynthesis of Tropane Alkaloids." In Tropane Alkaloids (Srivastava V., Mehrotra S., Mishra S., eds.) 2021: 21-50. The final authenticated version is available online at DOI: 10.1007/978-981-33-4535-5_2. Posted with permission.</p
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