2021
DOI: 10.1039/d0np00031k
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The scaffold-forming steps of plant alkaloid biosynthesis

Abstract: Plant alkaloids are central to both modern and traditional medicines. This review describes the progress made towards understanding the metabolic origins of these compounds, focussing on the common features of different biosynthetic pathways.

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Cited by 131 publications
(119 citation statements)
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References 213 publications
(313 reference statements)
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“…In some alkaloids the nitrogen atom is introduced into a preformed nucleus (e.g., terpenoid alkaloids). These pathway relationships and the breadth and depth of the metabolic pool are being actively pursued [34][35][36][37][38][39][40]. As biologically significant metabolites, alkaloids are often highly potent, and in some instances exclusive in their mode of action and application [2].…”
Section: Background and Originsmentioning
confidence: 99%
“…In some alkaloids the nitrogen atom is introduced into a preformed nucleus (e.g., terpenoid alkaloids). These pathway relationships and the breadth and depth of the metabolic pool are being actively pursued [34][35][36][37][38][39][40]. As biologically significant metabolites, alkaloids are often highly potent, and in some instances exclusive in their mode of action and application [2].…”
Section: Background and Originsmentioning
confidence: 99%
“…Besides engineering BIA pathways in heterogenous hosts, many enzymes (especially the C-C bond forming NCS and BBE) in the biosynthetic pathway could be engineered and evolved for the in vitro synthesis of novel THIQs. [247][248][249] NCS is wellknown for its broad scope for accepting different aldehydes to give THIQs. In 2017, Lichman et al discovered that the TfNCS from Thalictrum flavum catalysed the Pictet-Spengler reaction between dopamine and ketones, leading to novel chiral 1,1 0 -disubstituted and spiro-THIQs (Scheme 2B).…”
Section: Alkaloidsmentioning
confidence: 99%
“…In this category, alkaloids are grouped on the criteria of being biosynthesized from the same/similar biochemical precursors, which after going through certain chemical reactions gives rise to stable alkaloids ( Table 1 ). Tyrosine, tryptophan, ornithine, and lysine are amino acid precursors, which undergo enzymatically catalyzed chemical reactions giving rise to tetrahydroisoquinoline, indole, pyrrolizidine, and piperidine alkaloids, respectively [ 42 ]. For example, L-aspartate acts as a precursor for the biosynthesis of pyridine- and pyridinone-type alkaloids.…”
Section: Classification Of Plant Alkaloidsmentioning
confidence: 99%