Jayawardena Thilina U, Merindol Natacha, Liyanage Nuwan Sameera, Desgagné-Penix Isabel
Department of Chemistry, Biochemistry, and Physics, Université du Québec à Trois-Rivières, Trois-Rivières, QC, G8Z 4M3, Canada.
Plant Biology Research Group, Université du Québec à Trois-Rivières, Trois-Rivières, QC, Canada.
Nat Prod Rep. 2024 May 22;41(5):721-747. doi: 10.1039/d3np00044c.
Covering: 2017 to 2023 (now)Amaryllidaceae alkaloids (AAs) are a unique class of specialized metabolites containing heterocyclic nitrogen bridging that play a distinct role in higher plants. Irrespective of their diverse structures, most AAs are biosynthesized intramolecular oxidative coupling. The complex organization of biosynthetic pathways is constantly enlightened by new insights owing to the advancement of natural product chemistry, synthetic organic chemistry, biochemistry, systems and synthetic biology tools and applications. These promote novel compound identification, trace-level metabolite quantification, synthesis, and characterization of enzymes engaged in AA catalysis, enabling the recognition of biosynthetic pathways. A complete understanding of the pathway benefits biotechnological applications in the long run. This review emphasizes the structural diversity of the AA specialized metabolites involved in biogenesis although the process is not entirely defined yet. Moreover, this work underscores the pivotal role of synthetic and enantioselective studies in justifying biosynthetic conclusions. Their prospective candidacy as lead constituents for antiviral drug discovery has also been established. However, a complete understanding of the pathway requires further interdisciplinary efforts in which antiviral studies address the structure-activity relationship. This review presents current knowledge on the topic.
2017年至2023年(截至目前)
石蒜科生物碱(AAs)是一类独特的特殊代谢产物,含有杂环氮桥,在高等植物中发挥着独特作用。尽管其结构多样,但大多数AAs是通过分子内氧化偶联生物合成的。由于天然产物化学、合成有机化学、生物化学、系统和合成生物学工具及应用的发展,生物合成途径的复杂组织不断得到新的认识。这些促进了新型化合物的鉴定、痕量代谢物的定量、合成以及参与AA催化的酶的表征,从而有助于识别生物合成途径。从长远来看,对该途径的全面理解有利于生物技术应用。本综述强调了参与生物合成的AA特殊代谢产物的结构多样性,尽管该过程尚未完全明确。此外,这项工作强调了合成研究和对映选择性研究在证实生物合成结论方面的关键作用。它们作为抗病毒药物发现的先导成分的潜在候选地位也已确立。然而,要完全理解该途径需要进一步的跨学科努力,其中抗病毒研究要关注结构-活性关系。本综述介绍了关于该主题的当前知识。