{"id":207164,"date":"2025-02-24T14:17:54","date_gmt":"2025-02-24T20:17:54","guid":{"rendered":"https:\/\/lifeboat.com\/blog\/2025\/02\/a-concise-enzyme-cascade-enables-the-manufacture-of-natural-and-halogenated-protoberberine-alkaloids"},"modified":"2025-02-24T14:17:54","modified_gmt":"2025-02-24T20:17:54","slug":"a-concise-enzyme-cascade-enables-the-manufacture-of-natural-and-halogenated-protoberberine-alkaloids","status":"publish","type":"post","link":"https:\/\/lifeboat.com\/blog\/2025\/02\/a-concise-enzyme-cascade-enables-the-manufacture-of-natural-and-halogenated-protoberberine-alkaloids","title":{"rendered":"A concise enzyme cascade enables the manufacture of natural and halogenated protoberberine alkaloids"},"content":{"rendered":"<p><a class=\"aligncenter blog-photo\" href=\"https:\/\/lifeboat.com\/blog.images\/a-concise-enzyme-cascade-enables-the-manufacture-of-natural-and-halogenated-protoberberine-alkaloids.jpg\"><\/a><\/p>\n<p>Plant-derived alkaloids are an important class of natural products with various pharmacological properties<sup><a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Bui, V. H., Rodr\u00edguez-L\u00f3pez, C. E. & Dang, T. T. T. Integration of discovery and engineering in plant alkaloid research: recent developments in elucidation, reconstruction, and repurposing biosynthetic pathways. Curr. Opin. Plant Biol. 74, 102379 (2023).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR1\" id=\"ref-link-section-d20024660e449\">1<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Xiang, Z.-d et al. Protoberberine alkaloids: a review of the gastroprotective effects, pharmacokinetics, and toxicity. Phytomedicine 126, 155444 (2024).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR2\" id=\"ref-link-section-d20024660e449_1\">2<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Niu, Z. X., Wang, Y. T. & Wang, J. F. Recent advances in total synthesis of protoberberine and chiral tetrahydroberberine alkaloids. Nat. Prod. Rep. 41, 1457 (2024).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR3\" id=\"ref-link-section-d20024660e449_2\">3<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 4\" title=\"Debnath, B. et al. Role of plant alkaloids on human health: a review of biological activities. Mater. Today Chem. 9, 56&ndash;72 (2018).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR4\" id=\"ref-link-section-d20024660e452\">4<\/a><\/sup>, including Rotundine (<i>L<\/i>-tetrahydropalmatine), berberine, morphine, colchicine, galanthamine and hyoscyamine (Fig. <a data-track=\"click\" data-track-label=\"link\" data-track-action=\"figure anchor\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#Fig1\">1a<\/a>). Many of them have been used as traditional medicines in China, Native America, India and the Islamic region. For instance, Rotundine was first isolated from <i>Corydalis<\/i><sup><a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 5\" title=\"Chou, T. Q. The alkaloids of the Chinese Corydalis ambigua Cham, et Sch.(yen-hu-so). VI. Identification of corydalis D and corydalis M. Chin. J. Physiol 10507&ndash;511 (1936).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR5\" id=\"ref-link-section-d20024660e464\">5<\/a><\/sup>, a plant that has been used as traditional Chinese herbal medicine for over a thousand years, known for its analgesic, anti-inflammatory, neuroprotective, anti-addictive, and antitumor activities<sup><a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Du, Q. Y., Meng, X. L. & Wang, S. H. A comprehensive review on the chemical properties, plant sources, pharmacological activities, pharmacokinetic and toxicological characteristics of tetrahydropalmatine. Front. Pharmacol. 13, 890078 (2022).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR6\" id=\"ref-link-section-d20024660e468\">6<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Wang, J. B. & Mantsch, J. R. L-tetrahydropalamatine: a potential new medication for the treatment of cocaine addiction. Future Med. Chem. 4177&ndash;186 (2012).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR7\" id=\"ref-link-section-d20024660e468_1\">7<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 8\" title=\"Chu, H. Y., Jin, G. Z., Friedman, E. & Zhen, X. C. Recent development in studies of tetrahydroprotoberberines: mechanism in antinociception and drug addiction. Cell. Mol. Neurobiol. 28491&ndash;499 (2008).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR8\" id=\"ref-link-section-d20024660e471\">8<\/a><\/sup>. Today, it also serves as an alternative to anxiolytic and sedative drugs from the addictive benzodiazepine group, as well as analgesics<sup><a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 9\" title=\"Liu, L., Liu, M., Zhao, W., Zhao, Y. L. & Wang, Y. Levo-tetrahydropalmatine: a new potential medication for methamphetamine addiction and neurotoxicity. Exp. Neurol. 344, 113809 (2021).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR9\" id=\"ref-link-section-d20024660e476\">9<\/a><\/sup>. However, similar to many plant-derived natural products<sup><a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 10\" title=\"Zhang, H. L. & Tang, X. Y. Combining microbial and chemical syntheses for the production of complex natural products. Chin. J. Nat. Med. 20729&ndash;736 (2022).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR10\" id=\"ref-link-section-d20024660e480\">10<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 11\" title=\"Liu, S. Q., Yu, B. L., Dai, J. G. & Chen, R. D. Targeting the biological activity and biosynthesis of hyperforin: a mini-review. Chin. J. Nat. Med. 20721&ndash;728 (2022).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR11\" id=\"ref-link-section-d20024660e483\">11<\/a><\/sup>, the commercial use of plant-derived alkaloids still mainly relies on extraction from medicinal plants with low abundance<sup><a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Sun, S. J., Wei, Y. F., Wang, H., Tang, L. F. & Deng, B. Y. Simultaneous electrochemiluminescence determination of sinomenine, cepharanthine and tetrahydropalmatine in Stephania epigaea by capillary electrophoresis coupled with ultrasonic-assisted aqueous two-phase extraction. Int. J. Electrochem. Sci. 15, 5002&ndash;5017 (2020).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR12\" id=\"ref-link-section-d20024660e487\">12<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Tarabasz, D. & Kukula-Koch, W. Palmatine: a review of pharmacological properties and pharmacokinetics. Phytother. Res. 34, 33&ndash;50 (2020).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR13\" id=\"ref-link-section-d20024660e487_1\">13<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Neag, M. A. et al. Berberine: botanical occurrence, traditional uses, extraction methods, and relevance in cardiovascular, metabolic, hepatic, and renal disorders. Front. Pharmacol. 9,557 (2018).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR14\" id=\"ref-link-section-d20024660e487_2\">14<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 15\" title=\"Zhong, F. R. et al. Jatrorrhizine: a review of sources, pharmacology, pharmacokinetics and toxicity. Front. Pharmacol. 12, 783127 (2022).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR15\" id=\"ref-link-section-d20024660e490\">15<\/a><\/sup>, which is further affected by climate change, cultivation methods and location. Moreover, due to the lack of appropriate functional groups, derivatization of naturally occurring alkaloids to increase structural complexity and diversity through chemical methods remains challenging, restricting further drug development. Although chemical synthesis methods have been developed to overcome these issues, they often involve harsh conditions and heavy-metal catalysts<sup><a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 16\" title=\"Li, W. J. et al. Total synthesis of (-)-Canadine, (-)-Rotundine, (-)-Sinactine, and (-)-Xylopinine using a last-step enantioselective Ir-catalyzed hydrogenation. J. Org. Chem. 86, 8143&ndash;8153 (2021).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR16\" id=\"ref-link-section-d20024660e494\">16<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 17\" title=\"Gatland, A. E., Pilgrim, B. S., Procopiou, P. A. & Donohoe, T. J. Short and efficient syntheses of protoberberine alkaloids using palladium-catalyzed enolate arylation. Angew. Chem. Int. Ed. 53, 14555&ndash;14558 (2014).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR17\" id=\"ref-link-section-d20024660e497\">17<\/a><\/sup>. In addition, the structural complexity of alkaloids, with their chiral centers and regioselective modifications, often results in low yields.<\/p>\n<p>With the elucidation of the biosynthetic pathways of alkaloids and advancements in synthetic biology<sup><a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Galanie, S., Thodey, K., Trenchard, I. J., Filsinger Interrante, M. & Smolke, C. D. Complete biosynthesis of opioids in yeast. Science 349, 1095&ndash;1100 (2015).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR18\" id=\"ref-link-section-d20024660e541\">18<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Mehta, N., Meng, Y., Zare, R., Kamenetsky-Goldstein, R. & Sattely, E. A developmental gradient reveals biosynthetic pathways to eukaryotic toxins in monocot geophytes. Cell 187, 5620&ndash;5637 (2024).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR19\" id=\"ref-link-section-d20024660e541_1\">19<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Nett, R. S., Lau, W. & Sattely, E. S. Discovery and engineering of colchicine alkaloid biosynthesis. Nature 584148&ndash;153 (2020).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR20\" id=\"ref-link-section-d20024660e541_2\">20<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Wang, Y. J. et al. Discovery and engineering of the cocaine biosynthetic pathway. J. Am. Chem. Soc. 144, 22000&ndash;22007 (2022).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR21\" id=\"ref-link-section-d20024660e541_3\">21<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Wang, Y. J. et al. Genomic and structural basis for evolution of tropane alkaloid biosynthesis. Proc. Natl Acad. Sci. USA 120, e2302448120 (2023).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR22\" id=\"ref-link-section-d20024660e541_4\">22<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"He, S. M. et al. Identification and characterization of genes involved in benzylisoquinoline alkaloid biosynthesis in Coptis Species. Front. Plant Sci. 9,731 (2018).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR23\" id=\"ref-link-section-d20024660e541_5\">23<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Caputi, L. et al. Missing enzymes in the biosynthesis of the anticancer drug vinblastine in Madagascar periwinkle. Science 360, 1235&ndash;1238 (2018).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR24\" id=\"ref-link-section-d20024660e541_6\">24<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Kunjapur, A. M., Tarasova, Y. & Prather, K. L. J. Synthesis and accumulation of aromatic aldehydes in an engineered strain of Escherichia coli. J. Am. Chem. Soc. 136, 11644&ndash;11654 (2014).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR25\" id=\"ref-link-section-d20024660e541_7\">25<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Liao, D. Q. et al. Identification and developmental expression profiling of putative alkaloid biosynthetic genes in Corydalis yanhusuo bulbs. Sci. Rep. 6, 19460 (2016).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR26\" id=\"ref-link-section-d20024660e541_8\">26<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 27\" title=\"Galanie, S., Thodey, K., Trenchard, I. J., Interrante, M. F. & Smolke, C. D. Complete biosynthesis of opioids in yeast. Science 349, 1095&ndash;1100 (2015).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR27\" id=\"ref-link-section-d20024660e544\">27<\/a><\/sup>, many efforts have been made to biosynthesize natural and unnatural alkaloids in microorganisms, including <i>Saccharomyces cerevisiae<\/i> and <i>Escherichia coli<\/i><sup><a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Valentic, T. R., Payne, J. T. & Smolke, C. D. Structure-guided engineering of a scoulerine 9-O-methyltransferase enables the biosynthesis of tetrahydropalmatrubine and tetrahydropalmatine in yeast. ACS Catal. 10, 4497&ndash;4509 (2020).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR28\" id=\"ref-link-section-d20024660e553\">28<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Jiao, X. et al. De novo production of protoberberine and benzophenanthridine alkaloids through metabolic engineering of yeast. Nat. Commun. 15, 8759 (2024).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR29\" id=\"ref-link-section-d20024660e553_1\">29<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Minami, H. et al. Microbial production of plant benzylisoquinoline alkaloids. Proc. Natl Acad. Sci. USA 105, 7393&ndash;7398 (2008).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR30\" id=\"ref-link-section-d20024660e553_2\">30<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Gao, J. C. et al. Biosynthesis of catharanthine in engineered Pichia pastoris. Nat. Synth. 2231&ndash;242 (2023).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR31\" id=\"ref-link-section-d20024660e553_3\">31<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Zhang, J. et al. A microbial supply chain for production of the anti-cancer drug vinblastine. Nature 609341&ndash;347 (2022).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR32\" id=\"ref-link-section-d20024660e553_4\">32<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Han, J. N. & Li, S. J. De novo biosynthesis of berberine and halogenated benzylisoquinoline alkaloids in Saccharomyces cerevisiae. Commun. Chem. 6, 27 (2023).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR33\" id=\"ref-link-section-d20024660e553_5\">33<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Zhao, W. L. et al. Biosynthesis of plant-specific alkaloids tetrahydroprotoberberines in engineered Escherichia coli. Green Chem. 23, 5944&ndash;5955 (2021).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR34\" id=\"ref-link-section-d20024660e553_6\">34<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 35\" title=\"Galanie, S. & Smolke, C. D. Optimization of yeast-based production of medicinal protoberberine alkaloids. Microb. Cell Fact. 14, 1&ndash;13 (2015).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR35\" id=\"ref-link-section-d20024660e556\">35<\/a><\/sup> (Fig. <a data-track=\"click\" data-track-label=\"link\" data-track-action=\"figure anchor\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#Fig1\">1b<\/a>). However, challenges such as the complexity of their biosynthetic pathways, the difficulties in expressing plant-derived P450 enzyme<sup><a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Chang, M. C. Y., Eachus, R. A., Trieu, W., Ro, D. K. & Keasling, J. D. Engineering Escherichia coli for production of functionalized terpenoids using plant P450s. Nat. Chem. Biol. 3274&ndash;277 (2007).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR36\" id=\"ref-link-section-d20024660e563\">36<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" title=\"Li, S. J., Li, Y. R. & Smolke, C. D. Strategies for microbial synthesis of high-value phytochemicals. Nat. Chem. 10395&ndash;404 (2018).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR37\" id=\"ref-link-section-d20024660e563_1\">37<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 38\" title=\"Hawkins, K. M. & Smolke, C. D. Production of benzylisoquinoline alkaloids in Saccharomyces cerevisiae. Nat. Chem. Biol. 4564&ndash;573 (2008).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR38\" id=\"ref-link-section-d20024660e566\">38<\/a><\/sup> and berberine bridge enzyme (BBE)<sup><a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 29\" title=\"Jiao, X. et al. De novo production of protoberberine and benzophenanthridine alkaloids through metabolic engineering of yeast. Nat. Commun. 15, 8759 (2024).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR29\" id=\"ref-link-section-d20024660e571\">29<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 34\" title=\"Zhao, W. L. et al. Biosynthesis of plant-specific alkaloids tetrahydroprotoberberines in engineered Escherichia coli. Green Chem. 23, 5944&ndash;5955 (2021).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR34\" id=\"ref-link-section-d20024660e574\">34<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 39\" title=\"Zhang, Q., Wu, Y. H., Huang, X. S., Liu, H. L. & Wang, Y. Design and optimization for efficient production of (S)\u2011Canadine in Escherichia coli. ACS Sustainable Chem. Eng. 12, 6941&ndash;6951 (2024).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR39\" id=\"ref-link-section-d20024660e577\">39<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 40\" title=\"Gou, Y. et al. Intein-mediated temperature control for complete biosynthesis of sanguinarine and its halogenated derivatives in yeast. Nat. Commun. 15, 5238 (2024).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR40\" id=\"ref-link-section-d20024660e580\">40<\/a><\/sup>, and the cytotoxicity from the accumulation of alkaloids or its intermediates<sup><a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 34\" title=\"Zhao, W. L. et al. Biosynthesis of plant-specific alkaloids tetrahydroprotoberberines in engineered Escherichia coli. Green Chem. 23, 5944&ndash;5955 (2021).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR34\" id=\"ref-link-section-d20024660e584\">34<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 41\" title=\"Pinto, N. D. C. et al. Antimicrobial Annona muricata L. (soursop) extract targets the cell membranes of Gram-positive and Gram-negative bacteria. Ind. Crops Prod. 107332&ndash;340 (2017).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR41\" id=\"ref-link-section-d20024660e587\">41<\/a><\/sup> always results in low production titers<sup><a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 28\" title=\"Valentic, T. R., Payne, J. T. & Smolke, C. D. Structure-guided engineering of a scoulerine 9-O-methyltransferase enables the biosynthesis of tetrahydropalmatrubine and tetrahydropalmatine in yeast. ACS Catal. 10, 4497&ndash;4509 (2020).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR28\" id=\"ref-link-section-d20024660e591\">28<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 29\" title=\"Jiao, X. et al. De novo production of protoberberine and benzophenanthridine alkaloids through metabolic engineering of yeast. Nat. Commun. 15, 8759 (2024).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR29\" id=\"ref-link-section-d20024660e594\">29<\/a>,<a data-track=\"click\" data-track-action=\"reference anchor\" data-track-label=\"link\" data-test=\"citation-ref\" aria-label=\"Reference 34\" title=\"Zhao, W. L. et al. Biosynthesis of plant-specific alkaloids tetrahydroprotoberberines in engineered Escherichia coli. Green Chem. 23, 5944&ndash;5955 (2021).\" href=\"https:\/\/www.nature.com\/articles\/s41467-025-57280-0#ref-CR34\" id=\"ref-link-section-d20024660e597\">34<\/a><\/sup>, such as 16.9 mg L<sup>-1<\/sup> production in berberine and 68.6 mg L<sup>-1<\/sup> production in Rotundine in engineered yeasts, which still lack commercial viability. In fact, this remains a common manufacturing challenge for the heterologous biosynthesis of many plant-derived alkaloids in microorganisms.<\/p>\n<p>Recently, it was reported that a designed nine-enzyme catalytic cascade enabled the efficient biosynthesis of the HIV drug islatravir<sup>42<\/sup>, and therapeutic oligonucleotides could be produced through an enzyme cascade in a single operation<sup>43<\/sup>. These seminal examples suggest that the designed enzyme cascades will revolutionize drug synthesis and development. Furthermore, specific enzymes can control the stereo-and chemoselectivity of chiral compounds<sup>44,45<\/sup>. Importantly, the use of modular \u201cplug-and-play\u201d strategy allows the easy incorporation or removal of enzymes to tailor the cascade for synthesizing different target compounds<sup>46,47<\/sup>, thereby introducing structural complexity and diversity. As for plant-derived natural products, steps catalyzed by enzymes that are difficult to express in engineered cells or that are still not identified can be bypassed through the careful selection of substrates<sup>46<\/sup>, making the process more efficient or feasible.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Plant-derived alkaloids are an important class of natural products with various pharmacological properties1,2,3,4, including Rotundine (L-tetrahydropalmatine), berberine, morphine, colchicine, galanthamine and hyoscyamine (Fig. 1a). Many of them have been used as traditional medicines in China, Native America, India and the Islamic region. For instance, Rotundine was first isolated from Corydalis5, a plant that has been [\u2026]<\/p>\n","protected":false},"author":661,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1902,11,19],"tags":[],"class_list":["post-207164","post","type-post","status-publish","format-standard","hentry","category-bioengineering","category-biotech-medical","category-chemistry"],"_links":{"self":[{"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/posts\/207164","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/users\/661"}],"replies":[{"embeddable":true,"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/comments?post=207164"}],"version-history":[{"count":0,"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/posts\/207164\/revisions"}],"wp:attachment":[{"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/media?parent=207164"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/categories?post=207164"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/lifeboat.com\/blog\/wp-json\/wp\/v2\/tags?post=207164"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}