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1.中国科学院大学杭州高等研究院,化学与材料科学学院,浙江 杭州 310024
2.中国科学院上海有机化学研究所,生命过程小分子调控全国重点实验室,上海 200032
Received:30 November 2023,
Revised:2023-12-22,
Published:30 June 2024
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冯金, 潘海学, 唐功利. 近十年天然产物药物的生物合成研究进展[J]. 合成生物学, 2024, 5(3): 408-446
FENG Jin, PAN Haixue, TANG Gongli. Research advances in biosynthesis of natural product drugs within the past decade[J]. Synthetic Biology Journal, 2024, 5(3): 408-446
冯金, 潘海学, 唐功利. 近十年天然产物药物的生物合成研究进展[J]. 合成生物学, 2024, 5(3): 408-446 DOI: 10.12211/2096-8280.2023-092.
FENG Jin, PAN Haixue, TANG Gongli. Research advances in biosynthesis of natural product drugs within the past decade[J]. Synthetic Biology Journal, 2024, 5(3): 408-446 DOI: 10.12211/2096-8280.2023-092.
天然产物一直是潜在的先导药物的重要来源,天然产物及其结构类似物在历史上对疾病治疗做出了重大贡献,特别是对癌症和传染病的治疗。在过去两百年的时间里,天然产物的发现和研究经历了巨大的变化,由传统的分离鉴定为主的经典研究方法转为了基因组时代的多学科组合研究。虽然近二十年发现和挖掘了丰富的活性天然产物,但与自然界中巨大的天然产物合成潜力相比仍有不足,庞大的陆地和海洋天然产物资源尚待开发。同时,与传统的化学合成分子相比,天然产物具有丰富的骨架多样性和结构复杂性,在新药发现中展现了巨大的优势。虽然在天然产物的新药创新方面仍面临着种种挑战,但新的分析技术和挖掘策略的出现有望迎来天然产物发现的新阶段。本文总结了近十年(2014年1月—2023年10月)美国食品药品监督管理局批准成药的天然产物及源自天然产物的半合成药物,并对其中纯天然产物来源分子、重要的半合成天然产物前体的生物合成研究进展进行了详细总结。此外还简要总结了一些FDA批准的老药在过去十年中取得的重要生物合成研究进展。期望通过对成药天然产物生物合成途径及机制的深入理解,为更多天然产物创新药物的发现和研究提供借鉴。
Natural products have long been considered as an important source for potential drugs. In history
natural products and their structural analogs have contributed substantially to the treatment of various diseases
especially cancers and infectious diseases. After a long history of applications
people have gradually begun to explore active ingredients in natural products that truly exert therapeutic effects
and discovered a series of functional compounds
such as morphine
quinine
ephedrine
etc
. Over the past two hundred years
the discovery and research of natural products has undergone tremendous changes
from traditional identification and isolation methods to multidisciplinary approaches in the modern genomic era. Strategies for discovering natural products and tools for their prediction have been developed continuously. Although many novel and active natural products have been mined and discovered in the past two decades
considering the huge reserve of natural products in nature
a large number of genes or gene clusters encoding key enzymes for the biosynthesis of natural products have not yet been characterized
and both t
errestrial and marine natural product resources are to be explored. Compared with traditional chemically synthesized molecules
natural products possess diverse skeletons for structural complexity
which have shown remarkable advantages in the discovery of new drugs. While there are still many challenges in discovering new drugs from natural products
such as the effective mining of molecules with new structural features
identification and isolation of functional natural products with trace abundance
derivatization of natural product analogs for exploring connections between their structures and activities
and the complete synthesis of complicated active natural products at large scales
etc
.
the emergence of novel analytical technologies and mining strategies is expected to substantially renovate natural product discovery. This review comments on the natural product drugs and semisynthetic drugs derived from natural products approved by the U.S. Food and Drug Administration within the past decade from January 2014 to October 2023
and provides an overview on the research progress on the biosynthesis of these natural products and their precursors. In addition
important progress in the biosynthesis of some drugs approved by FDA before is also briefly summarized. An in-depth understanding of the biosynthetic pathways and mechanisms underlying their efficacy is expected to provide valuable insights for the discovery and research of more new drugs in the future.
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DIAS D A , URBAN S , ROESSNER U . A historical overview of natural products in drug discovery [J ] . Metabolites , 2012 , 2 ( 2 ): 303 - 336 .
VEERESHAM C . Natural products derived from plants as a source of drugs [J ] . Journal of Advanced Pharmaceutical Technology & Research , 2012 , 3 ( 4 ): 200 - 201 .
HUTCHINGS M I , TRUMAN A W , WILKINSON B . Antibiotics: past, present and future [J ] . Current Opinion in Microbiology , 2019 , 51 : 72 - 80 .
饶聪 , 云轩 , 虞沂 , 等 . 微生物药物的合成生物学研究进展 [J ] . 合成生物学 , 2020 , 1 ( 1 ): 92 - 102 .
RAO C , YUN X , YU Y , et al . Recent progress of synthetic biology applications in microbial pharmaceuticals research [J ] . Synthetic Biology Journal , 2020 , 1 ( 1 ): 92 - 102 .
张博 , 马永硕 , 尚轶 , 等 . 植物合成生物学研究进展 [J ] . 合成生物学 , 2020 , 1 ( 2 ): 121 - 140 .
ZHANG B , MA Y S , SHANG Y , et al . Recent advances in plant synthetic biology [J ] . Synthetic Biology Journal , 2020 , 1 ( 2 ): 121 - 140 .
赖奇龙 , 姚帅 , 查毓国 , 等 . 微生物组生物合成基因簇发掘方法及应用前景 [J ] . 合成生物学 , 2023 , 4 ( 3 ): 611 - 627 .
LAI Q L , YAO S , ZHA Y G , et al . Microbiome-based biosynthetic gene cluster data mining techniques and application potentials [J ] . Synthetic Biology Journal , 2023 , 4 ( 3 ): 611 - 627 .
KENSHOLE E , HERISSE M , MICHAEL M , et al . Natural product discovery through microbial genome mining [J ] . Current Opinion in Chemical Biology , 2021 , 60 : 47 - 54 .
LI L . Accessing hidden microbial biosynthetic potential from underexplored sources for novel drug discovery [J ] . Biotechnology Advances , 2023 , 66 : 108176 .
CRAGG G M , NEWMAN D J . Biodiversity: a continuing source of novel drug leads [J ] . Pure and Applied Chemistry , 2005 , 77 ( 1 ): 7 - 24 .
ATANASOV A G , WALTENBERGER B , PFERSCHY-WENZIG E M , et al . Discovery and resupply of pharmacologically active plant-derived natural products: a review [J ] . Biotechnology Advances , 2015 , 33 ( 8 ): 1582 - 1614 .
MATHUR S , HOSKINS C . Drug development: lessons from nature [J ] . Biomedical Reports , 2017 , 6 ( 6 ): 612 - 614 .
NEWMAN D J . Natural products and drug discovery [J ] . National Science Review , 2022 , 9 ( 11 ): nwac206 .
ATANASOV A G , ZOTCHEV S B , DIRSCH V M , et al . Natural products in drug discovery: advances and opportunities [J ] . Nature Reviews Drug Discovery , 2021 , 20 ( 3 ): 200 - 216 .
ZHU F , QIN C , TAO L , et al . Clustered patterns of species origins of nature-derived drugs and clues for future bioprospecting [J ] . Proceedings of the National Academy of Sciences of the United States of America , 2011 , 108 ( 31 ): 12943 - 12948 .
LIU X Y , QIN Y . Industrial total synthesis of natural medicines [J ] . Natural Product Reports , 2023 , 40 ( 11 ): 1694 - 1700 .
张发光 , 曲戈 , 孙周通 , 等 . 从化学合成到生物合成——天然产物全合成新趋势 [J ] . 合成生物学 , 2021 , 2 ( 5 ): 674 - 696 .
ZHANG F G , QU G , SUN Z T , et al . From chemical synthesis to biosynthesis: trends toward total synthesis of natural products [J ] . Synthetic Biology Journal , 2021 , 2 ( 5 ): 674 - 696 .
李晓军 , 张万斌 , 高栓虎 . 复杂天然产物全合成: 化学合成与生物合成结合的策略 [J ] . 有机化学 , 2018 , 38 ( 9 ): 2185 - 2198 .
LI X J , ZHANG W B , GAO S H . Total synthesis of complex natural products: combination of chemical synthesis and biosynthesis strategies [J ] . Chinese Journal of Organic Chemistry , 2018 , 38 ( 9 ): 2185 - 2198 .
贺俊斌 , 孟松 , 潘海学 , 等 . 多酶催化串联策略在复杂天然产物合成中的应用 [J ] . 合成生物学 , 2020 , 1 ( 2 ): 226 - 246 .
HE J B , MENG S , PAN H X , et al . Applications of the multienzyme-catalyzed tandem strategy in the synthesis of complex natural products [J ] . Synthetic Biology Journal , 2020 , 1 ( 2 ): 226 - 246 .
HARVEY A L , EDRADA-EBEL R , QUINN R J . The re-emergence of natural products for drug discovery in the genomics era [J ] . Nature Reviews Drug Discovery , 2015 , 14 ( 2 ): 111 - 129 .
NEWMAN D J , CRAGG G M . Natural products as sources of new drugs from 1981 to 2014 [J ] . Journal of Natural Products , 2016 , 79 ( 3 ): 629 - 661 .
NEWMAN D J , CRAGG G M . Natural products as sources of new drugs over the nearly four decades from 01/1981 to 09/2019 [J ] . Journal of Natural Products , 2020 , 83 ( 3 ): 770 - 803 .
THOMFORD N E , SENTHEBANE D A , ROWE A , et al . Natural products for drug discovery in the 21st century: innovations for novel drug discovery [J ] . International Journal of Molecular Sciences , 2018 , 19 ( 6 ): 1578 .
KHALAF K , TORNESE P , COCCO A , et al . Tauroursodeoxycholic acid: a potential therapeutic tool in neurodegenerative diseases [J ] . Translational Neurodegeneration , 2022 , 11 ( 1 ): 33 .
JOYCE S A , BRACHMANN A O , GLAZER I , et al . Bacterial biosynthesis of a multipotent stilbene [J ] . Angewandte Chemie International Edition , 2008 , 47 ( 10 ): 1942 - 1945 .
STANCZYK F Z , ARCHER D F . Biosynthesis of estetrol in human pregnancy: potential pathways [J ] . The Journal of Steroid Biochemistry and Molecular Biology , 2023 , 232 : 106359 .
TAHIR M N , SHAHBAZI F , RONDEAU-GAGNÉ S , et al . The biosynthesis of the cannabinoids [J ] . Journal of Cannabis Research , 2021 , 3 ( 1 ): 7 .
RIORDAN J F . Angiotensin Ⅱ: biosynthesis, molecular recognition, and signal transduction [J ] . Cellular and Molecular Neurobiology , 1995 , 15 ( 6 ): 637 - 651 .
AUCHUS R J . Overview of dehydroepiandrosterone biosynthesis [J ] . Seminars in Reproductive Medicine , 2004 , 22 ( 4 ): 281 - 288 .
MASSCHELEIN J , JENNER M , CHALLIS G L . Antibiotics from Gram-negative bacteria: a comprehensive overview and selected biosynthetic highlights [J ] . Natural Product Reports , 2017 , 34 ( 7 ): 712 - 783 .
ŠARENAC T M , MIKOV M . Bile acid synthesis: from nature to the chemical modification and synthesis and their applications as drugs and nutrients [J ] . Frontiers in Pharmacology , 2018 , 9 : 939 .
GARCIA-EFFRON G . Rezafungin-mechanisms of action, susceptibility and resistance: similarities and differences with the other echinocandins [J ] . Journal of Fungi , 2020 , 6 ( 4 ): 262 .
APGAR J M , WILKENING R R , PARKER D L JR , et al . Ibrexafungerp: an orally active β-1,3-glucan synthesis inhibitor [J ] . Bioorganic & Medicinal Chemistry Letters , 2021 , 32 : 127661 .
WANG Y . Voclosporin (Lupkynis), a macrocyclic peptide inhibitor of calcineurin for the treatment of lupus nephritis [M/OL ] // LI J J. Current drug synthesis . 1st ed . New York : Wiley , 2022 : 323 - 338 [2023-11-01] . https://onlinelibrary.wiley.com/doi/10.1002/9781119847281.ch17 https://onlinelibrary.wiley.com/doi/10.1002/9781119847281.ch17 .
PETERSON H , KIRCIK L , ARMSTRONG A W . Clascoterone cream 1%: mechanism of action, efficacy, and safety of a novel, first-in-class topical antiandrogen therapy for acne [J ] . Journal of Drugs in Dermatology , 2023 , 22 ( 6 ): SF350992 s 7 -SF350992s14.
PRESSER A , FEICHTINGER A , BUZZI S . A simplified and scalable synthesis of artesunate [J ] . Monatshefte Fur Chemie , 2017 , 148 ( 1 ): 63 - 68 .
MARTÍNEZ-MONTEAGUDO S I , ENTESHARI M , METZGER L . Lactitol: production, properties, and applications [J ] . Trends in Food Science & Technology , 2019 , 83 : 181 - 191 .
WATKINS R R , FILE T M . Lefamulin: a novel semisynthetic pleuromutilin antibiotic for community-acquired bacterial pneumonia [J ] . Clinical Infectious Diseases , 2020 , 71 ( 10 ): 2757 - 2762 .
XU L H , MA J , SHI L F , et al . Design, synthesis and characterizations of prodrugs of brexanolone [J ] . Bioorganic & Medicinal Chemistry Letters , 2023 , 90 : 129344 .
SENSI P . History of the development of rifampin [J ] . Clinical Infectious Diseases , 1983 , 5 ( Suppl 3 ): S402 - S406 .
DURÃES F , SOUSA E . Omadacycline: a newly approved antibacterial from the class of tetracyclines [J ] . Pharmaceuticals , 2019 , 12 ( 2 ): 63 .
CLARK J A , BURGESS D S . Plazomicin: a new aminoglycoside in the fight against antimicrobial resistance [J ] . Therapeutic Advances in Infectious Disease , 2020 , 7 : 2049936120952604 .
COBB R , BOECKH A . Moxidectin: a review of chemistry, pharmacokinetics and use in horses [J ] . Parasites & Vectors , 2009 , 2 ( S2 ): S5 .
RONN M , ZHU Z J , HOGAN P C , et al . Process R&D of eravacycline: the first fully synthetic fluorocycline in clinical development [J ] . Organic Process Research & Development , 2013 , 17 ( 5 ): 838 - 845 .
BUNICK C G , KERI J , TANAKA S K , et al . Antibacterial mechanisms and efficacy of sarecycline in animal models of infection and inflammation [J ] . Antibiotics , 2021 , 10 ( 4 ): 439 .
STONE R M , MANLEY P W , LARSON R A , et al . Midostaurin: its odyssey from discovery to approval for treating acute myeloid leukemia and advanced systemic mastocytosis [J ] . Blood Advances , 2018 , 2 ( 4 ): 444 - 453 .
NAGUNURI G C L , KATANGOOR V , SURIGILLA V , et al . Efficient process for obeticholic acid: synthesis, structural assignment, and control strategy for diastereoisomeric impurities [J ] . Organic Process Research & Development , 2022 , 26 ( 12 ): 3265 - 3275 .
BERRIO ESCOBAR J , PASTRANA RESTREPO M H , GALEANO JARAMILLO E , et al . Synthesis and cytotoxic activity of per-acetylated and halogenated derivatives of nucleosides in breast cancer cells [J ] . Ars Pharmaceutica , 2017 , 58 ( 4 ): 145 - 154 .
HUGHES D L . Patent review of manufacturing routes to fifth-generation cephalosporin drugs. Part 1, Ceftolozane [J ] . Organic Process Research & Development , 2017 , 21 ( 3 ): 430 - 443 .
SARAVOLATZ L D , STEIN G E . Oritavancin: a long-half-life lipoglycopeptide [J ] . Clinical Infectious Diseases , 2015 , 61 ( 4 ): 627 - 632 .
ZHANG D Z , ZHANG F , LIU W . A KAS-Ⅲ heterodimer in lipstatin biosynthesis nondecarboxylatively condenses C 8 and C 14 fatty acyl-CoA substrates by a variable mechanism during the establishment of a C 22 aliphatic skeleton [J ] . Journal of the American Chemical Society , 2019 , 141 ( 9 ): 3993 - 4001 .
SILVERBERG L J , DILLON J L , VEMISHETTI P , et al . Efficient synthesis of the anticancer drug etoposide 4′- phosphate: use of benzylic ether-protecting groups on the carbohydrate segment 1 [J ] . Organic Process Research & Development , 2000 , 4 ( 1 ): 34 - 42 .
ISHIKAWA H , COLBY D A , SETO S , et al . Total synthesis of vinblastine, vincristine, related natural products, and key structural analogues [J ] . Journal of the American Chemical Society , 2009 , 131 ( 13 ): 4904 - 4916 .
NETT R S , LAU W , SATTELY E S . Discovery and engineering of colchicine alkaloid biosynthesis [J ] . Nature , 2020 , 584 ( 7819 ): 148 - 153 .
DASTMALCHI M , CHEN X , HAGEL J M , et al . Neopinone isomerase is involved in codeine and morphine biosynthesis in opium poppy [J ] . Nature Chemical Biology , 2019 , 15 ( 4 ): 384 - 390 .
NOCQUET P A , OPATZ T . Total synthesis of (±)-scopolamine: challenges of the tropane ring [J ] . European Journal of Organic Chemistry , 2016 , 2016( 6 ): 1156 - 1164 .
WARREN M J , RAUX E , SCHUBERT H L , et al . The biosynthesis of adenosylcobalamin (vitamin B 12 ) [J ] . Natural Product Reports , 2002 , 19 ( 4 ): 390 - 412 .
HOWAT S , PARK B , OH I S , et al . Paclitaxel: biosynthesis, production and future prospects [J ] . New Biotechnology , 2014 , 31 ( 3 ): 242 - 245 .
STAELS B , FONSECA V A . Bile acids and metabolic regulation: mechanisms and clinical responses to bile acid sequestration [J ] . Diabetes Care , 2009 , 32 ( S2 ): S237 - S245 .
GUZIOR D V , QUINN R A . Review: microbial transformations of human bile acids [J ] . Microbiome , 2021 , 9 ( 1 ): 140 .
HONDA A , SALEN G , SHEFER S , et al . Regulation of 25- and 27-hydroxylation side chain cleavage pathways for cholic acid biosynthesis in humans, rabbits, and mice: assay of enzyme activities by high-resolution gas chromatography;-mass spectrometry [J ] . Journal of Lipid Research , 2000 , 41 ( 3 ): 442 - 451 .
KRIAA A , MARIAULE V , JABLAOUI A , et al . Bile acids: key players in inflammatory bowel diseases? [J ] . Cells , 2022 , 11 ( 5 ): 901 .
MARION S , DESHARNAIS L , STUDER N , et al . Biogeography of microbial bile acid transformations along the murine gut [J ] . Journal of Lipid Research , 2020 , 61 ( 11 ): 1450 - 1463 .
VANG S , LONGLEY K , STEER C J , et al . The unexpected uses of urso- and tauroursodeoxycholic acid in the treatment of non-liver diseases [J ] . Global Advances in Health and Medicine , 2014 , 3 ( 3 ): 58 - 69 .
AHN T K , KIM K T , JOSHI H P , et al . Therapeutic potential of tauroursodeoxycholic acid for the treatment of osteoporosis [J ] . International Journal of Molecular Sciences , 2020 , 21 ( 12 ): 4274 .
KUSACZUK M . Tauroursodeoxycholate-bile acid with chaperoning activity: molecular and cellular effects and therapeutic perspectives [J ] . Cells , 2019 , 8 ( 12 ): 1471 .
HUIJGHEBAERT S M , HOFMANN A F . Influence of the amino acid moiety on deconjugation of bile acid amidates by cholylglycine hydrolase or human fecal cultures [J ] . Journal of Lipid Research , 1988 , 27 ( 7 ): 742 - 752 .
FERRANDI E E , BERTOLESI G M , POLENTINI F , et al . In search of sustainable chemical processes: cloning, recombinant expression, and functional characterization of the 7α- and 7β-hydroxysteroid dehydrogenases from Clostridium absonum [J ] . Applied Microbiology and Biotechnology , 2012 , 95 ( 5 ): 1221 - 1233 .
SHONSEY E M , WHEELER J , JOHNSON M , et al . Synthesis of bile acid coenzyme A thioesters in the amino acid conjugation of bile acids [M/OL ] // Methods in enzymology . Amsterdam : Elsevier , 2005 , 400 : 360 - 373 [2023-11-01] . https://www.sciencedirect.com/science/article/abs/pii/S0076687905000212?via%3Dihub https://www.sciencedirect.com/science/article/abs/pii/S0076687905000212?via%3Dihub .
SHONSEY E M , SFAKIANOS M , JOHNSON M , et al . Bile acid coenzyme A: amino acid N -acyltransferase in the amino acid conjugation of bile acids [M/OL ] // Methods in enzymology . Amsterdam : Elsevier , 2005 , 400 : 374 - 394 [2023-11-01] . https://www.sciencedirect.com/science/article/abs/pii/S0076687905000224?via%3Dihub https://www.sciencedirect.com/science/article/abs/pii/S0076687905000224?via%3Dihub .
JI Q Z , TAN J , ZHU L C , et al . Preparing tauroursodeoxycholic acid (TUDCA) using a double-enzyme-coupled system [J ] . Biochemical Engineering Journal , 2016 , 105 : 1 - 9 .
SONG C , WANG B C , TAN J , et al . Discovery of tauroursodeoxycholic acid biotransformation enzymes from the gut microbiome of black bears using metagenomics [J ] . Scientific Reports , 2017 , 7 : 45495 .
XU Y P , YANG L , ZHAO S J , et al . Large-scale production of tauroursodeoxycholic acid products through fermentation optimization of engineered Escherichia coli cell factory [J ] . Microbial Cell Factories , 2019 , 18 ( 1 ): 34 .
JIN L N , YANG L , ZHAO S J , et al . A green strategy to produce potential substitute resource for bear bile using engineered Saccharomyces cerevisiae [J ] . Bioresources and Bioprocessing , 2022 , 9 ( 1 ): 32 .
SONG P , ZHANG X , FENG W , et al . Biological synthesis of ursodeoxycholic acid [J ] . Frontiers in Microbiology , 2023 , 14 : 1140662 .
ZHENG M M , CHEN K C , WANG R F , et al . Engineering 7β-hydroxysteroid dehydrogenase for enhanced ursodeoxycholic acid production by multiobjective directed evolution [J ] . Journal of Agricultural and Food Chemistry , 2017 , 65 ( 6 ): 1178 - 1185 .
ZHENG M M , CHEN F F , LI H , et al . Continuous production of ursodeoxycholic acid by using two cascade reactors with co-immobilized enzymes [J ] . ChemBioChem , 2018 , 19 ( 4 ): 347 - 353 .
YOU Z N , CHEN Q , SHI S C , et al . Switching cofactor dependence of 7β-hydroxysteroid dehydrogenase for cost-effective production of ursodeoxycholic acid [J ] . ACS Catalysis , 2019 , 9 ( 1 ): 466 - 473 .
GROBE S , BADENHORST C P S , BAYER T , et al . Engineering regioselectivity of a P450 monooxygenase enables the synthesis of ursodeoxycholic acid via 7β-hydroxylation of lithocholic acid [J ] . Angewandte Chemie International Edition , 2021 , 60 ( 2 ): 753 - 757 .
COELINGH BENNINK H J T , HOLINKA C F , DICZFALUSY E . Estetrol review: profile and potential clinical applications [J ] . Climacteric , 2008 , 11 ( Suppl 1 ): 47 - 58 .
GABAI G , MONGILLO P , GIARETTA E , et al . Do dehydroepiandrosterone (DHEA) and its sulfate (DHEAS) play a role in the stress response in domestic animals? [J ] . Frontiers in Veterinary Science , 2020 , 7 : 588835 .
MILLER K K M , CAI J , RIPP S L , et al . Stereo- and regioselectivity account for the diversity of dehydroepiandrosterone (DHEA) metabolites produced by liver microsomal cytochromes P450 [J ] . Drug Metabolism and Disposition , 2004 , 32 ( 3 ): 305 - 313 .
HOLINKA C F , DICZFALUSY E , COELINGH BENNINK H J T . Estetrol: a unique steroid in human pregnancy [J ] . The Journal of Steroid Biochemistry and Molecular Biology , 2008 , 110 ( 1-2 ): 138 - 143 .
CANTINEAU R , KREMERS P , DE GRAEVE J , et al . 15- and 16-hydroxylations of androgens and estrogens in the human fetal liver: a critical step in estetrol biosynthesis [J ] . Journal of Steroid Biochemistry , 1985 , 22 ( 2 ): 195 - 201 .
FURUE M , HASHIMOTO-HACHIYA A , TSUJI G . Aryl hydrocarbon receptor in atopic dermatitis and psoriasis [J ] . International Journal of Molecular Sciences , 2019 , 20 ( 21 ): 5424 .
BISSONNETTE R , VASIST L S , BULLMAN J N , et al . Systemic pharmacokinetics, safety, and preliminary efficacy of topical AhR agonist tapinarof: results of a phase 1 study [J ] . Clinical Pharmacology in Drug Development , 2018 , 7 ( 5 ): 524 - 531 .
BISSONNETTE R , STEIN GOLD L , RUBENSTEIN D S , et al . Tapinarof in the treatment of psoriasis: a review of the unique mechanism of action of a novel therapeutic aryl hydrocarbon receptor-modulating agent [J ] . Journal of the American Academy of Dermatology , 2021 , 84 ( 4 ): 1059 - 1067 .
ELEFTHERIANOS I , BOUNDY S , JOYCE S A , et al . An antibiotic produced by an insect-pathogenic bacterium suppresses host defenses through phenoloxidase inhibition [J ] . Proceedings of the National Academy of Sciences of the United States of America , 2007 , 104 ( 7 ): 2419 - 2424 .
LI J , CHEN G , WU H , et al . Identification of two pigments and a hydroxystilbene antibiotic from Photorhabdus luminescens [J ] . Applied and Environmental Microbiology , 1995 , 61 ( 12 ): 4329 - 4333 .
HU K J , LI J X , WEBSTER J M . Quantitative analysis of a bacteria-derived antibiotic in nematode-infected insects using HPLC-UV and TLC-UV methods [J ] . Journal of Chromatography B: Biomedical Sciences and Applications , 1997 , 703 ( 1-2 ): 177 - 183 .
FUCHS S W , BOZHÜYÜK K A , KRESOVIC D , et al . Formation of 1,3-cyclohexanediones and resorcinols catalyzed by a widely occuring ketosynthase [J ] . Angewandte Chemie International Edition , 2013 , 52 ( 15 ): 4108 - 4112 .
MORI T , AWAKAWA T , SHIMOMURA K , et al . Structural insight into the enzymatic formation of bacterial stilbene [J ] . Cell Chemical Biology , 2016 , 23 ( 12 ): 1468 - 1479 .
KAVAKLI S , GRAMMBITTER G L C , BODE H B . Biosynthesis of the multifunctional isopropylstilbene in Photorhabdus laumondii involves cross-talk between specialized and primary metabolism [J ] . Tetrahedron , 2022 , 128 : 133116 .
PARK H B , GODDARD T N , OH J , et al . Bacterial autoimmune drug metabolism transforms an immunomodulator into structurally and functionally divergent antibiotics [J ] . Angewandte Chemie International Edition , 2020 , 59 ( 20 ): 7871 - 7880 .
LAPRAIRIE R B , BAGHER A M , KELLY M E M , et al . Cannabidiol is a negative allosteric modulator of the cannabinoid CB 1 receptor [J ] . British Journal of Pharmacology , 2015 , 172 ( 20 ): 4790 - 4805 .
PERTWEE R G . The diverse CB 1 and CB 2 receptor pharmacology of three plant cannabinoids: Δ 9 -tetrahydrocannabinol, cannabidiol and Δ 9 -tetrahydrocannabivarin [J ] . British Journal of Pharmacology , 2008 , 153 ( 2 ): 199 - 215 .
ELSOHLY M A , SLADE D . Chemical constituents of marijuana: the complex mixture of natural cannabinoids [J ] . Life Sciences , 2005 , 78 ( 5 ): 539 - 548 .
LIVINGSTON S J , QUILICHINI T D , BOOTH J K , et al . Cannabis glandular trichomes alter morphology and metabolite content during flower maturation [J ] . The Plant Journal , 2020 , 101 ( 1 ): 37 - 56 .
TAURA F , TANAKA S , TAGUCHI C , et al . Characterization of olivetol synthase, a polyketide synthase putatively involved in cannabinoid biosynthetic pathway [J ] . FEBS Letters , 2009 , 583 ( 12 ): 2061 - 2066 .
GAGNE S J , STOUT J M , LIU E W , et al . Identification of olivetolic acid cyclase from Cannabis sativa reveals a unique catalytic route to plant polyketides [J ] . Proceedings of the National Academy of Sciences of the United States of America , 2012 , 109 ( 31 ): 12811 - 12816 .
TAN Z G , CLOMBURG J M , GONZALEZ R . Synthetic pathway for the production of olivetolic acid in Escherichia coli [J ] . ACS Synthetic Biology , 2018 , 7 ( 8 ): 1886 - 1896 .
KEARSEY L J , PRANDI N , KARUPPIAH V , et al . Structure of the Cannabis sativa olivetol-producing enzyme reveals cyclization plasticity in type Ⅲ polyketide synthases [J ] . The FEBS Journal , 2020 , 287 ( 8 ): 1511 - 1524 .
YANG X M , MATSUI T , KODAMA T , et al . Structural basis for olivetolic acid formation by a polyketide cyclase from Cannabis sativa [J ] . The FEBS Journal , 2016 , 283 ( 6 ): 1088 - 1106 .
TAURA F , SIRIKANTARAMAS S , SHOYAMA Y , et al . Cannabidiolic-acid synthase, the chemotype-determining enzyme in the fiber-type Cannabis sativa [J ] . FEBS Letters , 2007 , 581 ( 16 ): 2929 - 2934 .
FELLERMEIER M , ZENK M H . Prenylation of olivetolate by a hemp transferase yields cannabigerolic acid, the precursor of tetrahydrocannabinol [J ] . FEBS Letters , 1998 , 427 ( 2 ): 283 - 285 .
TAURA F , TANAYA R , SIRIKANTARAMAS S . Recent advances in cannabinoid biochemistry and biotechnology [J ] . ScienceAsia , 2019 , 45 ( 5 ): 399 .
PERROTIN-BRUNEL H , BUIJS W , VAN SPRONSEN J , et al . Decarboxylation of Δ 9 -tetrahydrocannabinol: kinetics and molecular modeling [J ] . Journal of Molecular Structure , 2011 , 987 ( 1-3 ): 67 - 73 .
WANG M , WANG Y H , AVULA B , et al . Decarboxylation study of acidic cannabinoids: a novel approach using ultra-high-performance supercritical fluid chromatography/photodiode array-mass spectrometry [J ] . Cannabis and Cannabinoid Research , 2016 , 1 ( 1 ): 262 - 271 .
LUO X Z , REITER M A , D’ESPAUX L , et al . Complete biosynthesis of cannabinoids and their unnatural analogues in yeast [J ] . Nature , 2019 , 567 ( 7746 ): 123 - 126 .
VALLIERE M A , KORMAN T P , ARBING M A , et al . A bio-inspired cell-free system for cannabinoid production from inexpensive inputs [J ] . Nature Chemical Biology , 2020 , 16 ( 12 ): 1427 - 1433 .
TORGERSON J S , HAUPTMAN J , BOLDRIN M N , et al . XENical in the prevention of diabetes in obese subjects (XENDOS) study: a randomized study of orlistat as an adjunct to lifestyle changes for the prevention of type 2 diabetes in obese patients [J ] . Diabetes Care , 2004 , 27 ( 1 ): 155 - 161 .
KUMAR P , DUBEY K K . Current trends and future prospects of lipstatin: a lipase inhibitor and pro-drug for obesity [J ] . RSC Advances , 2015 , 5 ( 106 ): 86954 - 86966 .
KRIDEL S J , AXELROD F , ROZENKRANTZ N , et al . Orlistat is a novel inhibitor of fatty acid synthase with antitumor activity [J ] . Cancer Research , 2004 , 64 ( 6 ): 2070 - 2075 .
WEIBEL E K , HADVARY P , HOCHULI E , et al . Lipstatin, an inhibitor of pancreatic lipase, produced by Streptomyces toxytricini . Ⅰ. Producing organism, fermentation, isolation and biological activity [J ] . The Journal of Antibiotics , 1987 , 40 ( 8 ): 1081 - 1085 .
EISENREICH W , KUPFER E , WEBER W , et al . Tracer studies with crude U- 13 C-lipid mixtures [J ] . Journal of Biological Chemistry , 1997 , 272 ( 2 ): 867 - 874 .
EISENREICH W , KUPFER E , STOHLER P , et al . Biosynthetic origin of a branched chain analogue of the lipase inhibitor, lipstatin [J ] . Journal of Medicinal Chemistry , 2003 , 46 ( 19 ): 4209 - 4212 .
GOESE M , EISENREICH W , KUPFER E , et al . Biosynthetic origin of hydrogen atoms in the lipase inhibitor lipstatin [J ] . The Journal of Biological Chemistry , 2000 , 275 ( 28 ): 21192 - 21196 .
GOESE M , EISENREICH W , KUPFER E , et al . Biosynthesis of lipstatin. Incorporation of multiply deuterium-labeled (5 Z , 8 Z )-tetradeca-5,8-dienoic acid and octanoic acid [J ] . The Journal of Organic Chemistry , 2001 , 66 ( 13 ): 4673 - 4678 .
SCHUHR C A , EISENREICH W , GOESE M , et al . Biosynthetic precursors of the lipase inhibitor lipstatin [J ] . The Journal of Organic Chemistry , 2002 , 67 ( 7 ): 2257 - 2262 .
BAI T L , ZHANG D Z , LIN S J , et al . Operon for biosynthesis of lipstatin, the beta-lactone inhibitor of human pancreatic lipase [J ] . Applied and Environmental Microbiology , 2014 , 80 ( 24 ): 7473 - 7483 .
KRASNER C N , MCMEEKIN D S , CHAN S , et al . A phase Ⅱ study of trabectedin single agent in patients with recurrent ovarian cancer previously treated with platinum-based regimens [J ] . British Journal of Cancer , 2007 , 97 ( 12 ): 1618 - 1624 .
TAVECCHIO M , NATOLI C , UBEZIO P , et al . Dynamics of cell cycle phase perturbations by trabectedin (ET-743) in nucleotide excision repair (NER)-deficient and NER-proficient cells, unravelled by a novel mathematical simulation approach [J ] . Cell Proliferation , 2007 , 40 ( 6 ): 885 - 904 .
WANG J L , WANG P F , ZENG Z , et al . Trabectedin in cancers: mechanisms and clinical applications [J ] . Current Pharmaceutical Design , 2022 , 28 ( 24 ): 1949 - 1965 .
PETEK B J , LOGGERS E T , POLLACK S M , et al . Trabectedin in soft tissue sarcomas [J ] . Marine Drugs , 2015 , 13 ( 2 ): 974 - 983 .
D’INCALCI M , BADRI N , GALMARINI C M , et al . Trabectedin, a drug acting on both cancer cells and the tumour microenvironment [J ] . British Journal of Cancer , 2014 , 111 ( 4 ): 646 - 650 .
SCHOFIELD M M , JAIN S , PORAT D , et al . Identification and analysis of the bacterial endosymbiont specialized for production of the chemotherapeutic natural product ET-743 [J ] . Environmental Microbiology , 2015 , 17 ( 10 ): 3964 - 3975 .
RATH C M , JANTO B , EARL J , et al . Meta-omic characterization of the marine invertebrate microbial consortium that produces the chemotherapeutic natural product ET-743 [J ] . ACS Chemical Biology , 2011 , 6 ( 11 ): 1244 - 1256 .
IRSCHIK H , TROWITZSCH-KIENAST W , GERTH K , et al . Saframycin Mx1, a new natural saframycin isolated from a myxobacterium [J ] . The Journal of Antibiotics , 1988 , 41 ( 8 ): 993 - 998 .
MIKAMI Y , TAKAHASHI K , YAZAWA K , et al . Biosynthetic studies on saframycin A, a quinone antitumor antibiotic produced by Streptomyces lavendulae [J ] . The Journal of Biological Chemistry , 1985 , 260 ( 1 ): 344 - 348 .
IKEDA Y , MATSUKI H , OGAWA T , et al . Safracins, new antitumor antibiotics. Ⅱ. Physicochemical properties and chemical structures [J ] . The Journal of Antibiotics , 1983 , 36 ( 10 ): 1284 - 1289 .
KLUEPFEL D , BAKER H A , PIATTONI G , et al . Naphthyridinomycin, a new broad-spectrum antibiotic [J ] . The Journal of Antibiotics , 1975 , 28 ( 7 ): 497 - 502 .
TOMITA F , TAKAHASHI K , TAMAOKI T . Quinocarcin, a novel antitumor antibiotic. 3. Mode of action [J ] . The Journal of Antibiotics , 1984 , 37 ( 10 ): 1268 - 1272 .
KOKETSU K , WATANABE K , SUDA H , et al . Reconstruction of the saframycin core scaffold defines dual Pictet-Spengler mechanisms [J ] . Nature Chemical Biology , 2010 , 6 ( 6 ): 408 - 410 .
PENG C , PU J Y , SONG L Q , et al . Hijacking a hydroxyethyl unit from a central metabolic ketose into a nonribosomal peptide assembly line [J ] . Proceedings of the National Academy of Sciences of the United States of America , 2012 , 109 ( 22 ): 8540 - 8545 .
FU C Y , TANG M C , PENG C , et al . Biosynthesis of 3-hydroxy-5-methyl- O -methyltyrosine in the saframycin/safracin biosynthetic pathway [J ] . Journal of Microbiology and Biotechnology , 2009 , 19 ( 5 ): 439 - 446 .
TANG M C , FU C Y , TANG G L . Characterization of SfmD as a heme peroxidase that catalyzes the regioselective hydroxylation of 3-methyltyrosine to 3-hydroxy-5-methyltyrosine in saframycin A biosynthesis [J ] . Journal of Biological Chemistry , 2012 , 287 ( 7 ): 5112 - 5121 .
DRAKE E J , GULICK A M . Structural characterization and high-throughput screening of inhibitors of PvdQ, an NTN hydrolase involved in pyoverdine synthesis [J ] . ACS Chemical Biology , 2011 , 6 ( 11 ): 1277 - 1286 .
LE V H , INAI M , WILLIAMS R M , et al . Ecteinascidins. A review of the chemistry, biology and clinical utility of potent tetrahydroisoquinoline antitumor antibiotics [J ] . Natural Product Reports , 2015 , 32 ( 2 ): 328 - 347 .
LAMOTH F . Novel therapeutic approaches to invasive candidiasis: considerations for the clinician [J ] . Infection and Drug Resistance , 2023 , 16 : 1087 - 1097 .
MIESEL L , LIN K Y , ONG V . Rezafungin treatment in mouse models of invasive candidiasis and aspergillosis: insights on the PK/PD pharmacometrics of rezafungin efficacy [J ] . Pharmacology Research & Perspectives , 2019 , 7 ( 6 ): e00546 .
BENZ F , KNÜSEL F , NÜESCH J , et al . Stoffwechselprodukte von Mikroorganismen 143. Mitteilung. echinocandin B, ein neuartiges polypeptid-antibioticum aus Aspergillus nidulans var. echinulatus: isolierung und bausteine [J ] . Helvetica Chimica Acta , 1974 , 57 ( 8 ): 2459 - 2477 .
SCHWARTZ R E , GIACOBBE R A , BLAND J A , et al . L-671,329, a new antifungal agent. Ⅰ. Fermentation and isolation [J ] . The Journal of Antibiotics , 1989 , 42 ( 2 ): 163 - 167 .
FROMTLING R A , ABRUZZO G K . L-671,329, a new antifungal agent. Ⅲ. In vitro activity, toxicity and efficacy in comparison to aculeacin [J ] . The Journal of Antibiotics , 1989 , 42 ( 2 ): 174 - 178 .
WICHMANN C F , LIESCH J M , SCHWARTZ R E . L-671,329, a new antifungal agent. Ⅱ. Structure determination [J ] . The Journal of Antibiotics , 1989 , 42 ( 2 ): 168 - 173 .
KELLER-JUSLÉN C , KUHN M , LOOSLI H R , et al . Struktur des cyclopeptid-antibiotikums sl 7810 (=echinocandinb) [J ] . Tetrahedron Letters , 1976 , 17 ( 46 ): 4147 - 4150 .
MIZUNO K , YAGI A , SATOI S , et al . Studies on aculeacin. Ⅰ. Isolation and characterization of aculeacin A [J ] . The Journal of Antibiotics , 1977 , 30 ( 4 ): 297 - 302 .
SATOI S , YAGI A , ASANO K , et al . Studies on aculeacin. Ⅱ. Isolation and characterization of aculeacins B, C, D, E, F and G [J ] . The Journal of Antibiotics , 1977 , 30 ( 4 ): 303 - 307 .
NORRIS T , VANALSTEN J , HUBBS S , et al . Commercialization and late-stage development of a semisynthetic antifungal API: anidulafungin/D-fructose (Eraxis) [J ] . Organic Process Research & Development , 2008 , 12 ( 3 ): 447 - 455 .
BALKOVEC J M , HUGHES D L , MASUREKAR P S , et al . Discovery and development of first in class antifungal caspofungin (CANCIDAS®) — a case study [J ] . Natural Product Reports , 2014 , 31 ( 1 ): 15 - 34 .
FUJIE A . Discovery of micafungin (FK463): a novel antifungal drug derived from a natural product lead [J ] . Pure and Applied Chemistry , 2007 , 79 ( 4 ): 603 - 614 .
CACHO R A , JIANG W , CHOOI Y H , et al . Identifica tion and characterization of the echinocandin B biosynthetic gene cluster from Emericella rugulosa NRRL 11440 [J ] . Journal of the American Chemical Society , 2012 , 134 ( 40 ): 16781 - 16790 .
HÜTTEL W , YOUSSAR L , GRÜNING B A , et al . Echinocandin B biosynthesis: a biosynthetic cluster from Aspergillus nidulans NRRL 8112 and reassembly of the subclusters Ecd and Hty from Aspergillus pachycristatus NRRL 11440 reveals a single coherent gene cluster [J ] . BMC Genomics , 2016 , 17 : 570 .
JIANG W , CACHO R A , CHIOU G , et al . EcdGHK are three tailoring iron oxygenases for amino acid building blocks of the echinocandin scaffold [J ] . Journal of the American Chemical Society , 2013 , 135 ( 11 ): 4457 - 4466 .
MATTAY J , HOUWAART S , HÜTTEL W . Cryptic production of trans -3-hydroxyproline in echinocandin B biosynthesis [J ] . Applied and Environmental Microbiology , 2018 , 84 ( 7 ): e02370-17 .
CHEN L , YUE Q , ZHANG X Y , et al . Genomics-driven discovery of the pneumocandin biosynthetic gene cluster in the fungus Glarea lozoyensis [J ] . BMC Genomics , 2013 , 14 : 339 .
WEI T Y , ZHENG Y , WAN M Y , et al . Analysis of FR901379 biosynthetic genes in Coleophoma empetri by clustered regularly interspaced short palindromic repeats/Cas9-based genomic manipulation [J ] . ACS Chemical Biology , 2022 , 17 ( 8 ): 2130 - 2141 .
FORTINEZ C M , BLOUDOFF K , HARRIGAN C , et al . Structures and function of a tailoring oxidase in complex with a nonribosomal peptide synthetase module [J ] . Nature Communications , 2022 , 13 ( 1 ): 548 .
LI Y , LAN N , XU L J , et al . Biosynthesis of pneumocandin lipopeptides and perspectives for its production and related echinocandins [J ] . Applied Microbiology and Biotechnology , 2018 , 102 ( 23 ): 9881 - 9891 .
YUE Q , CHEN L , ZHANG X L , et al . Evolution of chemical diversity in echinocandin lipopeptide antifungal metabolites [J ] . Eukaryotic Cell , 2015 , 14 ( 7 ): 698 - 718 .
HÜTTEL W . Structural diversity in echinocandin biosynthesis: the impact of oxidation steps and approaches toward an evolutionary explanation [J ] . Zeitschrift für Naturforschung C , 2017 , 72 ( 1/2 ): 1 - 20 .
LAN N , PERLATTI B , KVITEK D J , et al . Acrophiarin (antibiotic S31794/F-1) from Penicillium arenicola shares biosynthetic features with both Aspergillus - and Leotiomycete-type echinocandins [J ] . Environmental Microbiology , 2020 , 22 ( 6 ): 2292 - 2311 .
HÜTTEL W . Echinocandins: structural diversity, biosynthesis, and development of antimycotics [J ] . Applied Microbiology and Biotechnology , 2021 , 105 ( 1 ): 55 - 66 .
JIANG K L , LUO P , WANG X X , et al . Insight into advances for the biosynthetic progress of fermented echinocandins of antifungals [J ] . Microbial Biotechnology , 2023 , 17 ( 1 ): e14359 .
MEN P , WANG M , LI J D , et al . Establishing an efficient genetic manipulation system for sulfated echinocandin producing fungus Coleophoma empetri [J ] . Frontiers in Microbiology , 2021 , 12 : 734780 .
MEN P , GENG C , ZHANG X , et al . Biosynthesis mechanism, genome mining and artificial construction of echinocandin O -sulfonation [J ] . Metabolic Engineering , 2022 , 74 : 160 - 167 .
ZHOU Z , ZWELLING L A , GANAPATHI R , et al . Enhanced etoposide sensitivity following adenovirus-mediated human topoisomerase Ⅱ α gene transfer is independent of topoisomerase Ⅱ β [J ] . British Journal of Cancer , 2001 , 85 ( 5 ): 747 - 751 .
CANEL C , MORAES R M , DAYAN F E , et al . Podophyllotoxin [J ] . Phytochemistry , 2000 , 54 ( 2 ): 115 - 120 .
DINKOVA-KOSTOVA A T , GANG D R , DAVIN L B , et al . (+)-pinoresinol/(+)-lariciresinol redu ctase from Forsythia intermedia [J ] . Journal of Biological Chemistry , 1996 , 271 ( 46 ): 29473 - 29482 .
DAVIN L B , WANG H B , CROWELL A L , et al . Stereoselective bimolecular phenoxy radical coupling by an auxiliary (dirigent) protein without an active center [J ] . Science , 1997 , 275 ( 5298 ): 362 - 367 .
XIA Z Q , COSTA M A , PELISSIER H C , et al . Secoisolariciresinol dehydrogenase purification, cloning, and functional expression. Implications for human health protection [J ] . The Journal of Biological Chemistry , 2001 , 276 ( 16 ): 12614 - 12623 .
MARQUES J V , KIM K W , LEE C , et al . Next generation sequencing in predicting gene function in podophyllotoxin biosynthesis [J ] . The Journal of Biological Chemistry , 2013 , 288 ( 1 ): 466 - 479 .
LAU W , SATTELY E S . Six enzymes from mayapple that complete the biosynthetic pathway to the etoposide aglycone [J ] . Science , 2015 , 349 ( 6253 ): 1224 - 1228 .
SCHULTZ B J , KIM S Y , LAU W , et al . Total biosynthesis for milligram-scale production of etoposide intermediates in a plant chassis [J ] . Journal of the American Chemical Society , 2019 , 141 ( 49 ): 19231 - 19235 .
SALERNI B L , BATES D J , ALBERSHARDT T C , et al . Vinblastine induces acute, cell cycle phase-independent apoptosis in some leukemias and lymphomas and can induce acute apoptosis in others when Mcl-1 is suppressed [J ] . Molecular Cancer Therapeutics , 2010 , 9 ( 4 ): 791 - 802 .
DHAMODHARAN R , JORDAN M A , THROWER D , et al . Vinblastine suppresses dynamics of individual microtubules in living interphase cells [J ] . Molecular Biology of the Cell , 1995 , 6 ( 9 ): 1215 - 1229 .
HARRISON T S , LYSENG-WILLIAMSON K A . Vincristine sulfate liposome injection: a guide to its use in refractory or relapsed acute lymphoblastic leukemia [J ] . BioDrugs , 2013 , 27 ( 1 ): 69 - 74 .
O’CONNOR S E , MARESH J J . Chemistry and biology of monoterpene indole alkaloid biosynthesis [J ] . Natural Product Reports , 2006 , 23 ( 4 ): 532 - 547 .
DUGÉ DE BERNONVILLE T , CLASTRE M , BESSEAU S , et al . Phytochemical genomics of the Madagascar periwinkle : unravelling the last twists of the alkaloid engine [J ] . Phytochemistry , 2015 , 113 : 9 - 23 .
CAPUTI L , FRANKE J , FARROW S C , et al . Missing enzymes in the biosynthesis of the anticancer drug vinblastine in Madagascar periwinkle [J ] . Science , 2018 , 360 ( 6394 ): 1235 - 1239 .
ZHANG J , HANSEN L G , GUDICH O , et al . A microbial supply chain for production of the anti-cancer drug vinblastine [J ] . Nature , 2022 , 609 ( 7926 ): 341 - 347 .
GAO J C , ZUO Y M , XIAO F , et al . Biosynthesis of catharanthine in engineered Pichia pastoris [J ] . Nature Synthesis , 2023 , 2 : 231 - 242 .
CAMPBELL K B , CICCI T A , VORA A K , et al . Beyond gout: colchicine use in the cardiovascular patient [J ] . Hospital Pharmacy , 2015 , 50 ( 10 ): 859 - 867 .
LEUNG Y Y , YAO HUI L L , KRAUS V B . Colchicine — update on mechanisms of action and therapeutic uses [J ] . Seminars in Arthritis and Rheumatism , 2015 , 45 ( 3 ): 341 - 350 .
DALBETH N , LAUTERIO T J , WOLFE H R . Mechanism of action of colchicine in the treatment of gout [J ] . Clinical Therapeutics , 2014 , 36 ( 10 ): 1465 - 1479 .
BHATTACHARYYA B , PANDA D , GUPTA S , et al . Anti-mitotic activity of colchicine and the structural basis for its interaction with tubulin [J ] . Medicinal Research Reviews , 2008 , 28 ( 1 ): 155 - 183 .
SLOBODNICK A , SHAH B , PILLINGER M H , et al . Colchicine: old and new [J ] . The American Journal of Medicine , 2015 , 128 ( 5 ): 461 - 470 .
CHEN B , LIU X , HU Y J , et al . Enantioselective total synthesis of (-)-colchicine, (+)-demecolcinone and metacolchicine: determination of the absolute configurations of the latter two alkaloids [J ] . Chemical Science , 2017 , 8 ( 7 ): 4961 - 4966 .
LIANG X , LI L , WEI K , et al . Gram-scale, seven-step total synthesis of (-)-colchicine [J ] . Organic Letters , 2021 , 23 ( 7 ): 2731 - 2735 .
HERBERT R B . The biosynthesis of plant alkaloids and nitrogenous microbial metabolites [J ] . Natural Product Reports , 2003 , 20 ( 5 ): 494 - 508 .
LARSSON S , RØNSTED N . Reviewing Colchicaceae alkaloids — perspectives of evolution on medicinal chemistry [J ] . Current Topics in Medicinal Chemistry , 2014 , 14 ( 2 ): 274 - 289 .
WICKS C , HUDLICKY T , RINNER U . Morphine alkaloids: history, biology, and synthesis [M/OL ] // The alkaloids: chemistry and biology . Amsterdam : Elsevier , 2021 , 86 : 145 - 342 [2023-12-01] . https://www.sciencedirect.com/science/article/abs/pii/S1099483121000183?via%3Dihub https://www.sciencedirect.com/science/article/abs/pii/S1099483121000183?via%3Dihub .
BHANDARI M , BHANDARI A , BHANDARI A . Recent updates on codeine [J ] . Pharmaceutical Methods , 2011 , 2 ( 1 ): 3 - 8 .
WINZER T , KERN M , KING A J , et al . Morphinan biosynthesis in opium poppy requires a P450-oxidoreductase fusion protein [J ] . Science , 2015 , 349 ( 6245 ): 309 - 312 .
LAKSTYGAL A M , KOLESNIKOVA T O , KHATSKO S L , et al . DARK classics in chemical neuroscience: atropine, scopolamine, and other anticholinergic deliriant hallucinogens [J ] . ACS Chemical Neuroscience , 2019 , 10 ( 5 ): 2144 - 2159 .
KOHNEN-JOHANNSEN K L , KAYSER O . Tropane alkaloids: chemistry, pharmacology, biosynthesis and production [J ] . Molecules , 2019 , 24 ( 4 ): 796 .
HUANG J P , FANG C L , MA X Y , et al . Tropane alkaloids biosynthesis involves an unusual type Ⅲ polyketide synthase and non-enzymatic condensation [J ] . Nature Communications , 2019 , 10 ( 1 ): 4036 .
QIU F , ZENG J L , WANG J , et al . Functional genomics analysis reveals two novel genes required for littorine biosynthesis [J ] . The New Phytologist , 2020 , 225 ( 5 ): 1906 - 1914 .
QIU F , YANG C X , YUAN L N , et al . A phenylpyruvic acid reductase is required for biosynthesis of tropane alkaloids [J ] . Organic Letters , 2018 , 20 ( 24 ): 7807 - 7810 .
ZHAO T F , LI S Q , WANG J , et al . Engineering tropane alkaloid production based on metabolic characterization of ornithine decarboxylase in Atropa belladonna [J ] . ACS Synthetic Biology , 2020 , 9 ( 2 ): 437 - 448 .
QIU F , YAN Y J , ZENG J L , et al . Biochemical and metabolic insights into hyoscyamine dehydrogenase [J ] . ACS Catalysis , 2021 , 11 ( 5 ): 2912 - 2924 .
SRINIVASAN P , SMOLKE C D . Engineering a microbial biosynthesis platform for de novo production of tropane alkaloids [J ] . Nature Communications , 2019 , 10 ( 1 ): 3634 .
SRINIVASAN P , SMOLKE C D . Biosynthesis of medicinal tropane alkaloids in yeast [J ] . Nature , 2020 , 585 ( 7826 ): 614 - 619 .
ADHIKARY S , DUGGAL M K , NAGENDRAN S , et al . Lefamulin: a new hope in the field of community-acquired bacterial pneumonia [J ] . Current Pharmacology Reports , 2022 , 8 ( 6 ): 418 - 426 .
PAUKNER S , RIEDL R . Pleuromutilins: potent drugs for resistant bugs-mode of action and resistance [J ] . Cold Spring Harbor Perspectives in Medicine , 2017 , 7 ( 1 ): a027110 .
GOETHE O , HEUER A , MA X S , et al . Antibacterial properties and clinical potential of pleuromutilins [J ] . Natural Product Reports , 2019 , 36 ( 1 ): 220 - 247 .
ARIGONI D . Some studies in the biosynthesis of terpenes and related compounds [J ] . Pure and Applied Chemistry , 1968 , 17 ( 3/4 ): 331 - 348 .
BIRCH A J , HOLZAPFEL C W , RICKARDS R W . The structure and some aspects of the biosynthesis of pleuromutilin [J ] . Tetrahedron , 1966 , 22 : 359 - 387 .
LEMKE C , WHITHAM O , PETERS R J . Magnesium-specific ring expansion/contraction catalysed by the class Ⅱ diterpene cyclase from pleuromutilin biosynthesis [J ] . Organic & Biomolecular Chemistry , 2020 , 18 ( 29 ): 5586 - 5588 .
TSUKAGOSHI T , TOKIWANO T , OIKAWA H . Studies on the later stage of the biosynthesis of pleuromutilin [J ] . Bioscience, Biotechnology, and Biochemistry , 2007 , 71 ( 12 ): 3116 - 3121 .
BAILEY A M , ALBERTI F , KILARU S , et al . Identification and manipulation of the pleuromutilin gene cluster from Clitopilus passeckerianus for increased rapid antibiotic production [J ] . Scientific Reports , 2016 , 6 : 25202 .
ALBERTI F , KHAIRUDIN K , VENEGAS E R , et al . Heterologous expression reveals the biosynthesis of the antibiotic pleuromutilin and generates bioactive semi-synthetic derivatives [J ] . Nature Communications , 2017 , 8 ( 1 ): 1831 .
YAMANE M , MINAMI A , LIU C W , et al . Biosynthetic machinery of diterpene pleuromutilin isolated from Basidiomycete fungi [J ] . ChemBioChem , 2017 , 18 ( 23 ): 2317 - 2322 .
ALBERTI F , KHAIRUDIN K , DAVIES J A , et al . Biosynthesis of pleuromutilin congeners using an Aspergillus oryzae expression platform [J ] . Chemical Science , 2023 , 14 ( 14 ): 3826 - 3833 .
SCHAFHAUSER T , WIBBERG D , BINDER A , et al . Genome assembly and genetic traits of the pleuromutilin-producer Clitopilus passeckerianus DSM1602 [J ] . Journal of Fungi , 2022 , 8 ( 8 ): 862 .
GUO C , DAI H Q , ZHANG M T , et al . Molecular networking assisted discovery and combinatorial biosynthesis of new antimicrobial pleuromutilins [J ] . European Journal of Medicinal Chemistry , 2022 , 243 : 114713 .
BASSO N , TERRAGNO N A . History about the discovery of the renin-angiotensin system [J ] . Hypertension , 2001 , 38 ( 6 ): 1246 - 1249 .
LU H , CASSIS L A , KOOI C W V , et al . Structure and functions of angiotensinogen [J ] . Hypertension Research , 2016 , 39 ( 7 ): 492 - 500 .
STREATFEILD-JAMES R M A , WILLIAMSON D , PIKE R N , et al . Angiotensinogen cleavage by renin: i mportance of a structurally constrained N -terminus [J ] . FEBS Letters , 1998 , 436 ( 2 ): 267 - 270 .
FANG H , LI D , KANG J , et al . Metabolic engineering of Escherichia coli for de novo biosynthesis of vitamin B 12 [J ] . Nature Communications , 2018 , 9 ( 1 ): 4917 .
KANG Q , FANG H , XIANG M J , et al . A synthetic cell-free 36-enzyme reaction system for vitamin B 12 production [J ] . Nature Communications , 2023 , 14 ( 1 ): 5177 .
HU Y J , GU C C , WANG X F , et al . Asymmetric total synthesis of taxol [J ] . Journal of the American Chemical Society , 2021 , 143 ( 42 ): 17862 - 17870 .
BIGGS B W , LIM C G , SAGLIANI K , et al . Overcoming heterologous protein interdependency to optimize P450-mediated Taxol precursor synthesis in Escherichia coli [J ] . Proceedings of the National Academy of Sciences of the United States of America , 2016 , 113 ( 12 ): 3209 - 3214 .
LI J H , MUTANDA I , WANG K B , et al . Chloroplastic metabolic engineering coupled with isoprenoid pool enhancement for committed taxanes biosynthesis in Nicotiana benthamiana [J ] . Nature Communications , 2019 , 10 ( 1 ): 4850 .
XIONG X Y , GOU J B , LIAO Q G , et al . The Taxus genome provides insights into paclitaxel biosynthesis [J ] . Nature Plants , 2021 , 7 ( 8 ): 1026 - 1036 .
XU B F , LEI L , ZHU X C , et al . Identification and characterization of L-lysine decarboxylase from Huperzia serrata and its role in the metabolic pathway of lycopodium alkaloid [J ] . Phytochemistry , 2017 , 136 : 23 - 30 .
WANG J , ZHANG Z K , JIANG F F , et al . Deciphering the biosynthetic mechanism of pelletierine in Lycopodium alkaloid biosynthesis [J ] . Organic Letters , 2020 , 22 ( 21 ): 8725 - 8729 .
NETT R S , DHO Y , TSAI C , et al . Plant carbonic anhydrase-like enzymes in neuroactive alkaloid biosynthesis [J ] . Nature , 2023 , 624 ( 7990 ): 182 - 191 .
FORMAN V , LUO D , GEU-FLORES F , et al . A gene cluster in Ginkgo biloba encodes unique multifunctional cytochrome P450s that initiate ginkgolide biosynthesis [J ] . Nature Communications , 2022 , 13 ( 1 ): 5143 .
ADRIO J , CUEVAS C , MANZANARES I , et al . Total synthesis and biological evaluation of tamandarin B analogues [J ] . The Journal of Organic Chemistry , 2007 , 72 ( 14 ): 5129 - 5138 .
WHITE K M , ROSALES R , YILDIZ S , et al . Plitidepsin has potent preclinical efficacy against SARS-CoV-2 by targeting the host protein eEF1A [J ] . Science , 2021 , 371 ( 6532 ): 926 - 931 .
BARANOVA A A , ALFEROVA V A , KORSHUN V A , et al . Modern trends in natural antibiotic discovery [J ] . Life , 2023 , 13 ( 5 ): 1073 .
IMAI Y , MEYER K J , IINISHI A , et al . A new antibiotic selectively kills Gram-negative pathogens [J ] . Nature , 2019 , 576 ( 7787 ): 459 - 464 .
SHUKLA R , LAVORE F , MAITY S , et al . Teixobactin kills bacteria by a two-pronged attack on the cell envelope [J ] . Nature , 2022 , 608 ( 7922 ): 390 - 396 .
WANG Z Q , KOIRALA B , HERNANDEZ Y , et al . A naturally inspired antibiotic to target multidrug-resistant pathogens [J ] . Nature , 2022 , 601 ( 7894 ): 606 - 611 .
YUAN Y J , CHENG S , BIAN G K , et al . Efficient exploration of terpenoid biosynthetic gene clusters in filamentous fungi [J ] . Nature Catalysis , 2022 , 5 ( 4 ): 277 - 287 .
ZHANG M M , WONG F T , WANG Y J , et al . CRISPR-Cas9 strategy for activation of silent Streptomyces biosynthetic gene clusters [J ] . Nature Chemical Biology , 2017 , 13 ( 6 ): 607 - 609 .
MULLOWNEY M W , DUNCAN K R , ELSAYED S S , et al . Artificial intelligence for natural product drug discovery [J ] . Nature Reviews Drug Discovery , 2023 , 22 ( 11 ): 895 - 916 .
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