Strategies for engineering plant natural products: the iridoid-derived monoterpene indole alkaloids of Catharanthus roseus.
暂无分享,去创建一个
[1] H. Tokuyama,et al. Stereocontrolled total synthesis of (+)-vincristine. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[2] B. Hill,et al. Novel actions of the antitumor drugs vinflunine and vinorelbine on microtubules. , 2000, Cancer research.
[3] J. Memelink,et al. Geraniol 10‐hydroxylase1, a cytochrome P450 enzyme involved in terpenoid indole alkaloid biosynthesis , 2001, FEBS letters.
[4] S. O’Connor,et al. Chemoselective derivatization of alkaloids in periwinkle. , 2007, Chemical communications.
[5] K. Weissman. Mutasynthesis - uniting chemistry and genetics for drug discovery. , 2007, Trends in biotechnology.
[6] R. Verpoorte,et al. The iridoid glucoside secologanin is derived from the novel triose phosphate/pyruvate pathway in a Catharanthus roseus cell culture , 1998, FEBS letters.
[7] K. Rinehart,et al. Preparation of four new antibiotics from a mutant of Streptomyces fradiae. , 1969, Proceedings of the National Academy of Sciences of the United States of America.
[8] S. O’Connor,et al. Homolog of tocopherol C methyltransferases catalyzes N methylation in anticancer alkaloid biosynthesis , 2010, Proceedings of the National Academy of Sciences.
[9] S. O’Connor,et al. Chemistry and biology of monoterpene indole alkaloid biosynthesis. , 2006, Natural product reports.
[10] Jacob Pollier,et al. Combinatorial Biosynthesis in Plants: A (P)review on Its Potential and Future Exploitation , 2012 .
[11] R. Verpoorte,et al. The Catharanthus alkaloids: pharmacognosy and biotechnology. , 2004, Current medicinal chemistry.
[12] P. Waterhouse,et al. Constructs and methods for high-throughput gene silencing in plants. , 2003, Methods.
[13] M. Beljanski. Three alkaloids as selective destroyers of cancer cells in mice. Synergy with classic anticancer drugs. , 1986, Oncology.
[14] C. Marineau,et al. Molecular cloning and analysis of cDNA encoding a plant tryptophan decarboxylase: comparison with animal dopa decarboxylases. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[15] J. Koepke,et al. The Structure of Rauvolfia serpentina Strictosidine Synthase Is a Novel Six-Bladed β-Propeller Fold in Plant Proteins[W] , 2006, The Plant Cell Online.
[16] S. O’Connor,et al. Silencing of tryptamine biosynthesis for production of nonnatural alkaloids in plant culture , 2009, Proceedings of the National Academy of Sciences.
[17] R. Verpoorte,et al. Activity of the cytochrome P450 enzyme geraniol 10-hydroxylase and alkaloid production in plant cell cultures , 2002 .
[18] Xueyan Ma,et al. Heterologous expression of a Rauvolfia cDNA encoding strictosidine glucosidase, a biosynthetic key to over 2000 monoterpenoid indole alkaloids. , 2002, European journal of biochemistry.
[19] F. Gago,et al. Tubulin-based structure-affinity relationships for antimitotic Vinca alkaloids. , 2012, Anti-cancer agents in medicinal chemistry.
[20] D. Newman,et al. Plants as a source of anti-cancer agents. , 2005, Journal of ethnopharmacology.
[21] S. O’Connor,et al. Semi-synthesis of Secologanin Analogues , 2006 .
[22] K. San,et al. Characterization of an Inducible Promoter System in Catharanthus roseus Hairy Roots , 2002, Biotechnology progress.
[23] Sarah E O'Connor,et al. Directed biosynthesis of alkaloid analogs in the medicinal plant Catharanthus roseus. , 2006, Journal of the American Chemical Society.
[24] G. Cordell. The Alkaloids : Chemistry and biology , 2010 .
[25] S. O’Connor,et al. Metabolic reprogramming of periwinkle plant culture. , 2009, Nature chemical biology.
[26] J. Memelink,et al. Molecular Cloning and Analysis of Strictosidine β-d-Glucosidase, an Enzyme in Terpenoid Indole Alkaloid Biosynthesis in Catharanthus roseus * , 2000, The Journal of Biological Chemistry.
[27] V. De Luca,et al. The Leaf Epidermome of Catharanthus roseus Reveals Its Biochemical Specialization[W][OA] , 2008, The Plant Cell Online.
[28] D. Boger,et al. Direct coupling of catharanthine and vindoline to provide vinblastine: total synthesis of (+)- and ent-(-)-vinblastine. , 2008, Journal of the American Chemical Society.
[29] B. Trout,et al. Strictosidine synthase: mechanism of a Pictet-Spengler catalyzing enzyme. , 2008, Journal of the American Chemical Society.
[30] P. Facchini,et al. Alkaloid biosynthesis: metabolism and trafficking. , 2008, Annual review of plant biology.
[31] S. Irmler,et al. Indole alkaloid biosynthesis in Catharanthus roseus: new enzyme activities and identification of cytochrome P450 CYP72A1 as secologanin synthase. , 2000, The Plant journal : for cell and molecular biology.
[32] P. Facchini,et al. Plant aromatic L-amino acid decarboxylases: evolution, biochemistry, regulation, and metabolic engineering applications. , 2000, Phytochemistry.
[33] S. O’Connor,et al. Rapid identification of enzyme variants for reengineered alkaloid biosynthesis in periwinkle. , 2007, Chemistry & biology.
[34] Anna E Speers,et al. Activity-based protein profiling in vivo using a copper(i)-catalyzed azide-alkyne [3 + 2] cycloaddition. , 2003, Journal of the American Chemical Society.
[35] S. Panjikar,et al. Structure-based engineering of strictosidine synthase: auxiliary for alkaloid libraries. , 2007, Chemistry & biology.
[36] M. Clastre,et al. Cloning and expression of cDNAs encoding two enzymes of the MEP pathway in Catharanthus roseus. , 2000, Biochimica et biophysica acta.
[37] R. Noble. The discovery of the vinca alkaloids--chemotherapeutic agents against cancer. , 1990, Biochemistry and cell biology = Biochimie et biologie cellulaire.
[38] C. Khosla,et al. Combinatorial biosynthesis of 'unnatural' natural products: the polyketide example. , 1995, Chemistry & biology.
[39] M. Clastre,et al. 1-Deoxy-D-xylulose 5-phosphate synthase from periwinkle: cDNA identification and induced gene expression in terpenoid indole alkaloid-producing cells. , 2000 .