Synthesis of 11-carbon terpenoids in yeast using protein and metabolic engineering
暂无分享,去创建一个
Antonios M. Makris | M. Maffei | M. S. Motawia | A. Makris | Codruta Ignea | Sotirios C. Kampranis | S. Kampranis | Marianna Pontini | Mohammed S. Motawia | Massimo E. Maffei | Codruta Ignea | Marianna Pontini
[1] J. Chappell,et al. Engineering Triterpene and Methylated Triterpene Production in Plants Provides Biochemical and Physiological Insights into Terpene Metabolism1[OPEN] , 2015, Plant Physiology.
[2] P. Dewick. Medicinal Natural Products , 1997 .
[3] W. Schwab,et al. Monoterpene biosynthesis in lemon (Citrus limon). cDNA isolation and functional analysis of four monoterpene synthases. , 2002, European journal of biochemistry.
[4] E. Winterfeldt. Applications of Diisobutylaluminium Hydride (DIBAH) and Triisobutylaluminium (TIBA) as Reducing Agents in Organic Synthesis , 1975 .
[5] E. Pichersky,et al. The Biochemical and Molecular Basis for the Divergent Patterns in the Biosynthesis of Terpenes and Phenylpropenes in the Peltate Glands of Three Cultivars of Basil1 , 2004, Plant Physiology.
[6] A. Sutherland,et al. Stereoselective synthesis of the bicyclic guanidine alkaloid (+)-monanchorin. , 2010, Organic & biomolecular chemistry.
[7] P. Dewick,et al. Medicinal Natural Products: A Biosynthetic Approach , 1997 .
[8] Fabrice Foucher,et al. Biosynthesis of monoterpene scent compounds in roses , 2015, Science.
[9] C. Gatz,et al. Herbivore-induced and floral homoterpene volatiles are biosynthesized by a single P450 enzyme (CYP82G1) in Arabidopsis , 2010, Proceedings of the National Academy of Sciences.
[10] M. Komatsu,et al. Identification and functional analysis of genes controlling biosynthesis of 2-methylisoborneol , 2008, Proceedings of the National Academy of Sciences.
[11] Jeroen S. Dickschat,et al. A detailed view of 2-methylisoborneol biosynthesis. , 2013, Angewandte Chemie.
[12] Conrad C. Huang,et al. UCSF Chimera—A visualization system for exploratory research and analysis , 2004, J. Comput. Chem..
[13] R. Croteau,et al. Structure of limonene synthase, a simple model for terpenoid cyclase catalysis , 2007, Proceedings of the National Academy of Sciences.
[14] A. Makris,et al. Combined metabolome and transcriptome profiling provides new insights into diterpene biosynthesis in S. pomifera glandular trichomes , 2015, BMC Genomics.
[15] J. Noel,et al. Biosynthesis of Plant Volatiles: Nature's Diversity and Ingenuity , 2006, Science.
[16] D. Cane,et al. Biosynthesis of 2-methylisoborneol in cyanobacteria. , 2011, Environmental science & technology.
[17] D. Cane,et al. Biochemistry and molecular genetics of the biosynthesis of the earthy odorant methylisoborneol in Streptomyces coelicolor. , 2008, Journal of the American Chemical Society.
[18] R. Croteau,et al. cDNA isolation, functional expression, and characterization of (+)-α-pinene synthase and (−)-α-pinene synthase from loblolly pine (Pinus taeda): Stereocontrol in pinene biosynthesis , 2003 .
[19] C. Poulter,et al. Tris(tetrabutylammonium) hydrogen pyrophosphate. A new reagent for the preparation of allylic pyrophosphate esters , 1981 .
[20] E. Pichersky,et al. Characterization of Geraniol Synthase from the Peltate Glands of Sweet Basil1 , 2004, Plant Physiology.
[21] D. Cane,et al. Exploring biosynthetic diversity with trichodiene synthase. , 2007, Archives of biochemistry and biophysics.
[22] Jeroen S. Dickschat,et al. Biosynthesis of the off-flavor 2-methylisoborneol by the myxobacterium Nannocystis exedens. , 2007, Angewandte Chemie.
[23] P. Pendleton,et al. Dehydration products of 2-methylisoborneol , 1997 .
[24] M. Komatsu,et al. Terpene synthases are widely distributed in bacteria , 2014, Proceedings of the National Academy of Sciences.
[25] Jeroen S. Dickschat,et al. Bacterial terpene cyclases. , 2016, Natural product reports.
[26] Vassilios Roussis,et al. Carnosic acid biosynthesis elucidated by a synthetic biology platform , 2016, Proceedings of the National Academy of Sciences.
[27] O. Miyata,et al. Radical Cyclization in Heterocycle Synthesis. Part 10: A Concise Synthesis of (−)-Kainic Acid via Sulfanyl Radical Addition–Cyclization–Elimination Reaction , 2000 .
[28] A. Makris,et al. Rational Conversion of Substrate and Product Specificity in a Salvia Monoterpene Synthase: Structural Insights into the Evolution of Terpene Synthase Function[W] , 2007, The Plant Cell Online.
[29] J. Weissman,et al. A general lack of compensation for gene dosage in yeast , 2010, Molecular systems biology.
[30] Wei Gao,et al. Modular pathway engineering of diterpenoid synthases and the mevalonic acid pathway for miltiradiene production. , 2012, Journal of the American Chemical Society.
[31] Hans Jasper Genee,et al. Software-supported USER cloning strategies for site-directed mutagenesis and DNA assembly. , 2015, ACS synthetic biology.
[32] A. Makris,et al. Reconstructing the chemical diversity of labdane-type diterpene biosynthesis in yeast. , 2015, Metabolic engineering.
[33] J. Gershenzon,et al. Identification and Regulation of TPS04/GES, an Arabidopsis Geranyllinalool Synthase Catalyzing the First Step in the Formation of the Insect-Induced Volatile C16-Homoterpene TMTT[W] , 2008, The Plant Cell Online.
[34] A. Makris,et al. Positive genetic interactors of HMG2 identify a new set of genetic perturbations for improving sesquiterpene production in Saccharomyces cerevisiae , 2012, Microbial Cell Factories.
[35] C. Karahadian,et al. Volatile compounds from Penicillium sp. contributing musty-earthy notes to Brie and Camembert cheese flavors , 1985 .
[36] C. Poulter,et al. Farnesyl diphosphate synthase. Altering the catalytic site to select for geranyl diphosphate activity. , 2000, Biochemistry.
[37] J. Gershenzon,et al. The function of terpene natural products in the natural world. , 2007, Nature chemical biology.
[38] A. Makris,et al. Use of the de novo transcriptome analysis of silver-leaf nightshade (Solanum elaeagnifolium) to identify gene expression changes associated with wounding and terpene biosynthesis , 2015, BMC Genomics.
[39] J. Gershenzon,et al. Characterization of Biosynthetic Pathways for the Production of the Volatile Homoterpenes DMNT and TMTT in Zea mays[OPEN] , 2016, Plant Cell.
[40] H. Ikeda,et al. Cloning and characterization of Pfl_1841, a 2-methylenebornane synthase in Pseudomonas fluorescens PfO-1. , 2011, Tetrahedron.
[41] A. Makris,et al. Improving yeast strains using recyclable integration cassettes, for the production of plant terpenoids , 2011, Microbial cell factories.
[42] Joseph P Noel,et al. Formation of a Novel Macrocyclic Alkaloid from the Unnatural Farnesyl Diphosphate Analogue Anilinogeranyl Diphosphate by 5-Epi-Aristolochene Synthase. , 2015, ACS chemical biology.
[43] M. Maffei,et al. Engineering monoterpene production in yeast using a synthetic dominant negative geranyl diphosphate synthase. , 2014, ACS synthetic biology.
[44] D. Cane,et al. Biosynthesis of the earthy odorant geosmin by a bifunctional Streptomyces coelicolor enzyme. , 2007, Nature chemical biology.
[45] M C Peitsch,et al. ProMod and Swiss-Model: Internet-based tools for automated comparative protein modelling. , 1996, Biochemical Society transactions.
[46] M. O’Donnell,et al. Overproduction and analysis of eukaryotic multiprotein complexes in Escherichia coli using a dual-vector strategy. , 2003, Analytical biochemistry.
[47] D. Cane,et al. Structure of 2-methylisoborneol synthase from Streptomyces coelicolor and implications for the cyclization of a noncanonical C-methylated monoterpenoid substrate. , 2012, Biochemistry.
[48] Jeroen S. Dickschat,et al. Volatiles from nineteen recently genome sequenced actinomycetes. , 2015, Organic & biomolecular chemistry.