Two Herbivore-Induced Cytochrome P450 Enzymes CYP79D6 and CYP79D7 Catalyze the Formation of Volatile Aldoximes Involved in Poplar Defense[C][W]
暂无分享,去创建一个
M. Reichelt | J. Gershenzon | T. Köllner | B. Schneider | S. Unsicker | A. Schmidt | J. Schnitzler | Tobias G. Köllner | A. C. McCormick | A. Clavijo McCormick | Sandra Irmisch | G. A. Boeckler | Katja Block | A. Clavijo Mccormick | Andreas Boeckler
[1] G. Becker,et al. Land availability and potential biomass production with poplar and willow short rotation coppices in Germany , 2014 .
[2] Koichiro Tamura,et al. MEGA6: Molecular Evolutionary Genetics Analysis version 6.0. , 2013, Molecular biology and evolution.
[3] S. Bak,et al. Plant Defense against Insect Herbivores , 2013, International journal of molecular sciences.
[4] B. Hamberger,et al. Plant P450s as versatile drivers for evolution of species-specific chemical diversity , 2013, Philosophical Transactions of the Royal Society B: Biological Sciences.
[5] C. Olsen,et al. Biosynthesis of rhodiocyanosides in Lotus japonicus: rhodiocyanoside A is synthesized from (Z)-2-methylbutanaloxime via 2-methyl-2-butenenitrile. , 2012, Phytochemistry.
[6] J. Gershenzon,et al. Mixtures of plant secondary metabolites: Metabolic origins and ecological benefits , 2012 .
[7] Kirsten Jørgensen,et al. Genomic clustering of cyanogenic glucoside biosynthetic genes aids their identification in Lotus japonicus and suggests the repeated evolution of this chemical defence pathway. , 2011, The Plant journal : for cell and molecular biology.
[8] M. Nei,et al. MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. , 2011, Molecular biology and evolution.
[9] T. Beringer,et al. Bioenergy production potential of global biomass plantations under environmental and agricultural constraints , 2011 .
[10] Joshua S. Yuan,et al. Four terpene synthases produce major compounds of the gypsy moth feeding-induced volatile blend of Populus trichocarpa. , 2011, Phytochemistry.
[11] J. Gershenzon,et al. Herbivore-Induced SABATH Methyltransferases of Maize That Methylate Anthranilic Acid Using S-Adenosyl-l-Methionine1[W] , 2010, Plant Physiology.
[12] E. Glawischnig,et al. Evolution of camalexin and structurally related indolic compounds. , 2009, Phytochemistry.
[13] I. Major,et al. Expression profiling and functional analysis of Populus WRKY23 reveals a regulatory role in defense. , 2009, The New phytologist.
[14] J. Gershenzon,et al. Monoterpene and sesquiterpene synthases and the origin of terpene skeletal diversity in plants. , 2009, Phytochemistry.
[15] J. Gershenzon,et al. Protective perfumes: the role of vegetative volatiles in plant defense against herbivores. , 2009, Current opinion in plant biology.
[16] K. Kuča,et al. The Acute Toxicity of Acetylcholinesterase Reactivators in Mice in Relation to Their Structure , 2006, Neurotoxicity Research.
[17] M. Alam,et al. Comparison of Cytochrome P450 Genes from Six Plant Genomes , 2008, Tropical Plant Biology.
[18] Jay D Keasling,et al. Induction of multiple pleiotropic drug resistance genes in yeast engineered to produce an increased level of anti-malarial drug precursor, artemisinic acid , 2008, BMC biotechnology.
[19] R. Raguso. Wake Up and Smell the Roses: The Ecology and Evolution of Floral Scent , 2008 .
[20] J. Ton,et al. Long-distance signalling in plant defence. , 2008, Trends in plant science.
[21] G. Howe,et al. Plant immunity to insect herbivores. , 2008, Annual review of plant biology.
[22] A. Morse,et al. Transcript profiles of the cytokinin response regulator gene family in Populus imply diverse roles in plant development. , 2007, The New phytologist.
[23] J. Gershenzon,et al. Diversity and distribution of floral scent , 2006, The Botanical Review.
[24] Y. Di,et al. Difference in volatiles of poplar induced by various damages , 2004, Journal of Forestry Research.
[25] S. Marsh. Populus , 2007 .
[26] J. Bohlmann,et al. Transgenic, non-isoprene emitting poplars don't like it hot. , 2007, The Plant journal : for cell and molecular biology.
[27] J. Carlson,et al. Within-plant signalling via volatiles overcomes vascular constraints on systemic signalling and primes responses against herbivores. , 2007, Ecology letters.
[28] J. Glazebrook,et al. Arabidopsis Cytochrome P450 Monooxygenase 71A13 Catalyzes the Conversion of Indole-3-Acetaldoxime in Camalexin Synthesis[W] , 2007, The Plant Cell Online.
[29] M. Gribskov,et al. The Genome of Black Cottonwood, Populus trichocarpa (Torr. & Gray) , 2006, Science.
[30] J. D’Auria. Acyltransferases in plants: a good time to be BAHD. , 2006, Current opinion in plant biology.
[31] A. Müller,et al. Many roads lead to "auxin": of nitrilases, synthases, and amidases. , 2006, Plant biology.
[32] M. Marra,et al. Genomics of hybrid poplar (Populus trichocarpa× deltoides) interacting with forest tent caterpillars (Malacosoma disstria): normalized and full‐length cDNA libraries, expressed sequence tags, and a cDNA microarray for the study of insect‐induced defences in poplar , 2006, Molecular ecology.
[33] J. Gershenzon,et al. The products of a single maize sesquiterpene synthase form a volatile defense signal that attracts natural enemies of maize herbivores. , 2006, Proceedings of the National Academy of Sciences of the United States of America.
[34] L. Kang,et al. Volatiles released from bean plants in response to agromyzid flies , 2006, Planta.
[35] J. Noel,et al. Floral benzenoid carboxyl methyltransferases: from in vitro to in planta function. , 2005, Phytochemistry.
[36] Aijun Zhang,et al. Phenylacetaldehyde O-methyloxime: a volatile compound produced by grapefruit leaves infected with the citrus canker pathogen, Xanthomonas axonopodis pv. citri. , 2005, Journal of agricultural and food chemistry.
[37] Dongmei Li,et al. Highly efficient Beckmann rearrangement and dehydration of oximes , 2005 .
[38] J. Takabayashi,et al. Developmental stage of herbivorePseudaletia separata affects production of herbivore-induced synomone by corn plants , 1995, Journal of Chemical Ecology.
[39] T. A. Beek,et al. Leaf age affects composition of herbivore-induced synomones and attraction of predatory mites , 1994, Journal of Chemical Ecology.
[40] J. Takabayashi,et al. Variation in composition of predator-attracting allelochemicals emitted by herbivore-infested plants: Relative influence of plant and herbivore , 1991, CHEMOECOLOGY.
[41] Michael P. Cummings,et al. MEGA (Molecular Evolutionary Genetics Analysis) , 2004 .
[42] R. Last,et al. Application of a high-throughput HPLC-MS/MS assay to Arabidopsis mutant screening; evidence that threonine aldolase plays a role in seed nutritional quality. , 2004, The Plant journal : for cell and molecular biology.
[43] B. G. Hansen,et al. Camalexin is synthesized from indole-3-acetaldoxime, a key branching point between primary and secondary metabolism in Arabidopsis. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[44] S. Tabata,et al. Biosynthesis of the Nitrile Glucosides Rhodiocyanoside A and D and the Cyanogenic Glucosides Lotaustralin and Linamarin in Lotus japonicus1 , 2004, Plant Physiology.
[45] J. Bohlmann,et al. Forest tent caterpillars (Malacosoma disstria) induce local and systemic diurnal emissions of terpenoid volatiles in hybrid poplar (Populus trichocarpa x deltoides): cDNA cloning, functional characterization, and patterns of gene expression of (-)-germacrene D synthase, PtdTPS1. , 2004, The Plant journal : for cell and molecular biology.
[46] M. Cowles. Statistical Computing: An Introduction to Data Analysis using SPlus , 2004 .
[47] Søren Bak,et al. The presence of CYP79 homologues in glucosinolate-producing plants shows evolutionary conservation of the enzymes in the conversion of amino acid to aldoxime in the biosynthesis of cyanogenic glucosides and glucosinolates , 1998, Plant Molecular Biology.
[48] J. Leplé,et al. Transgenic poplars: expression of chimeric genes using four different constructs , 1992, Plant Cell Reports.
[49] T. V. van Beek,et al. Qualitative and Quantitative Variation Among Volatile Profiles Induced by Tetranychus urticae Feeding on Plants from Various Families , 2004, Journal of Chemical Ecology.
[50] Robert H. Kushler,et al. Statistical Computing: An Introduction to Data Analysis Using S-PLUS , 2003, Technometrics.
[51] D. Baulcombe,et al. An enhanced transient expression system in plants based on suppression of gene silencing by the p19 protein of tomato bushy stunt virus. , 2003, The Plant journal : for cell and molecular biology.
[52] B. Halkier,et al. Transgenic tobacco and Arabidopsis plants expressing the two multifunctional sorghum cytochrome P450 enzymes, CYP79A1 and CYP71E1, are cyanogenic and accumulate metabolites derived from intermediates in Dhurrin biosynthesis. , 2000, Plant physiology.
[53] Yasuhisa Asano,et al. Distribution of Aldoxime Dehydratase in Microorganisms , 2000, Applied and Environmental Microbiology.
[54] B. Halkier,et al. Cytochrome P450 CYP79A2 from Arabidopsis thaliana L. Catalyzes the Conversion of l-Phenylalanine to Phenylacetaldoxime in the Biosynthesis of Benzylglucosinolate* , 2000, The Journal of Biological Chemistry.
[55] B. Møller,et al. Cloning and expression of cytochrome P450 enzymes catalyzing the conversion of tyrosine to p-hydroxyphenylacetaldoxime in the biosynthesis of cyanogenic glucosides in Triglochin maritima. , 2000, Plant physiology.
[56] B. Møller,et al. Cytochromes P-450 from Cassava (Manihot esculentaCrantz) Catalyzing the First Steps in the Biosynthesis of the Cyanogenic Glucosides Linamarin and Lotaustralin , 2000, The Journal of Biological Chemistry.
[57] B. Møller,et al. Cytochromes P-450 from cassava (Manihot esculenta Crantz) catalyzing the first steps in the biosynthesis of the cyanogenic glucosides linamarin and lotaustralin. Cloning, functional expression in Pichia pastoris, and substrate specificity of the isolated recombinant enzymes. , 2000, The Journal of biological chemistry.
[58] Y. Asano,et al. A new enzymatic method of nitrile synthesis by Rhodococcus sp. strain YH3-3 1 Dedicated to Professor , 1999 .
[59] S. Dorn,et al. Herbivore‐induced emissions of maize volatiles repel the corn leaf aphid, Rhopalosiphum maidis , 1998 .
[60] A. Nussler,et al. Expression and Detection of Inducible Nitric Oxide Synthase in Experimental Models of Inflammation , 1996, Methods.
[61] B. Halkier,et al. Isolation of a Microsomal Enzyme System Involved in Glucosinolate Biosynthesis from Seedlings of Tropaeolum majus L , 1996, Plant physiology.
[62] D. Pompon,et al. Yeast expression of animal and plant P450s in optimized redox environments. , 1996, Methods in enzymology.
[63] B. Halkier,et al. Purification and characterization of recombinant cytochrome P450TYR expressed at high levels in Escherichia coli. , 1995, Archives of biochemistry and biophysics.
[64] D. Kleier,et al. Oxime Fungicides: Highly Active Broad-Spectrum Protectants , 1995 .
[65] B. Halkier,et al. Cytochrome P-450TYR Is a Multifunctional Heme-Thiolate Enzyme Catalyzing the Conversion of L-Tyrosine to p-Hydroxyphenylacetaldehyde Oxime in the Biosynthesis of the Cyanogenic Glucoside Dhurrin in Sorghum bicolor (L.) Moench (*) , 1995, The Journal of Biological Chemistry.
[66] D. Nelson,et al. Diversity and Evolution of Plant P450 and P450-Reductases , 1995, Drug metabolism and drug interactions.
[67] F. Durst,et al. Characterization of recombinant plant cinnamate 4-hydroxylase produced in yeast. Kinetic and spectral properties of the major plant P450 of the phenylpropanoid pathway. , 1994, European journal of biochemistry.
[68] R. Kaiser. On the Scent of Orchids , 1993 .
[69] R. Buttery,et al. Bioactive volatile compounds from plants , 1993 .
[70] B. Halkier,et al. The biosynthesis of cyanogenic glucosides in seedlings of cassava (Manihot esculenta Crantz). , 1992, Archives of biochemistry and biophysics.
[71] B. Halkier,et al. The biosynthesis of cyanogenic glucosides in higher plants. Identification of three hydroxylation steps in the biosynthesis of dhurrin in Sorghum bicolor (L.) Moench and the involvement of 1-ACI-nitro-2-(p-hydroxyphenyl)ethane as an intermediate. , 1990, The Journal of biological chemistry.
[72] J. Grootwassink,et al. Formation of sulfatoglucosides from exogenous aldoximes in plant cell cultures and organs , 1990 .
[73] B. Møller,et al. The biosynthesis of cyanogenic glucosides in higher plants. Channeling of intermediates in dhurrin biosynthesis by a microsomal system from Sorghum bicolor (linn) Moench. , 1980, The Journal of biological chemistry.
[74] M. Matsuo,et al. 1-Nitro-2-phenylethane, a possible intermediate in the biosynthesis of benzylglucosinolate , 1972 .
[75] H. Kindl,et al. Aldoximes as intermediates in the biosynthesis of tyrosol and tyrosol derivatives , 1971 .
[76] G. J. Karabatsos,et al. Structural studies by nuclear magnetic resonance—XVIII , 1968 .
[77] F. Vane,et al. Structural Studies by Nuclear Magnetic Resonance. III.syn-antiAssignments from Solvent Effects , 1963 .
[78] F. Vane,et al. Structural Studies by Nuclear Magnetic Resonance. IV. Conformations of syn-anti Isomers from Chemical Shifts and Spin-Spin Coupling Constants , 1963 .