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The organ-specific expression of terpene synthase genes contributes to the terpene hydrocarbon composition of chamomile essential oilsThe molecular basis of host plant selection in Melaleuca quinquenervia by a successful biological control agentA Latex Metabolite Benefits Plant Fitness under Root Herbivore AttackThe Eucalyptus terpene synthase gene familyMolecular and biochemical evolution of maize terpene synthase 10, an enzyme of indirect defense.Restoring a maize root signal that attracts insect-killing nematodes to control a major pest.The products of a single maize sesquiterpene synthase form a volatile defense signal that attracts natural enemies of maize herbivores.Identification and characterization of CYP79D6v4, a cytochrome P450 enzyme producing aldoximes in black poplar (Populus nigra).Functional and evolutionary relationships between terpene synthases from Australian Myrtaceae.The maize gene terpene synthase 1 encodes a sesquiterpene synthase catalyzing the formation of (E)-beta-farnesene, (E)-nerolidol, and (E,E)-farnesol after herbivore damage.Dynamic evolution of herbivore-induced sesquiterpene biosynthesis in sorghum and related grass crops.Positive Darwinian selection is a driving force for the diversification of terpenoid biosynthesis in the genus Oryza.Nonseed plant Selaginella moellendorffi [corrected] has both seed plant and microbial types of terpene synthases.The variability of sesquiterpenes emitted from two Zea mays cultivars is controlled by allelic variation of two terpene synthase genes encoding stereoselective multiple product enzymes.Terpene synthases and their contribution to herbivore-induced volatile emission in western balsam poplar (Populus trichocarpa).Recruitment of entomopathogenic nematodes by insect-damaged maize roots.Localization of sesquiterpene formation and emission in maize leaves after herbivore damage.The timing of herbivore-induced volatile emission in black poplar (Populus nigra) and the influence of herbivore age and identity affect the value of individual volatiles as cues for herbivore enemies.Protonation of a neutral (S)-beta-bisabolene intermediate is involved in (S)-beta-macrocarpene formation by the maize sesquiterpene synthases TPS6 and TPS11.Monoterpene and sesquiterpene synthases and the origin of terpene skeletal diversity in plants.The maize cytochrome P450 CYP79A61 produces phenylacetaldoxime and indole-3-acetaldoxime in heterologous systems and might contribute to plant defense and auxin formationOne amino acid makes the difference: the formation of ent-kaurene and 16α-hydroxy-ent-kaurane by diterpene synthases in poplarCYP79D enzymes contribute to jasmonic acid-induced formation of aldoximes and other nitrogenous volatiles in two Erythroxylum species.Beetle feeding induces a different volatile emission pattern from black poplar foliage than caterpillar herbivory.Covariation and phenotypic integration in chemical communication displays: biosynthetic constraints and eco-evolutionary implications.Novel family of terpene synthases evolved from trans-isoprenyl diphosphate synthases in a flea beetle.CYP79 P450 monooxygenases in gymnosperms: CYP79A118 is associated with the formation of taxiphyllin in Taxus baccata.Volatile squalene from a nonseed plant Selaginella moellendorffii: Emission and biosynthesis.A small, differentially regulated family of farnesyl diphosphate synthases in maize (Zea mays) provides farnesyl diphosphate for the biosynthesis of herbivore-induced sesquiterpenes.Herbivore-induced volatile emission in black poplar: regulation and role in attracting herbivore enemies.Two herbivore-induced cytochrome P450 enzymes CYP79D6 and CYP79D7 catalyze the formation of volatile aldoximes involved in poplar defense.Molecular and genomic basis of volatile-mediated indirect defense against insects in rice.A maize (E)-beta-caryophyllene synthase implicated in indirect defense responses against herbivores is not expressed in most American maize varieties.Four terpene synthases contribute to the generation of chemotypes in tea tree (Melaleuca alternifolia)A multiproduct terpene synthase from Medicago truncatula generates cadalane sesquiterpenes via two different mechanisms.Theoretical and experimental analysis of the reaction mechanism of MrTPS2, a triquinane-forming sesquiterpene synthase from chamomile.Gene coexpression analysis reveals complex metabolism of the monoterpene alcohol linalool in Arabidopsis flowers.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.The sesquiterpene hydrocarbons of maize (Zea mays) form five groups with distinct developmental and organ-specific distributions.Selinene Volatiles Are Essential Precursors for Maize Defense Promoting Fungal Pathogen Resistance.
P50
Q21261990-50E818C5-C712-4078-B59C-46BB88E72D11Q28285501-5999C490-F819-40E0-AD61-B834C38624A5Q28552040-2AD39F66-D498-4DEE-8F55-A96A755464D1Q30316464-F0ACC658-A489-4BDE-A1A7-DE9D71FE8795Q30319049-060929F6-A3A1-45B9-81C0-924E4C5F2B4FQ30489500-430CD027-C876-49DF-BD82-E2B56A3C2F1AQ33231825-C0B5F537-7D65-4805-9D21-AFC4445512A2Q33879540-796805F3-2194-4B06-84C7-9F4D55178AF9Q34110632-4100F650-DEFC-41BB-BDA8-6988CD5B41EDQ34164576-7CAA2074-363E-4CAE-9F89-7F041BB9F512Q34212121-D742239E-73EC-4F84-821D-C59F9F29F5E3Q34233849-07F52F18-E5FB-4327-BEDE-BF0DE36837C1Q34295094-6BFCFB87-4191-469A-BD31-997306A15D51Q34312400-DE60DD98-021D-47C3-8C18-01BC29E5726BQ34339910-53C7E7D4-D914-47D0-BB7B-96C015679035Q34409563-191706BD-9798-46B3-9907-34A8E42CBB6EQ34567475-58EC530E-70C9-49F4-926B-9BBA4676FD0DQ34676810-75D39813-3B78-40FD-9637-9AC883696C8FQ34784782-6366AAD0-BA9F-409C-8A00-96EE0D1A2B1AQ35005789-C26103BA-F9B4-454A-BCB9-2BD0BC704E3BQ35643591-D2E5D2F2-1843-446C-A464-3014EB54C01EQ35825345-6E540894-BCA7-4D6D-B3A3-34A38B706275Q36156533-F3167633-8933-4BDD-BD3E-C57E508BB580Q36216351-13ED6D87-3028-4DF3-87C3-D443997E1229Q36296355-3EED3AE2-87BB-45B4-8415-BB813E21C710Q36710462-AE3C7245-2270-4620-8B93-F7C6E7242A86Q38631147-01604322-785B-4C60-82BB-DB4CC6D5B21AQ40697605-47869F74-3C44-402C-8E45-4B0ED62DF2DFQ41438585-94037635-1437-41B7-9BD3-518DFF08EA82Q42004996-5C47DB9E-BB49-4122-8F86-003E644845EEQ42006015-A4C7FD69-C94B-4A05-9F0D-4676A8B40559Q42029528-DB4EFA40-8D84-473A-AB1B-27B278D63C87Q42030244-7C92E3FD-F6C4-4522-8422-75259F2F4FE4Q42278973-94270EB0-2D5C-46B8-9F02-CA7944666877Q42939648-15842467-C9C8-44F1-B4FB-1394EE77DAFCQ43654488-0DFB0691-CED2-4096-8C0E-76CED2FB3263Q43821770-26FE4B8D-CD7B-4A2F-A756-5F34ACBF0319Q44610427-FCDF2738-FE0A-42B0-A668-D49A15E252FDQ44997348-6DC2EC15-A377-42EC-A627-12DF63031185Q46078698-25DEE41C-1A29-4370-BB0D-F884B93A4F91
P50
description
hulumtues
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Tobias G Köllner
@ast
Tobias G Köllner
@en
Tobias G Köllner
@es
Tobias G Köllner
@nl
Tobias G Köllner
@sl
type
label
Tobias G Köllner
@ast
Tobias G Köllner
@en
Tobias G Köllner
@es
Tobias G Köllner
@nl
Tobias G Köllner
@sl
altLabel
Tobias Köllner
@en
prefLabel
Tobias G Köllner
@ast
Tobias G Köllner
@en
Tobias G Köllner
@es
Tobias G Köllner
@nl
Tobias G Köllner
@sl
P1053
H-3375-2014
P106
P21
P31
P3829
P496
0000-0002-7037-904X