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Laboratory of Biologically Active Compounds

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AmaranthusanatomyantioxidantsappleapplesArabidopsis thalianaarracachaautophagyautophagy-related genesautophagy.related genesbeechbeechnutcalcium oxalateCannabis sativacarotenoidsCell densityChenopodiumchitinasesCleavage polyembryonycytokinin derivativesdesiccationdevelopmentDisanthusdormancyDouglas-firDouglas firembryoembryogenesisembryogenic cultureFagus sylvaticaflavonoidsfloral iductionflow cytometryfloweringgene expressiongerminationglucanaseshemphistochemistryimage analysisimmunolabellinginductionin vitro regenerationmaritime pinemicropropagationmicroscopynon-embryogenic cellsNorway spruceorganogenesisoxidative stressphenolic acidsphenolsphotoperiodphytohormonesPicea abiespolyaminespolyphenolic compoundsproliferationProtein patternproteomePseudotsuga menziesiiputrescineResearchrootsignallingsomaclonal variationsomatic embryogenesisspermidinesperminestarch grainsstereologystorage compoundstissue culturestobacco cell culturetranscriptometransformationUV-B irradiationUV-B radiationVegetative propagationyaconzygotic embryoβ-1,3-glucanases

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Phenotypes of primary transformants of Arabidopsis Col-0 carrying CfFTL2–1 under the complex metoxyfenozide-inducible promoter (Vge:TM-2:5×m:cfftl2–1), which flowered without chemical induction. Plants started to bolt immediately after germination. Some of them formed minuscule flowers (a, b, c), others produced tiny flower buds with long trichomes (d). All the plantlets died without generating viable seed. Photo: Lukáš Synek.

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