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Laboratory of Biologically Active Compounds

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Amaranthusanatomyappleapplesarracachaautophagyautophagy-related genesautophagy.related genesbeechbeechnutcalcium oxalateCannabis sativacarotenoidsCell densityChenopodiumchitinasesCleavage polyembryonycytokinin derivativesdesiccationdevelopmentDisanthusdormancyDouglas-firDouglas firembryoembryogenesisembryogenic cultureFagus sylvaticafloral iductionflow cytometryfloweringgene expressiongerminationglucanaseshemphistochemistryimage analysisinductionin vitro regenerationmaritime pinemicropropagationmicroscopynon-embryogenic cellsNorway spruceorganogenesisoxidative stressphenolic acidsphotoperiodphytohormonesPicea abiespolyaminespolyphenolic compoundsproliferationProtein patternproteomePseudotsuga menziesiiputrescineResearchsignallingsomaclonal variationsomatic embryogenesisspermidinesperminestarch grainsstereologystorage compoundstissue culturestobacco cell culturetranscriptometransformationUV-B irradiationUV-B radiationVegetative propagationyaconzygotic embryoβ-1,3-glucanases

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Callus induction and plant regeneration of A. xanthorrhiza. (a) Callus with meristematic centres (bar = 3 mm) (b) Histological analysis of morphogenic callus (MC: Meristematic Centers) (bar = 200 µm ) (c) Shoots regeneration from callus (bar = 4 mm) (d) Germinated somatic embryo (bar = 1.2 mm) (e) Histological analysis of early cotyledonary somatic embryo (Ct: Cotyledon; Hy: Hypocotyl; Ra: Radicle; SA: Shoot Apex) (bar = 500 µm) (f) Plant recovered from callus (bar = 5 mm)

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