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Adventitious root formation (ARF) in the model plant Petunia hybrida cv. Mitchell has been analysed in terms of anatomy, gene expression, enzymatic activities and levels of metabolites. This study focuses on the involvement of wound response and primary metabolism.Microscopic techniques were complemented with targeted transcript, enzyme and metabolite profiling using real time polymerase chain reaction (PCR), Northern blot, enzymatic assays, chromatography and mass spectrometry.Three days after severance from the stock plants, first meristematic cells appeared which further developed into root primordia and finally adventitious roots. Excision of cuttings led to a fast and transient increase in the wound‐hormone jasmonic acid, followed by the expression of jasmonate‐regulated genes such as cell wall invertase. Analysis of soluble and insoluble carbohydrates showed a continuous accumulation during ARF. A broad metabolite profiling revealed a strong increase in organic acids and resynthesis of essential amino acids.Substantial changes in enzyme activities and metabolite levels indicate that specific enzymes and metabolites might play a crucial role during ARF. Three metabolic phases could be defined: (i) sink establishment phase characterized by apoplastic unloading of sucrose and being probably mediated by jasmonates; (ii) recovery phase; and (iii) maintenance phase, in which a symplastic unloading occurs.
Publikation
Zurbriggen, M. D.; Carrillo, N.; Tognetti, V. B.; Melzer, M.; Peisker, M.; Hause, B.; Hajirezaei, M.-R.;Chloroplast-generated reactive oxygen species play a major role in localized cell death during the non-host interaction between tobacco and Xanthomonas campestris pv. vesicatoriaPlant J.60962-973(2009)DOI: 10.1111/j.1365-313X.2009.04010.x
Attempted infection of plants by pathogens elicits a complex defensive response. In many non‐host and incompatible host interactions it includes the induction of defence‐associated genes and a form of localized cell death (LCD), purportedly designed to restrict pathogen advance, collectively known as the hypersensitive response (HR). It is preceded by an oxidative burst, generating reactive oxygen species (ROS) that are proposed to cue subsequent deployment of the HR, although neither the origin nor the precise role played by ROS in the execution of this response are completely understood. We used tobacco plants expressing cyanobacterial flavodoxin to address these questions. Flavodoxin is an electron shuttle present in prokaryotes and algae that, when expressed in chloroplasts, specifically prevents ROS formation in plastids during abiotic stress episodes. Infiltration of tobacco wild‐type leaves with high titres of Xanthomonas campestris pv. vesicatoria (Xcv ), a non‐host pathogen, resulted in ROS accumulation in chloroplasts, followed by the appearance of localized lesions typical of the HR. In contrast, chloroplast ROS build‐up and LCD were significantly reduced in Xcv ‐inoculated plants expressing plastid‐targeted flavodoxin. Metabolic routes normally inhibited by pathogens were protected in the transformants, whereas other aspects of the HR, including the induction of defence‐associated genes and synthesis of salicylic and jasmonic acid, proceeded as in inoculated wild‐type plants. Therefore, ROS generated in chloroplasts during this non‐host interaction are essential for the progress of LCD, but do not contribute to the induction of pathogenesis‐related genes or other signalling components of the response.