Geschmack ist vorhersagbar: Mit FlavorMiner. FlavorMiner heißt das Tool, das IPB-Chemiker und Partner aus Kolumbien jüngst entwickelt haben. Das Programm kann, basierend auf maschinellem Lernen (KI), anhand der…
Seit Februar 2021 bietet Wolfgang Brandt, ehemaliger Leiter der Arbeitsgruppe Computerchemie am IPB, sein Citizen Science-Projekt zur Pilzbestimmung an. Dafür hat er in regelmäßigen Abständen öffentliche Vorträge zur Vielfalt…
Ibdah, M.; Krins, A.; Seidlitz, H. K.; Heller, W.; Strack, D.; Vogt, T.;Spectral dependence of flavonol and betacyanin accumulation in Mesembryanthemum crystallinum under enhanced ultraviolet radiationPlant Cell Environ.251145-1154(2002)DOI: 10.1046/j.1365-3040.2002.00895.x
Mesembryanthemum crystallinum L. (Aizoaceae) is a drought‐ and salt‐tolerant halophyte that is able to endure harsh environmental conditions. Upon irradiation with high light irradiance (1200–1500 µ mol m−2 s−1) it displays a rapid cell‐specific accumulation of plant secondary metabolites in the upper leaf epidermis; a phenomenon that is not detectable with salt or drought treatment. The accumulation of these compounds, the betacyanins and acylated flavonol glycosides, increases if the plants are exposed to polychromatic radiation with a progressively decreasing short‐wave cut‐off in the ultraviolet range. The response is localized in the epidermal bladder cells on the tips of young leaves and epidermal layers of fully expanded leaves. It is demonstrated that the accumulation of flavonols and betacyanins can be described by a weakly sigmoid dose function in combination with an exponential decrease of the response function of the plant with increasing wavelength.
Publikation
Mikkat, S.; Milkowski, C.; Hagemann, M.;The gene sll 0273 of the cyanobacterium Synechocystis sp. strain PCC6803 encodes a protein essential for growth at low Na+/K+ ratiosPlant Cell Environ.23549-559(2000)DOI: 10.1046/j.1365-3040.2000.00565.x
A mutant of Synechocystis sp. strain PCC6803 was obtained by random cartridge mutagenesis, which could not grow at low sodium concentrations. Genetic analyses revealed that partial deletion of the sll 0273 gene, encoding a putative Na+ /H+ exchanger, was responsible for this defect. Physiological characterization indicated that the sll 0273 mutant exhibited an increased sensitivity towards K+ , even at low concentrations, which was compensated for by enhanced concentrations of Na+ . This enhanced Na+ demand could also be met by Li+ . Furthermore, addition of monensin, an ionophore mediating electroneutral Na+ /H+ exchange, supported growth of the mutant at unfavourable Na+ /K+ ratios. Measurement of internal Na+ and K+ contents of wild‐type and mutant cells revealed a decreased Na+ /K+ ratio in mutant cells pre‐incubated at a low external Na+ /K+ ratio, while it remained at the level of the wild type after pre‐incubation at a high external Na+ /K+ ratio. We conclude that the Sll0273 protein is required for Na+ influx, especially at low external Na+ concentrations or low Na+ /K+ ratios. This system may be part of a sodium cycle and may permit re‐entry of Na+ into the cells, if nutrient/Na+ symporters are not functional or operating.
Publikation
Leopold, J.; Hause, B.; Lehmann, J.; Graner, A.; Parthier, B.; Wasternack, C.;Isolation, characterization and expression of a cDNA coding for a jasmonate-inducible protein of 37 kDa in barley leavesPlant Cell Environ.19675-684(1996)DOI: 10.1111/j.1365-3040.1996.tb00402.x
In barley leaves, there is a dramatic alteration of gene expression upon treatment with jasmonates leading to the accumulation of newly formed proteins, designated as jasmonate‐inducible proteins (JIPs). In the present study, a new jasmonate‐inducible cDNA, designated pHvJS37, has been isolated by differential screening of a γgt10 cDNA library constructed from mRNA of jasmonate‐treated barley leaf segments. The open reading frame (ORF) encodes a 39‐9 kDa polypeptide which cross‐reacts with antibodies raised against the in vivo JIP‐37. The hydropathic plot suggests that the protein is mainly hydrophilic, containing two hydrophilic domains near the C‐terminus. Database searches did not show any sequence homology of pHv.JS37 to known sequences. Southern analysis revealed at least two genes coding for JIP‐37 which map to the distal portion of the long arm of chromosome 3 and are closely related to genes coding for JIP‐23. The expression pattern of the JIP‐37 genes over time shows differential responses to jasmonate, abscisic acid (ABA), osmotic stress (such as sorbitol treatment) and desiccation stress. No expression was found under salt stress. From experiments using an inhibitor and intermediates of jasmonate synthesis such as α‐linolenic acid and 12‐oxophytodienoic acid, we hypothesize that there is a stress‐induced lipid‐based signalling pathway in which an endogenous rise of jasmonate switches on JIP‐37 gene expression. Using immunocytochemical techniques, JIP‐37 was found to be simultaneously located in the nucleus, the cytoplasm and the vacuoles.