Unser 10. Leibniz Plant Biochemistry Symposium am 7. und 8. Mai war ein großer Erfolg. Thematisch ging es in diesem Jahr um neue Methoden und Forschungsansätze der Naturstoffchemie. Die exzellenten Vorträge über Wirkstoffe…
Omanische Heilpflanze im Fokus der Phytochemie IPB-Wissenschaftler und Partner aus Dhofar haben jüngst die omanische Heilpflanze Terminalia dhofarica unter die phytochemische Lupe genommen. Die Pflanze ist reich an…
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…
Sinelnikov, I. G.; Siedhoff, N. E.; Chulkin, A. M.; Zorov, I. N.; Schwaneberg, U.; Davari, M. D.; Sinitsyna, O. A.; Shcherbakova, L. A.; Sinitsyn, A. P.; Rozhkova, A. M.;Expression and refolding of the plant chitinase from Drosera capensis for applications as a sustainable and integrated pest managementFront. Bioeng. Biotechnol.9728501(2021)DOI: 10.3389/fbioe.2021.728501
Recently, the study of chitinases has become an important target of numerous research projects due to their potential for applications, such as biocontrol pest agents. Plant chitinases from carnivorous plants of the genus Drosera are most aggressive against a wide range of phytopathogens. However, low solubility or insolubility of the target protein hampered application of chitinases as biofungicides. To obtain plant chitinase from carnivorous plants of the genus Drosera in soluble form in E.coli expression strains, three different approaches including dialysis, rapid dilution, and refolding on Ni-NTA agarose to renaturation were tested. The developed « Rapid dilution » protocol with renaturation buffer supplemented by 10% glycerol and 2M arginine in combination with the redox pair of reduced/oxidized glutathione, increased the yield of active soluble protein to 9.5 mg per 1 g of wet biomass. A structure-based removal of free cysteines in the core domain based on homology modeling of the structure was carried out in order to improve the soluble of chitinase. One improved chitinase variant (C191A/C231S/C286T) was identified which shows improved expression and solubility in E. coli expression systems compared to wild type. Computational analyzes of the wild-type and the improved variant revealed overall higher fluctuations of the structure while maintaining a global protein stability. It was shown that free cysteines on the surface of the protein globule which are not involved in the formation of inner disulfide bonds contribute to the insolubility of chitinase from Drosera capensis. The functional characteristics showed that chitinase exhibits high activity against colloidal chitin (360 units/g) and high fungicidal properties of recombinant chitinases against Parastagonospora nodorum. Latter highlights the application of chitinase from D. capensis as a promising enzyme for the control of fungal pathogens in agriculture.
Publikation
Gorzolka, K.; Perino, E. H. B.; Lederer, S.; Smolka, U.; Rosahl, S.;Lysophosphatidylcholine 17:1 from the Leaf Surface of the Wild Potato Species Solanum bulbocastanum Inhibits Phytophthora infestansJ. Agr. Food Chem.695607-5617(2021)DOI: 10.1021/acs.jafc.0c07199
Late blight, caused by the oomycete Phytophthora infestans, is economically the most important foliar disease of potato. To assess the importance of the leaf surface, as the site of the first encounter of pathogen and host, we performed untargeted profiling by liquid chromatography–mass spectrometry of leaf surface metabolites of the susceptible cultivated potato Solanum tuberosum and the resistant wild potato species Solanum bulbocastanum. Hydroxycinnamic acid amides, typical phytoalexins of potato, were abundant on the surface of S. tuberosum, but not on S. bulbocastanum. One of the metabolites accumulating on the surface of the wild potato was identified as lysophosphatidylcholine carrying heptadecenoic acid, LPC17:1. In vitro assays revealed that both spore germination and mycelial growth of P. infestans were efficiently inhibited by LPC17:1, suggesting that leaf surface metabolites from wild potato species could contribute to early defense responses against P. infestans.
Publikation
Fayek, N. M.; Mekky, R. H.; Dias, C. N.; Kropf, M.; Heiss, A. G.; Wessjohann, L. A.; Farag, M. A.;UPLC-MS Metabolome-Based Seed Classification of 16 Vicia Species: A Prospect for Phyto-Equivalency and Chemotaxonomy of Different AccessionsJ. Agr. Food Chem.695252-5266(2021)DOI: 10.1021/acs.jafc.0c06054
Seeds of domesticated Vicia (vetch) species (family Fabaceae-Faboideae)
are produced and consumed worldwide for their nutritional value. Seed
accessions belonging to 16 different species of Vicia—both domesticated
and wild taxa—were subjected to a chemotaxonomic study using
ultraperformance liquid chromatography–mass spectrometry (UPLC-MS)
analyzed by chemometrics. A total of 89 metabolites were observed in the
examined Vicia accessions. Seventy-eight out of the 89 detected
metabolites were annotated. Metabolites quantified belonged to several
classes, viz., flavonoids, procyanidins, prodelphinidins, anthocyanins,
stilbenes, dihydrochalcones, phenolic acids, coumarins, alkaloids,
jasmonates, fatty acids, terpenoids, and cyanogenics, with flavonoids
and fatty acids amounting to the major classes. Flavonoids, fatty acids,
and anthocyanins showed up as potential chemotaxonomic markers in Vicia
species discrimination. Fatty acids were more enriched in Vicia faba specimens, while the abundance of flavonoids was the highest in Vicia parviflora. Anthocyanins allowed for discrimination between Vicia hirsuta and Vicia sepium.
To the best of our knowledge, this is the first report on employing
UPLC-MS metabolomics to discern the diversity of metabolites at the
intrageneric level among Vicia species.