Zum Einfluß des bakteriellen Phytotoxins Coronatin auf pflanzliche Zellsuspensionskulturen

Effect of the Bacterial Phytotoxin Coronatine on Plant Cell Cultures The influence of the bacterial phytotoxin coronatine on cell cultures of Lycopersicon peruvianum and Chenopodium album was studied. It was detectable that the cell culture L. peruvianum more related to the host plant of the phytopathogenic bacteria reacts more sensitive to coronatine. Concentrations of 3.5 ng coronatme/ml culture liquid mduce reductions in growth and the TTC-activity. In the case of the other used cell culture the critical amount of coronatine was higher than 7 ng/ml culture liquid. In further experiments the concentrations of free amino acids and proteins within the cell were followed. After 6–7 days of culture a slightly recovery of the cultures treated with coronatine was detectable.     

Morphological characterization of microencapsulated Penicillium raistrickii i 477

For the immobilization of spores of Penicillium raistrickii i 477 the formation of polyelectrolyte complexes using the sodium salt of cellulose sulphate as polyanion and poly-dimethyl-diallylammoniumchloride as polycation was used. Light and scanning electron microscopy have shown that during germination of spores the capsule walls do not cause effective limitations on hyphal growth and that there are no significant morphological changes of the mycelium detectable by an outgrowth of immobilized spores. By comparing the 15α-hydroxylation of 13-ethyl-gon-4-en-3,17-dione with free and encapsulated cells it was found that an increase of total dry biomass per immobilized system led to a higher product formation in relation to free cells.     

Type I interferon is required for T helper (Th) 2 induction by dendritic cells

Type 2 inflammation is a defining feature of infection with parasitic worms (helminths), as well as being responsible for widespread suffering in allergies. However, the precise mechanisms involved in T helper (Th) 2 polarization by dendritic cells (DCs) are currently unclear. We have identified a previously unrecognized role for type I IFN (IFN‐I) in enabling this process. An IFN‐I signature was evident in DCs responding to the helminth Schistosoma mansoni or the allergen house dust mite (HDM). Further, IFN‐I signaling was required for optimal DC phenotypic activation in response to helminth antigen (Ag), and efficient migration to, and localization with, T cells in the draining lymph node (dLN). Importantly, DCs generated from Ifnar1^?/? mice were incapable of initiating Th2 responses in vivo. These data demonstrate for the first time that the influence of IFN‐I is not limited to antiviral or bacterial settings but also has a central role to play in DC initiation of Th2 responses.     

Formation, derivatization and applications of bacterial cellulose

Acetobacter xylinum produces highly crystalline cellulose extracellulary using glucose as a carbon source. The polymer formed is free of other biogenic compounds, separable in a simple way and characterized by its high water-absorption capacity. Stepwise solvent exchange from water to unpolar solvents leads to a drastic decrease of the water content of the bacterial cellulose without decrease of the highly swollen and activated state. Heterogeneous as well as homogeneous derivatizations, e.g. carboxymethylation, silylation and acetylation, were performed on the wet or dried biopolymer. Furthermore, different methods for formation of hollow fibres during biosynthesis were investigated. Such tubes may have applications as biocompatible material in medicine.     

Effect of Coronatine on Ethylene Release and ATPase Activity of Tomato Cell Cultures

The effects of the phytotoxin coronatine formed by pathovars of Pseudomonas syringae on coronatine sensitive cell cultures of Lycopersicon peruvianum and Lycopersicon esculentum were investigated. The studied parameters were ethylene release, activity of membrane-bound ATPase and vitality using the TTC test. The cells of L. esculentum responded with an increase, the cells of L. peruvianum with a decrease of ethylene formation after application of different coronatine concentrations. These results indicate that the effect on ethylene release is not the primary effect of the toxin. The activity of membrane-bound ATPase was not affected by coronatine.