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Specific perception of subnanomolar concentrations of chitin fragments by tomato cells: induction of extracellular alkalinization, changes in protein phosphorylation, and establishment of a refractory state
Authors:Georg Felix  Martin Regenass  Thomas Boller
Institution:Friedrich Miescher-Institut, P.O.B. 2543, CH-4002 Basel, Switzerland
Abstract:Suspension-cultured tomato cells respond to yeast cell wall preparations with a rapid, transient alkalinization of the culture medium. Depending on the dose of the stimulus, the pH starts to increase after a lag period of about 0.5–2 min and reaches a transient maximum, up to 0.6 pH units above the initial value, after 2–4 min. Using this alkalinization response as a rapid and convenient assay, a sensitive perception system for small chitin fragments was revealed in the tomato cells. Chitin oligomers with four or more N -acetylglucosamine residues stimulated the alkalinization response significantly at concentrations below 10 pM and half-maximally at concentrations of 100 pM. About 10 000-fold higher concentrations of the trimer, N,N',N" -triacetylchitotriose, were required to elicit similar responses. For up to 8 h after a first treatment with 10 nM of the tetramer, N,N',N",N‴ -tetraacetyl-chitotetraose, cells did not respond to a second stimulation with any of the chitin fragments. Throughout this refractory period, however, cells remained fully responsive to preparations of fungal xylanase, another stimulus which induces a more permanent alkalinization after a lag phase of more than 2 min. The alkalinization response to these two qualitatively different stimuli was paralleled by the same characteristic changes in the pattern of protein phosphorylation, detected by in vivo pulse-labelling with 32P]phosphate for 30 sec. The onset of the alkalinization and of the changes in protein phosphorylation coincided in both cases, and both phenomena were blocked by the protein kinase inhibitor K-252a. Although the mechanism underlying the extracellular pH increase is unknown, activation of the alkalinization response provides a sensitive and convenient assay to investigate early events in chemoperception of microbial signals by plant cells.
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