Abstract
Transgenic soybean (Glycine max L.) cells expressing aequorin were used to monitor changes in cytosolic Ca(2+) concentrations in response to treatment with fungal elicitors. After an apparent lag phase of about 60 s, both chitin fragments and beta-glucan elicitors caused a rapid increase in cytosolic Ca concentration, which peaked within 2-2.5 min of treatment. The Ca(2+) concentration then decreased and reached the basal level after about 5 min in the case of the treatment with chitin fragments, while a second rise in the Ca(2+) concentration with a maximum occurring after about 7-8 min was observed in the case of beta-glucan treatment. Calibration of the signals showed that the elicitors enhanced the cytosolic Ca(2+) concentration from resting concentrations as low as 0.1 mu M to highest levels of about 2 mu M. Dose-response experiments showed that the concentration of elicitors giving a Ca(2+) response at the 50% level was 0.4 nM for the chitin fragment and 28 mu M and 72 mu M, respectively, for a synthetic hepta-beta-glucoside and a fungal beta-glucan fraction. The beta-glucan- or N,N'.N ",N"'-tetraacetyl chitotetratose (CH4)-induced Ca(2+) signals were inhibited by both the Ca(2+) chelator 1,2-bis-(2-aminophenoxy) ethane-N,N,N',N'-tetraacetic acid (BAPTA) and by the Ca(2+)-channel inhibitor La(3+). Neomycin, whose target in plant cells has not yet been clearly identified, reduced predominantly the expression of the second peak of the biphasic Ca(2+) curve following beta-glucan treatment. Bacterial cyclic beta-glucans known to elicitor-sensing mechanism of soybean cells, and is probably connected with the subsequent activation of defence responses.
