Plant Physiol, October 2000, Vol. 124, pp. 733-740
Nod Factors and Chitooligomers Elicit an Increase in Cytosolic
Calcium in Aequorin-Expressing Soybean
Cells1
Joachim
Müller,2*
Christian
Staehelin,2
Zhi-Ping
Xie,
Gabriele
Neuhaus-Url, and
Thomas
Boller
Friedrich-Miescher-Institut, P.O. Box 2543, CH-4002 Basel,
Switzerland (J.M., G.N.-U., T.B.); and Botanisches Institut der
Universität Basel, Hebelstrasse 1, CH-4056 Basel, Switzerland
(C.S., Z.-P.X., T.B.)
Rhizobial Nod factors (NFs) function as nodulation signals that
trigger symbiotic responses of leguminous host plants. NFs consist of a
chitin oligomer backbone carrying a fatty acid at the non-reducing end.
Depending on the rhizobial strain, NFs carry additional substituents,
which may determine host specificity. Transgenic suspension-cultured
soybean (Glycine max [L.] Merr.) cells expressing
aequorin have been used to record cytosolic [Ca2+]
changes upon treatment with purified NFs and chitin fragments. Both
compounds elicited an increase of cytosolic [Ca2+] at
nanomolar concentrations. The shape and amplitude of cytosolic [Ca2+] changes was similar to the response elicited by
un-derivatized chitin oligomers. Cells challenged first with NFs did
not respond to a subsequent treatment with chitin oligomers and vice
versa. Dose-response experiments showed that un-derivatized chitin
oligomers were more active compared with NFs. The capacity of NFs to
elicit the calcium response depended on their structure. The presence of reducing end substituents in methylfucosylated NFs from
Rhizobium sp. NGR234 and the O-acetyl
group at the non-reducing end in NFs from Sinorhizobium
meliloti attenuated the activity to cause the calcium changes.
The sulfate group in NFs from Rhizobium tropici did not
affect the elicitor activity. Pentameric S. meliloti NFs were more active than tetrameric molecules, whereas trimeric or dimeric
degradation products were inactive. Substituents in NFs may have the
function to avoid stimulation of defense reactions mediated by the
perception system for chitin oligomers.
1
This work was supported by the Swiss National
Foundation and by a Roche Foundation fellowship (to J.M.).
2
These authors contributed equally to the paper.
*
Corresponding author; e-mail joachim.mueller{at}unibas.ch; fax
41-61-697-45-27.
© 2000 American Society of Plant Physiologists