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ALLELOCHEMICALS FROM AGERATUM CONYZOIDES AND ORYZA SATIVA 203<br />

(Figure 8). They were produced in rice leaves and stems with M. grisea and R. solani.<br />

Phytocassanes A-E had high antifungal activity against the pathogenic fungi, M.<br />

grisea and R. solani (Koga et al., 1995; 1997). Their ED 50 values in prevention of<br />

spore germination and germ tube growth of M. grisea were very low (Figure 8).<br />

Sakuranetin is a flavonoid-type phytoalexin that was identified from rice plants. It<br />

had high antifungal activity and a large amount of accumulation in rice leaves<br />

(Nakazato et al., 2000).<br />

It has been shown in host-pathogen interactions that resistance reactions can be<br />

triggered by a large number of abiotic and biotic factors. Among the chemical factors,<br />

macromolecules of microbial origin are very important. Plant defense responses are<br />

stimulated by very low concentrations of these molecules (Darvill and Albersheim,<br />

1984). It was confirmed that a chemical for plant disease control might function by<br />

activating the natural resistance mechanisms of the host, for example, 2,2-dichloro-<br />

3,3-dimethyl cyclopropane carboxylic acid may exert its systemic fungicidal activity<br />

against the rice blast disease caused by P. oryzae (Cartwright et al., 1977). The<br />

application of methionine on wounded rice leaves induced the production of rice<br />

phytoalexins, sakuranetin and momilactone A. In the paddy field, methionine treatment<br />

has been demonstrated to reduce rice blast (Nakazato et al., 2000).<br />

An increasing number of studies have shown that rice phytoalexins are induced<br />

by elicitor that are produced by pathogenic microorganisms and make field disease<br />

control by inducing the pathogen defense mechanism in rice (Schaffrath et al., 1995;<br />

Tamogami et al., 1997a,b). Elicitors have been investigated extensively. It has been<br />

shown that jasmonic acid and its related compounds play important roles as the<br />

signaling molecules that elicit the production of phytoalexins in rice. Sakuranetin<br />

production may be elicited by exogenously applied jasmonic acid in rice leaves.<br />

Furthermore, sakuranetin production by exogenously applied jasmonic acid was<br />

significantly counteracted by amino acid, cytokinin, kinetin and zeatin (Tamogami et<br />

al., 1997a,b).<br />

4. CONCLUSION<br />

Many interactions between plant pathogens and their hosts are allelopathic.<br />

<strong>Allelochemicals</strong> can be applied in biological control of weeds and plant diseases (Rice,<br />

1995). Our research suggested that allelochemicals produced and released from A.<br />

conyzoides intercropping in citrus orchard did play important roles in integrated pest<br />

management. Many kinds of allelochemicals in rice not only inhibit the germination<br />

and growth of weeds, but also participate in the defense against pathogens. However,<br />

it remains unclear which allelochemicals in rice are predominantly involved in defense<br />

mechanisms against the pathogens. Therefore, further clarification of the resistance<br />

mechanism and multiple functions of rice allelochemicals are warranted.<br />

Acknowledgments : The author thanks Dr. Inderjit and anonymous reviewers for<br />

thoughtful criticisms and correcting English on earlier versions of the manuscript. The<br />

work was supported by National Natural Science Foundation of China (NSFC<br />

No.30170182; 30430460) and Hundreds-Talent Program of Chinese Academy of Sciences.

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