Skip to main content
Applied and Environmental Microbiology logoLink to Applied and Environmental Microbiology
. 1996 Aug;62(8):2811–2817. doi: 10.1128/aem.62.8.2811-2817.1996

Chemotactic Preferences and Strain Variation in the Response of Phytophthora sojae Zoospores to Host Isoflavones

B M Tyler, M Wu, J Wang, W Cheung, P F Morris
PMCID: PMC1388913  PMID: 16535375

Abstract

The zoospores of Phytophthora sojae are chemotactically attracted to the isoflavones genistein and daidzein that are released by soybean roots. In this study we have examined the response of P. sojae zoospores to a wide range of compounds having some structural similarity to genistein and daidzein, including isoflavones, flavones, chalcones, stilbenes, benzoins, benzoates, benzophenones, acetophenones, and coumarins. Of 59 compounds examined, 43 elicited some response. A comparison of the chemotactic responses elicited by the various compounds revealed a primary role for the phenolic 4(prm1)- and 7-hydroxyl groups on the isoflavone structure. A few compounds acted as repellents, notably methylated flavones with a hydrophobic B ring. The chemotactic response to many of the analogs was markedly different among different strains of P. sojae.

Full Text

The Full Text of this article is available as a PDF (257.7 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Banfalvi Z., Nieuwkoop A., Schell M., Besl L., Stacey G. Regulation of nod gene expression in Bradyrhizobium japonicum. Mol Gen Genet. 1988 Nov;214(3):420–424. doi: 10.1007/BF00330475. [DOI] [PubMed] [Google Scholar]
  2. Cameron J. N., Carlile M. J. Binding of isovaleraldehyde, an attractant, to zoospores of the fungus Phytophthora palmivora in relation to zoospore chemotaxis. J Cell Sci. 1981 Jun;49:273–281. doi: 10.1242/jcs.49.1.273. [DOI] [PubMed] [Google Scholar]
  3. Cunningham S., Kollmeyer W. D., Stacey G. Chemical control of interstrain competition for soybean nodulation by Bradyrhizobium japonicum. Appl Environ Microbiol. 1991 Jul;57(7):1886–1892. doi: 10.1128/aem.57.7.1886-1892.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Hermiller J. B., Tenaglia A. N., Kisslo K. B., Phillips H. R., Bashore T. M., Stack R. S., Davidson C. J. In vivo validation of compensatory enlargement of atherosclerotic coronary arteries. Am J Cardiol. 1993 Mar 15;71(8):665–668. doi: 10.1016/0002-9149(93)91007-5. [DOI] [PubMed] [Google Scholar]
  5. Hess K. M., Dudley M. W., Lynn D. G., Joerger R. D., Binns A. N. Mechanism of phenolic activation of Agrobacterium virulence genes: development of a specific inhibitor of bacterial sensor/response systems. Proc Natl Acad Sci U S A. 1991 Sep 1;88(17):7854–7858. doi: 10.1073/pnas.88.17.7854. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Kosslak R. M., Joshi R. S., Bowen B. A., Paaren H. E., Appelbaum E. R. Strain-Specific Inhibition of nod Gene Induction in Bradyrhizobium japonicum by Flavonoid Compounds. Appl Environ Microbiol. 1990 May;56(5):1333–1341. doi: 10.1128/aem.56.5.1333-1341.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Lerouge P., Roche P., Faucher C., Maillet F., Truchet G., Promé J. C., Dénarié J. Symbiotic host-specificity of Rhizobium meliloti is determined by a sulphated and acylated glucosamine oligosaccharide signal. Nature. 1990 Apr 19;344(6268):781–784. doi: 10.1038/344781a0. [DOI] [PubMed] [Google Scholar]
  8. Manson M. D. Bacterial motility and chemotaxis. Adv Microb Physiol. 1992;33:277–346. doi: 10.1016/s0065-2911(08)60219-2. [DOI] [PubMed] [Google Scholar]
  9. Rolfe B. G. Flavones and isoflavones as inducing substances of legume nodulation. Biofactors. 1988 Jan;1(1):3–10. [PubMed] [Google Scholar]
  10. Sekizaki H., Yokosawa R., Chinen C., Adachi H., Yamane Y. Studies on zoospore attracting activity. II. Synthesis of isoflavones and their attracting activity to Aphanomyces euteiches zoospore. Biol Pharm Bull. 1993 Jul;16(7):698–701. doi: 10.1248/bpb.16.698. [DOI] [PubMed] [Google Scholar]
  11. Winans S. C., Mantis N. J., Chen C. Y., Chang C. H., Han D. C. Host recognition by the VirA, VirG two-component regulatory proteins of agrobacterium tumefaciens. Res Microbiol. 1994 Jun-Aug;145(5-6):461–473. doi: 10.1016/0923-2508(94)90095-7. [DOI] [PubMed] [Google Scholar]
  12. Zambryski P. Basic processes underlying Agrobacterium-mediated DNA transfer to plant cells. Annu Rev Genet. 1988;22:1–30. doi: 10.1146/annurev.ge.22.120188.000245. [DOI] [PubMed] [Google Scholar]

Articles from Applied and Environmental Microbiology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES