Plant Physiol. Journal of Pharmacology and Experimental Therapeutics
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Plant Physiology 66:1008-1011 (1980)
© 1980 American Society of Plant Biologists

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Nes, W. D.
Right arrow Articles by Bean, G. A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Nes, W. D.
Right arrow Articles by Bean, G. A.
Agricola
Right arrow Articles by Nes, W. D.
Right arrow Articles by Bean, G. A.
Articles

Effect of Steric and Nuclear Changes in Steroids and Triterpenoids on Sexual Reproduction in Phytophthora cactorum1

William David Nes2, Glenn Wayne Patterson3 and George Albert Bean

Department of Botany, University of Maryland, College Park, Maryland 20742

The comparative biological activity of 21 naturally occurring or synthetically derived steroids, 7 tetracyclic and pentacylic triterpenoids, and antheridiol incubated with cultures of Phytophthora cactorum has been examined. There was greater dependence on precise steric features of the sterol side chain than on the extent of nuclear unsaturation in inducing oospore formation. There was no significant effect on oospore formation by changing nuclear unsaturation in ring B from {Delta}5 to {Delta}7 or to {Delta}5,7. Converting the unsaturated sterol to its corresponding stanol resulted in a significant reduction in the number of oospores produced. The effectiveness of sterols bearing different side chains in inducing oospores was found to be in the following relative order: 24{alpha}-ethyl = trans-{Delta}22-24{alpha}-ethyl > trans-{Delta}22-24{beta}-ethyl = 24{alpha}-E-ethylidene = 24{alpha}-methyl > 24{beta}-methyl = trans-{Delta}22-24{beta}-methyl = 26-methyl = saturated C7 side chain and C-20 R (17-{alpha}H, 20-{alpha}H, right-handed conformer) = cis-{Delta}22-C7 side chain and C-20 R > saturated C7 side chain and C-20 S (17-{alpha}H, 20-{beta}H, right-handed conformer) > no sterol = 29-hydroxyporiferasterol = 20{alpha}-hydroxycholesterol = 24{xi}-hydroxy-24-vinylcholesterol. Of the sterols examined the most significant stereochemical criterion for the induction of oospore formation was absence of bulk on the front face of C-20. This follows from the observation that 20-isocholesterol and 20{alpha}-hydroxycholesterol, in which a methyl and hydroxy group, respectively, project to the front in the right handed conformation, were inactive in stimulating production of oospores. None of the triterpenoids studied induced oospore formation to any significant degree. Oospore formation was not induced by antheridiol nor 29-hydroxyporiferasterol in combination or added separately to growing cultures of P. cactorum in the concentration range 0.01 - 10.0 milligrams per liter.


2 Present address: Department of Nutritional Sciences, University of California, Berkely, CA 94720

3 To whom correspondence should be addressed.

1 Scientific Article No. A2625 Contribution No. 5663 of the Maryland Agricultural Experiment Station.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
ASPB Publications PLANT PHYSIOLOGY® THE PLANT CELL
Copyright © 1980 by the American Society of Plant Biologists