July
1997
, Volume
10
, Number
5
Pages
537
-
549
Authors
Jerry D.
Reed
,
1
David L.
Edwards
,
2
and
Carlos F.
Gonzalez
1
Affiliations
1Department of Plant Pathology and Microbiology, Texas A&M University, College Station 77843-2132 U.S.A.; 2Ceres Technologies, Inc., San Antonio, TX 78230 U.S.A.
Go to article:
RelatedArticle
Accepted 18 March 1997.
Abstract
Synthetic combinatorial libraries were evaluated with an iterative process to identify a hexapeptide with broad-spectrum activity against selected phytopathogenic fungi. A D-amino acid hexapeptide (FRLKFH) and pentapeptide (FRLHF) exhibited activity against Fusarium oxysporum f. sp. lycopersici, Rhizoctonia solani (anastomosis group 1), Ceratocystis fagacearum, and Pythium ultimum. The peptides showed no hemolytic or mutagenic activity. Fluorescent microscopy studies with a membrane impermeant dye indicated that fungal cytoplasmic membranes were compromised rapidly and that the nuclear membrane was also affected.
JnArticleKeywords
Additional keywords:
antifungal,
synthetic peptide.
Page Content
ArticleCopyright
© 1997 The American Phytopathological Society