The antifungal protein AFP from Aspergillus giganteus inhibits chitin synthesis in sensitive fungi

被引:84
|
作者
Hagen, Silke
Marx, Florentine
Ram, Arthur F.
Meyer, Vera
机构
[1] Tech Univ Berlin, Inst Biotechnol, Dept Genet & Microbiol, D-13355 Berlin, Germany
[2] Leiden Univ, Inst Biol, Fungal Genet Res Grp, Leiden, Netherlands
[3] Univ Innsbruck, Bioctr, A-6020 Innsbruck, Austria
关键词
CELL-WALL STRESS; SACCHAROMYCES-CEREVISIAE; FUSARIUM-OXYSPORUM; CLASS-V; IN-VITRO; SYNTHASE; GROWTH; EXPRESSION; PERMEABILIZATION; RESISTANCE;
D O I
10.1128/AEM.02497-06
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The antifungal protein AFP from Aspergillus giganteus is highly effective in restricting the growth of major human- and plant-pathogenic filamentous fungi. However, a fundamental prerequisite for the use of AFP as an antifungal drug is a complete understanding of its mode of action. In this study, we performed several analyses focusing on the assumption that the chitin biosynthesis of sensitive fungi is targeted by AFP. Here we show that the N-terminal domain of AFP (amino acids 1 to 33) is sufficient for efficient binding of AFP to chitin but is not adequate for inhibition of the growth of sensitive fungi. AFP susceptibility tests and SYTOX Green uptake experiments with class III and class V chitin synthase mutants of Fusarium oxysporum and Aspergillus oryzae showed that deletions made the fungi less sensitive to AFP and its membrane permeabilization effect. In situ chitin synthase activity assays revealed that chitin synthesis is specifically inhibited by AFP in sensitive fungi, indicating that AFP causes cell wall stress and disturbs cell integrity. Further evidence that there was AFP-induced cell wall stress was obtained by using an Aspergillus niger reporter strain in which the cell wall integrity pathway was strongly induced by AFP.
引用
收藏
页码:2128 / 2134
页数:7
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