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Scientia Silvae Sinicae ›› 2012, Vol. 48 ›› Issue (9): 88-94.doi: 10.11707/j.1001-7488.20120914

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Inhibiting Effects and Mechanism of Trichoderma Strains to Cytospora chrysosperma

Li Chongwei1,2, Yang Libin1,3, Deng Xun4, Ilan Chet5, Song Ruiqing1   

  1. 1. College of Forestry, Northeast Forestry University Harbin 150040;2. Key Laboratory of Microbiology, College of Life Sciences, Heilongjiang University Harbin 150080;3. Heilongjiang Academy of Land Reclamation Sciences Harbin 150038;4. Forestry Protection Institute of Heilongjiang Forestry Academy Harbin 150040;5. Faculty of Agriculture, Hebrew University of Jerusalem Rehovot 76100 Israel
  • Received:2011-09-22 Revised:2012-02-11 Online:2012-09-25 Published:2012-09-25

Abstract:

Three Trichoderma strains, T-33,T-14,T-09, which have inhibiting effects on Cytospora chrysosperma, were derived from 29 domestic and foreign strains with methods of antagonistic culture and growth-inhibition. The extracts obviously inhibited mycelium growth and conidia germination of Cytospore chrysosperma were gained. The effect of the most highly efficient extract on pathogen’s cell physiological indicators and protective enzyme activities was systematically studied. The growth-inhibiting rate of the substances extracted from the fermented liquid of strain T-33 was 94%, and the extract also had an inhibiting effect on spore germination. The extract was able to increase the electrical conductivity and MDA content of the pathogen significantly, reduce the protein content and activity of SDH, PK, HK, LDH, MDH, and coenzyme I, and cause a sharp decline in Na+、K+-ATP, Mg2+-ATP and Ca2+-ATP enzymes activities. The results indicated that the pathogen cell membrane would be severely peroxided, and some metabolic pathways such as glycolysis, TCA cycle, electron transport and oxidative phosphorylation, would be restricted. Finally, the extract inhibited pathogen growth by destroying the pathogen’s protection system and metabolic pathways.

Key words: Trichoderma, extract, Cytospora chrysosperma, inhibiting mechanism

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