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Tytuł pozycji:

Antagonistic effects of Bacillus cereus strain B-02 on morphology, ultrastructure and cytophysiology of Botrytis cinerea

Tytuł:
Antagonistic effects of Bacillus cereus strain B-02 on morphology, ultrastructure and cytophysiology of Botrytis cinerea
Autorzy:
Li F.-X.
Ma H.-Q.
Liu J.
Zhang C.
Tematy:
antagonistic effect
Bacillus cereus
B-02 strain
morphology
ultrastructure
cytophysiology
Botrytis cinerea
Botrytis cereus
gray mould
greenhouse
tomato
chemical control
Język:
angielski
Dostawca treści:
AGRO
Artykuł
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The study on antagonistic mechanism of biocontrol strains gives the premise and basis for efficient and stable biological control. This study aimes to overcome of biocontrol agent in aspects of complicated and diversified mode of action, short-lasting and unstable efficacy in the production processes. This study elucidated the antagonistic mechanism of Bacillus cereus strain B-02 on Botrytis cinerea by detecting changes in morphology, ultrastructure and physiology in affected hyphae of Botrytis cinerea. Which provided certain theoretical and practical significance for biological control of gray mould caused by B. cinerea. B. cereus strain B-02 isolated from tomato rhizosphere mightily suppressed gray mold in tomato caused by B. cinerea. Spore germination and hyphal growth of B. cinerea were inhibited by B. cereus strain B-02. Changes of cell morphology such as distortion, shrinking and swelling were observed by SEM. TEM observation further indicated the ultrastructural alterations of hyphae, including mitochondrion reduction, un-membranous inclusion in cytoplasm, considerable thickening of cell walls, and electronic density enhancement. LSCM observation revealed the fluorescence intensity of nucleus DNA, mitochondrion DNA and reactive oxygen radical in treated hyphae were all stronger than control and the difference was significant (P < 0.01). These results indicated that the antagonistic effects of B. cereus strain B-02 on B. cinerea were likely due to a combination of abnormal synthesis of nucleus DNA and mitochondrion DNA and multifarious ultrastructural alterations in hyphal cell.

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