عنوان المقالة:Domiciliation of Trichoderma asperellum Suppresses Globiosporangium ultimum and Promotes Pea Growth, Ultrastructure, and Metabolic Features Domiciliation of Trichoderma asperellum Suppresses Globiosporangium ultimum and Promotes Pea Growth, Ultrastructure, and Metabolic Features
د زياد موسى عبد المعطي | Zeiad Moussa Abd El-Moati | 6803
- نوع النشر
- مقال علمي
- المؤلفون بالعربي
- الملخص الانجليزي
- The beneficial microorganisms represent a new and hopeful solution for a sustainable environment and development. In this investigation, Trichoderma asperellum ZNW, isolated from seeds, was domiciliated within the pea plant for improving growth, disease management, and enhancement of productivity. Globisporangium ultimum NZW was isolated from deformed pea seeds, representing the first record of the pathogen caused by pea damping-off. Both fungi were molecularly identified. T. asperellum ZNW produced several lytic enzymes and bioactive metabolites as detected by GC-MC. The SEM illustrated the mycoparasitic behavior of T. asperellum ZNW on G. ultimum NZW mycelia. In the pot experiment, T. asperellum domiciliated the root and grew as an endophytic fungus, leading to root vessel lignification. Under soil infection, T. asperellum reduced damping-off, by enhancing peroxidase, polyphenol, total phenols, and photosynthetic pigments content. The vegetative growth, yield, and soil dehydrogenase activity were improved, with an enhancement in the numerical diversity of the microbial rhizosphere. This work may enable more understanding of the plant-fungal interaction, yet, working on domiciliation is recommended as a new approach to plant protection and growth promotion under various ecological setups.
- تاريخ النشر
- 12/01/2023
- الناشر
- microorganisms mdpi
- رقم المجلد
- 11
- رقم العدد
- رابط DOI
- 10.3390/microorganisms11010198
- الصفحات
- 198
- رابط الملف
- تحميل (0 مرات التحميل)
- رابط خارجي
- https://www.mdpi.com/2076-2607/11/1/198
- الكلمات المفتاحية
- Globisporangium ultimum; hydrolytic enzymes; mycoparasitism; GC-MS; electron microscopy; dehydrogenase; microbial community