The Trichoderma viride F-00612 consortium tolerates 2-amino-3H-phenoxazin-3-one and degrades nitrated benzo[d]oxazol-2(3H)-one
Autor: | Laura Laschke, Vadim Schütz, Margot Schulz, Andrii P. Gryganskyi, Nataliya Voloshchuk |
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Rok vydání: | 2020 |
Předmět: |
0106 biological sciences
0303 health sciences food.ingredient biology medicine.drug_class Trichoderma viride Antibiotics Picolinic acid biology.organism_classification 01 natural sciences Biochemistry Microbiology 03 medical and health sciences chemistry.chemical_compound food chemistry Nitration medicine Agar Acinetobacter calcoaceticus Ecology Evolution Behavior and Systematics Allelopathy Bacteria 030304 developmental biology 010606 plant biology & botany |
Zdroj: | Chemoecology. 30:79-88 |
ISSN: | 1423-0445 0937-7409 |
DOI: | 10.1007/s00049-020-00300-w |
Popis: | Numerous allelopathic plant secondary metabolites impact plant–microorganism interactions by injuring plant-associated beneficial bacteria and fungi. Fungi belonging to the genus Trichoderma positively influence crops, including benzoxazinone-containing maize. However, benzoxazinones and their downstream metabolites such as benzoxazolinone and phenoxazinones are often fungitoxic. Specimen Trichoderma viride F-00612 was found to be insensitive to 100-µM phenoxazinone and 500-µM benzoxazolinone. Screening of 46 additional specimens of ascomycetes revealed insensitivity to phenoxazinones among fungi that cause disease in benzoxazinone-producing cereal crops, whereas many other ascomycetes were highly sensitive. In contrast, most of the screened fungi were insensitive to benzoxazolinone. T. viride F-00612 was associated with bacteria and, thus, existed as a consortium. By contrast, Enterobacter species and Acinetobacter calcoaceticus were prominent in the original specimen, and Bacillus species predominated after antibiotic application. Prolonged cultivation of T. viride F-00612 in liquid medium and on Czapek agar in the presence of T. viride F-00612 consortium may contribute to the ability to manage benzoxazinone downstream products and facilitate BOA-6-OH degradation via nitration. |
Databáze: | OpenAIRE |
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