Production of β-1,3-glucanase and chitosanase from clostridial strains isolated from the soil subjected to biological disinfestation
Autor: | Nobuo Kaku, Gen Ishioka, Katsuji Ueki, Toshiaki Takehara, Atsuko Ueki |
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Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: |
0106 biological sciences
lcsh:Biotechnology Biophysics lcsh:QR1-502 Polysaccharide 01 natural sciences Applied Microbiology and Biotechnology lcsh:Microbiology Microbiology Cell wall 03 medical and health sciences Anaerobic soil disinfestation 010608 biotechnology lcsh:TP248.13-248.65 Fusarium oxysporum Chitosanase Pathogen 030304 developmental biology chemistry.chemical_classification 0303 health sciences biology Chemistry β-1 3-Glucanase food and beverages Glucanase biology.organism_classification Anaerobic bacteria Clostridium beijerinckii Clostridium beijerinckii Fusarium oxysporum f. sp. spinaciae Original Article Biocontrol of soil-borne pathogen |
Zdroj: | AMB Express, Vol 9, Iss 1, Pp 1-14 (2019) AMB Express SC30202003180006 NARO成果DBa |
ISSN: | 2191-0855 |
Popis: | Biological soil disinfestation (BSD) or anaerobic (reductive) soil disinfestation (ASD/RSD) is a bioremediation method used to eliminate soil-borne plant pathogens by exploiting the activities of anaerobic bacteria in soil. In this study, two obligate anaerobic bacterial strains isolated from BSD-treated soil and identified as Clostridium beijerinckii were examined for their abilities to suppress the spinach wilt disease pathogen (Fusarium oxysporum f. sp. spinaciae) as a representative soil-borne fungal plant pathogen. Both strains degraded β-1,3-glucan and chitosan, two major polysaccharide components of ascomycetes fungal cell wall, supplemented in the medium. β-1,3-Glucanase was detected in the supernatants of cultures supplemented with different types of glucan. Similarly, chitosanase was detected in cultures supplemented with chitosan. Both the enzyme activities were also detected in cultures containing glucose as a substrate. Live cells of F. oxysporum f. sp. spinaciae that were co-incubated with each anaerobic strain under anaerobic conditions using glucose as a substrate died during incubation. Freeze-dried dead fungal biomass of the pathogen, when added to the culture, supported good growth of both anaerobes and production of both enzymes. Severe and nearly complete degradation of both live and dead fungal cells during incubation with anaerobic bacteria was observed by fluorescence microscopy. When individual anaerobic bacterial strain was co-incubated with live pathogenic fungal cells in wheat bran, a popular material for BSD-treatment, both the strains grew well and killed the fungal pathogen promptly by producing both enzymes. These results indicate that both the bacterial strains attack the fungal cells by releasing extracellular fungal cell wall-degrading enzymes, thereby eliminating the pathogen. |
Databáze: | OpenAIRE |
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