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Predominant secretion of cellobiohydrolases and endo-β-1,4-glucanases in nutrient-limited medium by Aspergillus spp. isolated from subtropical field
- Source :
- The Journal of Biochemistry. 168:243-256
- Publication Year :
- 2020
- Publisher :
- Oxford University Press (OUP), 2020.
-
Abstract
- Biological degradation of cellulose from dead plants in nature and plant biomass from agricultural and food-industry waste is important for sustainable carbon recirculation. This study aimed at searching diverse cellulose-degrading systems of wild filamentous fungi and obtaining fungal lines useful for cellooligosaccharide production from agro-industrial wastes. Fungal lines with cellulolytic activity were screened and isolated from stacked rice straw and soil in subtropical fields. Among 13 isolated lines, in liquid culture with a nutrition-limited cellulose-containing medium, four lines of Aspergillus spp. secreted 50–60 kDa proteins as markedly dominant components and gave clear activity bands of possible endo-β-1,4-glucanase in zymography. Mass spectroscopy (MS) analysis of the dominant components identified three endo-β-1,4-glucanases (GH5, GH7 and GH12) and two cellobiohydrolases (GH6 and GH7). Cellulose degradation by the secreted proteins was analysed by LC-MS-based measurement of derivatized reducing sugars. The enzymes from the four Aspergillus spp. produced cellobiose from crystalline cellulose and cellotriose at a low level compared with cellobiose. Moreover, though smaller than that from crystalline cellulose, the enzymes of two representative lines degraded powdered rice straw and produced cellobiose. These fungal lines and enzymes would be effective for production of cellooligosaccharides as cellulose degradation-intermediates with added value other than glucose.
- Subjects :
- Bodily Secretions
Cellobiose
Oligosaccharides
Biomass
Biochemistry
Fungal Proteins
03 medical and health sciences
chemistry.chemical_compound
Nutrient
Cellulase
Trioses
Cellulose 1,4-beta-Cellobiosidase
Zymography
Food science
Cellulose
Molecular Biology
Soil Microbiology
030304 developmental biology
chemistry.chemical_classification
0303 health sciences
Aspergillus
biology
030306 microbiology
Hydrolysis
Oryza
Nutrients
General Medicine
biology.organism_classification
Culture Media
Biodegradation, Environmental
Enzyme
Secretory protein
chemistry
Subjects
Details
- ISSN :
- 17562651 and 0021924X
- Volume :
- 168
- Database :
- OpenAIRE
- Journal :
- The Journal of Biochemistry
- Accession number :
- edsair.doi.dedup.....ea59963656b52a0dc7edc8532b60031a
- Full Text :
- https://doi.org/10.1093/jb/mvaa049