Screening of High Exopolysaccharide Yield Strain of Boletus edulis by UV Ray
Wenqiang Chen
Abstract
Wenqiang Chen
Abstract
To enhance the exopolysaccharide production by Boletus edulis,the strain was mutagenized by using UV-irradiation was performed,and the conditions for it s protoplast preparation and regeneration of the mycelium incubation time,enzyme concentration,enzyme temperature,enzyme time,and osmotic stabilizer were examined.The result s showed that the mycelia incubated for 56 h were most suitable for protoplast release.The mixture solution of 1% fiber enzyme/1% snail enzyme and(0.010 92) g/mL mannitol was the most effective osmotic stabilizer and was most favorable for protoplast preparation.The suitable incubation temperature and time for the release of protoplast was 30~35 ℃ and 2 h.With the optimum conditions,the protoplasts and the regeneration rate was 3.71×10~5 and 7.32%,respectively.Compared with that of parent strain,the yield of exopolysaccharide production by mutant strains increase 30.4%.
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To enhance the exopolysaccharide production by Boletus edulis,the strain was mutagenized by using UV-irradiation was performed,and the conditions for it s protoplast preparation and regeneration of the mycelium incubation time,enzyme concentration,enzyme temperature,enzyme time,and osmotic stabilizer were examined.The result s showed that the mycelia incubated for 56 h were most suitable for protoplast release.The mixture solution of 1% fiber enzyme/1% snail enzyme and(0.010 92) g/mL mannitol was the most effective osmotic stabilizer and was most favorable for protoplast preparation.The suitable incubation temperature and time for the release of protoplast was 30~35 ℃ and 2 h.With the optimum conditions,the protoplasts and the regeneration rate was 3.71×10~5 and 7.32%,respectively.Compared with that of parent strain,the yield of exopolysaccharide production by mutant strains increase 30.4%.
Key concepts: Protoplast, Mycelium, Mannitol, Strain (injury), Enzyme, Incubation, Enzyme assay, Yield (engineering)