Saccharomycete cell wall breaking method
A yeast and cell technology, applied in the field of microorganisms, can solve problems such as unfavorable food processing and production, and achieve the effects of low cost, simple operation and obvious effect.
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[0030] Example 1: Weigh 1.0 g of yeast, add reaction buffer to 5.0 mL, add 10 μL of toluene and mix for 2 min, shake at 37° C. and 120 rpm for 60 min to break the wall. That is, the toluene-broken enzyme liquid is obtained.
Example Embodiment
[0031] Example 2: Weigh 1.0 g of yeast, add reaction buffer to 5.0 mL, add 0.01 g / L complex enzyme and mix for 2 min, shake and break the wall at 37°C, pH 5.5, 120 rpm for 60 min. That is, the enzyme solution in which the composite enzyme is broken is obtained.
[0032] Wherein, the composition of each component in the compound enzyme is: 5% helicase, 70% lysozyme, 10% mannanase, and 15% dextranase.
Example Embodiment
[0033] Example 3: Weigh 1.0 g of yeast, add reaction buffer to 5.0 mL, add 0.02 g / L complex enzyme and mix for 2 min, shake and break the wall at 37°C, pH 5.5, 120 rpm for 60 min. That is, the enzyme solution in which the composite enzyme is broken is obtained.
[0034] Wherein, the composition of each component in the compound enzyme is: 5% helicase, 70% lysozyme, 10% mannanase, and 15% dextranase.
[0035] The enzyme activity after breaking the wall with toluene in Example 1 was calculated as 100%.
[0036] Yeast relative breaking rate (%)=(A / B)*100%
[0037] A: Compound Enzyme Breaking Fluid β-Galactosidase Enzyme Activity
[0038] B: β-galactosidase activity in toluene wall breaking solution
[0039] Table 1 Effect of 0.1% compound enzyme on yeast wall breaking
[0040]
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