Penicillium strain producing cellulase and application in cellulose enzymatic hydrolysis thereof
A technology of cellulase and cellulose, which is applied in the field of microorganisms, can solve the problems such as the limited ability of Penicillium to hydrolyze cellulose, and achieve the effect of improving activity and high activity
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Embodiment 1
[0037] Embodiment 1: the cultivation of departure bacterial strain
[0038] The Penicillium strain with cellulase production ability was subcultured, and after continuous activation for 3 times, it was inserted into the liquid medium and cultured with shaking at 30°C overnight.
[0039] The components and dosage in the medium are: bran 100g / L, glucose 10g / L, and the rest is water.
Embodiment 2
[0040] Embodiment 2: the pretreatment of bacterial classification
[0041] Centrifuge the bacterium solution obtained in Example 1 to remove the culture medium, resuspend the obtained bacterium with physiological saline to configure the bacterium suspension, and connect it to a sterilized Erlenmeyer flask covered with glass beads, at room temperature Shake for 5 minutes to disperse the bacterial cells, filter with sterilized gauze, serially dilute, count until the cell concentration is 106-107 / ml, and set aside.
Embodiment 3
[0042] Embodiment 3: UV mutagenesis
[0043] Turn on the UV lamp 20 minutes in advance to stabilize the light wave.
[0044] Get the bacterium suspension 5-6ml that embodiment 2 makes and join in the 9cm petri dish, guarantee the bacterium liquid thickness 2-3cm, put the petri dish on the magnetic stirrer, put into the aseptic stirrer in the petri dish.
[0045] Open the lid of the petri dish, 20-30cm away from the UV lamp, and irradiate for 30, 60, 90, 120, 150, 180s respectively while stirring.
[0046] Select 0.1ml of the bacterial suspension that has been irradiated by ultraviolet radiation for different periods of time, add it to 0.9ml sterile normal saline to dilute, and put it in an ice bath for 1-2h.
[0047] Take 0.1ml of the ice-bathed bacterial suspension and spread it on a flat plate containing 100g / L bran juice and 1-5g / L lithium chloride for preliminary screening and separation, and cultivate at 30°C for 3 days.
[0048] Select about 200 colonies of different s...
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