Method for degrading ligno-cellulose and special cellulose decomposing bacteria therefor
A technology of cellulolytic bacteria and lignocellulose, applied in the direction of using microorganisms, methods based on microorganisms, biochemical equipment and methods, etc., can solve the problems of difficult to achieve pure culture of microorganisms, obtain sample microbial population information, etc., to achieve Promote the development of animal husbandry, significant economic value and social significance, and the effect of maintaining soil fertility
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Embodiment 1
[0027] Embodiment 1, the acquisition of cellulolytic strain L-A
[0028] Each liter of medium contains the following components: yeast powder, 5g; casein peptone, 1.5g; K 2 HPO 4 , 1.5g; MgSO 4 ·7H 2 O, 0.5g; CaCl 2 ·H 2 O, 1 g; NaHCO 3 , 0.9g; NaCl, 0.6g; NH 4 Cl, 0.6g; FeCl 3 , 0.006g; pH7.2.
[0029] The preparation method of the medium is: FeCl 3 Prepared as a 1g / L storage solution. Weigh the remaining corresponding medicine in proportion and pour it into a beaker filled with tap water in advance. After the medicine is fully dissolved, dilute to 990ml with tap water, and add 6ml of FeCl 3 Store the solution, adjust the pH to 7.2, and finally adjust the volume to 1000ml.
[0030] Distribute each 10ml of culture medium into 18×180mm common test tubes (with 12×100mm filter paper strips placed in advance).
[0031] 1. Obtaining of cellulolytic strain L-A
[0032] 0.5 g of anaerobic activated sludge sample collected from Guangxi cassava alcohol waste liquid UASB-TL...
Embodiment 2
[0078] Embodiment 2, the culture temperature optimization of cellulolytic strain L-A
[0079] Each liter of medium contains the following components: yeast powder, 5g; casein peptone, 1.5g; K 2 HPO 4 , 1.5g; MgSO 4 ·7H 2 O, 0.5g; CaCl 2 ·H 2 O, 1 g; NaHCO 3 , 0.9g; NaCl, 0.6g; NH 4 Cl, 0.6g; FeCl 3 , 0.006g; pH7.2.
[0080] The preparation method of the medium is: FeCl 3 Prepared as a 1g / L storage solution. Weigh the remaining corresponding medicine in proportion and pour it into a beaker filled with tap water in advance. After the medicine is fully dissolved, dilute to 990ml with tap water, and add 6ml of FeCl 3 Store the solution, adjust the pH to 7.2, and finally adjust the volume to 1000ml.
[0081] Distribute each 10ml of culture medium into 18×180mm common test tubes (with 12×100mm filter paper strips placed in advance).
[0082] The cellulolytic strain L-A obtained in step 1 of Example 1 was inoculated into test tubes containing medium, the inoculum amount w...
Embodiment 3
[0084] Embodiment 3, cellulolytic strain L-A degrades lignocellulose
[0085]Each liter of medium contains the following components: yeast powder, 1g; casein peptone, 1g; K 2 HPO 4 , 0.1g; MgSO 4 ·7H 2 O, 0.1g; CaCl 2 ·H 2 O, 0.5g; NaHCO 3 , 0.2g; NaCl, 0.1g; NH 4 Cl, 0.1g; FeCl 3 , 0.001g; pH6.8.
[0086] The preparation method of the medium is: FeCl 3 Prepared as a 1g / L storage solution. Weigh the remaining corresponding medicine in proportion and pour it into a beaker filled with tap water in advance. After the medicine is fully dissolved, use tap water to make the volume to 990ml, and add 1ml of FeCl 3 Store the solution, adjust the pH to 6.8, and finally adjust the volume to 1000ml.
[0087] Distribute each 10ml of culture medium into 18×180mm common test tubes.
[0088] Take 30 test tubes filled with culture medium and divide them into three groups, 10 tubes in each group. Dried straw was added to the first set of test tubes (0.1 g of dried straw was added t...
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