Method for producing xylanase by anaerobic fermentation of corn straws
A technology of xylanase and anaerobic fermentation, which is applied in the field of anaerobic fermentation of corn stalks to produce xylanase, which can solve the problem of unsatisfactory effect of compound flora of artificial components, poor treatment effect of single microorganism, and long pretreatment time and other issues, to achieve important industrial application value and development prospects, high-efficiency lignocellulose degradation ability, and low equipment requirements
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Embodiment 1
[0028] Embodiment one, Piromyces Yak TZ +M. ruminantium Preparation of bacteria.
[0029] Draw 1mL Piromyces Yak TZ +M. ruminantium The co-culture was inoculated into 9 mL of anaerobic medium based on air-dried and pulverized wheat straw in a 20 mL Heinz anaerobic tube, and compound antibiotics were added at the same time to make the final concentration of the anaerobic medium solution be Penicillin 1600 IU / mL and streptomycin sulfate 2000 IU / mL. After anaerobic culture at 39°C for 72 hours, the growth peak is reached, and the fermentation broth is a high-activity bacterial agent at this time.
Embodiment 2
[0030] Example 2: Production of xylanase by anaerobic fermentation of corn stalks.
[0031] 45 mL of liquid basic medium was placed in a 100 mL volume anaerobic fermentation bottle, and 0.5 g of crushed and air-dried corn stover was used as the substrate. Deoxygenation. Sterilize. Subcultured for 72 h Piromyces Yak TZ +M. ruminantium Use a sterile syringe to draw 5 mL of the co-culture and inoculate it into the above-mentioned anaerobic medium with corn stalks. At the same time, add compound antibiotics so that the final concentration in the anaerobic medium solution is 1600 IU / mL of penicillin and streptomycin sulfate. 2000 IU / mL, cultured anaerobically at 39 °C for 7 days.
[0032] The fermentation broth of the co-culture was 1000× g After centrifugation for 10 min, the supernatant was taken as the crude enzyme solution, and the xylanase activity was determined by the DNS method with a spectrophotometer. The specific method is as follows: diluted crude enzyme solution...
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