A test paper for detecting alkaline xylanase activity and its preparation method
A technology for xylanase and xylan, which is applied to biochemical equipment and methods, measuring devices, and determination/inspection of microorganisms, can solve problems such as measurement difficulties, and achieves simple preparation process, easy operation, and good application prospects. Effect
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[0026] Taking the alkaline xylanase produced by the fermentation of modified Trichoderma reesei ATCC56765 as an example, the crude enzyme activity of the xylanase is 80-100U / mL, and the optimum pH is 7.8;
[0027] (1) Prepare DNS chromogenic reagent, sodium dihydrogen phosphate-disodium hydrogen phosphate buffer solution with pH=7.80, and on this basis prepare alkaline xylan standard solution, xylanase standard solution and different concentration gradients Alkaline xylanase solution;
[0028] The preparation method of the DNS developer is as follows: liquid A: dissolve 6.90 g of crystalline phenol in 15.2 mL of 10% NaOH solution, dilute to 69 mL with distilled water, and add 6.90 g of sodium bisulfite to the solution. Solution B: Dissolve 255 g of potassium sodium tartrate in 300 mL of 10% NaOH solution, and then add 880 mL of 1% 3,5-dinitrosalicylic acid solution. Mix the two solutions of A and B to obtain the yellow reagent, which is stored in a brown bottle for 7-10 days ...
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