Method for separating urokinase from human urinary trypsin inhibitor
A trypsin inhibition and separation method technology, applied in the separation field of urokinase and human urinary trypsin inhibitor, can solve the problems of large loss of activity, decreased product quality, long cycle, etc., and achieves improved specific activity, low cost, and time. short effect
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Embodiment 1
[0027] Mix 10 grams of UK crude product (31,500 U / g) and 10 grams of UTI crude product (23,300 U / g), add 100ml of deionized water, stir to dissolve, centrifuge to collect 92ml of supernatant, and use 1N NaOH solution to adjust the pH to 8.4; slowly add 16% (w / v) ammonium sulfate powder, while adding ammonium sulfate powder, stir to dissolve it, and protein precipitation appears in the solution, then add 4.6g ammonium sulfate powder, stir After dissolving, adjust the pH to 8.4 with 1N NaOH solution, and let it stand for 2 hours; centrifuge at 3000rpm for 10 minutes, collect the precipitate 1, continue to add ammonium sulfate powder to the supernatant to 60% (w / v), let it stand for 2 hours, 3000rpm Centrifuge for 10 minutes to collect pellet 2.
[0028] The activities of UK and UTI in precipitation 1 and precipitation 2 were determined, see Table 1.
[0029] Table 1:
[0030]
[0031] It can be seen from Table 1 that UK is mainly concentrated in Precipitation 1 with ...
Embodiment 2
[0033] Mix 10 grams of UK crude product (37,200 U / g) and 10 grams of UTI crude product (19,500 U / g), add 100ml of deionized water, stir to dissolve, centrifuge to collect 93ml of supernatant, and use 1N Adjust the pH to 9.6 with NaOH solution; slowly add 30% (w / v) ammonium sulfate powder, while adding ammonium sulfate powder, stir to dissolve it, then adjust the pH to 9.6 with 1N NaOH solution, and let it stand for 6 hours; 3000rpm Centrifuge for 10 minutes to collect the precipitate 1, continue to add ammonium sulfate powder to the supernatant to 55% (w / v), let stand for 2 hours, then centrifuge at 3000rpm for 10 minutes, and collect the precipitate 2.
[0034] The activities of UK and UTI in precipitation 1 and precipitation 2 were determined, see Table 2.
[0035] Table 2:
[0036]
[0037] It can be seen from Table 2 that UK is mainly concentrated in Precipitation 1 with a yield of about 95%, and UTI is mainly concentrated in Precipitation 2 with a yield of more...
Embodiment 3
[0039] Add 10.2kg of UK crude product mixed with UTI, add 50kg of deionized water, stir to dissolve, centrifuge to collect 46L of supernatant, adjust the pH of the supernatant to 9.0 with 1N NaOH solution; slowly add saturated ammonium sulfate solution, Stir while adding, until obvious protein precipitation appears in the solution, then add 3.5L saturated ammonium sulfate solution, adjust the pH to 9.0 with 1N NaOH solution, and let it stand for 2 hours; add diatomaceous earth for plate and frame filtration, and collect the precipitate 1 , add ammonium sulfate powder to the supernatant to 60% (w / v), let it stand for 6 hours, add diatomaceous earth for plate and frame filtration, and collect the precipitate 2. Ammonia solution can also be used to adjust the pH.
[0040] The activities of UK and UTI in precipitation 1 and precipitation 2 were determined, see Table 3.
[0041] table 3:
[0042]
[0043] It can be seen from Table 3 that UK is mainly concentrated in pre...
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