Method for extracting ice structuring proteins (ISPs) from winter wheat in cold region
A technology for ice-structured protein and winter wheat, which is applied in the preparation methods of peptides, chemical instruments and methods, plant peptides, etc., can solve the problems of high cost, limited raw materials for ice-structured protein extraction, and complicated extraction process, and achieves diverse and good shapes. Ice crystal modification properties, the effect of small ice crystal size
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specific Embodiment approach 1
[0024] Specific embodiment one: the present embodiment extracts the method for ice structure protein from winter wheat in cold region and carries out according to the following steps:
[0025] 1. Preparation of ice puck
[0026] Place glass balls in each ice hole of the silicone ice tray, pour distilled water into the ice holes, and then freeze in a -18°C refrigerator to obtain ice balls;
[0027] 2. Extraction of winter wheat ISPs in cold regions
[0028] According to the ratio of solid to liquid: 1g: (10-30mL), mix cold winter wheat flour with phosphate buffer solution, stir and extract at room temperature for 0.5-3.0h, and then centrifuge for 14-16min in a centrifuge to obtain a supernatant;
[0029] 3. Ice puck extraction
[0030] Add the ice ball prepared in step 1 to the supernatant of step 2, put it in a refrigerator at -18°C, and extract it on ice for 2 to 4 minutes. At this time, the ice structure protein adsorbed by the ice ball reaches saturation. extract, and ob...
specific Embodiment approach 2
[0039] Specific embodiment 2: The difference between this embodiment and specific embodiment 1 is: the diameter of the glass ball described in step 1 is 1 cm; the diameter of the obtained ice ball is 2 cm; the temperature resistance of the silica gel ice tray is -40°C Silicone ice tray, the silicone ice tray is plate-shaped, with a length of 24cm and a width of 7.3cm. There are 10×2 spherical ice holes on the plate, and the inner diameter of each ice hole is 2cm. Other steps and parameters are the same as those in the first embodiment.
specific Embodiment approach 3
[0040] Embodiment 3: The difference between this embodiment and Embodiment 1 or 2 is that the pH of the phosphate buffer solution in Step 2 is 7.2-8.0, and the phosphate concentration is 60-140 mmol / L. Other steps and parameters are the same as those in Embodiment 1 or 2.
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