Chitin nanofiber/Nisin composite preservative based on transglutaminase induced crosslinking and preparation method
A technology of transglutaminase and nanofibers, which is applied in fiber processing, animal fiber, biochemical fiber processing, etc., can solve the problems of non-compliance with green safety and safety to be verified, and achieve stable structure, safe source of raw materials, and improved The effect of antibacterial activity
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[0028] The invention provides a chitin nanofiber / Nisin composite preservative based on transglutaminase-induced crosslinking and a preparation method thereof, comprising the following steps:
[0029] Preparation of S1 chitin nanofibers:
[0030] Disperse the chitin powder in 33% (w / v) sodium hydroxide and 0.3% sodium borohydride (w / v), in a water bath at 90°C, magnetically stir for 4 hours, and the obtained chitin solution is suction filtered , washing, the obtained residue was dried in an oven at 45° C. for 1 h, dissolved with 1% (v / v) acetic acid solution, ultrasonically treated for 1 h, left to stand for 30 min, and the supernatant was taken out and freeze-dried to obtain chitin nanofibers;
[0031] Preparation of S2 transglutaminase-induced cross-linked chitin nanofiber / Nisin composite preservative:
[0032] Put the chitin nanofibers described in S1 in 1% glacial acetic acid solution (v / v), and use ultrasonic treatment for 1 h to prepare a chitin nanofiber solution with a...
Embodiment 1
[0041] Preparation of S1 chitin nanofibers:
[0042] The chitin powder was dispersed in 33% (w / v) sodium hydroxide and 0.3% sodium borohydride (w / v), in a water bath at 90°C, and magnetically stirred for 4 hours. The solution was suctioned, filtered, and washed with deionized water until the filtrate was clear and colorless. The collected residue was dried in an oven at 45° C. for 1 h, dissolved with 1% (v / v) acetic acid solution, ultrasonically treated for 1 h, allowed to stand for 30 min, and the supernatant was taken out and freeze-dried for 24 h to obtain chitin nanofibers.
[0043] Preparation of S2 transglutaminase-induced cross-linked chitin nanofiber / Nisin composite preservative:
[0044] The prepared chitin nanofibers were placed in 1% glacial acetic acid solution (v / v), and ultrasonically treated for 1 h to prepare a chitin nanofiber solution with a concentration of 2.4 mg / mL. Add Nisin and 0.4% transglutaminase (m / m, based on the dry matter of Nisin) to the above ...
Embodiment 2
[0046] Preparation of S1 chitin nanofibers:
[0047] The chitin powder was dispersed in 33% (w / v) sodium hydroxide and 0.3% sodium borohydride (w / v), in a water bath at 90°C, and magnetically stirred for 4 hours. The solution was suctioned, filtered, and washed with deionized water until the filtrate was clear and colorless. The collected residue was dried in an oven at 45° C. for 1 h, dissolved with 1% (v / v) acetic acid solution, ultrasonically treated for 1 h, allowed to stand for 30 min, and the supernatant was taken out and freeze-dried for 24 h to obtain chitin nanofibers.
[0048] Preparation of S2 transglutaminase-induced cross-linked chitin nanofiber / Nisin composite preservative:
[0049] The prepared chitin nanofibers were placed in 1% glacial acetic acid solution (v / v), and ultrasonically treated for 1 h to prepare a chitin nanofiber solution with a concentration of 2.4 mg / mL. Add Nisin and 0.4% transglutaminase (m / m, based on the dry matter of Nisin) to the above ...
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