Modified protocatechuic acid liposome for preservation and fresh keeping of shrimps and crabs, and preparation method and application of modified protocatechuic acid liposome
A catechin, storage and preservation technology, applied in biochemical equipment and methods, microorganism-based methods, preservation of meat/fish with acid, etc., can solve problems such as physical and chemical instability, particle size changes, core material leakage, etc. , to achieve the effect of improving chemical stability, increasing viscosity and preventing ice crystal damage
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Embodiment 1
[0073] Bacterial cellulose was prepared by the following steps:
[0074] (i) prepare culture medium according to the following formula:
[0075] Slant medium: glucose 20g / L, peptone 5g / L, yeast powder 5g / L, disodium hydrogen phosphate 2g / L, citric acid 1g / L, agar 20g / L, calcium carbonate 0.5g / L; pH 6.2; Sterilize at 121°C and 0.1MPa for 30 minutes;
[0076] Seed medium: 20g / L sucrose, 5g / L peptone, 5g / L yeast powder, 2g / L disodium hydrogen phosphate, 1g / L citric acid; pH is 6.2; sterilize at 121℃, 0.1MPa for 30min;
[0077] The fermentation medium includes the following components: sucrose 20g / L, peptone 8g / L, yeast powder 10.55g / L, disodium hydrogen phosphate 2.7g / L, citric acid 1g / L; pH is 6.2; 121°C, 0.1MPa Sterilize for 30 minutes;
[0078] (ii) Activation: Acetobacter xylinum was inoculated on the slant medium, and after culturing in a 29° C. incubator for 54 hours, an activated strain was obtained;
[0079] (iii) Seed culture: Pick the 3-ring activated strain and ino...
Embodiment 2
[0093] Bacterial cellulose was prepared by the following steps:
[0094] (i) prepare culture medium according to the following formula:
[0095] Slant medium: glucose 20g / L, peptone 5g / L, yeast powder 5g / L, disodium hydrogen phosphate 2g / L, citric acid 1g / L, agar 20g / L, calcium carbonate 0.5g / L; pH 6.0; Sterilize at 121°C and 0.1MPa for 30 minutes;
[0096] Seed medium: sucrose 20g / L, peptone 5g / L, yeast powder 5g / L, disodium hydrogen phosphate 2g / L, citric acid 1g / L; pH is 6.0; sterilize at 121℃, 0.1MPa for 30min;
[0097] The fermentation medium includes the following components: sucrose 20g / L, peptone 8g / L, yeast powder 10.55g / L, disodium hydrogen phosphate 2.7g / L, citric acid 1g / L; pH is 6.0; 121°C, 0.1MPa Sterilize for 30 minutes;
[0098] (ii) Activation: Acetobacter xylinum was inoculated on the slant medium, and after culturing in a 28° C. incubator for 48 hours, an activated strain was obtained;
[0099] (iii) Seed culture: Pick the 3-ring activated strain and ino...
Embodiment 3
[0113] Bacterial cellulose was prepared by the following steps:
[0114] (i) prepare culture medium according to the following formula:
[0115] Slant medium: glucose 20g / L, peptone 5g / L, yeast powder 5g / L, disodium hydrogen phosphate 2g / L, citric acid 1g / L, agar 20g / L, calcium carbonate 0.5g / L; pH 6.5; Sterilize at 121°C and 0.1MPa for 30 minutes;
[0116] Seed medium: sucrose 20g / L, peptone 5g / L, yeast powder 5g / L, disodium hydrogen phosphate 2g / L, citric acid 1g / L; pH is 6.5; sterilize at 121℃, 0.1MPa for 30min;
[0117] The fermentation medium includes the following components: sucrose 20g / L, peptone 8g / L, yeast powder 10.55g / L, disodium hydrogen phosphate 2.7g / L, citric acid 1g / L; pH is 6.5; 121°C, 0.1MPa Sterilize for 30 minutes;
[0118] (ii) Activation: Acetobacter xylinum was inoculated on the slant medium, and after culturing in a 30° C. incubator for 60 hours, an activated strain was obtained;
[0119] (iii) Seed culture: Pick 2 rings of activated strains and in...
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