Preparation methods of prodigiosin and biological stain as well as application of biological stain in fabric
A prodigiosin and dye technology, applied in the field of biological dyes, can solve problems such as waste and environmental pollution, and achieve the effects of convenient preparation, simple extraction process and good antibacterial properties
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Embodiment 1
[0044] (1) Activation of the original strain
[0045] According to the composition of the seed medium, weigh 3.0g of beef extract, 10.0g of peptone, 5.0g of NaCl, and 15g of agar, put them into a 1000mL beaker, add water to 1000mL, heat and stir to dissolve, and use 1mol / L of HCl and 1mol / L of NaOH Adjust the pH of the medium so that the pH is 7.4-7.6. Then it was divided into 250mL shake flasks, sterilized at 121°C for 20min with a sterilizer, and finally poured into a plate. After the plate is cooled, under aseptic conditions, use an inoculation needle to pick up the strains in the glycerol tube to scratch the plate, place it in a biochemical incubator, and incubate at 37°C for 12 hours to obtain activated Serratia, Staphylococcus aureus, Bacillus subtilis, put it in the refrigerator and save it for later use;
[0046] (2) Obtain inactivated Staphylococcus aureus and Bacillus subtilis
[0047] Weigh peptone 13.0g, glycerol 20.0g, MgSO 4 Add 1.2g, NaCl 5.0g, and Gly 2.0g ...
Embodiment 2
[0074] (1) Activation of the original strain
[0075] According to the composition of the seed medium, weigh 3.0g of beef extract, 10.0g of peptone, 5.0g of NaCl, and 15g of agar, put them into a 1000mL beaker, add water to 1000mL, heat and stir to dissolve, and use 1mol / L of HCl and 1mol / L of NaOH Adjust the pH of the medium so that the pH is 7.4-7.6. Then it was divided into 250mL shake flasks, sterilized at 121°C for 20min with a sterilizer, and finally poured into a plate. After the plate is cooled, under aseptic conditions, use an inoculation needle to pick up the strains in the glycerol tube to scratch the plate, place it in a biochemical incubator, and incubate at 37°C for 12 hours to obtain activated Serratia, Staphylococcus aureus, Bacillus subtilis, put it in the refrigerator and save it for later use;
[0076] (2) Obtain inactivated Staphylococcus aureus and Bacillus subtilis
[0077] Weigh peptone 13.0g, glycerol 20.0g, MgSO 4 Add 1.2g, NaCl 5.0g, and Gly 2.0g ...
Embodiment 3
[0085] (1) Activation of the original strain
[0086]According to the composition of the seed medium, weigh 3.0g of beef extract, 10.0g of peptone, 5.0g of NaCl, and 15g of agar, put them into a 1000mL beaker, add water to 1000mL, heat and stir to dissolve, and use 1mol / L of HCl and 1mol / L of NaOH Adjust the pH of the medium so that the pH is 7.4-7.6. Then it was divided into 250mL shake flasks, sterilized at 121°C for 20min with a sterilizer, and finally poured into a plate. After the plate is cooled, under aseptic conditions, use an inoculation needle to pick up the strains in the glycerol tube to scratch the plate, place it in a biochemical incubator, and incubate at 37°C for 12 hours to obtain activated Serratia, Staphylococcus aureus, Bacillus subtilis, put it in the refrigerator and save it for later use;
[0087] (2) Obtain inactivated Staphylococcus aureus and Bacillus subtilis
[0088] Weigh peptone 13.0g, glycerol 20.0g, MgSO 4 Add 1.2g, NaCl 5.0g, and Gly 2.0g i...
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