Acetobacter xylinum and method for preparing nano-cellulose skin tissue repair material by using the same
A technology of nanocellulose and Acetobacter xylinum, applied in the direction of microorganism-based methods, biochemical equipment and methods, bacteria, etc., can solve the problems of not being able to improve the mechanical properties of materials, infection or rejection, and poor water holding capacity , to achieve high social and economic benefits, low cost, and long-term moisture retention
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Embodiment 1
[0023] 1. Preparation of basement membrane of nanocellulose skin tissue repair materials
[0024] (1) Prepare a slant medium containing 5% glucose by mass percentage, 1% yeast powder, 2% calcium carbonate and 2% agar. The Acetobacter xylinum Y05 (Acetobacterxylinum Y05, CCTCC M207163) preserved on the slant is activated on the slant medium, and the activated bacterial classification is inoculated in a 250mL Erlenmeyer shaker flask, cultivated on a shaker as a first-class seed, and the first-class Seeds are inoculated in seed tanks, and after expanded cultivation, they are made into seed cultures for fermentation production.
[0025] (2) Prepare a liquid medium containing 10% glucose, add 1% yeast powder and 2% calcium carbonate, and its initial pH value is 5.5, and culture it statically for 7 days at a constant temperature of 30°C.
[0026] (3) Soak the cultured nanocellulose membrane in distilled water for 2 days, then put it into a NaOH solution with a mass concentration of...
Embodiment 2
[0031] 1. Preparation of basement membrane of nanocellulose skin tissue repair materials
[0032] (1) Prepare a slant medium containing 5% glucose by mass percentage, 1% yeast powder, 2% calcium carbonate and 2% agar. Acetobacter xylinum Y05 (Acetobacter xylinum Y05, CCTCC M 207163) preserved on the slant was activated on the slant medium, and the activated strain was inoculated in a 250mL Erlenmeyer shaker flask, cultivated on a shaker as a primary seed, and a The high-grade seeds are inoculated in the seed tanks, and after expanded cultivation, they are made into seed cultures for fermentation production.
[0033] (2) Prepare a liquid medium containing 12% glucose, add 1.5% yeast powder and 3% calcium carbonate, and its initial pH value is 3.5, and culture it statically at a constant temperature of 30° C. for 7 days.
[0034] 2. Combination of new nanocellulose skin tissue repair materials
[0035] Prepare a 2% collagen acetic acid solution and store at 4°C. Chitosan was ...
Embodiment 3
[0037] 1. Preparation of basement membrane of nanocellulose skin tissue repair materials
[0038] (1) Prepare slant culture medium containing 10% glucose by mass percentage, 1% yeast powder, 2% calcium carbonate and 2% agar. Acetobacter xylinum Y05 (Acetobacter xylinum Y05, CCTCC M 207163) preserved on the slant was activated on the slant medium, and the activated strain was inoculated in a 250mL Erlenmeyer shaker flask, cultivated on a shaker as a primary seed, and a The high-grade seeds are inoculated in the seed tanks, and after expanded cultivation, they are made into seed cultures for fermentation production.
[0039] (2) Prepare a liquid medium containing 15% glucose, add 2% yeast powder and 4% calcium carbonate, and its initial pH value is 6.0, and culture it statically at a constant temperature of 30° C. for 14 days.
[0040] 2. Combination of new nanocellulose skin tissue repair materials
[0041] Prepare a 2% collagen acetic acid solution and store at 4°C. Chitosa...
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