Construction method of microecosystem for microbial retting of ramie phloem
A technology of micro-ecosystem and construction method, which is applied in the field of construction of ramie bast fiber biological degumming micro-ecosystem, can solve the problems of high requirements for strain preparation process, weak enzyme degumming ability, and easy contamination of miscellaneous bacteria strains, etc. Achieve the effects of strong anti-bacteria ability, high affinity and fast degumming speed
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Embodiment 1
[0029] Embodiment 1: Construction of ramie mixed bacteria degumming micro-ecosystem
[0030] Bacteria collection and enrichment culture: Bacteria materials were collected from retting pond water, ramie degumming factory sludge, old hemp garden soil, and rotten hemp piles in Xianning, Hubei Province, and 1 L of retting pond water and ramie degumming factory sludge were collected respectively. Collect 1Kg of garden soil and rotten hemp stalks, and store materials in different habitats separately. After bringing them back to the laboratory, keep 100g (or 100ml) of the strain material for low temperature storage for later use. The remaining materials are directly used as inoculum and inoculated into 60L plastic barrels respectively. In each bucket, add 40L tap water, 5Kg ramie bast, compact and submerge, adjust the pH to 7.5 every 24 hours, let it stand for 12 days at 37°C, and then filter it with double-layer gauze to clean up the sediment and residue in the bucket. Keep 20L of c...
Embodiment 2
[0034] Embodiment 2: the preservation of ramie mixed bacteria degumming micro-ecosystem
[0035] In vivo subculture: In a 500ml Erlenmeyer flask, add 40g of raw hemp and 390ml of tap water, inoculate 10ml of domesticated and mature mixed bacterial culture solution, adjust the initial pH to 8.5, readjust the pH to 7.5 after 3 hours, and culture at 42°C for 3 days Afterwards, 10ml of the culture solution was left as the inoculum each time, and the subculture was repeated in the same way. Each subculture cycle was 3 days, and 3 copies of this living material were preserved in parallel.
[0036] Establish 16s rDNA molecular fingerprints: extract the total DNA of the flora after 407 days of domestication, and conduct 16srDNA analysis according to the well-known methods in the industry. That is, PCR (DNA polymerase chain reaction) amplifies the 16s rDNA sequence, denaturing gradient gel electrophoresis (DGGE) separates the 16s rDNA sequence of different bacteria, establishes a stand...
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