A Strain of Stenotrophomonas Efficiently Degrading Polybutylene Terephthalate/Adipate and Its Application
A polybutylene terephthalate and adipate technology, applied in bacteria, hydrolase, microorganism-based methods, etc., can solve the problems of small types and numbers of microorganisms, slow degradation, and low degradation rate, and achieve excellent Degradation effect, strong adaptability, widely distributed effect
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Embodiment 1
[0034] The isolation and identification of embodiment 1 bacterial strain
[0035] 1. Plate separation and screening of PBAT-degrading bacteria
[0036] Collect the soil of a farmland with PBAT mulch in Yanxia Town, Liquan County, Shaanxi Province, weigh 10g of soil in a 150mL triangular flask with 90mL of sterile water, and configure 10 -1 ~10 -6 The soil bacteria suspension with a series of concentration gradients was inoculated in the inorganic salt medium with PBAT as the only carbon source. After culturing in a constant temperature incubator at 37°C for 3 days, the growth of microorganisms on the medium was observed, and a single colony was picked. Continuously inoculated several times in PBAT as the only carbon source inorganic salt medium for isolation and purification until a strain of bacteria was isolated, and then the colony morphology was observed, as shown in figure 1 As shown, the colonies were orange-red, with flat edges and smooth surfaces.
[0037] 2. Identi...
Embodiment 2
[0040] Example 2 strain producing lipase ability identification
[0041] The Stenotrophomonas was inoculated on the oil medium, cultured at 37°C for 3 days, and there were obvious red hydrolysis circles under the colonies, which showed that the bacteria could produce lipase.
Embodiment 3
[0042]Example 3 Degradation experiment of strains on PBAT membrane and lipase production experiment.
[0043] 1. Preparation of PBAT membrane
[0044] Select 5 g of PBAT film with a molecular weight of 100,000, dissolve it in 95 mL of analytically pure chloroform, stir it thoroughly until it dissolves, pour it into a mold, wait for the chloroform to volatilize, prepare a PBAT film, and cut it into 1 *1cm 2 A small piece of the strain was used for the experiment of degrading the PBAT membrane.
[0045] 2. Preparation of Medium
[0046] On the basis of PBAT as the sole carbon source inorganic salt medium, 3% butanediol and other external carbon sources were added as the co-metabolism growth substrate of the bacteria.
[0047] 3. Preparation of Seed Solution
[0048] The purified strain was inoculated in 100 mL of LB medium, and cultured for 12 hours at 37°C with a shaker speed of 130 r / min to obtain OD 600 The bacterial solution with a value of 1.0 was used as the seed solu...
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