Molecular motor lipid vesicle composition as well as preparation method and application thereof
A technology of molecular motors and lipid vesicles, which is applied in the field of biological and polymer materials, can solve the problems of poor mechanical properties, limited life, and easy breakage, and achieve the effects of improving stability, improving delicate vitality, and promoting wound healing
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[0051]The present invention also provides a method of preparing a molecular motor lipid vesicle, the step of preparing:
[0052]1) Collection of bacteria;
[0053]The bacteria used in step 1) include a kind of thermophilic fungi, thermophilic bacteria, Beltophili, Bacillus, Slimophilic acid Soclastin, Slimophili, and Soilophilus.
[0054]Preferably, theophilic bacteria are thermophilicin.
[0055]2) Bacterial crushing: The bacterium obtained by step 1) is broken to obtain a cell fragmer;
[0056]The bacterial crush used in step 2) can be mechanically, for example: high-pressure homogenization method, oscillating bead crushing method, high speed mixing bead grinding method, ultrasonic crushing method, hit crushing method; or non-mechanical method, for example Osmotic pressure impact crushing method, freeze-thaw crushing method, enzyme-dissolving method, chemical crushing method.
[0057]In the present invention, in order to improve the anti-oxidation resistance of lipid vesicles, the lipid peroxidatio...
Embodiment 1
[0072]This embodiment provides a method of preparing a molecular motor lipid vesicle, and the preparation method thereof comprises:
[0073]1) Bacterial collection: In the culture of Botherophilic bacteria, cultured in 75 ° C to the latter period, collected bacteria;
[0074]2) Crushing of the bacteria: After the bacterium obtained in step 1) was preserved by -80 ° C, 500 g of the bacterium was taken into 1 liter buffer (80 mm Tris.HCl, pH 8.0, including 1.0 mMβ-thiol). Ethanol, 0.Lmm EDTA 0.25M sucrose, 4mmmmgCl2The solution is suspended, treated with ultrasonic treatment to achieve crushing;
[0075]3) Centrifugation, prepared heat-resistant SOD: centrifuge at high speed (20000 g) for 30 min, resulting in precipitate A and supernatant B. The precipitate A was added with 500 ml of buffer (15 mM Tris.HCl, pH 7.6, including 1.0 mMβ-mercaptoethanol, 0.LmMedta) to 20 m mgCl2The solution was 8 ml and DNasei 10 mg, and the reaction was reacted for 30 minutes under room temperature. After the DNas...
Embodiment 2
[0080]The present embodiment is the same as in Example 1, and the only difference is that the polyglymine is replaced with polyethyleneiocine.
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