Lactobacillus plantarum CW006 with antihypertensive function
A technology of Lactobacillus plantarum and strains, applied in the food processing and pharmaceutical industries, the field of new strains of Lactobacillus plantarum, can solve the problems of increased blood pressure, loss of diastolic vasoactive activity, increased blood pressure, etc.
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Embodiment 1
[0037] Example 1 Preliminary Screening
[0038] Taking traditional fermented food (douche, bean paste, yoghurt, Tibetan mushroom) as samples, lactic acid bacteria were separated, purified and preserved by Gram staining and catalase experiments. After culturing in MRS medium for 24 hours, transfer it to fresh MRS medium, culture under the same conditions for 12 hours, centrifuge the bacteria, resuspend with PBS buffer, add 1% to 10% skimmed milk (SKM), and ferment at 37°C For a certain period of time, the fermented milk was refrigerated and centrifuged at 8500×g at 4°C for 10 minutes, and the obtained supernatant was adjusted to pH 8.3 with 10mol / L NaOH, and stored at -70°C until testing. The method of Cushman and Cheung (1971) was used to measure the activity of inhibiting ACE in fermented milk.
[0039]
[0040] O.D. A is the absorbance value in the absence of inhibitor
[0041] O.D. B is the absorbance value in the presence of inhibitor and ACE
[0042] O.D. C Absor...
Embodiment 2
[0046] The acid and bile resistance characteristics of embodiment 2 lactic acid bacteria
[0047] The experimental strains were suspended in MRS medium with pH 2.0 and pH 3.0 respectively, cultured at 37°C for 3 hours, and the survival rate of viable bacteria was determined by plate counting method.
[0048] The experimental strains were inoculated into MRS and MRSO (MRS with 0.3% ox bile added) at 1% inoculation amount, cultured at 37°C, and the time difference between MRS and MRSO culture solution reaching 0.3 unit growth at A620nm was used as the evaluation of the bile tolerance of the strain in accordance with.
[0049] Strain number
[0050] Strain number
[0051] CW006
Embodiment 3
[0052] Example 3 Effect of Simulated Gastrointestinal Digestion on ACE Inhibitory Activity
[0053] The whey prepared above was subjected to ultrafiltration through a cellulose membrane with a molecular weight cut-off of 10,000 Da (permeate) for determination. According to Sandrine Parrot's method, adjust the whey pH to 2.0 with 1M hydrochloric acid, take 10ml of the sample solution and add 1ml of pepsin solution (0.1g of pepsin dissolved in 1L of 0.01M hydrochloric acid), where E / S is 1:200, at 37 ℃ water bath shaker (160 times / min) digestion reaction for 90min, then heated in 85℃ water bath for 5min to terminate the reaction, adjust the pH of the sample solution to 7.5 with 4% sodium hydroxide, add 0.2ml trypsin solution (0.5g trypsin solution In 1L deionized water), where E / S is about 1:200, reacted for 240min under the same conditions as above, and then heated in a water bath at 85°C for 5min to terminate the reaction. Samples were taken after pepsin digestion for 90min, ...
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