Method for improving enzyme activity of glutathion peroxidase in lactic acid bacteria
A technology of glutathione peroxide and lactic acid bacteria, applied in the direction of microorganism-based methods, biochemical equipment and methods, and adding compounds to stimulate growth, can solve the problem of low enzyme activity and achieve enhanced enzyme activity and expression The effect of volume increase
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Embodiment 1
[0046] Step 1, Activation of Strains
[0047] Inject 0.3 mL of the MRS broth medium sterilized by high temperature and high pressure into the freeze-dried tube of Lactobacillus rhamnosus, and gently blow it with a pipette gun to fully dissolve it into a bacterial suspension. Aspirate the bacterial suspension, put them all into 2 test tubes, and cultivate them under the specified conditions of the strains. After the activation is successful, in order to improve the activity of the strains, inoculate each strain into the MRS broth medium, and place them in a constant temperature incubator. Cultivate at 37°C for 24 hours, and activate three generations continuously.
[0048] Step 2, selenium-enriched culture of Lactobacillus rhamnosus
[0049] Prepare 0.17mg / mL sodium selenite solution and MRS liquid medium and pre-sterilize it. When in use, add sodium selenite solution into MRS liquid medium and dilute to a sodium selenite concentration of 20 μg / mL. Inoculate 1 mL of the above...
Embodiment 2-7
[0052] In embodiment 2-7, Lactobacillus rhamnosus is replaced by Lactobacillus acidophilus, Lactobacillus casei, Lactobacillus reuteri, Lactobacillus bulgaricus, Streptococcus thermophilus and Lactobacillus plantarum respectively, other conditions are identical with embodiment 1 .
Embodiment 8-14
[0054] The concentration of sodium selenite was adjusted to 40 μg / mL, 60 μg / mL, 80 μg / mL, 100 μg / mL, 120 μg / mL, 140 μg / mL, 160 μg / mL, and other conditions were the same as in Example 1.
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