Application of breast milk-derived lactobacillus reuteri in reducing fat and regulating fat metabolism rhythm
A Lactobacillus reuteri, lipid metabolism technology, applied in the field of microbial technology and food science, can solve problems such as side effects, achieve the effect of maintaining interaction, promoting phosphorylation of tight junction proteins, and enhancing mucosal barrier
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Embodiment 1
[0055] Example 1: Breast milk sample collection
[0056] Specific steps are as follows:
[0057] Select breastfeeding mothers who have been proved to be healthy by physical examination and sign survey, and start to collect breast milk after receiving the informed consent for sample collection; wash hands before collecting breast milk with a breast pump, use a breast shield of appropriate size, and place the nipple on the The central part of the breast shield should be kept airtight, and an appropriate pressure (170-60mmHg) should be selected; the breast milk should be stored in a breast storage bag, and transported to the analysis site within 2 hours on ice.
Embodiment 2
[0058] Example 2: Collection of human milk flora and analysis of Lactobacillus reuteri
[0059] Specific steps are as follows:
[0060] Centrifuge the breast milk at 8000-12000rpm for 15min (4°C), remove the liquid, and collect the solids at the bottom of the centrifuge tube; take part of the solids to extract DNA, and use Lactobacillus reuteri-specific PCR to analyze the presence of Lactobacillus reuteri Condition.
Embodiment 3
[0061] Example 3: IgA-binding bacteria enrichment
[0062] Specific steps are as follows:
[0063] Such as figure 1 , the solid matter obtained by centrifuging breast milk was suspended in peptone buffer, bovine serum albumin was added to block non-specific binding (final concentrations were 10%, 0.05-0.5%), biotin-labeled rabbit anti-human IgA serum was added, and incubated for 15 ~30min, then add streptavidin-modified magnetic beads (addition amount: 0.1-1.0mg / mL), absorb the bacteria with a magnet, wash twice with peptone buffer, and obtain the IgA-binding bacterial population.
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