Method for quickly, qualitatively and quantitatively measuring Lactobacillus plantarum in probiotic dairy products
A Lactobacillus plantarum, qualitative assay technology, applied in microorganism-based methods, microbial assay/inspection, biochemical equipment and methods, etc. limited issues
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Embodiment 1
[0105] Rapid qualitative detection of Lactobacillus plantarum in probiotic dairy products:
[0106] In this example, the plasmid pPT containing the target amplification fragment was used as a positive control; dH 2 O was used as a negative control; in addition, L.plantarum 1.2437, L.casei ATCC393, L.rhamnosus1.2134, L.acidophilus ATCC 4356, L.fermentum 1.1880, and traditional fermented milk yogurt samples 25# and 36# collected from Tibet were used as sample, see figure 2 .
[0107] Described L.rhamnosus 1.2134, L.plantarum 1.2437, L.coryniformis subsp.coryniformis 1.1879 were purchased from the China General Microorganism Culture Collection; L.acidophilus ATCC4356, L.casei ATCC393 were purchased from American Type Culture Collection. Bifidobacterium animalis Subsp.Lactis V9 and L.reuteri ZL 12-1-1 are preserved by the Ministry of Education Key Laboratory of "Dairy Biotechnology and Engineering" of Inner Mongolia Agricultural University.
[0108] a. Preparation of template ...
Embodiment 2
[0123] Quantitative determination of Lactobacillus plantarum in probiotic dairy products:
[0124] Quantitative determination of soymilk fermented by L. plantarum IMAU10156 preserved in our laboratory. The measurement steps are as follows:
[0125] a. Preparation of sample total RNA
[0126] Extraction by Trizol method: After grinding 500 mg of the sample in a mortar filled with liquid nitrogen, quickly add 1 mL of Trizol reagent, extract sample RNA according to the instructions of the Trizol kit, and then treat it with DNaseI twice to ensure that the DNA contamination in the RNA is completely eliminated. The purified RNA sample was obtained, the concentration was determined according to the method described in the specification of this application, and the RNA integrity was subjected to 1% agarose gel electrophoresis.
[0127] b. Reverse transcription amplification
[0128] Reaction system 10.0 μL: 2.0 μL 5× PrimerScript Buffer (TakaRa DRR063A), 0.5 μL PrimerScript RT Enzy...
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