Quantitative analysis method of lactic acid bacteria and bacilli in yeast microbial community
A microbial community, Bacillus technology, applied in the field of bioengineering, can solve the problems of lack of stability and reliability of detection results, time-consuming and labor-intensive, etc., to strengthen monitoring, improve detection efficiency, and simplify detection procedures.
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Embodiment 1
[0027] The preparation of embodiment 1 standard curve
[0028] 1. Synthesize specific primers for lactic acid bacteria and bacillus, and specifically amplify the lactic acid bacteria and bacillus screened in Daqu
[0029] Lactic acid bacteria specific primer sequence (5'→3'):
[0030] Lacto-F: AGAACACCAGTGGCGAAGG
[0031] Lacto-R: CAGGCGGAGTGCTTAATGC
[0032] Bacillus-specific primer sequence (5′→3′)
[0033] Bacil-F: ATGGCTGTCGTCAGCT
[0034] Bacil-R: ACGGGCGGTGTGTAC
[0035] 2. Screening of lactic acid bacteria and bacillus in Daqu and determination of standard strains:
[0036] a. Screening of lactic acid bacteria:
[0037] Screening medium for lactic acid bacteria: glucose 2%w / w, peptone 1%w / w, beef extract 1%w / w, yeast extract 0.5%w / w, K 2 HPO 4 0.2%w / w, Triammonium Citrate 0.2%w / w, Sodium Acetate 0.5%w / w, Tween 800.1%v / v, MgSO 4 ·7H 2 O0.05%w / w, MnSO 4 4H 2 O0.025%w / w, pH6.2~6.4, agar 1.5%w / w, 121℃, after 20min sterilization, add sterilized CaCO 3 Solution 2...
Embodiment 2
[0065] The extraction of microbial total DNA in the Daqu microbial flora of embodiment 2
[0066] 1. Daqu sample collection
[0067] Collect Daqu samples. If the DNA cannot be extracted in time after the sample is collected, it should be stored in a -80°C refrigerator immediately.
[0068] 2. Extraction of microbial total DNA from Daqu
[0069] Weigh 1 g of Daqu sample, add liquid nitrogen to the mortar and grind thoroughly, and transfer to a 50 mL centrifuge tube. Transfer to a centrifuge tube, add 1mL CTAB extract (2%CTAB, 5mol / L NaCl, 1mol / LTris-HCl(pH8.0), 0.5mol / L EDTA) and 20μL mercaptoethanol to the centrifuge tube, and mix at 65°C. Shake for 30min with a homogenizer, add 5μL of proteinase k (20mg / mL), centrifuge at 6000×g for 10min at 37°C at 220r / min, and collect the supernatant (1mL).
[0070] Add an equal volume of Tris-saturated phenol (500 μL) and chloroform-isoamyl alcohol (volume ratio 24:1) (500 μL), extract once, centrifuge at 12,000 rpm for 10 min, take th...
Embodiment 3
[0071] Quantitative Analysis of Lactic Acid Bacteria and Bacillus in Embodiment 3 Daqu Microflora
[0072] Quantification of lactic acid bacteria in Daqu samples: use the total DNA of Daqu obtained in Example 2, and use specific primers for lactic acid bacteria and Bacillus in Example 1. Daqu fluorescent quantitative PCR analysis was performed according to the fluorescent quantitative PCR reaction system and PCR program in Example 1.
[0073] According to the fluorescent quantitative PCR of lactic acid bacteria standard sample, the linear equation y=-0.3411x+14.07(R 2 =0.9978) to calculate the copy number of lactic acid bacteria in Daqu samples at different time points, so as to obtain the change trend of lactic acid bacteria biomass in Daqu (such as figure 1 Note as shown: figure 1 Days on the x-axis shown represent Daqu production and storage days).
[0074] Quantification of Bacillus in Daqu samples: according to the linear equation y=-0.3387x+13.152(R 2 =0.9974) to cal...
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