Induction of VBNC state of lactobacillus casei Zhang and detection method of cell fatty acid in VBNC state
A technology of Lactobacillus casei and cells, which is applied in the detection of fatty acids in VBNC cells and in the field of VBNC induction, can solve the problems of single induction method and few types of induction liquid, and achieve the effect of simple operation and strong stress resistance
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Embodiment 1
[0048] 1. Activation of Lb.casei Zhang
[0049] Lactobacillus casei Zhang (Lb.casei Zhang, CGMCC No.1697) preserved in vacuum freeze-drying was inoculated in liquid MRS medium, and activated for 18-24 hours at a temperature of 37°C. At the end of the logarithmic phase, activated lactobacilli were obtained. The said lactobacillus is Lactobacillus casei Zhang (Lb. casei Zhang), and the activation of the lactobacillus is carried out at a temperature of 37° C. for 18-24 hours.
[0050] Note: The probiotic Lb.casei Zhang was provided by the Lactic Acid Bacteria Culture Bank (LABCC), the Key Laboratory of "Dairy Biotechnology and Engineering" of the Ministry of Education, Inner Mongolia Agricultural University, LABCC number IMAU10048.
[0051] At the same time, it is also preserved in the China General Microbiological Culture Collection Center (China General Microbiological Culture Collection Center), and the preservation number is CGMCC No.1697.
[0052] 2. Inducing conditions
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Embodiment 2
[0065] 1. Extraction of cell membrane fatty acids of Lb.casei Zhang
[0066] Obtain lactic acid bacteria sludge: regularly take the bacteria in the induction solution in Example 1 (in the process of normal state and VBNC state, VBNC state bacteria), centrifuge at 4000rpm for 5min, wash with normal saline once, weigh about 0.5g of bacteria in 10mL sterile, In a centrifuge tube with a screw cap.
[0067] Fatty acid extraction: Take 0.5g of the normal state and VBNC state cells of Lactobacillus casei Zhang, mix with 1.9mL methanol: chloroform (2:1), shake at room temperature for 15min, add 0.63mL chloroform and 0.63mL ultrapure water, make the chloroform and methanol 1:1, then shaken for 15 minutes, fully broken and centrifuged, so that the chloroform layer contains all lipids, while the methanol layer does not contain lipids, and the purified lipid extract is separated to obtain a chloroform layer.
[0068] B) The chloroform phase of the lower layer was removed, and the concent...
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