Ganoderma amboinense bacterial liquid fermentation culture method
A technology of fermenting and cultivating Ganoderma lucidum, which is applied in the field of microorganisms, can solve problems such as long cycle time, low production efficiency, and large environmental impact, and achieve the effect of increasing production
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Embodiment 1
[0030] Embodiment 1 A kind of method for staghorn ganoderma liquid culture, concrete steps are as follows:
[0031] (1) Mother species expansion
[0032] Under aseptic conditions, cut out a small piece of the mother bell of staghorn ganoderma lucidum, transfer it to the slant medium, stopper it, put it in a constant temperature incubator, and cultivate it at 27°C for 7 days;
[0033] Slant medium: wash and peel the potatoes, weigh 200g, cut into small pieces, add 30g of wheat bran, add 1000mL of water to boil, keep for 30min, filter, add 20g of agar to the filtrate, heat it to melt it all, add 30g of glucose , Potassium dihydrogen phosphate 2g, magnesium sulfate 1g, pH is 7.0, put into test tubes separately, put into autoclave sterilization, the temperature is 121 ℃, the time is 30min, make the test tube slope (18mm * 180mm) standby;
[0034] (2) Preparation of seed solution
[0035] Take 1cm on the slant medium 2 The mycelium was inoculated in the seed liquid medium, and p...
Embodiment 2
[0040] Example 2 Evaluation of the ability of Ganoderma lucidum to produce Ganoderma lucidum polysaccharides and triterpenoids
[0041] Antler Ganoderma lucidum strain NCPSLZ1 is selected as the antler ganoderma, and the preservation number of the strain NCPSLZ1 is CCTCCNo.M2015796; the preservation unit is the China Center for Type Culture Collection; the preservation date is December 29, 2015; and the preservation address is Wuhan University, Wuhan, China.
[0042] The liquid fermentation medium that uses during assessment, the formula (by mass percentage) of medium is 15% potato juice, 3% wheat bran, 3% glucose, 0.2% potassium dihydrogen phosphate, 0.1% magnesium sulfate, and pH is 7.0 . The inoculum size was 5% (V / V), 500mL shake flask (filling liquid 250mL), 150r / min, 27±2°C constant temperature culture for 70h to obtain the fermentation broth for evaluation, and further obtain freeze-dried mycelium powder.
[0043]The determination of the mycelia biomass of bacterial st...
Embodiment 3
[0047] Embodiment 3 liquid fermentation condition optimization
[0048] 3.1 Mother species expansion
[0049] Wash and peel the potatoes, weigh 200g, cut into small pieces, boil with 30g of wheat bran, add 1000mL of water, keep for 30min, filter, add 20g of agar to the filtrate, heat it to make it all melt, add 30g of glucose, dihydrogen phosphate Potassium 2g, magnesium sulfate 1g, pH 7.0, divided into test tubes, placed in an autoclave for sterilization (temperature 121°C, time 30min), and made into a test tube slope (18mm×180mm) for later use.
[0050] Under sterile conditions, cut out the mother species of the small piece of strain NCPSLZ1, transfer it to the slant medium, plug it, put it in a constant temperature incubator, and cultivate it at 27°C. After the mycelium grows all over the slant, place the expanded mother species Store in a 4°C refrigerator until use.
[0051] 3.2 Preparation of seed solution
[0052] 15% potato juice, 3% wheat bran, 3% glucose, 0.2% pota...
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