Technology for producing lycopene by biological fermentation
A technology of lycopene and biological fermentation, applied in the direction of microorganism-based methods, fermentation, microorganisms, etc., can solve the problems of high production cost, inability to accumulate lycopene, low fermentation yield, etc., and achieve the effect of facilitating absorption
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Embodiment 1
[0037] This embodiment provides a process for producing lycopene by biological fermentation, which includes the following steps:
[0038] Step 1: Take 200g of peeled potatoes, add 1000mL of deionized water to boil and keep for 30min; after cooling, filter through two layers of gauze, take the filtrate, add deionized water to 1000mL, add 20g of glucose and 10g of agar; sterilize at 115°C After 30 minutes, potato culture medium (PDA) was prepared. Take ATCC 14271 (+) (hereinafter referred to as positive bacteria) and ATCC 14272 (-) (hereinafter referred to as negative bacteria) and spread them on PDA plates respectively, culture them in a constant temperature incubator at 26°C for 4 days, then lower the temperature to 16°C, Stimulate sporulation, and feed oxygen into the incubator at a rate of 2 L / min, and at the same time give light with an intensity of 4WLx to cultivate spores for 3 days.
[0039] Step 2: Connect positive bacteria spores and negative bacteria spores respectiv...
Embodiment 2
[0044] This embodiment provides a process for producing lycopene by biological fermentation, which includes the following steps:
[0045] Step 1: Take 200g of peeled potatoes, add 1000mL of deionized water to boil and keep for 30min; after cooling, filter through two layers of gauze, take the filtrate, add deionized water to 1000mL, add 20g of glucose and 10g of agar; sterilize at 115°C After 30 minutes, potato medium (PDA) was prepared. Take ATCC 14271 (+) (hereinafter referred to as positive bacteria) and ATCC 14272 (-) (hereinafter referred to as negative bacteria) and spread them on PDA plates respectively, culture them in a constant temperature incubator at 28°C for 3 days, then lower the temperature to 18°C, Stimulate spore formation, and feed oxygen into the incubator at a rate of 2 L / min, and at the same time give light with an intensity of 4WLx to cultivate spores for 2 days.
[0046] Step 2: Connect positive bacteria spores and negative bacteria spores respectively ...
Embodiment 3
[0051] This embodiment provides a process for producing lycopene by biological fermentation, which includes the following steps:
[0052] Step 1: Take 200g of peeled potatoes, add 1000mL of deionized water to boil and keep for 30min; after cooling, filter through two layers of gauze, take the filtrate, add deionized water to 1000mL, add 20g of glucose and 10g of agar; sterilize at 115°C After 30 minutes, potato medium (PDA) was prepared. Take ATCC 14271 (+) (hereinafter referred to as positive bacteria) and ATCC 14272 (-) (hereinafter referred to as negative bacteria) and spread them on PDA plates, culture them in a constant temperature incubator at 30°C for 2 days, then lower the temperature to 20°C, Stimulate spore formation, and feed oxygen into the incubator at a rate of 2L / min, and at the same time give light with an intensity of 4WLx to cultivate spores for 1d.
[0053] Step 2: Connect positive bacteria spores and negative bacteria spores respectively into a triangular ...
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