Preparation method for lactic acid bacterium nutrient enhancer for holothurian culture
A technology of lactic acid bacteria and enhancer, which is applied in the direction of bacteria, application, animal feed, etc., to achieve the effect of long storage time, simple processing process and low preparation cost
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Embodiment 1
[0020] (1) Strain recovery: Pick bacteria from a single colony of the standard strain of lactic acid bacteria and inoculate them into the lactic acid bacteria medium, and culture them at 35°C for 12 hours.
[0021] (2) Bacteria enrichment: Inoculate into lactic acid bacteria medium at a volume ratio of 4%, ferment at 35°C, and cultivate for 28 hours until the final concentration of the bacterial suspension is 10 8 cfu / g; obtained fermentation product;
[0022] Wherein, described lactic acid bacteria culture medium, its preparation method is as follows:
[0023] Take 10g of peptone, 10g of beef extract, 5g of yeast extract, 20g of glucose, 2g of diammonium citrate, 5g of sodium acetate, 2g of dipotassium hydrogen phosphate, 0.2g of magnesium sulfate heptahydrate, 0.05 of manganese sulfate heptahydrate, and 0.25 of manganese sulfate tetrahydrate. g, Tween-801mL, distilled water 1000mL, sterilized at 115°C for 20 minutes; after the medium is gradually cooled, adjust the pH of th...
Embodiment 2
[0029] (1) Strain recovery: pick bacteria from a single colony of the standard strain of lactic acid bacteria and inoculate them into the lactic acid bacteria medium, and culture at 35°C for 12 hours;
[0030] (2) Bacteria enrichment: Inoculate into lactic acid bacteria medium at a volume ratio of 5%, ferment at 35°C, and cultivate for 48 hours until the final concentration of the bacterial suspension is 10 10 cfu / g; obtained fermentation product;
[0031] Wherein, described lactic acid bacteria culture medium, its preparation method is as follows:
[0032] Take 10g of peptone, 10g of beef extract, 5g of yeast extract, 20g of glucose, 2g of diammonium citrate, 5g of sodium acetate, 2g of dipotassium hydrogen phosphate, 0.2g of magnesium sulfate heptahydrate, 0.05 of manganese sulfate heptahydrate, and 0.25 of manganese sulfate tetrahydrate. g, Tween-801mL, distilled water 1000mL, sterilized at 115°C for 20 minutes; after the medium is gradually cooled, adjust the pH of the so...
experiment example 3
[0038] (1) Strain recovery: Pick bacteria from a single colony of the standard strain of lactic acid bacteria and inoculate them into the lactic acid bacteria medium, and culture them at 35°C for 12 hours.
[0039] (2) Bacteria enrichment: Inoculate into lactic acid bacteria culture medium at a volume ratio of 3-5%, and carry out fermentation and cultivation at 35°C for 28 hours, until the final concentration of the bacterial suspension is 10 10 cfu / g; obtained fermentation product;
[0040] Wherein, described lactic acid bacteria culture medium, its preparation method is as follows:
[0041]Take 10g of peptone, 10g of beef extract, 5g of yeast extract, 20g of glucose, 2g of diammonium citrate, 5g of sodium acetate, 2g of dipotassium hydrogen phosphate, 0.2g of magnesium sulfate heptahydrate, 0.05 of manganese sulfate heptahydrate, and 0.25 of manganese sulfate tetrahydrate. g, Tween-801mL, distilled water 1000mL, sterilized at 115°C for 20 minutes; after the medium is gradua...
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