Aureobasidium pullulans strain and application thereof
A technology of Aureobasidium pullulans and strains, applied in the direction of fungi, microorganisms, biochemical equipment and methods, etc., can solve the problems of clear research on liamocin biosynthesis mechanism, complex liamocin biosynthesis pathway, and low yield of liamocin, and achieve a simplified later stage The treatment process and method are simple and easy, and the extraction method is simple
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Embodiment 1
[0045] The method that Aureobasidium pullulans strain of the present invention is used for fermentation to produce liamocin is as follows:
[0046] S1. Activation of strains: transfer the slant bacteria to PDA slant medium, and cultivate them in a constant temperature incubator at 26°C for 2 days;
[0047]S2. Seed cultivation: select 3 loops of well-cultured slant strains and inoculate them in 50 mL of seed culture medium, and cultivate them in a shaker at 26°C and 160r / min for 2 days;
[0048] Among them, the composition of the seed medium is: 5% glucose, 0.2% yeast extract, 0.5% KH 2 PO 4 , 0.04% MgSO 4 ·7H 2 O, 0.04% MnSO 4 ·H 2 O and 0.1% NaCl.
[0049] S3, fermentation culture: divided into two stages
[0050] (1) Inoculate the seed liquid cultivated in step S2 into the fermentation medium (1) at a ratio of 6%, and cultivate it in a shaker at 26° C. and 160 r / min for 3 days;
[0051] Wherein, the composition of fermentation medium (1) is: 5% glucose, 0.2% yeast ex...
Embodiment 2
[0056] The method that Aureobasidium pullulans strain of the present invention is used for fermentation to produce liamocin is as follows:
[0057] S1. Strain activation: transfer the slant bacteria to the PDA slant medium, and cultivate them in a constant temperature incubator at 28°C for 2.5 days;
[0058] S2. Seed culture: select the well-cultured slant strains in step S1, pick 2 loops and inoculate them in 50 mL of seed culture medium, and cultivate them in a shaker at 26° C. and 160 r / min for 2 days;
[0059] Among them, the composition of the seed medium is: 5% glucose, 0.2% yeast extract, 0.5% KH 2 PO 4 , 0.04% MgSO 4 ·7H 2 O, 0.04% MnSO 4 ·H 2 O and 0.1% NaCl.
[0060] S3, fermentation culture: divided into two stages:
[0061] (1) Inoculate the seed solution cultivated in step S2 into the fermentation medium (1) at a ratio of 10%, and cultivate it in a shaker at 28° C. and 200 r / min for 3 days;
[0062] Among them, the composition of fermentation medium (1) is...
Embodiment 3
[0067] The method that Aureobasidium pullulans strain of the present invention is used for fermentation to produce liamocin is as follows:
[0068] S1. Activation of strains: transfer the slant bacteria to PDA slant medium, and cultivate them in a constant temperature incubator at 26°C for 2 days;
[0069] S2. Seed culture: select the slant bacteria cultured well in step S1, pick 3 loops and inoculate them in the seed culture medium, and cultivate them in a shaker at 28°C and 200r / min for 2 days;
[0070] Among them, the composition of the seed medium is: 5% glucose, 0.2% yeast extract, 0.5% KH 2 PO 4 , 0.04% MgSO 4 ·7H 2 O, 0.04% MnSO 4 ·H 2 O and 0.1% NaCl.
[0071] S3, fermentation culture: divided into two stages
[0072] (1) Inoculate the seed solution cultivated in step S2 into the fermentation medium (1) at a ratio of 8%, and cultivate it in a shaker at 28° C. and 180 r / min for 3 days;
[0073] Among them, the composition of the fermentation medium (1) is: 7% ma...
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