Method for producing microbial oil through oil-producing microorganisms adopting jerusalem artichoke as raw materials
A technology for oil-producing microorganisms and microbial oils, which is applied in the direction of single-cell algae, bacteria, fungi, etc., can solve problems such as the inability to use nitrogen limitation regulation, difficulty in removing nitrogen elements from Jerusalem artichoke raw materials, and accumulation of oil, so as to improve oil production intensity and Substrate conversion rate, improving microbial oil fermentation technology economy, and improving the effect of utilization
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Embodiment 1
[0047] (1) Preparation of seed medium: Take 100 mesh inulin, 50g inulin and mix water with a mass ratio of 1:10, add water to make the volume 500ml, use 3mol / L hydrochloric acid to adjust the pH to 3.6; hydrolyze under saturated steam for 30min, adjust the pH To neutrality, obtain the Jerusalem artichoke hydrolyzate, prepare another part of Jerusalem artichoke hydrolyzate according to the same method, in order to use in step (3); Get wherein a part of Jerusalem artichoke hydrolyzate, add yeast powder to 10g / L, potassium dihydrogen phosphate to 1.0g / L, MgSO 4 ·7H 2 0 to 0.5g / L, sterilized to obtain the seed culture medium of microorganisms;
[0048] (2) Bacteria proliferation culture: with 10% (V / V) (OD 600nm =7.8) inoculum size Trichosporonfermentans CICC1368 (purchased from China General Microorganism Culture Collection Management Center) was connected to the seed medium prepared in step (1), 28°C, 100rpm, cultivated for 24h, and centrifuged to obtain Oleaginous microbial ...
Embodiment 2
[0058] (1) Preparation of seed medium: Take 50 mesh inulin, 70g inulin, and mix with water at a mass ratio of 1:4.3, add water to make the volume 300ml, use 3mol / L hydrochloric acid to adjust the pH to 2.0; hydrolyze under saturated steam for 20min, adjust the pH To neutrality, the Jerusalem artichoke hydrolyzate is obtained, and another part of the Jerusalem artichoke hydrolyzate is prepared in the same way for use in step (3); take one part of the Jerusalem artichoke hydrolyzate, add peptone 5g / L, and potassium dihydrogen phosphate to 1.0g / L,MgSO 4 ·7H 2 0 to 0.5g / L, sterilized to obtain the seed culture medium of microorganisms;
[0059] (2) Bacteria proliferation culture: with 10% (V / V) (OD 600nm =6.5) Inoculum size Cryptococcus curvatusATCC20509 (purchased from the American Type Culture Collection Center) was connected to the seed medium prepared in step (1), 24 ° C, 150 rpm, cultured for 24 hours, and centrifuged to obtain oil-producing microbial cells;
[0060] (3)...
Embodiment 3
[0069] (1) Preparation of seed medium: Take 200 mesh inulin, 100g inulin and mix with water at a mass ratio of 1:5, add water to make the volume 500ml, use 3mol / L hydrochloric acid to adjust the pH to 2.5; hydrolyze under saturated steam for 10min, adjust the pH To neutrality, obtain the Jerusalem artichoke hydrolyzate, prepare another part of Jerusalem artichoke hydrolyzate according to the same method, in order to use in step (3); Get wherein a part of Jerusalem artichoke hydrolyzate, add NH 4 NO 3 5g / L, potassium dihydrogen phosphate to 1.0g / L, MgSO 4 ·7H 2 0 to 0.5g / L, sterilized to obtain the seed culture medium of microorganisms;
[0070] (2) Bacteria proliferation culture: with 10% (V / V) (OD 600nm=5.0) inoculum size Rhodococcus opacus PD630 (purchased from the German Microorganism Culture Collection Center) was connected to the seed medium prepared in step (1), 30°C, 200rpm, cultivated for 48h, and centrifuged to obtain oil-producing microorganisms bacteria;
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