A method for promoting the accumulation of carotenoids and β-carotene in Dunaliella by utilizing β-ionone
A technology of carotene and ionone, applied in the field of food science, can solve the problems of limiting β-carotene production and long cycle, and achieve the effects of large-scale breeding, strong stress resistance, and increased production costs
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Embodiment 1
[0034] (1) Activation culture
[0035] First prepare Dunaliella liquid culture medium, its composition is: NaNO 3 0.420g / L, NaCl 87.690g / L, NaH 2 PO 4 2H 2 O 0.015g / L, NaHCO 3 0.840g / L, KCl 0.074g / L, MgSO 4 ·7H 2 O 1.230g / L, CaCl 2 2H 2 O 0.044g / L, Fe-EDTA solution (Na 2 EDTA 1.804g / L, FeCl 3 ·6H 2 O 0.483g / L) 0.5mL / L, A5 trace element solution (H 3 BO 3 2.860g / L, MnCl 2 4H 2 O 1.810g / L, ZnSO 4 ·7H 2 O 0.220g / L, CuSO 4 ·5H 2 O 0.079g / L, (NH 4 ) 6 Mo 7 o 24 4H 2 (0.039g / L) 1mL / L;
[0036] Then the cells of Dunaliella pasteurii were inoculated in the above-mentioned liquid medium, the light intensity was 8000Lx, the light-dark cycle was 14h:10h (14h light, 10h no light) (light-dark alternating culture), the temperature was 26°C, and the temperature was 26°C, with 50r / min speed vibration culture, to obtain synchronous growth of algae liquid.
[0037] (2) Induction culture
[0038] When the algal cells in the algal liquid are in the logarithmic growth...
Embodiment 2
[0049] (1) activation culture (with embodiment 1)
[0050] (2) Induction culture
[0051] Same as Example 1, except that the culture was continued for 6 hours after adding β-ionone.
[0052] (3) pigment extraction (with embodiment 1)
[0053] (4) Content determination
[0054] The method for determining the content of total carotenoids and β-carotene is the same as in Example 1, and it is found that adding 2 to 20 mg / L of β-ionone to treat Dunaliella pasteurii for 6 hours, the ratio of total carotenoids and β-carotene content The control group without β-ionone treatment increased by 9.3-33.0% and 16.2-38.1% respectively (see figure 2 ).
Embodiment 3
[0056] (1) activation culture (with embodiment 1)
[0057] (2) Induction culture
[0058] When Dunaliella pasteurii cells were in stationary phase (OD 630 =1.421), add 0, 1, 2, 5, 20 and 50mg / Lβ-ionone to the algae liquid respectively, and continue culturing for 4 days.
[0059] (3) pigment extraction (with embodiment 1)
[0060] (4) Content determination
[0061] After calculation, it was found that adding 1, 2 and 5 mg / L of β-ionone to treat Dunaliella pasteurii for 4 days, the content of total carotenoids and β-carotene increased by 13.9-13.9% compared with the control group without β-ionone. 28.6% and 31.0~39.3%, while the high concentration of 50mg / L β-ionone was treated for 4 days, the total carotenoid and β-carotene content was significantly higher than that of the control group due to the decrease in the cell biomass of Dunaliella pasteurii. reduce (see image 3 ). It shows that low concentration of β-ionone can promote the accumulation of total carotenoids and β...
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