Sporidiobolus pararoseus bacterial strain and application thereof
A yeast strain and lock-throwing technology, applied in fermentation, fungi and other directions, can solve the problems of short fermentation cycle, simple and extensive nutritional requirements, and easy to decline in traits.
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Embodiment 1
[0042] Example 1 Determination of the strain culture of Sporidiobolus pararoseus JD-2 and the fermentation process for enriching β-carotene.
[0043] The selected medium is as follows:
[0044] (1) Incline activation medium (g / L): glucose 20, peptone 1, yeast extract 1, pH 6.0.
[0045] (2) Liquid seed medium (g / L) enriched in β-carotene: glucose 40, corn steep liquor 20, (NH4) 2 SO 4 5. KH 2 PO 4 1. MgSO 4 ·7H 2 O 0.5, pH 6.0, 100mL / 500mL Erlenmeyer flask.
[0046] (3) Liquid fermentation medium enriched with β-carotene (g / L): glucose 40, corn steep liquor 20, (NH4) 2 8O 4 5. KH 2 PO 4 1. MgSO 4 ·7H 2 O 0.5, pH 6.0.
[0047] Fermentation culture method:
[0048] (1) Slant Activation Culture: The strain was transferred from the preserved slant to the activated slant medium, and cultured at 28° C. for 48 hours.
[0049] Liquid seed culture: the strains were inserted from the activated slant medium into the liquid seed medium, and cultured at 28° C. for 16 hou...
Embodiment 2
[0052] Example 2 The strain culture of Sporidiobolus pararoseus JD-2 and the determination of the fermentation process for enriching rhododromolene.
[0053] The selected medium is as follows:
[0054] (1) Incline activation medium (g / L): glucose 20, peptone 1, yeast extract 1, pH 6.0.
[0055] (2) Liquid seed medium (g / L) enriched with rhodozymene: glucose 40, yeast extract 20, (NH4) 2 SO 4 5. KH 2 PO 4 1. MgSO 4 ·7H 2 O 0.5, pH6.0, 100mL / 500mL Erlenmeyer flask.
[0056] (3) Liquid fermentation medium (g / L) enriched with rhododactylene: glucose 40, yeast extract 20, (NH4) 2 SO 4 5. KH 2 PO 4 1. MgSO 4 ·7H 2 O 0.5, pH 6.0.
[0057] Fermentation culture method:
[0058] (1) Slant Activation Culture: The strain was transferred from the preserved slant to the activated slant medium, and cultured at 28° C. for 48 hours.
[0059] Liquid seed culture: the strain was transferred from the activated slant medium into the liquid seed medium, and cultured at 28° C. for...
Embodiment 3
[0062] Example 3 Extraction of Carotenoids
[0063] The specific process for preparing the carotenoid extract in the aforementioned Examples 1 and 2 can be: centrifuge the bacterial solution containing Sporidiobolus pararoseus JD-2 at 4000r / min for 10min to obtain the bacterial cells, wash with deionized water Once, after centrifuging to remove water, add 0.6mol / L hydrochloric acid, raise the temperature in the sterilizing pot to 115°C, quickly deflate and reduce the pressure, centrifuge to remove hydrochloric acid, wash the precipitate with deionized water once, centrifuge again to remove water, add volume The mixture of alcohol and n-hexane with a ratio of 4:1 was shaken and extracted at room temperature for 30 minutes, then centrifuged (4000r / min, 10 minutes), and the supernatant was concentrated at 40°C and a vacuum of 0.1Mpa to obtain Carotene crude extract.
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