Rhodotorula mucilaginosa for producing beta-caroten, beta-caroten and its production method
A technology of carotene and Torula rhodozyme, applied in the direction of microorganism-based methods, biochemical equipment and methods, fermentation, etc., can solve the problem of low β-carotene content, achieve short growth cycle, high yield, temperature and Effects over a wide pH range
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[0028] Example 1: Isolation and identification of β-carotene-producing Rhodotorulamucilaginosa CGMCC No. 1536
[0029] 1. Sample collection
[0030] Soil samples were collected from abandoned gardens in Urumqi, Xinjiang. After screening, optimization and other technical means, they were placed on a plate suitable for yeast medium, such as YPD medium (20% glucose, 20% peptone, 10% yeast extract), and separated at 28°C. The XJU-1 strain of Rhodotorulamucilaginosa was obtained.
[0031] 2. Bacteria identification
[0032] They were identified by molecular taxonomy based on the base sequence of the D1 / D2 region in the large subunit 26S rDNA and the base sequence analysis of the small subunit 5.8S rDNA and two internal transcribed spacers (ITS1 and ITS2). Combined with morphological observation and determination of physiological and biochemical properties, it was accurately identified as Rhodotorula mucilaginosa CGMCC No.1536.
Example Embodiment
[0033] Example 2: Cultivation of β-carotene-producing Rhodotorulamucilaginosa CGMCC No. 1536 strain and determination of fermentation process.
[0034] The selected medium is as follows:
[0035] ①Slant activation medium: glucose 2%; peptone 2%; yeast powder 1%; pH 9.0.
[0036] ②Liquid seed medium: glucose 2%; peptone 2%; yeast powder 1%; pH 8.5.
[0037] ③Liquid fermentation medium: glucose 4%; peptone 2%; yeast powder 1%; pH 8.0.
[0038] The present invention adopts conventional culture medium, but has special requirements for pH, and conventional fermentation is carried out in a slightly acidic environment, while the strain of the present invention can produce high beta-carotene in a slightly alkaline condition.
[0039] Fermentation culture method (referring to accompanying drawing 1):
[0040] ①Slant activation culture: connect the strain from the preservation slant to the activated slant medium, and cultivate at 28°C for 48h.
[0041] ②Liquid seed culture: connecte...
Example Embodiment
[0044] Example 3: Process for producing β-carotene by fermentation of Rhodotorula mucilaginosa CGMCC No.1536 strain.
[0045] The fermentation process steps in Example 2 were repeated, and the specific parameters in the fermentation process were repeatedly verified. The long-preserved strain of the present invention was inoculated into potato agar medium, under the conditions of pH 7.0, temperature 25° C., and shaking speed of 150 r / min, after culturing on a solid slant for 48.2 hours, fermentation was performed, and the fermentation broth was centrifuged (3000 rPmin) After 10 minutes, the supernatant was discarded, the precipitate was washed with water, and then centrifuged again. The obtained yeast mud was dried and weighed, and subjected to post-processing such as concentration and crystallization to obtain β-carotene, and the yield was 368 μg / g.
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