Culture medium capable of increasing biomass of rhodotorula glutinis and application of culture medium
A technology of rhodotorula viscosus and culture medium, which is applied in the field of medium for increasing the biomass of rhodotorula viscoscens, which can solve problems such as waste of resources, slow cell proliferation rate, and difficulty in adapting to the industrial production of rhodotorula viscoscens, and achieve the effect of reducing costs
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0031] Embodiment 1 sticky rhodotorula culture medium preparation
[0032] (1) Dissolve 100g of malt extract powder in 1L of distilled water, centrifuge at 4000r / min for 15min, filter with filter paper, and dilute the supernatant 1×10 5 Pa autoclave for 15 minutes;
[0033] (2) Combine the centrifuged precipitate in step (1) and the precipitate formed during the sterilization process, stir with 4 times the volume of distilled water at a high speed of 2600r / min for 30min, and centrifuge the supernatant at 4000r / min for 20min Combine with the centrifuged supernatant of step (1), adjust the pH value of the solution to 5.0, and then pass through 1×10 5 Pa high-pressure sterilization again for 15 minutes to obtain Rhodotorula viscosus medium.
Embodiment 2
[0034] Embodiment 2 sticky rhodotorula culture medium preparation
[0035] (1) Dissolve 100g of malt extract powder in 1L of distilled water, centrifuge at 3000r / min for 15min, filter with filter paper, and dilute the supernatant 1×10 5 Pa autoclave for 30min;
[0036] (2) Combine the centrifuged sediment in step (1) and the precipitate formed in the sterilization process, use 2 times the volume of distilled water for ultrasonic treatment at 800W for 15 minutes, and centrifuge the supernatant at 3000r / min for 15 minutes with step ( 1) Combine the centrifuged supernatants, adjust the pH value of the solution to 5.5, and then pass through 1×10 5 Pa high-pressure sterilization again for 30 minutes to obtain Rhodotorula viscosus medium.
Embodiment 3
[0037] Embodiment 3 sticky rhodotorula culture medium preparation
[0038] (1) Dissolve 100g of malt extract powder in 1L of distilled water, centrifuge at 6000r / min for 15min, filter with filter paper, and dilute the supernatant 1×10 5 Pa autoclave for 20min;
[0039] (2) Combine the centrifugal sediment in step 1) and the sediment formed in the sterilization process, carry out high-speed 800r / min stirring with 5 times the volume of distilled water for 60min, and centrifuge at 6000r / min for 15min with the supernatant The centrifuged supernatant of step (1) was combined, and the pH value of the solution was adjusted to 5.3, and then subjected to 1×10 5 Pa high-pressure sterilization again for 20 minutes to obtain Rhodotorula viscosus medium.
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 