Method for producing lycopene through fermentation of blakeslea trispora and lycopene
A technology of Blakeslea trispora and lycopene, which is applied in the field of fermentation engineering, can solve the problems of reduced metabolic flux of carotenoids, weakened metabolic flux of lycopene, insufficient phosphorylation level, etc., and achieve the exemption of sugar control process , Simplify operation and reduce production cost
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Embodiment 1
[0052] B. trispora positive bacteria and B. trispora negative bacteria were respectively inoculated on the slant surface containing PDA medium, cultured at 28°C for 6 days, then transferred to seed medium, at 28°C, Cultivate for 48 hours under the condition of 220rpm, and feed air at a flow rate of 1.5vvm during the cultivation process.
[0053] The cultured B. trispora positive bacteria and B. trispora negative bacteria were divided into two parts respectively, one part was used for simultaneous inoculation and fermentation with B. trispora of opposite sex, and the other part continued to be cultured. Wherein, the simultaneous inoculation is to inoculate the cultured B. trispora positive bacteria and B. trispora negative bacteria in a weight ratio of 1:5 in a fermenter containing a fermentation medium. The biomass dry weight of B. trispora positive bacteria and B. trispora negative bacteria were both 15g / L at the time of inoculation.
[0054] Simultaneously after the inocula...
Embodiment 2
[0060] B. trispora positive bacteria and B. trispora negative bacteria were respectively inoculated on the slope containing PDA medium, cultured at 26°C for 8 days, then transferred to seed medium, and grown at 26°C, Cultivate for 52 hours under the condition of 200rpm, and feed air at a flow rate of 1vvm during the cultivation process.
[0061] The cultured B. trispora positive bacteria and B. trispora negative bacteria were divided into two parts respectively, one part was used for simultaneous inoculation and fermentation with B. trispora of opposite sex, and the other part continued to be cultured. Wherein, the simultaneous inoculation is to inoculate the cultured B. trispora positive bacteria and B. trispora negative bacteria in a weight ratio of 1:3 in a fermenter containing a fermentation medium. The biomass dry weight of B. trispora positive bacteria and B. trispora negative bacteria was 12g / L at the time of inoculation.
[0062] Simultaneously after the inoculation, ...
Embodiment 3
[0068] B. trispora positive bacteria and B. trispora negative bacteria were respectively inoculated on the slant surface containing PDA medium, cultured at 30°C for 4 days, then transferred to seed medium, at 30°C, Cultivate for 44 hours under the condition of 240rpm, and feed air at a flow rate of 2vvm during the cultivation process.
[0069] The cultured B. trispora positive bacteria and B. trispora negative bacteria were divided into two parts respectively, one part was used for simultaneous inoculation and fermentation with B. trispora of opposite sex, and the other part continued to be cultured. Wherein, the simultaneous inoculation is to inoculate the cultured B. trispora positive bacteria and B. trispora negative bacteria in a weight ratio of 1:7 in a fermenter containing a fermentation medium. The biomass dry weight of B. trispora positive bacteria and B. trispora negative bacteria was 10g / L at the time of inoculation.
[0070] Simultaneously after the inoculation, fe...
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