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

Active Publication Date: 2018-07-13
HEFEI INSTITUTES OF PHYSICAL SCIENCE - CHINESE ACAD OF SCI +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Use KH 2 PO 4 or K 2 HPO 4 Contain PO 4 3+ If the amount of salt is too small, the phosphorylation level will be insufficient, which will greatly reduce the metabolic flux of carotenoids, and if it is too much, it will bring a large amount of K + , so that the cell membrane permeability of the bacteria becomes too strong, resulting in the precipitation of internal substances such as the target product lycopene into the fermentation clear night
[0003] At the ...

Method used

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  • Method for producing lycopene through fermentation of blakeslea trispora and lycopene
  • Method for producing lycopene through fermentation of blakeslea trispora and lycopene

Examples

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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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Abstract

The invention relates to a method for producing lycopene through fermentation of blakeslea trispora and lycopene, and belongs to the field of fermentation engineering. The method comprises the following steps: respectively culturing positive fungi and negative fungi of the blakeslea trispora, and taking a part of cultured positive fungi and negative fungi of the blakeslea trispora and simultaneously carrying out inoculation; performing fermentation, controlling a pH value of a fermentation system to reach 5.8 to 6.2 by using a regulating agent in a fermentation process, supplementing materialsin a period of 40 to 100 hours after beginning of fermentation, continuously fermenting to 120 hours, and then releasing from a tank, wherein the regulating agent is an acidic substance which contains PO4<3+> and does not contain metallic ions or salt; a fermentation culture medium contains starch phosphate ester substances. The method has the advantages of simpleness and low cost; a fermentationpH value is controlled by the acidic substance which contains PO4<3+> and does not contain metallic ions or salt and PO4<3+> is provided, so that introduction of excessive amount of K<+> is avoided;through cooperative application of the starch phosphate ester substances, the output of the lycopene is increased; therefore, the output of the lycopene is higher, and the method is suitable for industrial production.

Description

technical field [0001] The invention relates to the field of fermentation engineering, and in particular to a method for producing lycopene by B. trispora fermentation and lycopene. Background technique [0002] Existing fermentation methods usually use KH 2 PO 4 or K 2 HPO 4 Contain PO 4 3+ salt to increase phosphorylation levels and provide K + , enhance the permeability of cell membrane, and benefit the entry of nutrients into cells. Use KH 2 PO 4 or K 2 HPO 4 Contain PO 4 3+ If the amount of salt is too small, the phosphorylation level will be insufficient, which will greatly reduce the metabolic flux of carotenoids, and if it is too much, it will bring a large amount of K + , so that the cell membrane permeability of the bacteria becomes too strong, resulting in the precipitation of internal substances such as the target product lycopene into the fermentation clear night. [0003] At the same time, due to the need to add an alkaline blocking agent during t...

Claims

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Application Information

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IPC IPC(8): C12P5/02C12R1/645
CPCC12P5/007
Inventor 刘洋李翔宇姚建铭
Owner HEFEI INSTITUTES OF PHYSICAL SCIENCE - CHINESE ACAD OF SCI
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