Hydroxy alkanoic acid polymer and its producing method

A technology of hydroxyalkanoic acid and production method, applied in bacteria, fermentation and other directions, can solve the problems of increasing production cost, increasing the difficulty of product extraction by PHA, and high price

Inactive Publication Date: 2006-11-08
SHANXI UNIV
View PDF2 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

In addition, genetically recombinant bacteria are generally not used as production strains in the production process of food and medical products to avoid biosafety problems
(4) In the relevant research on hydroxyalkanoic acid polymers similar to the present invention, the main raw materials used are olive oil and oleic acid, soybean oil and lauric acid, sodium gluconate and lauric acid, etc., and no downstream extraction has been reported. and processing
Generally speaking, using oil as a carbon source to ferment and produce PHA will increase the difficulty of product extraction and often affect the quality of PHA
However, using sodium gluconate as a fermentation raw material will increase production costs and affect its application range due to its high price.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Hydroxy alkanoic acid polymer and its producing method
  • Hydroxy alkanoic acid polymer and its producing method
  • Hydroxy alkanoic acid polymer and its producing method

Examples

Experimental program
Comparison scheme
Effect test

example 1

[0072] Example 1 takes glucose as the fermentative production of carbon source synthesis P (HBHO)

[0073] (1) Inclined plane and shake flask seed culture

[0074] Inoculate the preserved S. fredii strain on the slant medium, activate it twice in an incubator at 30°C, transfer it to a shake flask containing a shake flask seed medium, and activate it twice again, and wait for the next stage of shaking Flask cultured for 14 hours, when the bacterial cell concentration reached 1.53g stem cells / L (OD 600 When the value is 3.0), the cell growth is still in the logarithmic growth phase, which is used as the seed liquid of the seed tank for subsequent use.

[0075] (2) Seed tank seed culture

[0076] Take a 10L self-control tank as the seed tank, use fermented seed culture medium, the filling coefficient is 0.7, insert the seed solution, the inoculum amount is 8%, cultivate at 30°C, adjust and control the pH to 7.0-7.2 through 8mol NaOH solution, and keep the solution When the oxy...

Embodiment 2

[0084] Embodiment 2 uses starch hydrolyzate as the fermentative production of carbon source synthesis P (HBHO)

[0085] (1) Inclined plane and shake flask seed culture

[0086] Inoculate the preserved S. fredii strain on the slant medium, activate it twice in an incubator at 28°C, transfer it to a shake flask containing a shake flask seed medium, and activate it twice again, and wait for the next stage of shaking Flask cultured for 16 hours, when the bacterial cell concentration reached 2.3g stem cells / L (OD 600 When the value is 4.5), the cell growth is still in the logarithmic growth phase, and it is used as the seed liquid of the seed tank for subsequent use.

[0087] (2) Seed tank seed culture

[0088] A 10L self-control tank is used as the seed tank, a fermented seed medium is used, the filling coefficient is 0.7, the seed solution is inserted, the inoculation amount is 8%, and the culture is carried out at 28°C, and the pH is adjusted and controlled by 8 mol of NaOH so...

Embodiment 3

[0094] Embodiment 3, use waste molasses as the fermentative production of carbon source synthesis P (HBHO)

[0095] (1) Inclined plane and shake flask seed culture

[0096] Inoculate the preserved S. fredii strain on the slant medium, activate it twice in an incubator at 32°C, transfer it to a shake flask containing a shake flask seed medium, and activate it twice again, and wait for the next stage of shaking Flask cultured for 18h, when the bacterial cell concentration reached 2.85g stem cells / L (OD 600 When the value is 5.5), the cell growth is still in the logarithmic growth phase, and it is used as the seed liquid of the seed tank for subsequent use.

[0097] (2) Seed tank seed culture

[0098] Use a 10L self-control tank as the seed tank, use a fermented seed medium with a loading coefficient of 0.7, insert the seed liquid, and inoculate the amount of 10%, cultivate at 32°C, adjust and control the pH to 7.0-7.2 through 8mol NaOH solution, and maintain the solution. Whe...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The invention discloses a polymer of hydroxyalkanoic acid, that is, a polymer of 3-hydroxybutyric acid and 3-hydroxyoctanoic acid [P(3-HB-co-3-HO), hereinafter referred to as P(HBHO)]. The production method is as follows: select Sinorhizobium fredii as the production strain, use carbohydrates as the carbon source, ammonium salt as the nitrogen source, under the optimum medium and culture conditions, through high-density fermentation and lauric acid Regulation of salt metabolism to obtain P(HBHO) products. And the fermentation management method, separation and purification method and quality detection method of P(HBHO) were established. The output of P(HBHO) produced by this method reaches 14.4g / L~22.1g / L, and its molecular weight is controlled at 11.2×10 4 Da~18.5×10 4 Between Da, the endotoxin content can be controlled at 4EU / g~6EU / g, which is lower than the minimum standard of 20EU / g stipulated by the US FDA. Therefore, this new nanoscale lipid material can be used in biomedicine and medical tissue engineering .

Description

technical field [0001] The invention relates to a polymer compound obtained by forming a carboxylate bond on a polymer main chain, and specifically belongs to a hydroxyalkanoic acid polymer (hereinafter referred to as PHA) and a production method thereof. Background technique [0002] PHA is a kind of high molecular polymer with simple structure biosynthesized, and it is the main carbon source and energy storage material of prokaryotes. Under the condition of unbalanced metabolism, prokaryotes will use the remaining nutrients to synthesize PHA and distribute it discretely in the cells in the form of particles, and its content can reach up to 90% of the dry weight of the cells. Decomposition and utilization. It is precisely because of this biological characteristic that endows this kind of material with biorenewability and biodegradability. [0003] Studies have shown that PHA has very similar physical and chemical properties to general-purpose plastics, such as polypropyle...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Patents(China)
IPC IPC(8): C08G63/06C12P7/42C12N1/20
Inventor 赵良启冯涛肖婧凡王海宾
Owner SHANXI UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap