Method for increasing yield of bacterium curdlan by using acinetobacter

A technology of Acinetobacter lwedenii and bacteria is applied in the field of increasing the yield of keratin, which can solve the problem of high price of keratin and achieve the effect of increasing the yield of keratin.

Active Publication Date: 2015-09-09
DONGHUA UNIV +1
View PDF3 Cites 4 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the price of curdlan gum is still relatively high at present, increasing the output of curdlan gum and reducing production costs are the main direction of curdlan fermentation production

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

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0022] (1) Acinetobacter ruckeri CGMCC 1.3778 was selected and purchased from China General Microorganism Culture Collection Center (CGMCC). Get a ring of bacteria from the slant of Acinetobacter ruckeri and inoculate it into a 250ml Erlenmeyer flask with 50ml seed culture medium, and cultivate it by shaking at 28°C and 200rpm for 20h, and use it as a seed solution; wherein, the composition of the medium (g / L) is : Peptone 10g, yeast extract 2g and MgSO 4 ·7H 2 O 1g;

[0023] (2) The curdlan-producing fungus Rhizobium ATCC 31750 was selected and purchased from the American ATCC Culture Collection. Take a ring of strains from the rhizobia slant and inoculate them into a 250ml Erlenmeyer flask containing 50ml of seed medium, and culture them with shaking at 28°C for 20 hours at a speed of 150rpm to obtain curdlan gum-producing bacteria seed liquid; wherein, the composition of the medium Same as step (1);

[0024] (3) the seed liquid of Acinetobacter ruckeri prepared in step ...

Embodiment 2

[0028] (1) Acinetobacter ruckeri CGMCC 1.3778 was selected and purchased from China General Microorganism Culture Collection Center (CGMCC). Get a ring of bacteria from the slant of Acinetobacter ruckeri and inoculate it into a 250ml Erlenmeyer flask with 50ml of seed culture medium, and cultivate it by shaking at 32°C and 150rpm for 22h, and use it as a seed solution; wherein, the composition of the culture medium is the same as in Example 1;

[0029] (2) The curdlan-producing bacterium Agrobacterium ATCC 31749 was selected and purchased from the American ATCC Culture Collection. Take a ring of strains from the slant of Agrobacterium and inoculate them into a 250ml Erlenmeyer flask containing 50ml of seed medium, shake and culture at 32°C for 16h, with a rotation speed of 240rpm, to obtain the seed liquid of curdlan producing bacteria; wherein, the composition of the medium Same as step (1);

[0030] (3) The seed solution of Acinetobacter ruckeri prepared in step (1) and the...

Embodiment 3

[0034] (1) Acinetobacter ruckeri CGMCC 1.3778 was selected and purchased from China General Microorganism Culture Collection Center (CGMCC). Get a ring of bacteria from the slant of Acinetobacter ruckeri and inoculate it into a 250ml Erlenmeyer flask with 50ml of seed culture medium, and cultivate it by shaking at 30°C and 240rpm for 24h, and use it as a seed solution; wherein, the composition of the culture medium is the same as in Example 1;

[0035] (2) The curdlan-producing fungus Rhizobium ATCC 31750 was selected and purchased from the American ATCC Culture Collection. Take a ring of bacteria from the rhizobia slant and inoculate it into a 250ml Erlenmeyer flask with 50ml of seed medium, and culture it at 30°C for 20 hours with shaking at a speed of 200rpm to obtain the curdlan producing bacteria seed solution; wherein, the composition of the medium Same as step (1);

[0036] (3) The seed solution of Acinetobacter ruckeri prepared in step (1) and the seed solution of cur...

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 relates to a method for increasing the yield of bacterium curdlan by using acinetobacter. The method comprises the step of co-culturing acinetobacter lwoffii and curdlan producing bacteria to obtain the bacterium curdlan. By using the method disclosed by the invention, the yield of the curdlan producing bacteria is increased, and a novel method for producing curdlan through microbial fermentation is provided.

Description

technical field [0001] The invention belongs to the field of methods for increasing the yield of curdlan, in particular to a method for increasing the yield of curdlan by using Acinetobacter. Background technique [0002] Curdlan, also known as thermal gel, is a microbial exopolysaccharide mainly produced by bacteria of the genus Agrobacterium sp. and Rhizobium sp. Curdlan gum molecule is a linear molecule composed of glucose structural units connected by β-1,3 glycosidic bonds, without branches, and the relative molecular mass is about 5.3×10 4 ~2.0×10 6 . [0003] Curdlan gum has unique properties such as rheology, thermal gelation and simple structure, and can be widely used in food, biomedicine and other fields. Curdlan gum has the characteristic of heating and solidifying into gel, and the formed gel can be divided into low-grade gel and high-grade gel. Heat the aqueous dispersion of curdlan gum to 55-65°C and then lower the temperature to form a thermally reversibl...

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 Applications(China)
IPC IPC(8): C12P39/00C12P19/04C12R1/01C12R1/41
Inventor 杨雪霞刘毅超付雅欣步国建
Owner DONGHUA 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