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Method for constructing microorganism co-culture system for producing bacterial cellulose

A technology of co-cultivation system and bacterial cellulose, which is applied in the field of microbial co-cultivation system construction, can solve the problems of consumption and high viscosity, and achieve the effects of strong operability, optimized growth conditions, and simple procedures

Active Publication Date: 2016-06-15
NANJING UNIV OF SCI & TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The method uses Acetobacter xylinum to secrete acetic acid during the fermentation process, and Chlamydomonas is a microorganism with acetic acid as a carbon source, which can consume acetic acid in the fermentation broth and maintain the pH of the environment at an appropriate level. The co-cultivation of the two microorganisms can achieve Mutual benefit and symbiosis solves the problem of dissolved oxygen caused by high viscosity in the later stage of fermentation. At the same time, it can maintain a stable pH during the fermentation process and increase the yield of bacterial cellulose from 3.67g / L to 5.21g / L.

Method used

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  • Method for constructing microorganism co-culture system for producing bacterial cellulose
  • Method for constructing microorganism co-culture system for producing bacterial cellulose
  • Method for constructing microorganism co-culture system for producing bacterial cellulose

Examples

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Effect test

Embodiment 1

[0025] The present invention is a method for improving bacterial cellulose production by constructing a microbial co-cultivation system:

[0026] The first step: the two microorganisms are respectively expanded and cultivated in the seed liquid. Acetobacter xylinum was cultured on a shaker at 30°C and 160 rpm for 36 hours, and Chlamydomonas was cultured in a light incubator at 22°C and 160 rpm for 36 hours to prepare various microbial seed solutions;

[0027] Step 2: After the Chlamydomonas seed liquid is concentrated by centrifugation, add 10mL of 0.8% (w / v) sodium alginate sol, mix evenly, and use a syringe pump to control the flow rate to 200mL / h and inject to a concentration of 1%. (w / v) immobilized in calcium chloride solution, the disposable syringe needle volume used for immobilizing Chlamydomonas is 10mL, and inner diameter is 0.4mm, and Chlamydomonas is fixed in the linear gel;

[0028] The third step: after Acetobacter xylinum is inoculated into the fermentation med...

Embodiment 2

[0031] The present invention is a method for improving bacterial cellulose production by constructing a microbial co-cultivation system:

[0032] The first step: the two microorganisms are respectively expanded and cultivated in the seed liquid. Acetobacter xylinum was cultured on a shaker at 29°C and 150 rpm for 36 hours, and Chlamydomonas was cultured in a light incubator at 23°C and 160 rpm for 36 hours to prepare various microbial seed solutions;

[0033] Step 2: After the Chlamydomonas seed liquid is concentrated by centrifugation, add 10mL of 1.0% (w / v) sodium alginate sol, mix evenly, and use a syringe pump to control the flow rate to 200mL / h and inject to a concentration of 0.8% (w / v) immobilized in calcium chloride solution, the disposable syringe needle volume used for immobilizing Chlamydomonas is 10mL, and inner diameter is 0.4mm, and Chlamydomonas is fixed in the linear gel;

[0034] Step 3: After Acetobacter xylinum is inoculated into the fermentation medium wit...

Embodiment 3

[0037] The present invention is a method for improving bacterial cellulose production by constructing a microbial co-cultivation system:

[0038] The first step: the two microorganisms are respectively expanded and cultivated in the seed solution. Acetobacter xylinum was cultured on a 29°C 160rpm shaker for 36h, and Chlamydomonas was cultured in a light incubator at 22°C 160rpm for 36h to prepare various microbial seed solutions;

[0039] Step 2: after the Chlamydomonas seed liquid is concentrated by centrifugation, add 10mL of 0.8% (w / v) sodium alginate sol, mix evenly, and use a syringe pump to control the flow rate to 200mL / h and inject to a concentration of 1.0% (w / v) immobilized in calcium chloride solution, the disposable syringe needle volume used for immobilizing Chlamydomonas is 10mL, and inner diameter is 0.4mm, and Chlamydomonas is fixed in the linear gel;

[0040] Step 3: After Acetobacter xylinum is inoculated into the fermentation medium with 10% inoculation amo...

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Abstract

The invention discloses a method for constructing a microorganism co-culture system for producing bacterial cellulose. The method comprises the following steps: conducting seed amplification culture on acetobacter xylinum NUST4.2 and chlamydomonas in a separated mode, immobilizing chlamydomonas cells in calcium alginate by virtue of a micro-fluidic technique, and then conducting co-culture; and after culture, removing acetobacter xylinum cells and the chlamydomonas, so that pure bacterial cellulose is obtained. The chlamydomonas, as an oxygen producing microorganism adopted by the invention, can provide oxygen to the production of the bacterial cellulose in the later fermentation period, so that the problem of dissolving of oxygen caused by viscosity is solved. In addition, the acetobacter xylinum can secrete acetic acid during fermenting, and the chlamydomonas, which is a microorganism taking the acetic acid as a carbon source, can consume the acetic acid in a fermentation broth, so that ambient pH value is kept at an appropriate level. According to the scheme, a feasible solution is provided for solving the problem of dissolving of oxygen caused by excessive viscosity in the later fermentation period and for keeping the pH value stable during fermenting is provided, and a method for constructing a microorganism co-culture system for producing bacterial cellulose is provided.

Description

technical field [0001] The present invention improves the yield of bacterial cellulose by constructing a co-cultivation system of Acetobacter xylinum NUST4.2 (abbreviated as Ax.4.2) and Chlamydomonas, and realizes precise control of the cellulose micro-nano scale assembly process, specifically It involves the construction of a microbial co-culture system. Background technique [0002] Bacterial Cellulose (BC) is a new type of high-performance microbial synthetic material biosynthesized by Acetobacter xylinum. Compared with other forms of cellulose, although it has the same chemical composition, it also has special properties. Physicochemical and biological characteristics, especially the diversity of fermentation substrates and microorganisms that can be adjusted during the fermentation process. [0003] As a new biofunctional material, the production of bacterial cellulose has been industrialized. But so far, there are still many problems to be solved in the industrial pr...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12P39/00C12P19/04C12R1/02C12R1/89
Inventor 孙东平张衡杨加志朱春林陈春涛黄洋陈啸
Owner NANJING UNIV OF SCI & TECH
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