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
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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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