Preparation of composite bacteria

A production method and technology of composite bacteria, applied in the direction of using microorganisms, methods based on microorganisms, biochemical equipment and methods, etc., can solve the problems of inability to grasp the composition of bacteria, low decomposition efficiency, unstable effect, etc., to achieve The effect of good stability and practical value

A production method and technology of composite bacteria, applied in the direction of using microorganisms, methods based on microorganisms, biochemical equipment and methods, etc., can solve the problems of inability to grasp the composition of bacteria, low decomposition efficiency, unstable effect, etc., to achieve The effect of good stability and practical value

CN101481676BInactive Publication Date: 2011-01-19BIOGAS SCI RES INST MIN OF AGRI

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  • Preparation of composite bacteria
  • Preparation of composite bacteria
  • Preparation of composite bacteria

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0029] The following 13 strains were mixed and inoculated in a cellulose-containing culture solution, sealed and allowed to stand and cultivated at a culture temperature of 40°C and a pH of 6.5. The ratio of the number of cells of each strain to the total number of complex bacteria in the 13 strains was respectively They are: Cytophaga fermentans 10%, Clostridium papyrosolvens 25%, Desulfovibrio vulgaris 1%, Butyrivibrio fibrisolvens 5%, Acetobacterium woodii 5%, Cellulomonas flavigena 1%, Clostridium termitidis 1%, Clostridium cellobioparum 2.5% Wolfei 5%, Methanosarcina barkeri 19%, Methanobrevibacter arboriphilicus 15%, Methanosphaera stadtmaniae 8%, and Methanococcus vannielii 2.5%. The formula of the above-mentioned cellulose-containing culture solution is as follows: NaCl 3‰, cellulose (straw) 5‰, urea 1‰, peptone 1‰, yeast powder 0.5‰, CaCO 3 2‰, with water as solvent, the above content refers to CaCO 3 The ratio of the quality of NaCl, cellulose, urea, peptone, and yeas...

Embodiment 2

[0033] The following 13 strains were mixed and inoculated in a cellulose-containing culture solution, sealed and allowed to stand and cultivated at a culture temperature of 40°C and a pH of 6.5. The ratio of the number of cells of each strain to the total number of complex bacteria in the 13 strains was respectively Cytophaga fermentans accounted for 7.5%, Clostridium papyrosolvens accounted for 35%, Desulfovibrio vulgaris accounted for 3%, Butyrivibrio fibrisolvens 4%, Acetobacterium woodii accounted for 5%, Cellulomonas flavigena accounted for 5%, Clostridium termitidis accounted for 3%, and Clostridium cellobioparum accounted for 5%. Wolfei 5%, Methanosarcina barkeri 10%, Methanobrevibacter arboriphilicus 10%, Methanosphaera stadtmaniae 5%, and Methanococcus vannielii 2.5%. The formula of the above-mentioned cellulose-containing culture solution is as follows: NaCl 5‰, cellulose (straw) 8‰, urea 2‰, peptone 2‰, yeast powder 1‰, CaCO 3 2‰, with water as solvent, the above con...

Embodiment 3

[0038] The following 13 strains were mixed and inoculated in a cellulose-containing culture solution, sealed and allowed to stand and cultivated at a culture temperature of 40°C and a pH of 6.5. The ratio of the number of cells of each strain to the total number of complex bacteria in the 13 strains was respectively As follows: Cytophaga fermen tans accounted for 5%, Clostridium papyrosolvens accounted for 30%, Desulfovibrio vulgaris accounted for 1%, Butyrivibrio fibrisolvens 5%, Acetobacterium woodii accounted for 5%, Cellulomonas flavigena accounted for 5%, Clostridium termitidis accounted for 2%, Clostridium celloparitidis accounted for 2%, Syntrophomonas Wolfei 6%, Methanosarcina barkeri 20%, Methanobrevibacter arboriphilicus 10%, Methanosphaera stadtmaniae 5%, and Methanococcus vannielii 3%. The formula of the above-mentioned cellulose-containing culture solution is as follows: NaCl 7‰, cellulose (straw) 10‰, urea 4‰, peptone 3‰, yeast powder 1.5‰, CaCO 3 2‰, with water a...

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Abstract

The invention discloses a method for preparing composite bacterium, comprising the following steps: inoculating microorganism of zymogenous bacteria, hydrogen-producing acetogenic bacteria and methanogen respectively belonging to facultative anaerobic bacteria and strict anaerobic bacteria which are mixed according to a certain proportion into a culture solution containing cellulose, sealing and keeping standing to culture at a temperature of between 30 to 50 DEG C and pH value of 3 to 10, wherein the culture solution containing cellulose contains CaCO3, 0.3 to 0.7 percent of NaCl, 0.5 to 1 percent of cellulose, 0.1 to 0.4 percent of urea, 0.1 to 0.3 percent of peptone and 0.05 to 0.15 percent of yeast powder, and water is used as a solvent. The composite bacterium having effective cellulose degrading property and capable of generating methane is prepared by the method.

Description

Technical field [0001] The invention relates to the technical field of cellulose degradation and energy utilization, in particular to a manufacturing method of a composite bacteria that degrades cellulose and produces methanogen. Background technique [0002] Natural fiber materials are the most abundant biomass on earth. Except for a small part of it is used, most of them exist in the natural environment in the form of waste. In order to make full use of this kind of abundant renewable resources, scholars began to study the biodegradation of cellulose as early as 1883 and 1886, especially because the price of fossil energy such as petroleum and coal has been rising in recent years, and the bio-transformation of cellulose into The issue of new energy has received extensive attention from scholars at home and abroad. [0003] In the natural state, the complete degradation of cellulose is the result of the long-term interaction of multiple microorganisms in the microbial system. Thi...

Claims

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Application Information

Patent Timeline
19 Jan 2011
Publication
CN101481676B
IPC
C12N1/22; C12R1/145; C12R1/63; C12R1/02; C12R1/01
Inventors
邓宇; 马诗淳