Prepn process of high-concentration photosynthesis bacterial prepn
A photosynthetic bacteria preparation and technology of photosynthetic bacteria, applied in the direction of bacteria, etc., can solve the problems affecting the quality of the bacteria agent, the cumbersome operation process, and the difficulty in guaranteeing the quality, and achieve the effects of shortening the production time, increasing the yield of bacteria, and improving production efficiency
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0016] 1. Prepare bacterial strains: photosynthetic bacteria adopt Rhodopseudomonas capsulata and Rhodopseudomonas palustris Rps.Palustris, respectively culture these two strains and mix them at a volume ratio of 1:1 to obtain a mixed strain;
[0017] 2. Preparation of culture medium: Weigh 1.5kg of yeast extract, 0.5kg of potassium dihydrogen phosphate, 0.3kg of magnesium sulfate, 2.5kg of sodium acetate, and 0.8kg of fulvic acid, dissolve them in 1000kg of water, add 1kg of papaya extract, and adjust The pH value is 7.0;
[0018] 3. Cultivate strains: Add 180kg of mixed strains into the culture medium, mix evenly, put it into a transparent plastic bucket, plug it with a cotton plug, and cultivate it under the conditions of temperature 32-35°C and light intensity 2000LX for 3-5 days , Shake well every 5 hours during the cultivation process, and when the concentration of viable bacteria in the bacterial solution reaches more than 3 billion / ml, it will be made into a photosynth...
Embodiment 2
[0020] 1. Prepare strains: photosynthetic bacteria adopt Rhodobacter capsulatus, Rhodobacter palustris Rps.rutila and Rhodopseudomonas globosa Rps.Globiformis. The three bacterial strains are cultured separately and mixed according to the volume ratio of 1:1:1 to obtain the mixed strain;
[0021] 2. Preparation of culture medium: Weigh 2kg of yeast extract, 0.5kg of potassium dihydrogen phosphate, 0.5kg of magnesium sulfate, 3kg of sodium acetate, and 0.5kg of fulvic acid, dissolve them in 1000kg of water, then add 1.5kg of papaya extract to adjust the pH Value is 7.0;
[0022] 3. Cultivation of strains: Add 200kg of mixed strains into the culture medium, mix evenly, put them into a transparent plastic bucket, plug them with cotton plugs, and cultivate them for 4 days at a temperature of 32-35°C and a light intensity of 2500LX. Shake once every 5 hours during the process, and when the concentration of viable bacteria in the bacterial solution reaches more than 3 billion / ml, i...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More