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Preparation technique of photosynthetic bacteria preparation

A photosynthetic bacteria preparation and preparation technology technology, applied in the biological field, can solve the problems of low production efficiency, low bacterial content in the culture solution, easy to contaminate bacteria, etc., and achieve the effects of reducing production cost, shortening production time, and improving growth efficiency.

Inactive Publication Date: 2009-04-15
GUANGZHOU INST OF GEOCHEMISTRY - CHINESE ACAD OF SCI
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, a variety of methods and devices for cultivating photosynthetic bacteria have been developed. These methods are mainly based on the principle that photosynthetic bacteria can grow under anaerobic light conditions. The facilities are usually glass containers, plastic film bags, etc., and the facilities are simple. , the investment is small, and the existing problems are mainly that the cultivation time is long (generally 4-7 days), the production efficiency is low, the bacterial content of the culture solution is small (generally only 3 billion / mL), and it is easy to be contaminated. Unstable quality
Although some people have carried out the test of cultivating photosynthetic bacteria with aerated fermentation, it is still difficult to standardize, scale and industrialize the production of photosynthetic bacteria preparations due to the lack of perfect technology such as medium formula and culture process conditions.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0017] Preparation of medium:

[0018] According to following composition and proportioning (mass ratio), prepare the substratum of shaker culture and ventilated fermenter culture aerobic culture:

[0019] Glucose 0.9%, urea 0.04%, dipotassium hydrogen phosphate (K 2 HPO 4 )0.02%, potassium dihydrogen phosphate (KH 2 PO 4 ) 0.02%, magnesium sulfate (MgSO 4 ·7H 2 O) 0.02%, sodium chloride (NaCl) 0.20%, calcium chloride (CaCl 2 ) 0.03%, water 98.77%. Then, based on the total weight of the above medium, 0.20% of fulvic acid was added.

[0020] The culture medium used for slant seed culture is a solid culture medium made by adding 1.5% agar (mass ratio) on the basis of shaker culture and ventilated fermenter culture medium.

[0021] All media are sterilized.

[0022] Preparation process:

[0023] Inoculate Rhodopseudomonas palustris on the slant solid medium for activation, cultivate the slant at a temperature of 33°C for 48 hours to obtain slant seeds, insert the activa...

Embodiment 2

[0025] Preparation of medium:

[0026] According to following composition and proportioning (mass ratio), prepare the substratum of shaker culture and ventilated fermenter culture aerobic culture:

[0027] Glucose 1.0%, urea 0.06%, dipotassium hydrogen phosphate (K 2 HPO 4 )0.025%, potassium dihydrogen phosphate (KH 2 PO 4 ) 0.025%, magnesium sulfate (MgSO 4 ·7H 2 O) 0.025%, sodium chloride (NaCl) 0.25%, calcium chloride (CaCl 2 ) 0.03%, water 98.58%. Based on the total weight of the above medium, add 0.10% fulvic acid.

[0028] The culture medium that is used for slant seed culture is to add 1.5% agar (weight ratio) on the basis of shaker culture and aerated fermenter medium, and is made into a solid medium for slant culture.

[0029] All media are sterilized.

[0030] Preparation Process Engineering:

[0031] Inoculate Rhodopseudomonas palustris on the slant solid medium for activation, cultivate the slant at 34°C for 48 hours to obtain slant seeds, insert the acti...

Embodiment 3

[0033] Preparation of medium:

[0034] According to following composition and proportioning (mass ratio), prepare the substratum of shaker culture and ventilated fermenter culture aerobic culture:

[0035] Glucose 1.1%, urea 0.06%, dipotassium hydrogen phosphate (K 2 HPO 4 )0.03%, potassium dihydrogen phosphate (KH 2 PO 4 )0.03%, magnesium sulfate (MgSO 4 ·7H 2 O) 0.03%, sodium chloride (NaCl) 0.3%, calcium chloride (CaCl 2 ) 0.05%, water 98.40%. Based on the weight of the above medium, 0.30% (weight ratio) of fulvic acid was added as a growth promoter.

[0036] The culture medium that is used for slant seed culture is to add 1.5% agar (weight ratio) on the basis of shaker culture and aerated fermenter medium, and is made into a solid medium for slant culture.

[0037] All media are sterilized.

[0038] Preparation process:

[0039] Inoculate Rhodopseudomonas palustris on the slant solid medium for activation, cultivate the slant at 32°C for 48 hours to obtain slant ...

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Abstract

The invention discloses a preparation technique of a photosynthetic bacteria reagent, which comprises rhodopseudomonas palustris strain cultivation steps that include activated strain cultivation with an inclined plane, strain cultivation with a shaking table, cultivation with an aerated fermenting jar and the like, and adopts the culture medium comprising a basic culture medium and a growth promoting agent. The basic culture medium comprises following components by mass: 0.9 to 1.1 percent of glucose, 0.04 to 0.06 percent of carbamide, 0.02 to 0.03 percent of dipotassium hydrogen phosphate, 0.02 to 0.03 percent of monopotassium phosphate, 0.02 to 0.03 percent of magnesium sulfate, 0.20 to 0.30 percent of sodium chloride, 0.03 to 0.05 percent of calcium chloride and 98.40 to 98.77 percent of water. The added growth promoting agent is 0.10 to 0.30 percent of fulvic acid by mass referring to the basic culture medium. The photosynthetic bacteria reagent that is obtained by the preparation technique can reach the lysate concentration of 4000 to 6000 million per milliliter, and can be used in multiple fields of aquiculture, wastewater processing, crop production and the like.

Description

Technical field: [0001] The invention belongs to the field of biological technology, and relates to a preparation process of photosynthetic bacteria preparation. Background technique: [0002] Photosynthetic bacteria are a group of bacteria that can use organic matter as oxygen provider and carbon source under anaerobic light or aerobic dark conditions. Photosynthetic bacteria are widely used in aquaculture, wastewater treatment, planting and other fields. At present, a variety of methods and devices for cultivating photosynthetic bacteria have been developed. These methods are mainly based on the principle that photosynthetic bacteria can grow under anaerobic light conditions. The facilities are usually glass containers, plastic film bags, etc., and the facilities are simple. , the investment is small, and the existing problems are mainly that the cultivation time is long (generally 4-7 days), the production efficiency is low, the bacterial content of the culture solution ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12N1/20C12R1/01
Inventor 陈繁忠付广义余旭录
Owner GUANGZHOU INST OF GEOCHEMISTRY - CHINESE ACAD OF SCI
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