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Curdlan high-efficiency fermentation control method

A curdlan and control method technology, applied in the field of bioengineering, can solve the problems of wasteful acid production, lack of high-efficiency fermentation control methods of curdlan, and inability to effectively control the generation of metabolic by-products, etc., to achieve the effect of efficient fermentation process

Active Publication Date: 2019-03-01
康彤(上海)生物研发有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] To sum up, there is currently a lack of high-efficiency fermentation control methods for curdlan in this field. Because the generation of metabolic by-products cannot be effectively controlled when using glucose for fermentation, the waste of glucose and acid production during the fermentation process reduces the yield. Therefore, it is urgent to develop a method. On-line control method of curdlan fermentation with stable, high yield and low energy consumption

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0020] The first step, primary seed culture: 500mL shake flask, 100mL medium, medium formula: 4g sucrose, 0.5g potassium dihydrogen phosphate, 0.3g calcium carbonate, 0.8g diammonium hydrogen phosphate, 0.1g magnesium sulfate heptahydrate, 0.2g corn steep liquor, pH7.2. Sterilize at 115°C for 15min. Take an inclined test tube, add 6mL of physiological saline to wash the bacteria, take 2mL to inoculate into a shaker flask, and incubate at 32°C, 200rpm for 12h.

[0021] The second step, secondary seed cultivation: 15L fermenter, the added volume is 9L, medium formula: 400g sucrose, 80g diammonium hydrogen phosphate, 50g potassium dihydrogen phosphate, 5g magnesium sulfate heptahydrate, 5g calcium carbonate, 10g chloride Sodium, 20g corn steep liquor. Sterilization conditions: 115°C, 15min. Inoculate 300mL of primary seed liquid into secondary seed fermenter at 32°C, tank pressure 0.05MPa, pH 6.8, rotation speed 600rpm, ventilation ratio 1.2:1, cultivate for 13 hours, DO rises ...

Embodiment 2

[0027] The first step, primary seed culture: 500mL shake flask, 100mL medium, medium formula: 4g sucrose, 0.5g potassium dihydrogen phosphate, 0.3g calcium carbonate, 0.8g diammonium hydrogen phosphate, 0.1g magnesium sulfate heptahydrate, 0.2g corn steep liquor, pH7.2. Sterilize at 115°C for 15min. Take an inclined test tube, add 6mL of physiological saline to wash the bacteria, take 2mL and inoculate it into a shaker flask, and incubate at 32°C, 200rpm for 12 hours.

[0028] The second step, secondary seed cultivation: 15L fermenter, the added volume is 9L, medium formula: 400g sucrose,

[0029] 80g diammonium hydrogen phosphate, 50g potassium dihydrogen phosphate, 5g magnesium sulfate heptahydrate, 5g calcium carbonate, 10g sodium chloride, 20g corn steep liquor. Sterilization conditions: 115°C, 15min. Inoculate 300mL of the primary seed liquid into the secondary seed fermentation tank at 32°C, tank pressure 0.05MPa, pH 6.8, rotation speed 600rpm, ventilation ratio 1.2:1,...

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Abstract

The invention discloses an efficient fermentation control method for gel polysaccharide. The method comprises the first step of first-level seed culture, the second step of second-level seed culture, the third step of fermentation and the fourth step of fermentation control, wherein in the procedure of the third step, according to zymophyte concentration detected online, a nutrient solution with the glucose content of 500 g / L is automatically supplied, the nutrient solution is automatically supplemented when the glucose content in the fermentation liquid is lower than 5 g / L, the zymophyte concentration is maintained between 100 g / L and 150 g / L, and in other words, the nutrient solution starts to be supplemented when the zymophyte concentration is lower than 100 g / L and stops being supplemented when the zymophyte concentration is higher than 150 g / L. According to the control method, the adding speed and adding amount of the nutrient solution is controlled in real time according to the numerical value of the zymophyte concentration, and the gel polysaccharide fermentation process is directly and accurately controlled in real time and becomes stable and efficient.

Description

technical field [0001] The invention relates to the field of bioengineering, in particular to a high-efficiency fermentation control method of curdlan. Background technique [0002] Curdlan is a new microbial polysaccharide with many unique functions. In December 1996, after long-term safety and food toxicology tests, the FDA in the United States proved that curdlan is safe for use in food, and approved curdlan as a direct additive for food; curdlan Therefore, it is called the third food polysaccharide approved by FDA after xanthan gum and gellan gum. In addition to being used in the food industry, some scientists have recently studied the use of curdlan instead of dextran as the filler in the column for the chemical industry, and achieved better separation results. In the cosmetic industry, curdlan is also very effective as a thickener, suspending agent, stabilizer, moisturizer and rheology modifier, so it can be used in various types of cosmetics. According to analysis,...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C12P19/04
Inventor 赵伟曹大鹏陈文娜崔巍巍张曰辉杨梅玉
Owner 康彤(上海)生物研发有限公司