Bacillus coagulans solid-state fermentation production method

A technology of Bacillus coagulans and solid-state fermentation, applied in the field of microbial fermentation, can solve the problems of post-treatment sewage discharge, low spore formation rate, long fermentation period, etc., and achieve the effects of cost saving, simple process and high bacterial count.

Inactive Publication Date: 2015-04-22
湖北华扬科技发展有限公司
View PDF4 Cites 5 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] In recent years, with the vigorous development of microecological preparations, a group of Bacillus coagulans manufacturers and researchers have emerged. However, most of the production methods at home and abroad currently use liquid fermentation technology. However, liquid fermentation has many disadvantages, such as long fermentation period, Low spore formation rate, serious post-treatment sewage discharge, high cost and other problems, however, solid-state fermentation production method, high spore number and spore rate, simple process, low investment, easy operation, simple post-treatment, etc., have been widely accepted and research
Aiming at the industrialization of Bacillus coagulans, scholars at home and abroad have conducted in-depth research on the high-density culture of Bacillus coagulans liquid fermentation, and believe that the accumulation of lactic acid generated by Bacillus coagulans through homozygous fermentation in the fermentation liquid will cause a drop in pH value and damage the bacteria. The growth and the formation of spores have a strong inhibitory effect. For solid-state fermentation, there is also such a problem. How to more effectively increase the number and spore rate of Bacillus coagulans in solid-state fermentation

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0023] (1) First-level seed preparation: take 0.5ml of a bacterial strain preserved in a glycerol tube, put it into a bottle of YPD liquid medium (300ml / 1000ml), prepare 5 bottles of a total of 1500ml seed liquid; cultivate at 40°C and 150r / min 17h, that is, the first-class seed liquid.

[0024] (2) Secondary solid seed medium preparation: prepare 2.5kg solid seed medium: weigh 2250g of bran, 250g of soybean meal and mix for later use; weigh 25g of glucose, 50g of urea, and 50g of calcium carbonate; ℃ hot water, pour it into the weighed solid material and mix well until it is completely wet, put it into a cloth bag, tie it up, and sterilize it in a laboratory sterilizer at 121 ℃ for 50 minutes.

[0025] (3) Two-stage solid seed inoculation method: naturally cool the sterilized solid material to about 50°C, and at the same time put the plastic film and 35cm*45cm*15cm white pot under the ultraviolet light for 30 minutes to sterilize, and wait for the solid material to cool down ...

Embodiment 2

[0031] In order to better prove that the fermentation formula can stabilize the pH value in the fermentation process, the formulas with and without urea were compared.

[0032] (1) The process of adding urea formula: Weigh 900g of bran and 100g of soybean meal and mix them for use. First, dissolve 1.4g of manganese sulfate in 400ml, then add 10g of glucose and 20g of urea to dissolve, and finally add 20g of calcium carbonate. Mix well with the solid material until it is completely wet, put it in a cloth bag, sterilize at 121°C for 50 minutes, cool the sterilized solid material to about 50°C naturally, pour it into the fermentation container after the solid material is cooled, and take 600ml of the primary liquid seed in Example 1, adjust the pH value to 8.0, mix with the solid material, put it into the cultivation room for cultivation at 45°C, monitor the change of the pH value during the cultivation process, cultivate it for 3 days, and dry it at low temperature for detection....

Embodiment 3

[0039] (1) First-level seed preparation: take 0.5ml of a bacterial strain preserved in a glycerol tube, put it into a bottle of YPD liquid medium (300ml / 1000ml), prepare 5 bottles of a total of 1500ml seed liquid; cultivate at 40°C and 150r / min 17h, that is, the first-class seed liquid.

[0040] (2) Secondary solid seed medium preparation: prepare 2.5kg solid seed medium: weigh 2250g of bran, 250g of soybean meal and mix for later use, weigh 2.5g of glucose, 2.5g of urea, and 2.5g of calcium carbonate, dissolve in 1250ml In hot water at 50-60°C, pour it into the weighed solid material and mix well until it is completely wet, put it into a cloth bag, tie it up, and sterilize it in a laboratory sterilizer at 121°C for 50 minutes.

[0041] (3) Two-stage solid seed inoculation method: naturally cool the sterilized solid material to about 50°C, and at the same time put the plastic film and 35cm*45cm*15cm white pot under the ultraviolet light for 30 minutes to sterilize, and wait fo...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The invention relates to the field of microbial fermentation, and in particular relates to a bacillus coagulans solid-state fermentation production method. The method comprises the following steps: (1) first-stage seed preparation; (2) second-stage solid-state seed inoculation; (3) third-stage solid-state seed inoculation; and (4) solid-state fermentation inoculation, wherein a formula of a solid-state fermentation material comprises the following components in percentage by mass: 70-99% of wheat bran, 1-30% of soybean meal, 0.1-10% of glucose, 0.1-10% of urea, 0.1-10% of calcium carbonate and 0.1-5% of manganese sulfate, and accessory materials are added corresponding to the mass of the wheat bran and the soybean meal. According to the method disclosed by the invention, the solid-state fermentation inoculation quantity can be reduced by 50-95% compared with that of the prior art, and a pH value is kept between 7 and 8 in a fermentation process; moreover, a high bacterium number can be achieved, dominant populations can be formed for fermentation, bacterial contamination cannot be easily caused, relatively high spore numbers and spore rates can be achieved, the spore number is 1*10<9>CFU / g to 1*10<11>CFU / g, and the maximum spore rate can reach 99%; and the method is easy in production and promotion.

Description

technical field [0001] The invention relates to the field of microbial fermentation, in particular to a solid-state fermentation production method of bacillus coagulans. Background technique [0002] Bacillus coagulans has been included in the new feed and new feed additives within the protection period in the Ministry of Agriculture Announcement No. 1126 of the People's Republic of China "Feed Additives Category Catalog" (2008), and its approved use time is May 2004 In March, the scope of application is broiler chickens and growing and finishing pigs, indicating that its safety, effectiveness, economy and impact on the environment have passed the review of the National Feed Review Committee and approved by the Ministry of Agriculture. The U.S. FDA has also recognized it as a "generally recognized as safe" bacillus, and the application research of this bacillus in human and animal production has become a hot spot, and the effect is remarkable. [0003] The abuse of antibiot...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Applications(China)
IPC IPC(8): C12N1/20C12R1/07
CPCC12N1/20
Inventor 陶敏詹志春周樱顾爱玲余乐
Owner 湖北华扬科技发展有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products