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Microbial solid inocula, and preparation and use thereof

A solid bacterial agent and microbial technology, applied in the field of FGR solid bacterial agent, can solve the problems of complex preparation process, application limitation, complex production process, etc., achieve high concentration of bacterial liquid cells, save equipment and energy, and fast bacterial cell reproduction Effect

Inactive Publication Date: 2009-04-15
甘肃盛亚肽生物科技有限责任公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Its disadvantages are: the cost of raw materials used is high, the production process is complicated, and energy cannot be saved.
[0003] Most of the microbial strains used in the preparation of traditional microbial strains are: strains isolated and screened from national or local strain banks or directly from nature. The disadvantages are: 1. The activity of microbial strains is poor; 2. To organic matter The ability to decompose and transform is weak; 3. The bacterial agents prepared by these strains have a small number of viable cells, most of which are within 10 8 pcs / g
Its disadvantages are: complex preparation process, long fermentation cycle, high cost and limited application

Method used

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  • Microbial solid inocula, and preparation and use thereof
  • Microbial solid inocula, and preparation and use thereof
  • Microbial solid inocula, and preparation and use thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0030] (1) Cultivation of liquid strains in test tubes, take fresh tofu waste water and boil for 10 minutes to naturally precipitate to get 100ml of supernatant, add (NH 4 ) 2 SO 4 0.1g, H 3 PO 4 0.05ml, fully dissolved and adjusted to pH 5.5-6.5, packaged in 15×1.5cm dry test tubes, autoclaved at 112°C for 30 minutes, cooled to 32°C, and inoculated with F306 yeast fusion bacteria and G361 Geotrichum candidum respectively , and R. rhizopus in the test-tube liquid medium, cultured at 28-32°C for 24-48 hours, that is, the test-tube liquid strain (first-class strain)

[0031] (2) Cultivation of liquid strains in Erlenmeyer flasks

[0032] Take fresh tofu waste water and boil for 10 minutes to naturally precipitate, take 1000ml of supernatant, add (NH 4 ) 2 SO 4 1g, H 3 PO 4 0.5ml, after fully dissolving, adjust the pH to 5.5~6.5, and pack it into a 500ml Erlenmeyer flask, the amount of which is 1 / 4 of the total amount of the bottle, then autoclave at 112°C for 30 minu...

Embodiment 2

[0039] (1) Cultivation of test tube liquid strains, take 100ml of fresh vermicelli wastewater, add (NH 4 ) 2 SO 4 0.1g, H 3 PO 4 0.05ml, fully dissolved and adjusted to pH 5.5-6.5, packed in 15×1.2cm dry test tubes, sterilized by autoclaving at 112°C for 30 minutes, cooled to 32°C, inoculated with F306 yeast fusion bacteria and G361 Geotrichum candidum respectively , and R. rhizopus in the test-tube liquid medium, cultured at 28-32°C for 24-48 hours, that is, the test-tube liquid strain (first-class strain)

[0040] (2) Cultivation of liquid strains in Erlenmeyer flasks

[0041] Take 1000ml of fresh vermicelli waste water, add (NH 4 ) 2 SO 4 1g, H 3 PO 4 0.5ml, after fully dissolving, adjust the pH to 5.5~6.5, and pack it into a 500ml Erlenmeyer flask, the amount of which is 1 / 4 of the total amount of the bottle, then autoclave at 112°C for 30 minutes, cool to 32°C, The test-tube liquid strain is inoculated into the liquid conical flask medium, and cultured at 28...

Embodiment 3

[0048] (1) Cultivation of liquid strains in test tubes, take fresh cornstarch wastewater, boil for 10 minutes to get natural precipitation to take 100ml of supernatant, add (NH 4 ) 2 SO 4 0.1g, H 3 PO 4 0.05ml, fully dissolved and adjusted to pH 5.5-6.5, packed in 15×1.2cm dry test tubes, sterilized by autoclaving at 112°C for 30 minutes, cooled to 32°C, inoculated with F306 yeast fusion bacteria and G361 Geotrichum candidum respectively , and R. rhizopus in the test-tube liquid medium, cultured at 28-32°C for 24-48 hours, that is, the test-tube liquid strain (first-class strain)

[0049] (2) Cultivation of liquid strains in Erlenmeyer flasks

[0050] Get fresh cornstarch wastewater, get 1000ml of supernatant after boiling for 10 minutes, and add (NH) 4 ) 2 SO 4 1g, H 3 PO 4 0.5ml, after fully dissolving, adjust the pH to 5.5~6.5, and pack it into a 500ml Erlenmeyer flask, the amount of which is 1 / 4 of the total amount of the bottle, then autoclave at 112°C for 30...

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Abstract

The invention mainly relates to microorganism fermenting methods, in particular to a method which prepares a solid FGR microbial inoculum that combines yeast fusion strain (F306), geotrichum candidum link (G361) and rhizopus stolonifer strain (R) by utilizing wastewater and waste residue generated in food industries as well as application thereof. A solid culture medium of the solid microorganism microbial inoculum comprises following dry components by weight percentage: 50 to 80 percent of scum residue, 15 to 30 percent of corncob powder, 8 to 12 percent of bran coat, 0.5 to 0.8 percent of corn meal, 0.1 to 3 percent of ureophil and 0.2 to 4 percent of ammonium sulfate, fresh wastewater of bean curd, bean vermicelli, corn starch or yam starch is added for leading the weight percentage of water to be 45 to 65 percent, limewater with the concentration of 1 percent is used to adjust pH value between 5.5 and 6.5, a mixed strain liquid of the yeast fusion strain, the geotrichum candidum link and the rhizopus stolonifer strain with the weight 8 to 12 percent of the total dry components is added and completely agitated, ventilated agitation and fermentation are implemented in a fermenting pool with dual purposes of fermenting and drying at the temperature of 28 to 32 DEG C for 18 to 24 hours, and hot air is led into the fermenting pool at the temperature of 40 to 60 DEG C for drying, thus producing the solid microbial inoculum that has great application effect in addition agents of beast and bird feedstuff.

Description

Technical field: [0001] The invention mainly relates to a fermentation method for microorganisms, in particular to a method and application for preparing the FGR solid inoculum of the combination of yeast fusion bacteria (F306), ground mold (G361) and rhizopus (R) by utilizing waste liquid and waste residue produced in the food industry . Background technique: [0002] In the traditional preparation method of microbial inoculum, the raw materials used are glucose, peptone, molasses, beef extract, vitamins, inorganic salts and water are prepared into a liquid medium, and the bacterial moss is scraped from the slanted surface of the test tube and inoculated in the liquid medium, It is prepared into a liquid bacterial agent by aerobic or anaerobic culture, or the liquid bacterial strain is inoculated on a solid medium composed of corn flour, bran, soybean flour, seed cake, soybean meal and rice bran, and then fermented to prepare solid bacteria. agent. The disadvantages are: ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12N1/00C12N1/16C12N1/14A23K1/16C12R1/645C12R1/845A23K10/18
Inventor 孙荣高
Owner 甘肃盛亚肽生物科技有限责任公司
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