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Highly efficient and low-cost microbiological feed proteins based on vinegar residue and miscellaneous meal

A technology of microbial feed and vinegar grains, applied in animal feed, animal feed, applications, etc., can solve the problems of insignificant degradation of lignin and cellulose, poor fermentation, and low addition amount

Inactive Publication Date: 2014-04-09
泉州华惠生物科技有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The second is that bio-fermented feed based on grain or common industrial fermentation raw materials also needs low-temperature drying or freeze-drying storage treatment. Generally speaking, the cost is high, the amount of feed is small, and the biological activity is not obvious! Such as invention patents (CN1682599A), (CN1806659A), (CN101190003A), (CN102204632A)
The third is based on straw, distiller's grains and other wastes, treated with Trichoderma or cellulase, or fermented with probiotics, and dried at low temperature for storage. The raw materials also need to be sterilized, which is costly, but the active ingredients are not easy to preserve, and the effect of probiotics is not obvious. , such as invention patents (CN101897381B), (CN100337555C)
[0008] In previous studies, such as invention patents (CN1285156A), (CN101491290A), (CN101366445A), fresh distiller's grains were partially dried, which consumed a lot of energy, and was inoculated with a Geotrichum candidum or Paecilomyces for degradation, but the lignin effect Not obvious, the product has no probiotic effect
Another example is the invention patent (CN101919490A) (CN101756009A) and (CN101756044A), the vinegar grains are not pretreated by flora rich in ligninase and cellulase, and only by adding cellulase, etc., the cost is high and the effect is not obvious. Moreover, aerobic probiotics and anaerobic probiotics are not fermented in stages, resulting in poor fermentation on both sides
Invention patent (CN101756012A) has a second-stage fermentation, but the first-stage Aspergillus niger enzyme does not degrade lignin and cellulose significantly, and the second-stage is also aerobic fermentation without probiotic fermentation
The products of the above three inventions must be dried at low temperature, which consumes a lot of energy and has a low preservation rate of bacterial enzymes.
Therefore, the production cost is high, and the feeding effect is not obvious, which is not conducive to the promotion of industrialization

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0057] The first phase of biological pretreatment fermentation

[0058] (1) Neurospora seed culture and production medium.

[0059] Slant medium and plate medium: 200 g potato, 20 g sucrose, 20 g agar, in a constant volume of 1 L, pH 5.0, sterilized at 110°C for 30 min. Inoculate at 30°C and culture for 7-10 days.

[0060] Seed liquid medium: KH 2 PO 4 2g, MgSO 4 0.3g, CaCl 2 0.3g, peptone 5g, yeast extract 3g, wort 3g, FeSO 4 ·7H 2 O 0.005g, ZnSO 4 0.0014g, MnSO 4 .4H 2 O 0.0016g, CoCl 2 0.002 g, dilute to 1 L, pH 5.0. Add 100 ml culture medium to a 500 ml Erlenmeyer flask, and sterilize at 110°C for 30 minutes.

[0061] Solid-state fermentation production seed medium and production medium: crushed wet vinegar grains 76%, cottonseed meal 18%, ammonium nitrate 2%, urea 1%, calcium carbonate 2%, potassium dihydrogen phosphate 1%, magnesium sulfate 0.1%, The final water content of the medium was 58%.

[0062] (2) Cultivation method

[0063] Neurospora crass...

Embodiment 2

[0065] The second stage of fermentation

[0066] (1) Bacillus culture medium

[0067] Bacillus slant and plate culture medium: peptone 10g, beef extract powder 5g, sodium chloride 5g, agar 15g, glucose 20g, distilled water 1000ml, final pH7.0±0.2. Sterilize at 110°C for 30min;

[0068] Bacillus shake flask seed medium and seed tank medium: beef extract 5.0g / L, peptone 20.0g / L, glucose 5.0g / L, FeCl 2 6H2O 0.07g / L, MnC1 2 ·7H 2 O 0.01g / L, MgSO 4 ·7H 2 O 0.15g / L, pH 7.0, sterilized at 110°C for 30min.

[0069] (2) Yeast medium

[0070] Yeast slant medium and plate culture medium (100 ml): 2 g glucose, 1 g yeast extract, 2 g peptone, 2 g agar, pH value about 6.0.

[0071] Shake flask seed medium and seed tank medium: the composition is the same as that of the slant medium, without agar.

[0072] (3) The second-stage fermentation medium is composed of the solid bacterial agent pretreated by the first-stage fermentation plus 20% cotton meal, and the water content is 49%. To...

Embodiment 3

[0080] The third stage of fermentation

[0081] (1) Lactic acid bacteria medium

[0082] MRS slant medium (g / L): peptone 10, yeast powder 5, beef extract 5, glucose 20, diammonium citrate 2, Tween 80 1.0 ml, sodium acetate 25, K 2 HPO 4 2. MgSO 4 7 hours 2 O 0.58, MnSO 4 4H 2 O 0.25, Agar 20, pH 7.0.

[0083] Shake flask and seed tank lactic acid bacteria seed medium (g / L): 2.25% soybean oligosaccharides, 2.00% glucose, 1.25% peptone, 1.25% yeast powder, 6.50% tomato juice, 80.10% Tween, 0.20 dipotassium hydrogen phosphate %. pH 6.5, 200 ml in a 1L Erlenmeyer flask.

[0084] After the above medium was prepared, all of them were autoclaved at 115°C for 30 minutes.

[0085] (2) Culture medium for bifidobacteria

[0086] MRS slant medium (g / L): peptone 10, yeast powder 5, beef extract 5, glucose 20, diammonium citrate 2, Tween 80 1.0 ml, sodium acetate 25, K 2 HPO 4 2. MgSO 4 7 hours 2 O 0.58, MnSO 4 4H 2 O 0.25, Agar 20, pH 7.0.

[0087] Anaerobic bottle and s...

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PUM

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Abstract

The invention relates to the field of producing highly efficient and low-cost microbiological feed proteins based on the three-stage fermentation of vinegar residue and miscellaneous meal by using probiotics. The vinegar residue used as a main carbon source and the cottonseed meal used as a main nitrogen source as well as a partial carbon source are subjected to the first-stage fermentation pretreatment by using food-grade mould, the product is subjected to the second-stage fermentation by using bacillus and yeast as zymocytes and adding partial cottonseeds, and finally the product is added with partial soybean meal and rapeseed meal used as a nitrogen source as well as a partial carbon source, inoculated with lactobacillus and acid-resisting bifidobacterium and uniformly mixed, and then the product is subpackaged in one-way membrane bio-bags for sealed storage, namely the finished products are obtained by the three-stage fermentation. The microbiological feed proteins are extremely low in production cost and can be used as a feed component, and the adding amount reaches 5 to 40 percent. Because the finished products do not need drying treatment, the finished products have more viable bacteria as well as enzymes, few other bacteria and an obvious feeding effect; moreover, the microbiological feed proteins also have the advantages of greatly improving the utilization rate of livestock and poultry feed, increasing yield, improving intestinal environment, improving immunity and resistance, replacing antibiotics and improving quality of animal products.

Description

technical field [0001] The invention belongs to the field of microbial feed additives, in particular to novel microbial feed protein or microbial feed additives based on fibrous brewing waste with high efficiency and low cost. Background technique [0002] At present, the profit of the feed industry is very low, and most of them use grain as the raw material, so the cost is difficult to reduce. The microbial feed that can fully improve the utilization rate of feed and reduce the cost of feed brings new hope to the feed industry and aquaculture industry. As we all know, there are a large number of microorganisms in the gastrointestinal tract of animals. These microorganisms, as well as between microorganisms and animals, form an inseparable whole that is interdependent and interacting—the microecosystem. Probiotics are the main live bacteria component of this micro-ecosystem, and are of great significance to the growth, development, digestion, absorption, nutrition and immuni...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A23K1/06A23K1/14A23K10/38
CPCY02P60/87
Inventor 陈华友李萍萍杨胜利谢永明崔恒林齐向辉倪忠崔凤杰朱道辰王浩森
Owner 泉州华惠生物科技有限公司
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