CN104961582A - High-protein efficient clitocybe maxima culture medium prepared from water-chestnut residues and preparation method for high-protein efficient clitocybe maxima culture medium - Google Patents
High-protein efficient clitocybe maxima culture medium prepared from water-chestnut residues and preparation method for high-protein efficient clitocybe maxima culture medium Download PDFInfo
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- 241000307222 Clitocybe maxima Species 0.000 title claims abstract description 18
- 235000003283 Pachira macrocarpa Nutrition 0.000 title claims abstract description 18
- 235000014364 Trapa natans Nutrition 0.000 title claims abstract description 18
- 235000009165 saligot Nutrition 0.000 title claims abstract description 18
- 239000001963 growth medium Substances 0.000 title claims abstract description 14
- 240000001085 Trapa natans Species 0.000 title abstract 2
- 238000002360 preparation method Methods 0.000 title description 4
- 239000000843 powder Substances 0.000 claims abstract description 31
- 241001083492 Trapa Species 0.000 claims abstract description 16
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 15
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 claims abstract description 14
- 229910052901 montmorillonite Inorganic materials 0.000 claims abstract description 14
- 238000003756 stirring Methods 0.000 claims abstract description 14
- QJZYHAIUNVAGQP-UHFFFAOYSA-N 3-nitrobicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid Chemical compound C1C2C=CC1C(C(=O)O)C2(C(O)=O)[N+]([O-])=O QJZYHAIUNVAGQP-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000004021 humic acid Substances 0.000 claims abstract description 10
- 108090000790 Enzymes Proteins 0.000 claims abstract description 8
- 102000004190 Enzymes Human genes 0.000 claims abstract description 8
- 238000010521 absorption reaction Methods 0.000 claims abstract description 8
- 241000228245 Aspergillus niger Species 0.000 claims abstract description 7
- 241000193830 Bacillus <bacterium> Species 0.000 claims abstract description 7
- 229920000742 Cotton Polymers 0.000 claims abstract description 7
- 244000168141 Geotrichum candidum Species 0.000 claims abstract description 7
- 235000017388 Geotrichum candidum Nutrition 0.000 claims abstract description 7
- 240000007594 Oryza sativa Species 0.000 claims abstract description 7
- 235000007164 Oryza sativa Nutrition 0.000 claims abstract description 7
- 241000191998 Pediococcus acidilactici Species 0.000 claims abstract description 7
- 235000009566 rice Nutrition 0.000 claims abstract description 7
- 238000006243 chemical reaction Methods 0.000 claims abstract description 6
- 239000000203 mixture Substances 0.000 claims description 25
- 239000002893 slag Substances 0.000 claims description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 21
- 238000002156 mixing Methods 0.000 claims description 15
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 12
- ODINCKMPIJJUCX-UHFFFAOYSA-N Calcium oxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims description 12
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 claims description 12
- 230000004913 activation Effects 0.000 claims description 10
- 238000001816 cooling Methods 0.000 claims description 9
- 108090000623 proteins and genes Proteins 0.000 claims description 9
- 102000004169 proteins and genes Human genes 0.000 claims description 9
- 239000010902 straw Substances 0.000 claims description 7
- 235000007516 Chrysanthemum Nutrition 0.000 claims description 6
- 235000009917 Crataegus X brevipes Nutrition 0.000 claims description 6
- 235000013204 Crataegus X haemacarpa Nutrition 0.000 claims description 6
- 235000009685 Crataegus X maligna Nutrition 0.000 claims description 6
- 235000009444 Crataegus X rubrocarnea Nutrition 0.000 claims description 6
- 235000009486 Crataegus bullatus Nutrition 0.000 claims description 6
- 235000017181 Crataegus chrysocarpa Nutrition 0.000 claims description 6
- 235000009682 Crataegus limnophila Nutrition 0.000 claims description 6
- 235000004423 Crataegus monogyna Nutrition 0.000 claims description 6
- 240000000171 Crataegus monogyna Species 0.000 claims description 6
- 235000002313 Crataegus paludosa Nutrition 0.000 claims description 6
- 235000009840 Crataegus x incaedua Nutrition 0.000 claims description 6
- 244000017020 Ipomoea batatas Species 0.000 claims description 6
- 235000002678 Ipomoea batatas Nutrition 0.000 claims description 6
- 241000283973 Oryctolagus cuniculus Species 0.000 claims description 6
- 229910019142 PO4 Inorganic materials 0.000 claims description 6
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 6
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 6
- 229920002494 Zein Polymers 0.000 claims description 6
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 6
- 239000000292 calcium oxide Substances 0.000 claims description 6
- 235000012255 calcium oxide Nutrition 0.000 claims description 6
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 claims description 6
- 239000004202 carbamide Substances 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 229910001629 magnesium chloride Inorganic materials 0.000 claims description 6
- 239000000463 material Substances 0.000 claims description 6
- 239000002609 medium Substances 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 230000000050 nutritive effect Effects 0.000 claims description 6
- 239000010452 phosphate Substances 0.000 claims description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 6
- 239000011591 potassium Substances 0.000 claims description 6
- 229910052700 potassium Inorganic materials 0.000 claims description 6
- 230000001737 promoting effect Effects 0.000 claims description 6
- 238000001179 sorption measurement Methods 0.000 claims description 6
- 230000001954 sterilising effect Effects 0.000 claims description 6
- 235000013311 vegetables Nutrition 0.000 claims description 6
- 238000010792 warming Methods 0.000 claims description 6
- 239000002699 waste material Substances 0.000 claims description 6
- 235000015099 wheat brans Nutrition 0.000 claims description 6
- 239000005019 zein Substances 0.000 claims description 6
- 229940093612 zein Drugs 0.000 claims description 6
- 239000012467 final product Substances 0.000 claims description 4
- 239000004698 Polyethylene Substances 0.000 claims description 3
- 239000003085 diluting agent Substances 0.000 claims description 3
- 238000011177 media preparation Methods 0.000 claims description 3
- 229920003023 plastic Polymers 0.000 claims description 3
- 239000004033 plastic Substances 0.000 claims description 3
- -1 polyethylene Polymers 0.000 claims description 3
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- 238000005086 pumping Methods 0.000 claims description 3
- 238000007789 sealing Methods 0.000 claims description 3
- 244000189548 Chrysanthemum x morifolium Species 0.000 claims 2
- 239000013067 intermediate product Substances 0.000 abstract description 5
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- 230000015572 biosynthetic process Effects 0.000 abstract description 2
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- 241000521553 Pichia fermentans Species 0.000 abstract 1
- 241000223261 Trichoderma viride Species 0.000 abstract 1
- 230000001105 regulatory effect Effects 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 229940088598 enzyme Drugs 0.000 description 5
- 235000001674 Agaricus brunnescens Nutrition 0.000 description 4
- 241000723353 Chrysanthemum Species 0.000 description 4
- 241000233866 Fungi Species 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 108010059892 Cellulase Proteins 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
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- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 229940106157 cellulase Drugs 0.000 description 1
- 238000012258 culturing Methods 0.000 description 1
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- 230000007812 deficiency Effects 0.000 description 1
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- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 230000035764 nutrition Effects 0.000 description 1
- AZQWKYJCGOJGHM-UHFFFAOYSA-N para-benzoquinone Natural products O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
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- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Abstract
The invention discloses high-protein efficient clitocybe maxima culture medium prepared from water-chestnut residues. The high-protein efficient clitocybe maxima culture medium is characterized by comprising the following components in parts by weight: 30 to 40 parts of water chestnut residues, 20 to 30 parts of cotton seed hulls, 10 to 20 parts of rice chaff, 3 to 5 parts of montmorillonite powder, 2 to 3 parts of diatomite, 0.01 to 0.03 parts of trichoderma viride, 0.03 to 0.05 parts of aspergillus niger, 0.03 to 0.05 parts of geotrichum candidum, 0.1 to 0.3 parts of Candida lambica, 0.4 to 0.6 parts of bacillus and 0.3 to 0.5 parts of pediococcus acidilactici. The high-protein efficient clitocybe maxima culture medium adopts enzyme carried on montmorillonite and activated zymophyte carried and loaded on diatomite to respectively degrade and ferment insoluble organic substances, so that the degradation and fermentation speeds are effectively regulated, and the formation of an intermediate product is promoted; and finally, by virtue of high-temperature stirring reaction, reaction of the intermediate product is promoted to form high-activity biochemical humic acid, so that the absorption and the metabolism of clitocybe maxima are convenient, and efficient cultivation of the clitocybe maxima is realized.
Description
Technical field
The invention belongs to breed of edible fungus field, be specifically related to a kind of adopt water chestnut slag to prepare clitocybe maxima high protein efficient culture medium and preparation method.
Background technology
Edible mushrooms has abundant nutrition and good nourishing function because of it, enjoys the parent of people to look at.In recent years, edible mushrooms market scale constantly expands, and in order to meet the need of market, China's Edible Fungi is just towards the future development of industrialization, mass-producing and batch production.The edible fungus culturing fertilizer of green high-efficient has become an urgent demand of edible mushrooms development.Meanwhile, also to there is raw material availability low for Edible Fungi.Output needs the problem improved further.
Biochemical humic acid is by chemistry with microorganism fermentation process makes is a kind of organism by agricultural crop straw, wood chip etc., except containing except active xanthohumic acid, amino acid also containing some amount and abundant carboxyl, hydroxyl, phenolic hydroxyl group, quinone hydroxyl isoreactivity group, compared with mineral humic acid, have the following advantages: 1, molecular weight is little, seepage force is strong, more easily absorbed by crops and utilization; 2, active group rich content, physiologically active and chemically reactive stronger; 3, composition variation, active high, effect is more excellent.
Summary of the invention
The present invention is directed to the artificial culture demand of edible mushrooms, propose a kind of adopt water chestnut slag to prepare clitocybe maxima high protein efficient culture medium and preparation method.
The technical solution used in the present invention is as follows:
A kind of clitocybe maxima high protein efficient culture medium adopting water chestnut slag to prepare, it is characterized in that, comprise following parts by weight of component: water chestnut slag 30-40, cotton seed hulls 20-30, rice chaff 10-20, unslaked lime 2-4, vegetable seed straw powder 10-20, wheat bran 10-20, calcium carbonate 2-3, terra alba 5-7, Zein powder 10-20, montmorillonite powder 3-5, diatomite 2-3, hawthorn powder 15-20, dry rabbit excrement 3-5, sweet potato waste 10-20, chrysanthemum slag 12-14, viride 0.01-0.03, aspergillus niger 0.03-0.05, geotrichum candidum 0.03-0.05, the comparable candiyeast 0.1-0.3 of youth, genus bacillus 0.4-0.6, pediococcus acidilactici 0.3-0.5, urea 1-2, potassium primary phosphate 0.6-0.8, magnesium chloride 0.5-0.7, organic chelated leaven promoting agent 1-2, appropriate water.
The clitocybe maxima high protein efficient culture medium preparation method adopting water chestnut slag to prepare, is characterized in that, comprise the following steps:
(1) get water chestnut slag, cotton seed hulls, the mixing of vegetable seed straw powder, after adopting unslaked lime 100 times of water diluents to soak 2-3h, adopt High Temperature High Pressure decompressor process 2-3min, obtain expansion activated camplex for subsequent use;
(2) get montmorillonite powder, Zein powder, viride, aspergillus niger, geotrichum candidum and gross weight 1-2 water mix and blend 5-10min doubly to evenly, leave standstill 4-6h, obtaining montmorillonite powder absorption, to carry enzyme for subsequent use; Get diatomite, wheat bran, the comparable candiyeast of youth, genus bacillus, pediococcus acidilactici and gross weight 1-2 water mix and blend 6-8min doubly to evenly, leave standstill 2-3h, obtain the activation zymophyte that diatomite adsorption carries for subsequent use;
(3) get expansion activated camplex, enzyme mixing is carried in montmorillonite powder absorption, and add gross weight 3-5 water doubly, airtight stirring 20-30min is extremely even, airtight placement 2-3d at 38-42 DEG C afterwards, and the activation degraded mixture that must expand is for subsequent use;
(4) get rice chaff, activation zymophyte mixing that hawthorn powder, dry rabbit excrement, sweet potato waste, chrysanthemum slag, diatomite adsorption carry, and after adding gross weight 4-8 water mixing doubly, sealing and fermenting 20-30d, pumping into afterwards expands activates degraded mixture and stirs, leave standstill 2-3d, 80-90 DEG C of stirring reaction 30-50min in closed environment, cooling, obtains biochemical humic acid mixture for subsequent use;
(5) get calcium carbonate, terra alba, urea, potassium primary phosphate, magnesium chloride, organic chelated leaven promoting agent and gross weight 2-3 water doubly to mix to evenly, obtain nutritive medium for subsequent use;
(6) get biochemical humic acid mixture, nutritive medium mixing and stirring, and adjust the 50-60% that moisture content is gross weight, obtain culture material for subsequent use;
(7) be divided in polyethylene plastic bag by culture material, put into the steamer of band high-pressure valve and cooling valve afterwards, first vigorous fire is warming up to 100 DEG C, sterilizing 1-2h, being cooled to rapidly 0 DEG C by cooling valve, is warming up to 100 DEG C at secondary vigorous fire, sterilizing 30-50min, is cooled to room temperature, to obtain final product.
Beneficial effect of the present invention is embodied in:
The activation zymophyte that the enzyme that the present invention adopts polynite to carry and diatomite carry loading carries out organic degraded hard to tolerate and fermentation respectively, effectively have adjusted degraded and fermenting speed, facilitate the formation of intermediate product, finally reacted by high-temperature stirring, facilitate the reaction of intermediate product, form highly active biochemical humic acid, be convenient to absorption and the metabolism of clitocybe maxima, realize the Efficient Cultivation of clitocybe maxima.Avoid the intermediate product dullness that simple cellulase degradation causes, can not provide for final product the defect and deficiency enriching source.
Embodiment
Embodiment
Clitocybe maxima high protein efficient culture medium prepared by the employing water chestnut slag described in the present embodiment, it is characterized in that, comprise following parts by weight of component: water chestnut slag 35, cotton seed hulls 25, rice chaff 15, unslaked lime 3, vegetable seed straw powder 15, wheat bran 15, calcium carbonate 2.5, terra alba 6, Zein powder 15, montmorillonite powder 4, diatomite 2.5, hawthorn powder 17.5, dry rabbit excrement 4, sweet potato waste 15, chrysanthemum slag 13, viride 0.02, aspergillus niger 0.04, geotrichum candidum 0.04, the comparable candiyeast 0.2 of youth, genus bacillus 0.5, pediococcus acidilactici 0.4, urea 1.5, potassium primary phosphate 0.7, magnesium chloride 0.6, organic chelated leaven promoting agent 1.5, appropriate water.
Clitocybe maxima high protein efficient culture medium preparation method prepared by the employing water chestnut slag described in the present embodiment, is characterized in that, comprise the following steps:
(1) get water chestnut slag, cotton seed hulls, the mixing of vegetable seed straw powder, after adopting unslaked lime 100 times of water diluents to soak 2-3h, adopt High Temperature High Pressure decompressor process 2-3min, obtain expansion activated camplex for subsequent use;
(2) get montmorillonite powder, Zein powder, viride, aspergillus niger, geotrichum candidum and gross weight 1-2 water mix and blend 5-10min doubly to evenly, leave standstill 4-6h, obtaining montmorillonite powder absorption, to carry enzyme for subsequent use; Get diatomite, wheat bran, the comparable candiyeast of youth, genus bacillus, pediococcus acidilactici and gross weight 1-2 water mix and blend 6-8min doubly to evenly, leave standstill 2-3h, obtain the activation zymophyte that diatomite adsorption carries for subsequent use;
(3) get expansion activated camplex, enzyme mixing is carried in montmorillonite powder absorption, and add gross weight 3-5 water doubly, airtight stirring 20-30min is extremely even, airtight placement 2-3d at 38-42 DEG C afterwards, and the activation degraded mixture that must expand is for subsequent use;
(4) get rice chaff, activation zymophyte mixing that hawthorn powder, dry rabbit excrement, sweet potato waste, chrysanthemum slag, diatomite adsorption carry, and after adding gross weight 4-8 water mixing doubly, sealing and fermenting 20-30d, pumping into afterwards expands activates degraded mixture and stirs, leave standstill 2-3d, 80-90 DEG C of stirring reaction 30-50min in closed environment, cooling, obtains biochemical humic acid mixture for subsequent use;
(5) get calcium carbonate, terra alba, urea, potassium primary phosphate, magnesium chloride, organic chelated leaven promoting agent and gross weight 2-3 water doubly to mix to evenly, obtain nutritive medium for subsequent use;
(6) get biochemical humic acid mixture, nutritive medium mixing and stirring, and adjust the 50-60% that moisture content is gross weight, obtain culture material for subsequent use;
(7) be divided in polyethylene plastic bag by culture material, put into the steamer of band high-pressure valve and cooling valve afterwards, first vigorous fire is warming up to 100 DEG C, sterilizing 1-2h, being cooled to rapidly 0 DEG C by cooling valve, is warming up to 100 DEG C at secondary vigorous fire, sterilizing 30-50min, is cooled to room temperature, to obtain final product.
Claims (2)
1. the clitocybe maxima high protein efficient culture medium adopting water chestnut slag to prepare, it is characterized in that, comprise following parts by weight of component: water chestnut slag 30-40, cotton seed hulls 20-30, rice chaff 10-20, unslaked lime 2-4, vegetable seed straw powder 10-20, wheat bran 10-20, calcium carbonate 2-3, terra alba 5-7, Zein powder 10-20, montmorillonite powder 3-5, diatomite 2-3, hawthorn powder 15-20, dry rabbit excrement 3-5, sweet potato waste 10-20, chrysanthemum slag 12-14, viride 0.01-0.03, aspergillus niger 0.03-0.05, geotrichum candidum 0.03-0.05, the comparable candiyeast 0.1-0.3 of youth, genus bacillus 0.4-0.6, pediococcus acidilactici 0.3-0.5, urea 1-2, potassium primary phosphate 0.6-0.8, magnesium chloride 0.5-0.7, organic chelated leaven promoting agent 1-2, appropriate water.
2. the clitocybe maxima high protein efficient culture medium preparation method adopting water chestnut slag to prepare, is characterized in that, comprise the following steps:
(1) get water chestnut slag, cotton seed hulls, the mixing of vegetable seed straw powder, after adopting unslaked lime 100 times of water diluents to soak 2-3h, adopt High Temperature High Pressure decompressor process 2-3min, obtain expansion activated camplex for subsequent use;
(2) get montmorillonite powder, Zein powder, viride, aspergillus niger, geotrichum candidum and gross weight 1-2 water mix and blend 5-10min doubly to evenly, leave standstill 4-6h, obtaining montmorillonite powder absorption, to carry enzyme for subsequent use; Get diatomite, wheat bran, the comparable candiyeast of youth, genus bacillus, pediococcus acidilactici and gross weight 1-2 water mix and blend 6-8min doubly to evenly, leave standstill 2-3h, obtain the activation zymophyte that diatomite adsorption carries for subsequent use;
(3) get expansion activated camplex, enzyme mixing is carried in montmorillonite powder absorption, and add gross weight 3-5 water doubly, airtight stirring 20-30min is extremely even, airtight placement 2-3d at 38-42 DEG C afterwards, and the activation degraded mixture that must expand is for subsequent use;
(4) get rice chaff, activation zymophyte mixing that hawthorn powder, dry rabbit excrement, sweet potato waste, chrysanthemum slag, diatomite adsorption carry, and after adding gross weight 4-8 water mixing doubly, sealing and fermenting 20-30d, pumping into afterwards expands activates degraded mixture and stirs, leave standstill 2-3d, 80-90 DEG C of stirring reaction 30-50min in closed environment, cooling, obtains biochemical humic acid mixture for subsequent use;
(5) get calcium carbonate, terra alba, urea, potassium primary phosphate, magnesium chloride, organic chelated leaven promoting agent and gross weight 2-3 water doubly to mix to evenly, obtain nutritive medium for subsequent use;
(6) get biochemical humic acid mixture, nutritive medium mixing and stirring, and adjust the 50-60% that moisture content is gross weight, obtain culture material for subsequent use;
(7) be divided in polyethylene plastic bag by culture material, put into the steamer of band high-pressure valve and cooling valve afterwards, first vigorous fire is warming up to 100 DEG C, sterilizing 1-2h, being cooled to rapidly 0 DEG C by cooling valve, is warming up to 100 DEG C at secondary vigorous fire, sterilizing 30-50min, is cooled to room temperature, to obtain final product.
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Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104016776A (en) * | 2014-05-07 | 2014-09-03 | 合肥福泉现代农业科技有限公司 | Hypsizigus marmoreus culture medium prepared from chestnut shell and preparation method thereof |
| CN104030777A (en) * | 2014-05-07 | 2014-09-10 | 合肥福泉现代农业科技有限公司 | Needle mushroom medium with peanut shell as raw material, and preparation method thereof |
| CN104256057A (en) * | 2014-10-01 | 2015-01-07 | 青岛嘉瑞生物技术有限公司 | Method for preparing feed proteins by utilizing alcohol waste liquor and crop straws |
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Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104016776A (en) * | 2014-05-07 | 2014-09-03 | 合肥福泉现代农业科技有限公司 | Hypsizigus marmoreus culture medium prepared from chestnut shell and preparation method thereof |
| CN104030777A (en) * | 2014-05-07 | 2014-09-10 | 合肥福泉现代农业科技有限公司 | Needle mushroom medium with peanut shell as raw material, and preparation method thereof |
| CN104256057A (en) * | 2014-10-01 | 2015-01-07 | 青岛嘉瑞生物技术有限公司 | Method for preparing feed proteins by utilizing alcohol waste liquor and crop straws |
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