CN100370015C - Culture for caterpillar and cordycepin - Google Patents

Culture for caterpillar and cordycepin Download PDF

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Publication number
CN100370015C
CN100370015C CNB2005100110479A CN200510011047A CN100370015C CN 100370015 C CN100370015 C CN 100370015C CN B2005100110479 A CNB2005100110479 A CN B2005100110479A CN 200510011047 A CN200510011047 A CN 200510011047A CN 100370015 C CN100370015 C CN 100370015C
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fungus
cordyceps
culture medium
paste
substratum
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CN1778890A (en
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邓杰华
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Abstract

The present invention provides a method for culturing aweto fungus and Chinese caterpillar fungus, which is characterized in that a culture medium is prepared from the components of the following proportion by mass: 1% to 1.5% of milk powder, 2% to 2.5% of soybean flour, 2% to 4% of corn flour, 2% to 4% of wheat flour, 1% to 2% of glucose, 1% to 2% of sucrose, 0.05% to 0.08% of potassium dihydrogen phosphate, 0.05% to 0.2% of defoaming agent and 85% to 88% of water; the components are boiled into paste and put into a bottle, and after the paste is autoclaved, the paste is inoculated; the paste is cultured for 22 to 32 days at the temperature of 10 DEG C to 30 DEG C, so that mycelium which is crisp, thick, fragrant, delicious and rich in nutrition is obtained, can completely make up for the defects of natural products; not only various health products and medicines with high nutrient value and strong medicinal efficiency can be prepared by using the present invention, but also the diversity and the uniqueness of eating the present invention can be fully embodied. The culture medium provided by the present invention has a scientific and reasonable formula, and can enable the nutrient components of the culture medium to be distributed more uniformly after the culture medium is cooked, so that strains are easy to grow, the requirement of the culture process is not high and strict, the difficulty of the culture process is not large, and the culture medium is favorable for industrialized production and scale production.

Description

The cultural method of Cordyceps fungus or Cordyceps militaris (L.) Link. fungus
Technical field
The present invention relates to a kind of cultural method of biological bacteria, especially the cultural method of Cordyceps fungus, Cordyceps militaris (L.) Link. fungus belongs to biological technical field.
Background technology
Cordyceps sinensis is All Pure Nature high-grade nourishing nutritious prod and the rare traditional Chinese medicine that people generally acknowledge.Because of it is subjected to the influence of natural growthing condition bigger, makes the natural product limited amount, and cost an arm and a leg.For this reason, people's demand be satisfied, the artificial culture technology must be greatly developed.Cordyceps fungus, Cordyceps militaris (L.) Link. fungus are Mycophyta, belong to Cordyceps, and its mycelium is the vegetative organ of dietotherapeutic fungi, also are the main bodys of dietotherapeutic fungi.Last century the seventies, develop meticulously through domestic expert, can from natural cs, isolate multiple bacterial classification, use the submerged fermentation technology and turn out Cordyceps mycelium, and be that raw material is allocated general excipient substance into this tunning, make various medicinal preparationss and healthcare products.But the product that adopts the submerged fermentation technology to obtain can not keep original local flavor of its sporophore and quality, and off-odor is arranged, and can not directly eat, and the equipment used of submerged fermentation technology in addition is huge, technical sophistication, thus limited production and the development of this class fungi.Therefore, be necessary prior art is improved.
Summary of the invention
For overcoming yielding poorly that prior art exists, ingredient is impure, and local flavor and quality are not good to wait deficiency, the invention provides a kind of suitable for mass production, and the cultural method of the Cordyceps fungus of quality better, Cordyceps militaris (L.) Link. fungus.
The present invention realizes by following technical proposal: the cultural method of a kind of Cordyceps fungus or Cordyceps militaris (L.) Link. fungus is characterized in that comprising the following steps:
A, substratum
A, the following quality proportioning of employing: milk powder 1~1.5%, analysis for soybean powder 2~2.5%, Semen Maydis powder 2~4%, flour 2~4%, glucose 1~2%, sucrose 1~2%, potassium primary phosphate 0.05~0.08%, defoamer 0.05~0.2%, water 85~88%;
B, through following technology: after above-mentioned raw materials mixed, in whipping process, boil into scattered paste shape;
B, cultivation
A, the scattered paste shape substratum that the A step is obtained are packed in the culturing bottle, behind the sealing bottleneck, are under 0.12~0.2Mpa at pressure, and steam sterilizing 30~40 minutes treats that pressure reduces to zero, when temperature is reduced to below 60 ℃, takes out culturing bottle;
B, the amount of pressing every 100ml inoculation 2~4ml are injected liquid spawn in the bottle that substratum is housed, and under 10~30 ℃ of temperature, cultivate 22~32 days, get thalline;
C, thalline is put into 60~75 ℃ of warm water soaked 3~8 minutes, clean with clear water afterwards, promptly get bright product.
Described defoamer is a soybean oil.
Described milk powder is milk powder.
The present invention has following advantage and effect: adopt such scheme; it is thick to obtain the crisp meat of matter; flavor is fragrant good to eat; the thalline that nutritive substance is abundant; can compare favourably with natural sporophore; well sold and in short supply at natural cs; output is very limited; expensive current society; be undoubtedly a kind of preferred substitute; can remedy the deficiency of natural product fully; not only can be made into the various healthcare products that are of high nutritive value with it; the medicine that medicinal efficacy is strong; can also demonstrate fully diversity and uniqueness when eating; cultural method provided by the invention; remove that to have equipment simple, invest for a short time, raw material is easy to get; the output height; production link is common, and is easy to control, easy to operate; be not subject to seasonal restrictions etc. outside the characteristics; the main not only scientific formulation of substratum that also is; rationally, and more even through its nutritive ingredient is distributed, the very easily growth of bacterial classification; in the whole culturing process; culture condition such as temperature; humidity etc. are less demanding; not tight, difficulty is little, therefore; help industrialization; large-scale production is the good yeast culture technology of an ideal popularizing application prospect in fact.
Following table provides with the Cordyceps fungus of the present invention's method acquisition and the aminoacids content measurement result of Cordyceps militaris (L.) Link. fungus.
Sequence number Title Cordyceps sinensis (mg/g) Cordyceps militaris (L.) Link. (mg/g)
1 ASP Aspartic acid 0.11 1.07
2 GLU L-glutamic acid 0.160 1.18
3 SER Serine 0.26
4 GLY Glycine 0.64
5 HIS Histidine 0.15 1.58
6 ARG Arginine 0.19 0.32
7 THR Threonine 0.13 0.33
8 ALA L-Ala 0.21 0.56
9 PRO Proline(Pro) 0.91 1.90
10 TYR Tyrosine 0.07 0.04
11 VAL Xie Ansuan 0.13 0.36
12 MET Methionine(Met) 0.05 0.07
13 CYS Cysteine 0.06 0.16
14 ILE Isoleucine 0.08 0.12
15 LEU Leucine 0.09 0.20
16 PHE Phenylalanine 0.06 0.07
17 LYS Methionin 0.05 0.18
Embodiment
Embodiment 1
1, takes off the row raw material: milk powder 1kg, analysis for soybean powder 2.5kg, Semen Maydis powder 3kg, flour 3.3kg, glucose 2kg, sucrose 1kg, potassium primary phosphate 0.08kg, soybean oil 0.12kg, water 87kg;
2, through following technology: soybean oil is gone into pot smear, milk powder, analysis for soybean powder, Semen Maydis powder, flour, glucose, sucrose, potassium primary phosphate are put into container to be mixed, be in harmonious proportion evenly with small amount of water, add enough water afterwards, go into pot behind the stirring and evenly mixing, in whipping process, boil the scattered paste shape substratum;
3, scattered paste shape substratum branch is packed into bottle, every bottled 100ml with poly-third plastics film sealing bottleneck, puts into high-pressure steam sterilizing pan, under 0.12Mpa, high pressure steam sterilization 40 minutes treats that pressure reduces to zero naturally, when temperature drops to 59 ℃, take out, put into transfer room;
4, with the syringe of the bacterium of going out Cordyceps sinensis liquid spawn 2ml is injected bottled substratum after the above-mentioned sterilization, behind medical proof fabric sealing pin hole, put into the culturing room of ultraviolet lamp sterilization;
5, under 10 ℃ of temperature, cultivated 32 days, get thalline;
6, thalline is put into 60 ℃ of warm water and soaked 8 minutes, clean with clear water afterwards, promptly getting thickness is the bright product of Cordyceps fungus of 10mm.
Embodiment 2
1, takes off the row raw material: milk powder 1.5kg, analysis for soybean powder 2.3kg, Semen Maydis powder 4kg, flour 3kg, glucose 2kg, sucrose 2kg, potassium primary phosphate 0.05kg, soybean oil 0.15, water 85kg;
2, through following technology: soybean oil is gone into pot smear, milk powder, analysis for soybean powder, Semen Maydis powder, flour, glucose, sucrose, potassium primary phosphate are put into container to be mixed, be in harmonious proportion evenly with small amount of water, add enough water afterwards, go into pot behind the stirring and evenly mixing, in whipping process, boil the scattered paste shape substratum;
3, scattered paste shape substratum branch is packed into bottle, every bottled 100ml with poly-third plastics film sealing bottleneck, puts into high-pressure steam sterilizing pan, under 0.2Mpa, high pressure steam sterilization 30 minutes treats that pressure reduces to zero naturally, when temperature drops to 40 ℃, take out, put into transfer room;
4, with the syringe of the bacterium of going out Cordyceps militaris (L.) Link. liquid spawn 4ml is injected bottled substratum after the above-mentioned sterilization, behind medical proof fabric sealing pin hole, put into the culturing room of ultraviolet lamp sterilization;
5, under 30 ℃ of temperature, cultivated 22 days, get thalline;
6, thalline is put into 75 ℃ of warm water and soaked 3 minutes, clean with clear water afterwards, promptly getting thickness is the bright product of Cordyceps militaris (L.) Link. fungus of 12mm.
Embodiment 3
1, takes off the row raw material: milk powder 1.2kg, analysis for soybean powder 2.2kg, Semen Maydis powder 2.5kg, flour 2.5kg, glucose 1.5kg, sucrose 1.9kg, potassium primary phosphate 0.06kg, soybean oil 0.14kg, water 88kg;
2, through following technology: soybean oil is gone into pot smear, milk powder, analysis for soybean powder, Semen Maydis powder, flour, glucose, sucrose, potassium primary phosphate are put into container to be mixed, be in harmonious proportion evenly with small amount of water, add enough water afterwards, go into pot behind the stirring and evenly mixing, in whipping process, boil the scattered paste shape substratum;
3, scattered paste shape substratum branch is packed into bottle, every bottled 100ml with poly-third plastics film sealing bottleneck, puts into high-pressure steam sterilizing pan, under 0.15Mpa, high pressure steam sterilization 35 minutes treats that pressure reduces to zero naturally, when temperature drops to 50 ℃, take out, put into transfer room;
4, with the syringe of the bacterium of going out Cordyceps sinensis liquid spawn 3ml is injected bottled substratum after the above-mentioned sterilization, behind medical proof fabric sealing pin hole, put into the culturing room of ultraviolet lamp sterilization;
5, under 20 ℃ of temperature, cultivated 28 days, get thalline;
6, thalline is put into 70 ℃ of warm water and soaked 5 minutes, clean with clear water afterwards, promptly getting thickness is the bright product of Cordyceps fungus of 15mm.

Claims (3)

1. the cultural method of Cordyceps fungus or Cordyceps militaris (L.) Link. fungus is characterized in that comprising the following steps:
A, substratum
A, the following quality proportioning of employing: milk powder 1~1.5%, analysis for soybean powder 2~2.5%, Semen Maydis powder 2~4%, flour 2~4%, glucose 1~2%, sucrose 1~2%, potassium primary phosphate 0.05~0.08%, defoamer 0.05~0.2%, water 85~88%;
B, through following technology: after above-mentioned raw materials mixed, in whipping process, boil into scattered paste shape;
B, cultivation
A, the scattered paste shape substratum that the A step is obtained are packed in the culturing bottle, behind the sealing bottleneck, are under 0.12~0.2Mpa at pressure, and steam sterilizing 30~40 minutes treats that pressure reduces to zero, when temperature is reduced to below 60 ℃, takes out culturing bottle;
B, the amount of pressing every 100ml inoculation 2~4ml are injected liquid spawn in the bottle that substratum is housed, and under 10~30 ℃ of temperature, cultivate 22~32 days, get thalline;
C, thalline is put into 60~75 ℃ of warm water soaked 3~8 minutes, clean with clear water afterwards, promptly get bright product.
2. the cultural method of Cordyceps fungus according to claim 1 or Cordyceps militaris (L.) Link. fungus is characterized in that described defoamer is a soybean oil.
3. the cultural method of Cordyceps fungus according to claim 1 or Cordyceps militaris (L.) Link. fungus is characterized in that described milk powder is milk powder.
CNB2005100110479A 2005-09-30 2005-09-30 Culture for caterpillar and cordycepin Expired - Fee Related CN100370015C (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101293791A (en) * 2008-06-13 2008-10-29 上海浦东天厨菇业有限公司 Liquid bacterial culture medium for industrial preparation of hypsizygus marmoreus and preparation method thereof
CN101971764A (en) * 2010-03-22 2011-02-16 陈顺志 Industrial energy-saving and low-carbon method for cultivating cordyceps militaris

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102150561B (en) * 2011-01-01 2013-05-15 臧向明 Method for cultivating cordyceps sinensis
CN103553755B (en) * 2013-11-13 2015-05-27 青海洲龙生物科技有限责任公司 Cordyceps sinensis bacterial powder and production method thereof as well as special culture medium

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN85107991A (en) * 1985-11-01 1987-05-06 北京市营养源研究所 The industrial process of Cordyceps mycelium
CN1059457A (en) * 1991-10-22 1992-03-18 北京市营养源研究所 The manufacture method of nutriment from " Xianggu mushroom
CN1136393A (en) * 1996-01-19 1996-11-27 济南科贝尔生物工程有限公司 Agricultural chemical for preventing and controlling plant virus prepared by liquid fermentation and its producing technology
CN1271514A (en) * 2000-05-23 2000-11-01 曾树生 Process for preparing mushroom-shaped cordyceps mycelium
CN1275403A (en) * 1999-09-01 2000-12-06 朱宏图 Method for preparation of fungus powder medicine of artificial cultivated cordyceps
CN1362513A (en) * 2001-01-04 2002-08-07 怀化市益康生物高科技有限公司 Artificial cordyceps culturing medium
CN1445360A (en) * 2002-03-20 2003-10-01 中国科学院沈阳应用生态研究所 Method of artificial planting northerly Chinese caterpillar fungus for increasing content of physiologically active substance
CN1651568A (en) * 2004-02-03 2005-08-10 李勇 Edible fungus liquid culture submerged fermentation technology

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN85107991A (en) * 1985-11-01 1987-05-06 北京市营养源研究所 The industrial process of Cordyceps mycelium
CN1059457A (en) * 1991-10-22 1992-03-18 北京市营养源研究所 The manufacture method of nutriment from " Xianggu mushroom
CN1136393A (en) * 1996-01-19 1996-11-27 济南科贝尔生物工程有限公司 Agricultural chemical for preventing and controlling plant virus prepared by liquid fermentation and its producing technology
CN1275403A (en) * 1999-09-01 2000-12-06 朱宏图 Method for preparation of fungus powder medicine of artificial cultivated cordyceps
CN1271514A (en) * 2000-05-23 2000-11-01 曾树生 Process for preparing mushroom-shaped cordyceps mycelium
CN1362513A (en) * 2001-01-04 2002-08-07 怀化市益康生物高科技有限公司 Artificial cordyceps culturing medium
CN1445360A (en) * 2002-03-20 2003-10-01 中国科学院沈阳应用生态研究所 Method of artificial planting northerly Chinese caterpillar fungus for increasing content of physiologically active substance
CN1651568A (en) * 2004-02-03 2005-08-10 李勇 Edible fungus liquid culture submerged fermentation technology

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
冬虫夏草液体培养基的筛选和液体发酵技术研究. 张伟等.中国医学生物技术应用杂志. 2004 *
数理统计法优化冬虫夏草发酵培养基的研究. 武忠伟等.食品科学,第25卷第12期. 2004 *
胡昭更谈蛹虫草及米饭栽培. 徐摘.中国技术市场报. 2001 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101293791A (en) * 2008-06-13 2008-10-29 上海浦东天厨菇业有限公司 Liquid bacterial culture medium for industrial preparation of hypsizygus marmoreus and preparation method thereof
CN101971764A (en) * 2010-03-22 2011-02-16 陈顺志 Industrial energy-saving and low-carbon method for cultivating cordyceps militaris

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