CN107541470A - A kind of culture medium for bringing back to life pleurotus eryngii quel strains and its preparation method and application - Google Patents

A kind of culture medium for bringing back to life pleurotus eryngii quel strains and its preparation method and application Download PDF

Info

Publication number
CN107541470A
CN107541470A CN201711001075.1A CN201711001075A CN107541470A CN 107541470 A CN107541470 A CN 107541470A CN 201711001075 A CN201711001075 A CN 201711001075A CN 107541470 A CN107541470 A CN 107541470A
Authority
CN
China
Prior art keywords
pleurotus eryngii
life
culture medium
quel strains
eryngii quel
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201711001075.1A
Other languages
Chinese (zh)
Inventor
陈红霞
韦静宜
龙琦
何叶
田时炳
郭军
郑勇
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Chongqing Academy of Agricultural Sciences
Original Assignee
Chongqing Academy of Agricultural Sciences
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Chongqing Academy of Agricultural Sciences filed Critical Chongqing Academy of Agricultural Sciences
Priority to CN201711001075.1A priority Critical patent/CN107541470A/en
Publication of CN107541470A publication Critical patent/CN107541470A/en
Pending legal-status Critical Current

Links

Landscapes

  • Micro-Organisms Or Cultivation Processes Thereof (AREA)

Abstract

A kind of culture medium for bringing back to life pleurotus eryngii quel strains and its preparation method and application, is related to edible mushroom culture technique field.A kind of culture medium for bringing back to life pleurotus eryngii quel strains provided by the invention, counts, is mainly made up of following raw material in parts by weight:20~40 parts of carrot, 1~5 part of glucose, 1~5 part of agar.The culture medium is brought back to life to pleurotus eryngii quel strains, effect of rejuvenation is good, and culture raw material sources are wide, are easy to get, and cost is cheap.A kind of preparation method for the culture medium for bringing back to life pleurotus eryngii quel strains, including:Raw material is mixed with water.Preparation technology is simple, easy to operate.

Description

A kind of culture medium for bringing back to life pleurotus eryngii quel strains and its preparation method and application
Technical field
The present invention relates to edible mushroom culture technique field, and more particularly to it is a kind of bring back to life pleurotus eryngii quel strains culture medium and its Preparation method and application.
Background technology
Pleurotus eryngii also known as pleurotus eryngii, cap is plump, and quality is tender and crisp, because it has the fragrance of almond and the mouth such as abalone Feel and gain the name.Pleurotus eryngii has reducing blood lipid, norcholesterol, promotes gastro-intestinal digestion, strengthen body immunity, prevent cardiovascular disease And other effects, pole is liked by people.It is the Rare edible fungus kind that collection is edible, medicine is used for one.
Strain refers to the propagating materials of edible mushroom mycelium and its growth substrate composition.Culture presevation is with dry, low The means of gentle isolation air, reduce the rate of metabolism of microorganism fungus kind, the vital movement of strain is in semipermanent Resting state.Atoleine method is usually 2~3 years for the storage life of edible fungus species, past more than the strain of storage life Toward being difficult to bring back to life by conventional medium, or resuscitable strain, its growth rate is slow, and vigor is low, it is impossible to meet production and Scientific research requirements, the loss and waste of microorganism resource are caused, great loss is brought to production and scientific research breeding work.
The content of the invention
It is an object of the invention to provide a kind of culture medium for bringing back to life pleurotus eryngii quel strains, the culture medium is answered pleurotus eryngii quel strains Work, effect of rejuvenation are good, and culture raw material sources are wide, are easy to get, and cost is cheap.
Another object of the present invention is to provide a kind of preparation method for the culture medium for bringing back to life pleurotus eryngii quel strains, preparation technology Simply, it is easy to operate.
A further object of the present invention is the application for providing the culture medium of above-mentioned resurrection pleurotus eryngii quel strains.
The present invention is solved its technical problem and realized using following technical scheme:
The present invention proposes a kind of culture medium for bringing back to life pleurotus eryngii quel strains, counts, is mainly made up of following raw material in parts by weight: 20~40 parts of carrot, 1~5 part of glucose, 1~5 part of agar.
The present invention proposes a kind of preparation method for the culture medium for bringing back to life pleurotus eryngii quel strains, including:Raw material is mixed with water.
The present invention proposes application of the culture medium of above-mentioned resurrection pleurotus eryngii quel strains in edible mushroom is brought back to life.
A kind of beneficial effect of the culture medium of resurrection pleurotus eryngii quel strains of the embodiment of the present invention and its preparation method and application It is:
A kind of culture medium for bringing back to life pleurotus eryngii quel strains, using carrot, glucose and agar as raw material, carrot contains albumen Matter, carbohydrate, fat, carrotene, vitamin A, vitamin B1, vitamin B2, anthocyanidin, calcium, iron, sodium, potassium etc. are a variety of Nutritional ingredient, the necessary material brought back to life is provided for pleurotus eryngii quel strains, improves the resurrection rate of pleurotus eryngii quel strains.Simultaneously, there is provided apricot Bao Nutrition needed for mushroom strains growth, breeding.Glucose provides energy to strain, and auxiliary promotes the resurrection of strain, there is provided pleurotus eryngii Energy necessary to strain grows after bringing back to life.Agar is the polysaccharide body extracted in marine alga.After water extraction, nutrition is more easy to be inhaled carrot Receive.Obtained culture medium is brought back to life to pleurotus eryngii quel strains, effect of rejuvenation is good, and culture raw material sources are wide, are easy to get, and cost is cheap.It is a kind of The preparation method of the culture medium of pleurotus eryngii quel strains is brought back to life, preparation technology is simple, easy to operate.
Embodiment
, below will be in the embodiment of the present invention to make the purpose, technical scheme and advantage of the embodiment of the present invention clearer Technical scheme be clearly and completely described.Unreceipted actual conditions person, builds according to normal condition or manufacturer in embodiment The condition of view is carried out.Agents useful for same or the unreceipted production firm person of instrument, it is the conventional production that can be obtained by commercially available purchase Product.
Culture medium of a kind of resurrection pleurotus eryngii quel strains of the embodiment of the present invention and its preparation method and application is carried out below Illustrate.
A kind of culture medium for bringing back to life pleurotus eryngii quel strains provided in an embodiment of the present invention, is counted, mainly by following in parts by weight Raw material is made:20~40 parts of carrot, 1~5 part of glucose, 1~5 part of agar.Such as can take carrot 21,22,24,36, 36.5th, 39 parts, glucose 1.2,1.8,3.5,4.3 parts, agar 3.7,4.2,4.5 parts.
Further, in present pre-ferred embodiments, count in parts by weight, raw material includes:25~35 parts of carrot, Portugal 1~3 part of grape sugar, 1~3 part of agar.Such as can take carrot 27,29,31,34 parts, glucose 1.1,1.4,2.4 parts, agar 1.5th, 2.6 parts.
Further, in present pre-ferred embodiments, count in parts by weight, raw material includes:30 parts of carrot, glucose 2 Part, 2 parts of agar.
Carrot is rich in carbohydrate, protein, carbohydrate, fat, carrotene, vitamin A, vitamin B1, vitamin The nutritional ingredients such as B2, anthocyanidin, calcium, iron, sodium, potassium.In every 100 grams of carrots, containing about 0.6 gram of protein, 0.3 gram of fat, carbohydrate 7.6~8.3 grams, 0.6 milligram of iron, 1.35~17.25 milligrams of provitamin A (carrotene), vitaminB10 .02~0.04 is in the least Gram, 0.04~0.05 milligram of vitamin B2,12 milligrams of vitamin C, the kilojoule of heat 150.7, separately containing pectin, starch, inorganic salts and Several amino acids.
In the present invention, the raw material using carrot as culture medium, the nutriment enriched in carrot is to pleurotus eryngii quel strains The necessary material brought back to life is provided, improves the resurrection rate of pleurotus eryngii quel strains.Meanwhile the nutriment in carrot causes pleurotus eryngii bacterium Fast-growth, breeding after kind is brought back to life.
Glucose is a kind of important monose, is a kind of polyhydroxy aldehyde.Glucose is the energy source of living cells and new old Metabolic intermediate, it is the main Energy supply material of biology.Glucose easily absorbs as carbon source, strain, promotes the growth of strain. During pleurotus eryngii quel strains are brought back to life, glucose auxiliary carrot promotes the resurrection of strain, and provides pleurotus eryngii quel strains resurrection Energy necessary to grow afterwards.
Agar is one kind of natural plant gum, is the polysaccharide body extracted in marine alga.In the present invention, the solidification as culture medium Agent.
A kind of preparation method of culture medium for bringing back to life pleurotus eryngii quel strains provided in an embodiment of the present invention, including:
Mass ratio according to carrot, glucose, agar and water is 15~20:1:1:40~50.Weigh raw material.
Carrot is cleaned, dried, is cut into small pieces, preferably, carrot is smashed.Carrot block or carrot disintegrating slag are carried out Extraction.The nutriment in carrot is extracted by extraction so that pleurotus eryngii quel strains are more easy to absorb.Of the invention real Apply in example, extracted by the way of boiling.Specifically, carrot block or carrot disintegrating slag are boiled into 15~25min in boiling water, filter Take filtrate.Carrot filtrate is mixed with glucose, agar and water.Obtained Medium's PH Value is neutrality.
In order to ensure the pure of culture medium, the resurrection of the microbiological effect pleurotus eryngii quel strains such as bacterium, fungi is prevented, will be mixed Thing is 115~125 DEG C in temperature, and under conditions of pressure is 0.07~0.15MPa, sterilize 15~25min.
The culture medium provided by the invention for bringing back to life pleurotus eryngii quel strains has preferable On Reactivation, and it is edible to can apply to resurrection Bacterium.Edible mushroom includes pleurotus eryngii quel strains, it is preferable that pleurotus eryngii quel strains are the strain of preservation 10 years.
The feature and performance of the present invention are described in further detail with reference to embodiments.
Embodiment 1
A kind of culture medium for bringing back to life pleurotus eryngii quel strains is present embodiments provided, raw material includes:Carrot 200g, glucose 10g, agar 10g, water.
Main be prepared by the following method forms:
Carrot is cut into block, 20min is boiled in boiling water, filters to take filtrate.
Filtrate is mixed with glucose, agar, adds water to be settled to 1L.
By mixture under conditions of 115 DEG C, 0.1MPa, sterilize 15min, obtains culture medium.
Embodiment 2
A kind of culture medium for bringing back to life pleurotus eryngii quel strains is present embodiments provided, raw material includes:Carrot 400g, glucose 10g, agar 20g, water.
Main be prepared by the following method forms:
Carrot is cut into block, 15min is boiled in boiling water, filters to take filtrate.
Filtrate is mixed with glucose, agar, adds water to be settled to 1L.
By mixture under conditions of 125 DEG C, 0.15MPa, sterilize 25min, obtains culture medium.
Embodiment 3
A kind of culture medium for bringing back to life pleurotus eryngii quel strains is present embodiments provided, raw material includes:Carrot 250g, glucose 15g, agar 15g, water.
Main be prepared by the following method forms:
Carrot is cut into block, 20min is boiled in boiling water, filters to take filtrate.
Filtrate is mixed with glucose, agar, adds water to be settled to 1L.
By mixture under conditions of 121 DEG C, 0.11MPa, sterilize 20min, obtains culture medium.
Embodiment 4
A kind of culture medium for bringing back to life pleurotus eryngii quel strains is present embodiments provided, raw material includes:Carrot 250g, glucose 10g, agar 20g, water.
Main be prepared by the following method forms:
Carrot is cut into block, 15min is boiled in boiling water, filters to take filtrate.
Filtrate is mixed with glucose, agar, adds water to be settled to 1L.
By mixture under conditions of 118 DEG C, 0.09MPa, sterilize 15min, obtains culture medium.
Embodiment 5
A kind of culture medium for bringing back to life pleurotus eryngii quel strains is present embodiments provided, raw material includes:Carrot 400g, glucose 20g, agar 10g, water.
Main be prepared by the following method forms:
Carrot is cut into block, 20min is boiled in boiling water, filters to take filtrate.
Filtrate is mixed with glucose, agar, adds water to be settled to 1L.
By mixture under conditions of 120 DEG C, 0.11MPa, sterilize 20min, obtains culture medium.
Embodiment 6
A kind of culture medium for bringing back to life pleurotus eryngii quel strains is present embodiments provided, raw material includes:Carrot 300g, glucose 20g, agar 20g, water.
Main be prepared by the following method forms:
Carrot is cut into block, 20min is boiled in boiling water, filters to take filtrate.
Filtrate is mixed with glucose, agar, adds water to be settled to 1L.
By mixture under conditions of 121 DEG C, 0.11MPa, sterilize 20min, obtains culture medium.
Comparative example 1
This comparative example provides PDA culture medium, i.e. potato dextrose agar.
Comparative example 2
This comparative example provides CPDA culture mediums, i.e. potato dextrose agar complete medium.
Test example
The strain block that 8 block sizes about 0.5cm × 0.5cm preserves in atoleine is taken with inoculation shovel, strain block is being tried Gently it is switched to embodiment 1~6, comparative example 1, comparative example 2 by reducing the vasoliniment of absorption under several on tube wall and provides In test tube slant culture medium, silica gel plug is stoppered, the lucifuge culture under conditions of 25 DEG C, observes and records growing state, it is as a result as follows Table:
The pleurotus eryngii parent species sprouting situation of table 1
Sprout time Hypha form
Embodiment 1 About 2 days It is pure white sparse
Embodiment 2 About 2 days It is pure white sparse
Embodiment 3 About 1 day It is pure white dense
Embodiment 4 About 1 day It is pure white dense, it is energetic
Embodiment 5 About 1 day It is pure white dense, it is energetic
Embodiment 6 About 1 day It is pure white dense, it is energetic
Comparative example 1 About 3 days Hyphae length is few, tiny
Comparative example 2 About 3 days Hyphae length is few, tiny
As shown in Table 1, compared to comparative example 1 and comparative example 2, the culture medium for the resurrection pleurotus eryngii quel strains that embodiment 1~6 provides There is preferable On Reactivation to pleurotus eryngii parent species, sprout time is shorter.Wherein, the resurrection pleurotus eryngii that embodiment 4~6 provides More preferably, the parent species mycelia of resurrection is pure white dense, energetic for the On Reactivation of the culture medium of strain.Embodiment 6 brings back to life the mother of culture Kind is compared with the parent species that comparative example 1 and comparative example 2 are cultivated, and the parent species sprout time that embodiment 6 is brought back to life shortens 160%, and growth is fast Rate improves 72%, illustrates that resurrection ability of the culture medium of the offer of embodiment 6 to pleurotus eryngii quel strains is significantly better than conventional PDA cultures Base and CPDA culture mediums.Therefore, the formula of the culture medium for the resurrection pleurotus eryngii quel strains that embodiment 6 provides and preparation method more section It is reasonable to learn.
In summary, the culture medium provided in an embodiment of the present invention for bringing back to life pleurotus eryngii quel strains, with carrot, glucose and fine jade Fat as raw material, carrot contain protein, carbohydrate, fat, carrotene, vitamin A, vitamin B1, vitamin B2, The multiple nutritional components such as anthocyanidin, calcium, iron, sodium, potassium, to provide the necessary material brought back to life to pleurotus eryngii quel strains, improve pleurotus eryngii The resurrection rate of strain.Simultaneously, there is provided the nutrition needed for pleurotus eryngii quel strains growth, breeding.Glucose is auxiliary to provide energy to strain Carrot is helped to promote the resurrection of strain, there is provided energy necessary to pleurotus eryngii quel strains grow after bringing back to life.Agar be extracted in marine alga it is more Sugared body, it is culture medium curing agent.After water extraction, nutrition is more easy to be absorbed carrot.Obtained culture medium is answered pleurotus eryngii quel strains Work, effect of rejuvenation are good, and culture raw material sources are wide, are easy to get, and cost is cheap.
Embodiments described above is the part of the embodiment of the present invention, rather than whole embodiments.The present invention's The detailed description of embodiment is not intended to limit the scope of claimed invention, but is merely representative of the selected reality of the present invention Apply example.Based on the embodiment in the present invention, those of ordinary skill in the art are obtained under the premise of creative work is not made Every other embodiment, belong to the scope of protection of the invention.

Claims (10)

1. a kind of culture medium for bringing back to life pleurotus eryngii quel strains, it is characterised in that count, be mainly made up of following raw material in parts by weight: 20~40 parts of carrot, 1~5 part of glucose, 1~5 part of agar.
2. the culture medium according to claim 1 for bringing back to life pleurotus eryngii quel strains, it is characterised in that count in parts by weight, it is described Raw material includes:25~35 parts of the carrot, 1~3 part of the glucose, 1~3 part of the agar.
3. the culture medium according to claim 2 for bringing back to life pleurotus eryngii quel strains, it is characterised in that count in parts by weight, it is described Raw material includes:30 parts of the carrot, 2 parts of the glucose, 2 parts of the agar.
4. a kind of preparation method for the culture medium for bringing back to life pleurotus eryngii quel strains as claimed any one in claims 1 to 3, its feature It is, including:The raw material is mixed with water.
5. the preparation method of the culture medium according to claim 4 for bringing back to life pleurotus eryngii quel strains, it is characterised in that described in mixing Before raw material, the carrot boiling, filtering mix carrot filtrate with the glucose, the agar and the water.
6. the preparation method of the culture medium according to claim 5 for bringing back to life pleurotus eryngii quel strains, it is characterised in that the Hu trailing plants The mass ratio of fore-telling, the glucose, the agar and the water is 15~20:1:1:40~50.
7. the preparation method of the culture medium according to claim 6 for bringing back to life pleurotus eryngii quel strains, it is characterised in that the raw material After being mixed with the water, in addition to mixture sterilized.
8. the preparation method of the culture medium according to claim 7 for bringing back to life pleurotus eryngii quel strains, it is characterised in that the side of sterilizing Method includes:It it is 115~125 DEG C in temperature, under conditions of pressure is 0.07~0.15MPa, sterilize 15~25min.
9. application of the culture medium of the resurrection pleurotus eryngii quel strains as described in any one of claims 1 to 3 in edible mushroom is brought back to life.
10. application of the culture medium according to claim 9 for bringing back to life pleurotus eryngii quel strains in edible mushroom is brought back to life, its feature exist In the edible mushroom includes preserving the pleurotus eryngii quel strains of at least 10 years.
CN201711001075.1A 2017-10-24 2017-10-24 A kind of culture medium for bringing back to life pleurotus eryngii quel strains and its preparation method and application Pending CN107541470A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201711001075.1A CN107541470A (en) 2017-10-24 2017-10-24 A kind of culture medium for bringing back to life pleurotus eryngii quel strains and its preparation method and application

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201711001075.1A CN107541470A (en) 2017-10-24 2017-10-24 A kind of culture medium for bringing back to life pleurotus eryngii quel strains and its preparation method and application

Publications (1)

Publication Number Publication Date
CN107541470A true CN107541470A (en) 2018-01-05

Family

ID=60968094

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201711001075.1A Pending CN107541470A (en) 2017-10-24 2017-10-24 A kind of culture medium for bringing back to life pleurotus eryngii quel strains and its preparation method and application

Country Status (1)

Country Link
CN (1) CN107541470A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108419606A (en) * 2018-01-30 2018-08-21 山东惠民齐发果蔬有限责任公司 The application of a kind of preparation method and carrot culture medium of carrot culture medium in edible mushroom Mother culture

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105505797A (en) * 2016-01-11 2016-04-20 黄山学院 Culture medium for pleurotus eryngii strain cultivation

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105505797A (en) * 2016-01-11 2016-04-20 黄山学院 Culture medium for pleurotus eryngii strain cultivation

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
方白玉 等: "杏鲍菇母种培养基的优化初探", 《食用菌》 *
谢春芹 等: "杏鲍菇母种最适固化培养基的筛选", 《江苏农业科学》 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108419606A (en) * 2018-01-30 2018-08-21 山东惠民齐发果蔬有限责任公司 The application of a kind of preparation method and carrot culture medium of carrot culture medium in edible mushroom Mother culture

Similar Documents

Publication Publication Date Title
CN104030845B (en) A kind of glossy ganoderma substituting stuff cultivation substratum that with the addition of Grosvenor Momordica
CN103109679B (en) Method for cultivating antrodia camphorate sporocarp basswood in the second stage
CN104193462A (en) Agaric culture medium
CN103027293A (en) Method for preparing antrodia camphorata ferment
CN105284520A (en) Method promoting fig cuttage rooting
CN105379561A (en) High-yield cultivation method for edible mushrooms
CN111248026B (en) Quercus matsutake culture medium and application thereof
CN102301914B (en) Technology for culturing Pleurotus eryngii
CN107721589A (en) A kind of Agrocybe cylindracea culture medium of low tannin content and preparation method thereof
CN107125735A (en) A kind of matrimony vine composite enzyme and preparation method thereof
CN107873391B (en) Fungus inhibiting culture medium for cultivating agaric and cultivation method thereof
CN103299822A (en) Schizophyllum commune Fr high-yield fruiting body strain and three-dimensional ecology-returning cultivation method
CN107541470A (en) A kind of culture medium for bringing back to life pleurotus eryngii quel strains and its preparation method and application
CN108610167B (en) Edible fungus cultivation nutrient for improving lignin conversion rate and method for cultivating edible fungus by using nutrient
CN105237144A (en) Agaricus blazei culture medium and preparation method thereof
CN108713449A (en) A kind of cultural method of Poria cocos
CN107226735A (en) A kind of oyster mushroom culture medium matter and preparation method thereof
CN107114768A (en) Blueberry ferment and preparation method thereof
CN109076881B (en) Culture method and application of selenium-rich hericium erinaceus mycelium
CN107417338A (en) A kind of culture medium of edible fungus and preparation method thereof
CN106386172A (en) Method for cultivating high-yield high-quality Lentinus edodes having sweet-scented osmanthus fragrance
CN105622256A (en) Cultivation method of ganoderma lucidum antler substitute material
CN105347987A (en) Culture medium for substitute cultivation of ganoderma lucidum antler
KR20160033386A (en) Cultivatio-n method of Fermented phelleniuse linteus using the Cudrania tricuspida-ta and germinated brown rice
CN108558476A (en) A kind of dendrobium candidum water planting domestication hardening nutrient solution and its application

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication

Application publication date: 20180105

RJ01 Rejection of invention patent application after publication