CN109680017A - A kind of solid medium for being conducive to improve flavones content in phellinus igniarius mycelium - Google Patents

A kind of solid medium for being conducive to improve flavones content in phellinus igniarius mycelium Download PDF

Info

Publication number
CN109680017A
CN109680017A CN201910055052.1A CN201910055052A CN109680017A CN 109680017 A CN109680017 A CN 109680017A CN 201910055052 A CN201910055052 A CN 201910055052A CN 109680017 A CN109680017 A CN 109680017A
Authority
CN
China
Prior art keywords
parts
culture
conducive
potato
glucose
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.)
Withdrawn
Application number
CN201910055052.1A
Other languages
Chinese (zh)
Inventor
劳以军
操时英
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.)
Hangzhou Fairview Workshop Arts & Crafts Co ltd
Original Assignee
Hangzhou Fairview Workshop Arts & Crafts Co ltd
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 Hangzhou Fairview Workshop Arts & Crafts Co ltd filed Critical Hangzhou Fairview Workshop Arts & Crafts Co ltd
Priority to CN201910055052.1A priority Critical patent/CN109680017A/en
Publication of CN109680017A publication Critical patent/CN109680017A/en
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N1/00Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
    • C12N1/14Fungi; Culture media therefor
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P17/00Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
    • C12P17/02Oxygen as only ring hetero atoms
    • C12P17/06Oxygen as only ring hetero atoms containing a six-membered hetero ring, e.g. fluorescein

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Health & Medical Sciences (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Genetics & Genomics (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biotechnology (AREA)
  • General Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • General Engineering & Computer Science (AREA)
  • Microbiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Botany (AREA)
  • Mycology (AREA)
  • Medicinal Chemistry (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Virology (AREA)
  • Biomedical Technology (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)

Abstract

The invention discloses a kind of solid mediums for being conducive to improve flavones content in phellinus igniarius mycelium; its raw material includes: 20-30 parts of glucose, 20-30 parts of potato, 10-20 parts of soybean powder, 10-20 parts of casein, 5-10 parts of peptone, 5-8 parts of magnesium sulfate, 1-5 parts of calcium chloride, 1-5 parts of sodium chloride, 4-9 parts of saccharomycete, 20-26 parts of weed tree sawdust and 5-10 parts of fresh pig dung by weight; the casein is using fresh milk degreasing, and the present invention relates to edible mushroom culture technique fields.This is conducive to the solid medium for improving flavones content in phellinus igniarius mycelium; achieve the purpose that carry out fermentation using animal waste and weed tree sawdust and prepare culture substrate; realization directlys adopt the culture substrate that glucose, soybean powder, dry ferment and magnesium sulfate make high nutrition composition; substantially increase Phellinus bacterium culture medium matter nutrient content; the growth demand of Phellinus bacterium is met well; flavones content is lower in the Phellinus bacterium that culture substrate can be made to turn out, to be advantageous to the culture of Phellinus bacterium.

Description

A kind of solid medium for being conducive to improve flavones content in phellinus igniarius mycelium
Technical field
The present invention relates to edible mushroom culture technique field, specially one kind is conducive to improve flavones content in phellinus igniarius mycelium Solid medium.
Background technique
Phellinus category Basidiomycotina, Hymenomycetes, Aphyllophorales, Hymenochaetaceae, Phellinus be phelliuns igniarius and P .linteus, Phellinus are the perennial precious medicinal fungis of one kind developed in recent years, there is the laudatory title of " forest gold ", The gynecological diseases such as metrorrhagia, blood strangury, leukorrhagia, amenorrhoea can be controlled, modern medicine study shows that Phellinus has antitumor, antibacterial, anti-fiber Change, is anti-oxidant and the remarkable results such as improve the immunity of the human body, being the rare of biological antitumous effect first internationally recognized at present Medicinal fungi, is widely used in the industries such as medicine, food, daily-use chemical industry, health care product, and the disease that the world today is most difficult to capture is cancer Disease, due to the side effect of chemotherapeutics, the research of natural anti-cancer drugs is the hot spot of drug worker concern always, a large amount of popular Disease learns investigation, zoopery and experiment in vitro result of study and shows that flavonoids has extensive suppression cancer and protective effect on cancer risk, especially Think that cancer related with human body estrogen secretion, such as breast cancer, oophoroma, prostate cancer have preferable effect to some, What is played a major role in Phellinus is flavonoids, and flavonoids is one of main active in nature medicinal plant, by its structure It is divided into flavones, flavonols, flavanones, dioxy flavonols, isoflavones etc., current identified bioflavonoid has more than 6400 kinds, There is flavonoids physiological activity, the Phellinus bacterium such as adjusting blood lipid, elimination oxygen radical, anti-oxidant, antitumor, antiviral to cultivate It needs to be cultivated using unique culture medium in journey.
Current Phellinus bacterium culture medium matter nutrient content is lower, is not able to satisfy the growth demand of Phellinus bacterium, and existing culture Flavones content is lower in the Phellinus bacterium that matrix is turned out, and can not achieve and is improved to Phellinus culture substrate to realize to Phellinus bacterium It is cultivated well, is unable to reach and the purpose that fermentation prepares culture substrate, Bu Nengshi are carried out using animal waste and weed tree sawdust The culture substrate that glucose, soybean powder, dry ferment and magnesium sulfate make high nutrition composition is now directlyed adopt, to give Phellinus bacterium Culture bring greatly it is unfavorable.
Summary of the invention
(1) the technical issues of solving
In view of the deficiencies of the prior art, be conducive to improve flavones content in phellinus igniarius mycelium the present invention provides a kind of and consolidate Body culture medium, it is lower to solve existing Phellinus bacterium culture medium matter nutrient content, is not able to satisfy the growth demand of Phellinus bacterium, and existing Flavones content is lower in the Phellinus bacterium for having culture substrate to turn out, and can not achieve and is improved to Phellinus culture substrate to realize pair Phellinus bacterium is cultivated well, is unable to reach and carries out the purpose that fermentation prepares culture substrate using animal waste and weed tree sawdust, It can not achieve and directly adopt the problem of glucose, soybean powder, dry ferment and magnesium sulfate make high nutrition composition culture substrate.
(2) technical solution
In order to achieve the above object, the present invention is achieved by the following technical programs: one kind is conducive to improve phellinus liteus The solid medium of flavones content in body, raw material include: 20-30 parts of glucose, 20-30 parts of potato, Huang by weight 10-20 parts of bean powder, 10-20 parts of casein, 5-10 parts of peptone, 5-8 parts of magnesium sulfate, 1-5 parts of calcium chloride, 1-5 parts of sodium chloride, ferment Female bacterium 4-9 parts, 20-26 parts of weed tree sawdust and 5-10 parts of fresh pig dung.
Preferably, raw material includes following component: 25 parts of glucose, 25 parts of potato, 15 parts of soybean powder, casein 15 Part, 7 parts of peptone, 6 parts of magnesium sulfate, 3 parts of calcium chloride, 3 parts of sodium chloride, 6 parts of saccharomycete, 23 parts of weed tree sawdust and 7 parts of fresh pig dung.
Preferably, raw material includes following component: 20 parts of glucose, 20 parts of potato, 10 parts of soybean powder, casein 10 Part, 5 parts of peptone, 5 parts of magnesium sulfate, 1 part of calcium chloride, 1 part of sodium chloride, 4 parts of saccharomycete, 20 parts of weed tree sawdust and 5 parts of fresh pig dung.
Preferably, raw material includes following component: 30 parts of glucose, 30 parts of potato, 20 parts of soybean powder, casein 20 Part, 10 parts of peptone, 8 parts of magnesium sulfate, 5 parts of calcium chloride, 5 parts of sodium chloride, 9 parts of saccharomycete, 26 parts of weed tree sawdust and 10 parts of fresh pig dung.
Preferably, the casein is to be added lactic acid using fresh milk degreasing, pH is adjusted to 4.6, made casein protomere It loses charge and solidifies precipitating.
Preferably, the glucose be select take off dry corn by smashing and grinding equipment obtain corn flour, then to corn Water is added in powder and amylase stirs 2-3h, filters filter residue, can be obtained required glucose.
Preferably, the solid medium preparation method specifically includes the following steps:
S1, the weed tree sawdust of selection and fresh pig dung successively poured into pulverizer first, is sufficiently crushed, then will crushed Material afterwards pours into mixing and blending machine, stirs 1-2h with the revolving speed of 400-600r/min, fills weed tree sawdust with fresh pig dung Divide mixing, obtain culture material, the saccharomycete of selection is inoculated in culture material later, is stirred with the revolving speed of 500-600r/min Mixing 20-30min is mixed, 20-25d is sealed by fermentation, can be obtained Nutrious fermented matrix;
S2, the potato of selection is first subjected to peeling processing, then potato is put into boiler plus water submerged, heating are boiled Boiling, persistently boils 10-20min, later smashs cooked potato in boiler to pieces, and 20-25min is boiled in heating again, then Air-cooled 30-40min is stood, potato nutritional suspension can be obtained;
S3, the nutrition suspension that S2 is obtained is poured into the Nutrious fermented Medium Culture in S1, is stirred with revolving speed for 400-600r/min 30-40min is mixed, then by the glucose of selection, soybean powder, casein, peptone, magnesium sulfate, calcium chloride and sodium chloride are successively It is added in mixing and blending machine, 1-2h is stirred with the revolving speed of 700-900r/min, can be obtained culture medium;
S4, the culture medium raw material for obtaining S3 thermal dehydration to the moisture content at 37-48 DEG C are the 50- of total weight 66%, it is then wrapped up using aseptic thin-film, 10-25min is handled using 88-100 DEG C of vapor high pressure sterilization later, can be obtained Solid medium.
(3) beneficial effect
The present invention provides a kind of solid mediums for being conducive to improve flavones content in phellinus igniarius mycelium.With the prior art Compared to have it is following the utility model has the advantages that this be conducive to improve phellinus igniarius mycelium in flavones content solid medium, by its original Material includes: 20-30 parts of glucose, 20-30 parts of potato, 10-20 parts of soybean powder, 10-20 parts of casein, albumen by weight 5-10 parts of peptone, 5-8 parts of magnesium sulfate, 1-5 parts of calcium chloride, 1-5 parts of sodium chloride, 4-9 parts of saccharomycete, 20-26 parts of weed tree sawdust and fresh pig 5-10 parts of excrement, casein is added lactic acid, pH is adjusted to 4.6 using fresh milk degreasing, make casein protomere lose charge and Solidification precipitating, glucose be select take off dry corn by smashing and grinding equipment obtain corn flour, water is then added into corn flour 2-3h is stirred with amylase, filter residue is filtered, can be obtained required glucose, the preparation method of solid medium specifically includes following Step: S1, successively pouring into the weed tree sawdust of selection and fresh pig dung in pulverizer first, sufficiently crushed, after then crushing Material pour into mixing and blending machine, 1-2h is stirred with the revolving speed of 400-600r/min, carries out weed tree sawdust and fresh pig dung abundant Mixing obtains culture material, the potato of selection first S2, is carried out peeling processing, then potato is put into boiler and adds water It floods, heating is boiled, and 10-20min is persistently boiled, and later smashs cooked potato in boiler to pieces, and 20- is boiled in heating again 25min is then allowed to stand air-cooled 30-40min, and potato nutritional suspension can be obtained, the nutrition suspension that S2 is obtained S3, is poured into S1 In Nutrious fermented Medium Culture, with revolving speed be 400-600r/min stir 30-40min, then by the glucose of selection, soya bean Powder, casein, peptone, magnesium sulfate, calcium chloride and sodium chloride are added sequentially in mixing and blending machine, with 700-900r/min's Revolving speed stirs 1-2h, can be obtained culture medium, S4, the culture medium raw material for obtaining S3 at 37-48 DEG C thermal dehydration to moisture Content is the 50-66% of total weight, is then wrapped up using aseptic thin-film, later using 88-100 DEG C of vapor high pressure sterilization processing Solid medium can be obtained, it can be achieved that being improved to Phellinus culture substrate to realize and carry out very to Phellinus bacterium in 10-25min Good culture achievees the purpose that fermentation is carried out using animal waste and weed tree sawdust prepares culture substrate, and realization directlys adopt grape Sugar, soybean powder, dry ferment and magnesium sulfate make the culture substrate of high nutrition composition, substantially increase Phellinus bacterium culture medium matter battalion Content to be supported, meets the growth demand of Phellinus bacterium well, flavones content is lower in the Phellinus bacterium that culture substrate can be made to turn out, To be advantageous to the culture of Phellinus bacterium.
Specific embodiment
The technical scheme in the embodiments of the invention will be clearly and completely described below, it is clear that described implementation Example is only a part of the embodiment of the present invention, instead of all the embodiments.Based on the embodiments of the present invention, this field is common Technical staff's every other embodiment obtained without making creative work belongs to the model that the present invention protects It encloses.
The embodiment of the present invention provides three kinds of technical solutions: a kind of solid for being conducive to improve flavones content in phellinus igniarius mycelium The preparation method of culture medium, specifically includes following embodiment:
Embodiment 1
S1,23 parts of weed tree sawdusts of selection and 7 parts of fresh pig dungs are successively poured into pulverizer first, is sufficiently crushed, so Smashed material is poured into mixing and blending machine afterwards, 1.5h is stirred with the revolving speed of 500r/min, make weed tree sawdust and fresh pig dung into Row is sufficiently mixed, and obtains culture material, and 6 parts of saccharomycete of selection are inoculated in culture material later, with turning for 550r/min Speed is stirred 25min, is sealed by fermentation 23d, can be obtained Nutrious fermented matrix;
S2,25 portions of potatos of selection are first subjected to peeling processing, then potato is put into boiler and adds water submerged, adds Heat is boiled, and 15min is persistently boiled, and later smashs cooked potato in boiler to pieces, and 23min is boiled in heating again, then quiet Cold 35min is emptied, potato nutritional suspension can be obtained;
S3, the nutrition suspension that S2 is obtained is poured into the Nutrious fermented Medium Culture in S1, is 500r/min stirring with revolving speed 35min, then by 25 parts of glucose of selection, 15 parts of soybean powders, 15 parts of casein, 7 parts of peptones, 6 parts of magnesium sulfate, 3 parts of chlorine Change calcium and 3 parts of sodium chloride are added sequentially in mixing and blending machine, 1.5h is stirred with the revolving speed of 800r/min, can be obtained culture Base;
S4, the culture medium raw material for obtaining S3 thermal dehydration to the moisture content at 43 DEG C are the 60% of total weight, then It is wrapped up using aseptic thin-film, handles 18min using 93 DEG C of vapor high pressure sterilizations later, solid medium can be obtained.
Embodiment 2
S1,20 parts of weed tree sawdusts of selection and 5 parts of fresh pig dungs are successively poured into pulverizer first, is sufficiently crushed, so Smashed material is poured into mixing and blending machine afterwards, 1h is stirred with the revolving speed of 400r/min, carries out weed tree sawdust and fresh pig dung It is sufficiently mixed, obtains culture material, the saccharomycete of selection is inoculated in culture material later, is stirred with the revolving speed of 500r/min 20min is mixed, 20d is sealed by fermentation, can be obtained Nutrious fermented matrix;
S2,20 portions of potatos of selection are first subjected to peeling processing, then potato is put into boiler and adds water submerged, adds Heat is boiled, and 10min is persistently boiled, and later smashs cooked potato in boiler to pieces, and 20min is boiled in heating again, then quiet Cold 30min is emptied, potato nutritional suspension can be obtained;
S3, the nutrition suspension that S2 is obtained is poured into the Nutrious fermented Medium Culture in S1, is 400r/min stirring with revolving speed 30min, then by 20 parts of glucose of selection, 10 parts of soybean powders, 10 parts of casein, 5 parts of peptones, 5 parts of magnesium sulfate, 1 part of chlorine Change calcium and 1 part of sodium chloride is added sequentially in mixing and blending machine, 1h is stirred with the revolving speed of 700r/min, can be obtained culture medium;
S4, the culture medium raw material for obtaining S3 thermal dehydration to the moisture content at 37 DEG C are the 50% of total weight, then It is wrapped up using aseptic thin-film, handles 10min using 88 DEG C of vapor high pressure sterilizations later, solid medium can be obtained.
Embodiment 3
S1,26 parts of weed tree sawdusts of selection and 10 parts of fresh pig dungs are successively poured into pulverizer first, is sufficiently crushed, so Smashed material is poured into mixing and blending machine afterwards, 2h is stirred with the revolving speed of 600r/min, carries out weed tree sawdust and fresh pig dung It is sufficiently mixed, obtains culture material, the saccharomycete of selection is inoculated in culture material later, is stirred with the revolving speed of 600r/min 30min is mixed, 25d is sealed by fermentation, can be obtained Nutrious fermented matrix;
S2,30 portions of potatos of selection are first subjected to peeling processing, then potato is put into boiler and adds water submerged, adds Heat is boiled, and 20min is persistently boiled, and later smashs cooked potato in boiler to pieces, and 25min is boiled in heating again, then quiet Cold 40min is emptied, potato nutritional suspension can be obtained;
S3, the nutrition suspension that S2 is obtained is poured into the Nutrious fermented Medium Culture in S1, is 600r/min stirring with revolving speed 40min, then by 30 parts of glucose of selection, 20 parts of soybean powders, 20 parts of casein, 10 parts of peptones, 8 parts of magnesium sulfate, 5 parts of chlorine Change calcium and 5 parts of sodium chloride are added sequentially in mixing and blending machine, 2h is stirred with the revolving speed of 900r/min, can be obtained culture medium;
S4, the culture medium raw material for obtaining S3 thermal dehydration to the moisture content at 48 DEG C are the 66% of total weight, then It is wrapped up using aseptic thin-film, handles 25min using 100 DEG C of vapor high pressure sterilizations later, solid medium can be obtained.
Effect example
Certain cultivating edible family can be marked respectively using the solid culture matrix of 1-3 of embodiment of the present invention preparation Phellinus bacterium For No.1 culture substrate, No. two culture substrates and No. three culture substrates, then respectively to No.1 culture substrate, No. two culture substrates Phellinus bacterium are inoculated with No. three culture substrates, culture is then carried out and respectively obtains No.1 Phellinus strain, No. two Phellinus strains and No. three Phellinus strain carries out flavones detection, detection knot to No.1 Phellinus strain, No. two Phellinus strains and No. three Phellinus strains respectively later Fruit shows that the content of flavones in No.1 Phellinus strain is higher than the content of flavones in No. two Phellinus strains and No. three Phellinus strains, therefore Phellinus bacterium culture medium matter prepared by embodiment 1 is best.
It should be noted that, in this document, relational terms such as first and second and the like are used merely to a reality Body or operation are distinguished with another entity or operation, are deposited without necessarily requiring or implying between these entities or operation In any actual relationship or order or sequence.Moreover, the terms "include", "comprise" or its any other variant are intended to Non-exclusive inclusion, so that the process, method, article or equipment including a series of elements is not only wanted including those Element, but also including other elements that are not explicitly listed, or further include for this process, method, article or equipment Intrinsic element.
It although an embodiment of the present invention has been shown and described, for the ordinary skill in the art, can be with A variety of variations, modification, replacement can be carried out to these embodiments without departing from the principles and spirit of the present invention by understanding And modification, the scope of the present invention is defined by the appended.

Claims (7)

1. a kind of solid medium for being conducive to improve flavones content in phellinus igniarius mycelium, it is characterised in that: its raw material is by weight Part ratio includes: 20-30 parts of glucose, 20-30 parts of potato, 10-20 parts of soybean powder, 10-20 parts of casein, peptone 5-10 Part, 5-8 parts of magnesium sulfate, 1-5 parts of calcium chloride, 1-5 parts of sodium chloride, 4-9 parts of saccharomycete, 20-26 parts of weed tree sawdust and fresh pig dung 5-10 Part.
2. a kind of solid medium for being conducive to improve flavones content in phellinus igniarius mycelium according to claim 1, special Sign is: its raw material includes following component: 25 parts of glucose, 25 parts of potato, 15 parts of soybean powder, 15 parts of casein, peptone 7 Part, 6 parts of magnesium sulfate, 3 parts of calcium chloride, 3 parts of sodium chloride, 6 parts of saccharomycete, 23 parts of weed tree sawdust and 7 parts of fresh pig dung.
3. a kind of solid medium for being conducive to improve flavones content in phellinus igniarius mycelium according to claim 1, special Sign is: its raw material includes following component: 20 parts of glucose, 20 parts of potato, 10 parts of soybean powder, 10 parts of casein, peptone 5 Part, 5 parts of magnesium sulfate, 1 part of calcium chloride, 1 part of sodium chloride, 4 parts of saccharomycete, 20 parts of weed tree sawdust and 5 parts of fresh pig dung.
4. a kind of solid medium for being conducive to improve flavones content in phellinus igniarius mycelium according to claim 1, special Sign is: its raw material includes following component: 30 parts of glucose, 30 parts of potato, 20 parts of soybean powder, 20 parts of casein, peptone 10 parts, 8 parts of magnesium sulfate, 5 parts of calcium chloride, 5 parts of sodium chloride, 9 parts of saccharomycete, 26 parts of weed tree sawdust and 10 parts of fresh pig dung.
5. a kind of solid training for being conducive to improve flavones content in phellinus igniarius mycelium according to any one of claims 1-4 Support base, it is characterised in that: the casein is to be added lactic acid using fresh milk degreasing, pH is adjusted to 4.6, made the micro- glue of casein Grain loses charge and solidifies precipitating.
6. a kind of solid training for being conducive to improve flavones content in phellinus igniarius mycelium according to any one of claims 1-4 Support base, it is characterised in that: the glucose be select take off dry corn by smashing and grinding equipment obtain corn flour, then to corn Water is added in powder and amylase stirs 2-3h, filters filter residue, can be obtained required glucose.
7. a kind of solid training for being conducive to improve flavones content in phellinus igniarius mycelium described in -6 any one according to claim 1 Support base, it is characterised in that: the preparation method of the solid medium specifically includes the following steps:
S1, the weed tree sawdust of selection and fresh pig dung successively poured into pulverizer first, is sufficiently crushed, it then will be smashed Material pours into mixing and blending machine, stirs 1-2h with the revolving speed of 400-600r/min, carries out weed tree sawdust and fresh pig dung sufficiently mixed It closes, obtains culture material, the saccharomycete of selection is inoculated in culture material later, it is mixed with the revolving speed stirring of 500-600r/min 20-30min is closed, 20-25d is sealed by fermentation, can be obtained Nutrious fermented matrix;
S2, the potato of selection is first subjected to peeling processing, then potato is put into boiler plus water submerged, heating are boiled, 10-20min is persistently boiled, later smashs cooked potato in boiler to pieces, 20-25min is boiled in heating again, is then allowed to stand Potato nutritional suspension can be obtained in air-cooled 30-40min;
S3, the nutrition suspension that S2 is obtained is poured into the Nutrious fermented Medium Culture in S1, is that 400-600r/min stirs 30- with revolving speed 40min, then by the glucose of selection, soybean powder, casein, peptone, magnesium sulfate, calcium chloride and sodium chloride are added sequentially to In mixing and blending machine, 1-2h is stirred with the revolving speed of 700-900r/min, can be obtained culture medium;
S4, the culture medium raw material for obtaining S3 thermal dehydration to the moisture content at 37-48 DEG C are the 50-66% of total weight, so It is wrapped up afterwards using aseptic thin-film, 10-25min is handled using 88-100 DEG C of vapor high pressure sterilization later, solid training can be obtained Support base.
CN201910055052.1A 2019-01-21 2019-01-21 A kind of solid medium for being conducive to improve flavones content in phellinus igniarius mycelium Withdrawn CN109680017A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201910055052.1A CN109680017A (en) 2019-01-21 2019-01-21 A kind of solid medium for being conducive to improve flavones content in phellinus igniarius mycelium

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201910055052.1A CN109680017A (en) 2019-01-21 2019-01-21 A kind of solid medium for being conducive to improve flavones content in phellinus igniarius mycelium

Publications (1)

Publication Number Publication Date
CN109680017A true CN109680017A (en) 2019-04-26

Family

ID=66192482

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201910055052.1A Withdrawn CN109680017A (en) 2019-01-21 2019-01-21 A kind of solid medium for being conducive to improve flavones content in phellinus igniarius mycelium

Country Status (1)

Country Link
CN (1) CN109680017A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112195104A (en) * 2020-07-17 2021-01-08 江苏科技大学 Culture medium for identifying phellinus igniarius of mulberry tree and preparation method and application thereof
CN114369539A (en) * 2022-01-11 2022-04-19 吉林大学 Preparation method of culture medium taking agricultural wastes as raw materials, culture medium and application
TWI766394B (en) * 2020-10-19 2022-06-01 葡萄王生技股份有限公司 Use of phellinus linteus for preparing composition of improving sarcopenia

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112195104A (en) * 2020-07-17 2021-01-08 江苏科技大学 Culture medium for identifying phellinus igniarius of mulberry tree and preparation method and application thereof
CN112195104B (en) * 2020-07-17 2021-08-31 江苏科技大学 Culture medium for identifying phellinus igniarius of mulberry tree and preparation method and application thereof
TWI766394B (en) * 2020-10-19 2022-06-01 葡萄王生技股份有限公司 Use of phellinus linteus for preparing composition of improving sarcopenia
US11944659B2 (en) 2020-10-19 2024-04-02 Grape King Bio Ltd Method for improving sarcopenia by using Phellinus linteus
CN114369539A (en) * 2022-01-11 2022-04-19 吉林大学 Preparation method of culture medium taking agricultural wastes as raw materials, culture medium and application

Similar Documents

Publication Publication Date Title
CN105191667B (en) Hickory chick nutrient formulation, nutrient bag and preparation method thereof and hickory chick cultural method
CN102429163A (en) Method for preparing tartary buckwheat monascus and application thereof
CN101451096A (en) Method for preparing Chinese caterpillar fungus health wine
CN109680017A (en) A kind of solid medium for being conducive to improve flavones content in phellinus igniarius mycelium
CN107164237A (en) Selenium-enriched cordceps militaris and its cultural method and application
CN103393094A (en) Preparation method of ganoderma lucidum mycelium slices
CN104068377A (en) Cordyceps taishanensis ferment product and production method thereof
CN101305792A (en) Toadstool beverage and its preparation method
CN104694342B (en) A kind of manufacture method of balsam pear health-care wine
CN106036320A (en) Method for preparing mushroom mycelial fermentation broth original drink
CN103299824B (en) Method for preparing phellinus igniarius sclertium from fresh, tender and sweet corn
CN105875196A (en) Culture medium for culturing phellinus igniarius mycelium and culture method of phellinus igniarius mycelium
CN108771116A (en) A kind of processing method of multi-functional composite rice
CN111543254A (en) Culture method of phellinus igniarius mycelium, drink and application of phellinus igniarius mycelium
CN1556193A (en) Method of producing edible fungus and its health protection product using malt saccharification liquid
CN108566988A (en) Method for preparing novel selenium-rich rice and bean compound beverage
CN103404608B (en) A kind of vanilla fermented bean curd
CN104542862B (en) Agropyron dietary-fiber biscuit and preparation method thereof
CN105918642A (en) Method for preparing feed from cottonseed meal
CN105962033A (en) Processing method of digestible formula wheat flour
CN106690249B (en) Preparation method of black bean calcareous soy sauce
CN108813340A (en) A kind of lipid-loweringing spirulina noodles and preparation method thereof
CN101856049B (en) Grain amaranth lactobacillus fermented yogurt
CN109674000B (en) Method for preparing pure fermented soybean sour soup
CN105602860A (en) Gastrodia elata armillaria mellea strain culture medium and preparation method thereof

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
WW01 Invention patent application withdrawn after publication

Application publication date: 20190426

WW01 Invention patent application withdrawn after publication