CN101015258A - Pseudo-wild cultivating method for pholiota adiposa - Google Patents
Pseudo-wild cultivating method for pholiota adiposa Download PDFInfo
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- CN101015258A CN101015258A CN 200710013258 CN200710013258A CN101015258A CN 101015258 A CN101015258 A CN 101015258A CN 200710013258 CN200710013258 CN 200710013258 CN 200710013258 A CN200710013258 A CN 200710013258A CN 101015258 A CN101015258 A CN 101015258A
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Abstract
The invention discloses a method for cultivating Pholiota Adiposa artificially. The method imitates wild growing condition for Pholiota Adiposa growth, disintegrating willow peel, leaves or branch, then mixing with bean cake powder. Bran flour and wood dust to make culture medium; then inoculating Pholiota Adiposa on said culture medium. The method is characterized by little bacteria pollution, high rate of finished products and high productivity of fruiting body, fast growth of mycelium, reduced mature and production period for mycelium, and high content of water-soluble polysaccharide and alcohol-soluble chemical element.
Description
Technical field
The present invention relates to a kind of medicine/edible fungus cultivation method, be specifically related to a kind of pseudo-wild cultivating method for pholiota adiposa.
Background technology
Yellow umbrella [Pholiota.adipose (Fr) Quel] has another name called Liu Ding, willow mushroom, yellow mushroom, is the basidiomycetes steel, Agaricales, Stropharia rugoso-annulata section, a kind of famous and precious food medicine dual-purpose fungi of Pholiota.Yellow umbrella matter is crisp delicious, nutritious, has higher edible and medical value, tumour and the lung disease of being used for the treatment of among the people.
Yellow umbrella Chang Yesheng is on partly withered or withered willow trunk, all there is distribution in most of area in China, but because this bacterium wild resource rareness, so domestic and international (mainly being China and Japan) has some research reports about its biological property and artificial domesticating cultivation in recent years.Though and existing cultivation method sporophore shape of use and the yellow umbrella of wild type do not have significant difference, cultivate yield rate sterilization is required height, be unfavorable for promoting, whether also unknown planting pholiota adipose nutrition is consistent with chemical composition and wild type.
Summary of the invention
For solving the problem of above existence, the invention provides a kind of pseudo-wild cultivating method for pholiota adiposa.This method is a raw material with natural willow composition, carries out pseudo-wild cultivating with adding natural willow raw meal in the conventional medium.Its concrete technical step of taking is as follows:
(1) with natural willow composition raw material through cut short and drying after, pulverize, make natural willow raw meal;
(2) be that 5~40% natural willow raw meal, 5~10% bean cake powder, 20~25% wheat bran and 25~40% wood chips are mixed and made into medium with shared weight, and be that 1: 1.0~1.5 material-water ratio adds water by weight in medium, pack behind the mixing, carry out high-temperature sterilization;
(3) yellow agaric silk is inoculated in the cooling back naturally, places 24~30 ℃ of cultivations of incubator;
(4) turning every day is checked 1-2 time, after treating to cover with mycelium in the bag, dredges heap and ventilates, and regulates temperature to 20-25 ℃, after waiting to grow strumae, takes off bag and cultivates;
(5) treat to gather when sporophore growth is ripe.
Natural willow composition raw material can adopt willow bark, Folium Pterocaryae or band leaf willow branch, and the drying means of step (1) can adopt and dry, dries or 40~80 ℃ of oven dry.
The beneficial effect that the present invention had is: the present invention is a raw material with natural willow structural constituent, to yellow umbrella pseudo-wild cultivating, expanded the artificial domesticating cultivation approach of yellow umbrella, when effectively utilizing the abundant willow structural constituent resource of natural world, replenish and substitute more and more rare wild yellow umbrella resource.Compare with other yellow umbrella artificial cultivation technique, living contaminants is few, can improve the output (improving approximately about 1 times) of the tame bacterium bag of yellow umbrella yield rate (bringing up to more than 90% by 60%) and yellow destroying angel; Can improve the growth rate of pholiota adiposa mycelium, and shorten the ripe needed time of fruit body, therefore shorten the whole artificial cultivation cycle (about 20~50%) greatly.
The present invention is a raw material with natural willow structural constituent, to yellow umbrella pseudo-wild cultivating, can reduce the cost of yellow umbrella artificial cultivation medium.Adopt the resulting yellow umbrella of this cultivation method, its polyoses content, water-soluble and pure melt into divide content all than the control group height, and some active constituent content increases obviously.
Embodiment
Below in conjunction with embodiment the present invention is described further.
Embodiment one:
The willow branch of getting the band leaf dries, and cuts short to 3~5cm, pulverizes with Chinese herbal medicine pulverizing machine.Take by weighing willow branch powder 600g, add bean cake powder 100g, wheat bran 500g, wood chip 800g adds entry 2600g in 1: 1.3 ratio, mixing, the polypropylene plastics pocket of packing into, every bag of about 600g of weight in wet base.Put 0.1MPa sterilization 1h in the autoclave sterilizer, naturally the yellow agaric silk of cooling back inoculation.Place 25 ℃ of cultivations of incubator.Average inoculation promptly grew the white hypha body in the back pkt. in 5 days, shifted to an earlier date 3-4 days than control group (not adding willow branch powder).Turning every day is checked 1-2 time.Cover with mycelium in the average 25 days back pkt.s, none bag dyes assorted bacterium, and bacterium bag yield rate reaches 100%, and control group microbiological contamination rate reaches 40%, and mycelial growth is slow.Dredge heap and ventilate, regulate temperature, continue to cultivate, after waiting to grow strumae, take off bag and cultivate (average 52 days, control group is 20 days in advance) to 22-23 ℃.Treat to gather after the fruit body maturation, obtain fruit body weight in wet base 2100g altogether, and control group is had to 1200g.
Embodiment two:
Folium Pterocaryae is dried, pulverize.Take by weighing Folium Pterocaryae powder 300g, add bean cake powder 50g, wheat bran 250g, wood chip 400g adds entry 1200g in 1: 1.2 ratio, mixing, the polypropylene plastics pocket of packing into, every bag of about 550g of weight in wet base.Put 0.1MPa sterilization 1h in the autoclave sterilizer, inoculation yellow agaric silk in cooling back places 25 ℃ of cultivations of incubator naturally.Turning every day is checked 1-2 time.4 bags are all covered with mycelium after 25 days, and none bag dyes assorted bacterium, and bacterium bag yield rate reaches 100%.Crude polysaccharides content (160mg/g) in the yellow umbrella of analysis pseudo-wild cultivating group than control group (85mg/g) height, shows with the contrast of capillary electrophoresis fingerprint method its 80% alcohol extractive, behind the adding Folium Pterocaryae, can obviously increase the content of some composition.
Embodiment three:
Earlier willow bark being shredded is the fritter of 3~5 * 3~5cm, puts into 60~80 ℃ of oven dry of baking oven of tape drum blower fan then and spends the night, and pulverizes with Chinese herbal medicine pulverizing machine.Take by weighing willow bark powder 3500g, add bean cake powder 500g, wheat bran 2000g, wood chip 4000g adds entry 12000g in 1: 1.2 ratio, mixing, the polypropylene plastics pocket of packing into, every bag of about 550g of weight in wet base.Put 0.1MPa sterilization 1h in the autoclave sterilizer, inoculation yellow agaric silk in cooling back places 25 ℃ of cultivations of incubator naturally.Turning every day is checked 1-2 time.40 bags are all covered with mycelium after 23 days, and none bag dyes assorted bacterium, and bacterium bag yield rate reaches 100%.Dredge heap and ventilate, regulate temperature, cultivate and grow strumae after 48 days, take off bag and cultivate to 22-23 ℃.Treat to gather after the fruit body maturation, obtain fruit body weight in wet base 10Kg altogether, and control group is had to 5Kg.
Claims (3)
1, a kind of pseudo-wild cultivating method for pholiota adiposa is characterized in that this method adopts following processing step:
(1) with natural willow composition raw material through cut short and drying after, pulverize, make natural willow raw meal;
(2) be that 5~40% natural willow raw meal, 5~10% bean cake powder, 20~25% wheat bran and 25~40% wood chips are mixed and made into medium with shared weight, be that 1: 1.0~1.5 material-water ratio adds water then by weight in medium, pack behind the mixing, carry out high-temperature sterilization;
(3) yellow agaric silk is inoculated in the cooling back naturally, places 24~30 ℃ of cultivations of incubator;
(4) turning every day is checked 1-2 time, after treating to cover with mycelium in the bag, dredges heap and ventilates, and regulates temperature to 20-25 ℃, after waiting to grow strumae, takes off bag and cultivates;
(5) treat to gather when sporophore growth is ripe.
2, a kind of pseudo-wild cultivating method for pholiota adiposa according to claim 1 is characterized in that, described natural willow composition raw material is willow bark, willow or band leaf willow branch.
3, a kind of pseudo-wild cultivating method for pholiota adiposa according to claim 1 and 2, the drying that it is characterized in that natural willow composition raw material can adopt dries, dries and or 40~80 ℃ of oven dry.
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CNB2007100132585A CN100506017C (en) | 2007-01-18 | 2007-01-18 | Pseudo-wild cultivating method for pnoliota adiposa |
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CNB2007100132585A CN100506017C (en) | 2007-01-18 | 2007-01-18 | Pseudo-wild cultivating method for pnoliota adiposa |
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CN101015258A true CN101015258A (en) | 2007-08-15 |
CN100506017C CN100506017C (en) | 2009-07-01 |
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102172169A (en) * | 2011-01-19 | 2011-09-07 | 新疆农业科学院植物保护研究所 | Artificial rearing method for Pholiota adiposa |
CN102584451A (en) * | 2012-02-21 | 2012-07-18 | 山东省农业科学院农业资源与环境研究所 | Method for producing mushroom sticks by using bark waste as main material |
CN102668885A (en) * | 2012-05-30 | 2012-09-19 | 北京市农林科学院 | Pholiota adipose new strain and method for cultivating fruiting body of pholiota adiposa new strain |
CN103688745A (en) * | 2013-12-02 | 2014-04-02 | 兴化市板桥食用菌有限公司 | Pholiota adiposa cultivating method |
CN103918481A (en) * | 2014-04-08 | 2014-07-16 | 德州学院 | Liquid pholiota adipose strain mixing cultivation process |
-
2007
- 2007-01-18 CN CNB2007100132585A patent/CN100506017C/en not_active Expired - Fee Related
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102172169A (en) * | 2011-01-19 | 2011-09-07 | 新疆农业科学院植物保护研究所 | Artificial rearing method for Pholiota adiposa |
CN102584451A (en) * | 2012-02-21 | 2012-07-18 | 山东省农业科学院农业资源与环境研究所 | Method for producing mushroom sticks by using bark waste as main material |
CN102668885A (en) * | 2012-05-30 | 2012-09-19 | 北京市农林科学院 | Pholiota adipose new strain and method for cultivating fruiting body of pholiota adiposa new strain |
CN102668885B (en) * | 2012-05-30 | 2013-06-05 | 北京市农林科学院 | Pholiota adipose new strain and method for cultivating fruiting body of pholiota adiposa new strain |
CN103688745A (en) * | 2013-12-02 | 2014-04-02 | 兴化市板桥食用菌有限公司 | Pholiota adiposa cultivating method |
CN103688745B (en) * | 2013-12-02 | 2015-10-28 | 兴化市板桥食用菌有限公司 | A kind of yellow umbrella mushroom cultivation method |
CN103918481A (en) * | 2014-04-08 | 2014-07-16 | 德州学院 | Liquid pholiota adipose strain mixing cultivation process |
CN103918481B (en) * | 2014-04-08 | 2016-04-06 | 德州学院 | Yellow umbrella liquid spawn mixes bacteria cultivation technique |
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CN100506017C (en) | 2009-07-01 |
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