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CN107915528A - Cultivation method of morchella - Google Patents

Cultivation method of morchella Download PDF

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Publication number
CN107915528A
CN107915528A CN201711278207.5A CN201711278207A CN107915528A CN 107915528 A CN107915528 A CN 107915528A CN 201711278207 A CN201711278207 A CN 201711278207A CN 107915528 A CN107915528 A CN 107915528A
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parts
cultivation
cultivation method
culture medium
water
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张福喧
陈天明
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Huili Tianze Industrial Co ltd
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Huili Tianze Industrial Co ltd
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    • CCHEMISTRY; METALLURGY
    • C05FERTILISERS; MANUFACTURE THEREOF
    • C05BPHOSPHATIC FERTILISERS
    • C05B7/00Fertilisers based essentially on alkali or ammonium orthophosphates
    • CCHEMISTRY; METALLURGY
    • C05FERTILISERS; MANUFACTURE THEREOF
    • C05GMIXTURES OF FERTILISERS COVERED INDIVIDUALLY BY DIFFERENT SUBCLASSES OF CLASS C05; MIXTURES OF ONE OR MORE FERTILISERS WITH MATERIALS NOT HAVING A SPECIFIC FERTILISING ACTIVITY, e.g. PESTICIDES, SOIL-CONDITIONERS, WETTING AGENTS; FERTILISERS CHARACTERISED BY THEIR FORM
    • C05G3/00Mixtures of one or more fertilisers with additives not having a specially fertilising activity

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pest Control & Pesticides (AREA)
  • Fodder In General (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)

Abstract

The invention discloses a cultivation method of morel, which comprises the following steps: (1) preparing a culture medium, (2) inoculating and culturing in a bag, (3) cultivating a field, and (4) harvesting, wherein the culture medium uses raw materials including wheat grains, wood chips, bamboo strips, corn flour, wheat bran, glutamic acid, vitamin C, citric acid, gypsum, potassium dihydrogen phosphate, dipotassium hydrogen phosphate, fine sand, water, ethanol and ethyl orthosilicate. The invention can obtain high-quality morchella in a shorter period by artificial cultivation.

Description

一种羊肚菌的培育方法A kind of cultivation method of hickory chick

技术领域technical field

本发明涉及羊肚菌的培育方法的技术领域。The present invention relates to the technical field of the cultivation method of hickory chick.

背景技术Background technique

羊肚菌是一种珍稀的食用菌品种,其食用和药用价值均较高,其菌盖部分含有异亮氨酸、亮氨酸、赖氨酸、蛋氨酸、苯丙氨酸、苏氨酸和缬氨酸7种人体必需的氨基酸,整体含粗蛋白20%、粗脂肪26%、碳水化合物38.1%,多种氨基酸,特别是谷氨酸含量高达1.76 %,同时还至少含有8种维生素,包括维生素B1、维生素B2、维生素B12、烟酸、泛酸、吡哕醇、生物素、叶酸等。Morchella is a rare species of edible fungus with high edible and medicinal value. Its cap contains isoleucine, leucine, lysine, methionine, phenylalanine and threonine. Valine and 7 kinds of essential amino acids for human body, the whole contains 20% crude protein, 26% crude fat, 38.1% carbohydrates, a variety of amino acids, especially glutamic acid content as high as 1.76%, and at least 8 kinds of vitamins, Including vitamin B1, vitamin B2, vitamin B12, niacin, pantothenic acid, pyridoxine, biotin, folic acid, etc.

市面上的羊肚菌价格高昂,供不应求,主要因为用于出售的羊肚菌基本来自野生,数量有限,获取困难,大量的野生资源开采同时也会对环境造成破坏。The price of morels on the market is high, and the supply is in short supply. The main reason is that the morels for sale are basically wild, the quantity is limited, and it is difficult to obtain. The exploitation of a large number of wild resources will also cause damage to the environment.

发明内容Contents of the invention

本发明的目的在于提出一种可通过人工栽培、在较短的周期内获得高质量的羊肚菌的羊肚菌培育方法。The object of the present invention is to propose a kind of hickory chick cultivation method that can obtain high-quality hickory chick in a short cycle by artificial cultivation.

本发明的技术方案如下:Technical scheme of the present invention is as follows:

一种羊肚菌的培育方法,其包括以下过程:A kind of cultivation method of hickory chick, it comprises following process:

(1)培养基制备:(1) Culture medium preparation:

A.将麦粒、木屑、竹丝粉碎,得到备用的粉碎料;A. Grinding wheat grains, sawdust, and bamboo shreds to obtain spare crushed materials;

B.另取玉米粉、麦麸、谷氨酸、维生素C、柠檬酸与水及乙醇混合均匀,其后加入正硅酸乙酯,在加热条件下持续搅拌,混合物中形成微球,将微球滤出、洗净;B. Separately take corn flour, wheat bran, glutamic acid, vitamin C, citric acid and mix them with water and ethanol evenly, then add tetraethyl orthosilicate, keep stirring under heating conditions, microspheres are formed in the mixture, and the microspheres The ball is filtered out and washed;

C.将粉碎料、微球及石膏、磷酸二氢钾、磷酸氢二钾、细沙、水混合均匀,静置后得到培养基;C. Mix crushed materials, microspheres, gypsum, potassium dihydrogen phosphate, dipotassium hydrogen phosphate, fine sand, and water evenly, and obtain a culture medium after standing;

(2)接种及袋内培养:(2) Inoculation and bag culture:

将培养基装入袋内,装料完成后将菌袋封口、灭菌,其后接入梯棱羊肚菌菌种,在无菌避光条件下培养5~7天;Put the culture medium into the bag, seal the bacteria bag after filling, and sterilize it, then insert the morel strains, and cultivate it for 5-7 days under sterile light-proof conditions;

(3)田地培育:(3) Field cultivation:

选择土壤pH值为6.5~7.5的田地进一步培育,将该田地首先进行整理、翻挖、消毒,其后在田地上挖出填埋沟,在沟底铺洒草木灰,其后将菌袋放置在填埋沟内,再覆盖秸秆,在秸秆上再铺洒一层细土,其后日常对填埋沟进行浇灌,保持土壤湿润;Select a field with a soil pH value of 6.5-7.5 for further cultivation. Firstly, the field is sorted, dug, and disinfected. Then, a landfill ditch is dug on the field, plant ash is spread on the bottom of the ditch, and then the fungus bag is placed in the Fill the ditch, then cover the straw, spread a layer of fine soil on the straw, and then water the ditch daily to keep the soil moist;

(4)采收(4) Harvesting

田地培育90~180天对成熟羊肚菌进行采收即可。Field cultivation takes 90 to 180 days to harvest mature morels.

优选的是:所述培养基的原料按质量份计,包括麦粒30~40份,木屑20~30份,竹丝15~25份,玉米粉10~15份,麦麸10~15份,谷氨酸5~10份,5~10份维生素C,1~3份柠檬酸,1~5份石膏,0.1~1.0份磷酸二氢钾,0.1~1.0份磷酸氢二钾,15~25份细沙。Preferably: the raw materials of the medium include 30-40 parts of wheat grains, 20-30 parts of sawdust, 15-25 parts of bamboo shreds, 10-15 parts of corn flour, and 10-15 parts of wheat bran in parts by mass. 5~10 parts of glutamic acid, 5~10 parts of vitamin C, 1~3 parts of citric acid, 1~5 parts of gypsum, 0.1~1.0 parts of potassium dihydrogen phosphate, 0.1~1.0 parts of dipotassium hydrogen phosphate, 15~25 parts fine sand.

另外优选的是:所述步骤B中乙醇与水的体积比为1:1~5。In addition, preferably: the volume ratio of ethanol to water in the step B is 1:1-5.

另外优选的是:所述正硅酸乙酯与所述乙醇的质量比为1:1~3。In addition, preferably: the mass ratio of the ethyl orthosilicate to the ethanol is 1:1~3.

另外优选的是:所述步骤B中加热温度为30~40℃。In addition, preferably: the heating temperature in the step B is 30-40°C.

另外优选的是:所述步骤C中所述水的质量为所述粉碎料质量的10~50%。In addition, preferably: the mass of the water in the step C is 10-50% of the mass of the pulverized material.

本发明具备以下有益效果:The present invention has the following beneficial effects:

(1)本发明的培养基可在袋内培养、田地培育的全过程中持续、稳定地为羊肚菌的生长提供必要的营养成分,营养成分的释放速率均一稳定、持久;(1) The culture medium of the present invention can continuously and stably provide necessary nutrients for the growth of Morchella in the whole process of bag cultivation and field cultivation, and the release rate of nutrients is uniform, stable and long-lasting;

(2)本发明的培养基在培养羊肚菌的过程中,可有效地将营养成分与羊肚菌生长产生的代谢废物相隔离,避免部分代谢废物对羊肚菌的进一步生长产生障碍;(2) In the process of cultivating morels, the medium of the present invention can effectively isolate the nutritional components from the metabolic wastes produced by the growth of morels, so as to avoid some metabolic wastes from hindering the further growth of morels;

(3)本发明可实现羊肚菌的规模化种植,具有极大的经济效益;(3) The present invention can realize the large-scale cultivation of hickory chick, and has great economic benefits;

(4)本发明可实现羊肚菌的高质量人工栽培;(4) The present invention can realize high-quality artificial cultivation of hickory chick;

(5)本发明可显著缩短羊肚菌培育周期。(5) The invention can significantly shorten the morel culture period.

具体实施方式Detailed ways

以下通过实施例对本发明作进一步的详细说明,但不应将此理解为本发明的范围仅限于以下的实例。在不脱离本发明上述方法思想的情况下,根据本领域普通技术知识和惯用手段做出的各种替换或变更,均应包含在本发明的范围内。The present invention will be further described in detail through the following examples, but this should not be construed as limiting the scope of the present invention to the following examples. Without departing from the idea of the above-mentioned method of the present invention, various replacements or changes made according to common technical knowledge and conventional means in this field shall be included within the scope of the present invention.

实施例1Example 1

(1)培养基制备:(1) Culture medium preparation:

A.将麦粒、木屑、竹丝粉碎,得到备用的粉碎料;A. Grinding wheat grains, sawdust, and bamboo shreds to obtain spare crushed materials;

B.另取玉米粉、麦麸、谷氨酸、维生素C、柠檬酸与水及乙醇混合均匀,其后加入正硅酸乙酯,在加热条件下持续搅拌,混合物中形成微球,将微球滤出、洗净;B. Separately take corn flour, wheat bran, glutamic acid, vitamin C, citric acid and mix them with water and ethanol evenly, then add tetraethyl orthosilicate, keep stirring under heating conditions, microspheres are formed in the mixture, and the microspheres The ball is filtered out and washed;

C.将粉碎料、微球及石膏、磷酸二氢钾、磷酸氢二钾、细沙、水混合均匀,静置后得到培养基,其中培养基的原料按质量份计,包括麦粒30份,木屑20份,竹丝15份,玉米粉10份,麦麸10份,谷氨酸5份,5份维生素C,1份柠檬酸,1份石膏,0.1份磷酸二氢钾,0.1份磷酸氢二钾,15份细沙,所述步骤B中乙醇与水的体积比为1:1,步骤B中正硅酸乙酯与乙醇的质量比为1:1,步骤B中加热温度为30℃,步骤C中的水的质量为粉碎料的质量的10%;C. Mix crushed materials, microspheres and gypsum, potassium dihydrogen phosphate, dipotassium hydrogen phosphate, fine sand, and water evenly, and obtain a culture medium after standing still, wherein the raw materials of the culture medium are calculated in parts by mass, including 30 parts of wheat grains , 20 parts of sawdust, 15 parts of bamboo shreds, 10 parts of corn flour, 10 parts of wheat bran, 5 parts of glutamic acid, 5 parts of vitamin C, 1 part of citric acid, 1 part of gypsum, 0.1 part of potassium dihydrogen phosphate, 0.1 part of phosphoric acid Dipotassium hydrogen, 15 parts of fine sand, the volume ratio of ethanol to water in the step B is 1:1, the mass ratio of tetraethyl orthosilicate to ethanol in the step B is 1:1, and the heating temperature in the step B is 30°C , the quality of the water in the step C is 10% of the quality of pulverized material;

(2)接种及袋内培养:(2) Inoculation and bag culture:

将培养基装入袋内,装料完成后将菌袋封口、灭菌,其后接入梯棱羊肚菌菌种,在无菌避光条件下培养5天;Put the culture medium into the bag, seal and sterilize the fungus bag after the filling is completed, then insert the morel strains of the stepper rib, and cultivate it for 5 days under sterile light-proof conditions;

(3)田地培育:(3) Field cultivation:

选择土壤pH值为6.5~7.5的田地进一步培育,将该田地首先进行整理、翻挖、消毒,其后在田地上挖出填埋沟,在沟底铺洒草木灰,其后将菌袋放置在填埋沟内,再覆盖秸秆,在秸秆上再铺洒一层细土,其后日常对填埋沟进行浇灌,保持土壤湿润;Select a field with a soil pH value of 6.5-7.5 for further cultivation. Firstly, the field is sorted, dug, and disinfected. Then, a landfill ditch is dug on the field, plant ash is spread on the bottom of the ditch, and then the fungus bag is placed in the Fill the ditch, then cover the straw, spread a layer of fine soil on the straw, and then water the ditch daily to keep the soil moist;

(4)采收(4) Harvesting

田地培育90天对成熟羊肚菌进行采收即可。After 90 days of cultivation in the field, the mature morels can be harvested.

实施例2Example 2

(1)培养基制备:(1) Culture medium preparation:

A.将麦粒、木屑、竹丝粉碎,得到备用的粉碎料;A. Grinding wheat grains, sawdust, and bamboo shreds to obtain spare crushed materials;

B.另取玉米粉、麦麸、谷氨酸、维生素C、柠檬酸与水及乙醇混合均匀,其后加入正硅酸乙酯,在加热条件下持续搅拌,混合物中形成微球,将微球滤出、洗净;B. Separately take corn flour, wheat bran, glutamic acid, vitamin C, citric acid and mix them with water and ethanol evenly, then add tetraethyl orthosilicate, keep stirring under heating conditions, microspheres are formed in the mixture, and the microspheres The ball is filtered out and washed;

C.将粉碎料、微球及石膏、磷酸二氢钾、磷酸氢二钾、细沙、水混合均匀,静置后得到培养基,其中培养基的原料按质量份计,包括麦粒40份,木屑30份,竹丝25份,玉米粉15份,麦麸15份,谷氨酸10份, 10份维生素C, 3份柠檬酸, 5份石膏,1.0份磷酸二氢钾, 1.0份磷酸氢二钾,25份细沙,所述步骤B中乙醇与水的体积比为1:5,步骤B中正硅酸乙酯与乙醇的质量比为1:3,步骤B中加热温度为40℃,步骤C中的水的质量为粉碎料的质量的50%;C. Mix crushed material, microspheres and gypsum, potassium dihydrogen phosphate, dipotassium hydrogen phosphate, fine sand, and water evenly, and obtain a culture medium after standing still, wherein the raw materials of the culture medium are calculated in parts by mass, including 40 parts of wheat grains , 30 parts of wood chips, 25 parts of bamboo shreds, 15 parts of corn flour, 15 parts of wheat bran, 10 parts of glutamic acid, 10 parts of vitamin C, 3 parts of citric acid, 5 parts of gypsum, 1.0 parts of potassium dihydrogen phosphate, 1.0 parts of phosphoric acid Dipotassium hydrogen, 25 parts of fine sand, the volume ratio of ethanol to water in the step B is 1:5, the mass ratio of ethyl orthosilicate to ethanol in the step B is 1:3, and the heating temperature in the step B is 40°C , the quality of the water in the step C is 50% of the quality of pulverized material;

(2)接种及袋内培养:(2) Inoculation and bag culture:

将培养基装入袋内,装料完成后将菌袋封口、灭菌,其后接入梯棱羊肚菌菌种,在无菌避光条件下培养7天;Put the culture medium into the bag, seal and sterilize the fungus bag after the filling is completed, then insert the morel strains of the stepper rib, and cultivate it for 7 days under sterile light-proof conditions;

(3)田地培育:(3) Field cultivation:

选择土壤pH值为6.5~7.5的田地进一步培育,将该田地首先进行整理、翻挖、消毒,其后在田地上挖出填埋沟,在沟底铺洒草木灰,其后将菌袋放置在填埋沟内,再覆盖秸秆,在秸秆上再铺洒一层细土,其后日常对填埋沟进行浇灌,保持土壤湿润;Select a field with a soil pH value of 6.5-7.5 for further cultivation. Firstly, the field is sorted, dug, and disinfected. Then, a landfill ditch is dug on the field, plant ash is spread on the bottom of the ditch, and then the fungus bag is placed in the Fill the ditch, then cover the straw, spread a layer of fine soil on the straw, and then water the ditch daily to keep the soil moist;

(4)采收(4) Harvesting

田地培育180天对成熟羊肚菌进行采收即可。After 180 days of field cultivation, the mature morels can be harvested.

实施例3Example 3

(1)培养基制备:(1) Culture medium preparation:

A.将麦粒、木屑、竹丝粉碎,得到备用的粉碎料;A. Grinding wheat grains, sawdust, and bamboo shreds to obtain spare crushed materials;

B.另取玉米粉、麦麸、谷氨酸、维生素C、柠檬酸与水及乙醇混合均匀,其后加入正硅酸乙酯,在加热条件下持续搅拌,混合物中形成微球,将微球滤出、洗净;B. Separately take corn flour, wheat bran, glutamic acid, vitamin C, citric acid and mix them with water and ethanol evenly, then add tetraethyl orthosilicate, keep stirring under heating conditions, microspheres are formed in the mixture, and the microspheres The ball is filtered out and washed;

C.将粉碎料、微球及石膏、磷酸二氢钾、磷酸氢二钾、细沙、水混合均匀,静置后得到培养基,其中培养基的原料按质量份计,包括麦粒35份,木屑25份,竹丝20份,玉米粉15份,麦麸15份,谷氨酸8份,6份维生素C,1份柠檬酸,5份石膏,0.3份磷酸二氢钾,0.3份磷酸氢二钾,20份细沙,所述步骤B中乙醇与水的体积比为1:3,步骤B中正硅酸乙酯与乙醇的质量比为1:1~2,步骤B中加热温度为30℃,步骤C中的水的质量为粉碎料的质量的30%;C. Mix crushed materials, microspheres, gypsum, potassium dihydrogen phosphate, dipotassium hydrogen phosphate, fine sand, and water evenly, and obtain a culture medium after standing still, wherein the raw materials of the culture medium are calculated in parts by mass, including 35 parts of wheat grains , 25 parts of sawdust, 20 parts of bamboo shreds, 15 parts of corn flour, 15 parts of wheat bran, 8 parts of glutamic acid, 6 parts of vitamin C, 1 part of citric acid, 5 parts of gypsum, 0.3 parts of potassium dihydrogen phosphate, 0.3 parts of phosphoric acid Dipotassium hydrogen, 20 parts of fine sand, the volume ratio of ethanol and water is 1:3 in the described step B, and the mass ratio of tetraethyl orthosilicate and ethanol is 1:1~2 in the step B, and heating temperature is in the step B 30 DEG C, the quality of the water in the step C is 30% of the quality of pulverized material;

(2)接种及袋内培养:(2) Inoculation and bag culture:

将培养基装入袋内,装料完成后将菌袋封口、灭菌,其后接入梯棱羊肚菌菌种,在无菌避光条件下培养6天;Put the culture medium into the bag, seal and sterilize the fungus bag after the filling is completed, then insert the strain of morel spp., and cultivate it under sterile light-proof conditions for 6 days;

(3)田地培育:(3) Field cultivation:

选择土壤pH值为6.5~7.5的田地进一步培育,将该田地首先进行整理、翻挖、消毒,其后在田地上挖出填埋沟,在沟底铺洒草木灰,其后将菌袋放置在填埋沟内,再覆盖秸秆,在秸秆上再铺洒一层细土,其后日常对填埋沟进行浇灌,保持土壤湿润;Select a field with a soil pH value of 6.5-7.5 for further cultivation. Firstly, the field is sorted, dug, and disinfected. Then, a landfill ditch is dug on the field, plant ash is spread on the bottom of the ditch, and then the fungus bag is placed in the Fill the ditch, then cover the straw, spread a layer of fine soil on the straw, and then water the ditch daily to keep the soil moist;

(4)采收(4) Harvesting

田地培育150天对成熟羊肚菌进行采收即可。After 150 days of field cultivation, the mature morels can be harvested.

Claims (6)

1.一种羊肚菌的培育方法,其特征在于:所述培育方法包括以下过程:1. a cultivation method of hickory chick, is characterized in that: described cultivation method comprises the following processes: (1)培养基制备:(1) Culture medium preparation: A.将麦粒、木屑、竹丝粉碎,得到备用的粉碎料;A. Grinding wheat grains, sawdust, and bamboo shreds to obtain spare crushed materials; B.另取玉米粉、麦麸、谷氨酸、维生素C、柠檬酸与水及乙醇混合均匀,其后加入正硅酸乙酯,在加热条件下持续搅拌,混合物中形成微球,将微球滤出、洗净;B. Separately take corn flour, wheat bran, glutamic acid, vitamin C, citric acid and mix them with water and ethanol evenly, then add tetraethyl orthosilicate, keep stirring under heating conditions, microspheres are formed in the mixture, and the microspheres The ball is filtered out and washed; C.将粉碎料、微球及石膏、磷酸二氢钾、磷酸氢二钾、细沙、水混合均匀,静置后得到培养基;C. Mix crushed materials, microspheres, gypsum, potassium dihydrogen phosphate, dipotassium hydrogen phosphate, fine sand, and water evenly, and obtain a culture medium after standing; (2)接种及袋内培养:(2) Inoculation and bag culture: 将培养基装入袋内,装料完成后将菌袋封口、灭菌,其后接入梯棱羊肚菌菌种,在无菌避光条件下培养5~7天;Put the culture medium into the bag, seal the bacteria bag after filling, and sterilize it, then insert the morel strains, and cultivate it for 5-7 days under sterile light-proof conditions; (3)田地培育:(3) Field cultivation: 选择土壤pH值为6.5~7.5的田地进一步培育,将该田地首先进行整理、翻挖、消毒,其后在田地上挖出填埋沟,在沟底铺洒草木灰,其后将菌袋放置在填埋沟内,再覆盖秸秆,在秸秆上再铺洒一层细土,其后日常对填埋沟进行浇灌,保持土壤湿润;Select a field with a soil pH value of 6.5-7.5 for further cultivation. Firstly, the field is sorted, dug, and disinfected. Then, a landfill ditch is dug on the field, plant ash is spread on the bottom of the ditch, and then the fungus bag is placed in the Fill the ditch, then cover the straw, spread a layer of fine soil on the straw, and then water the ditch daily to keep the soil moist; (4)采收(4) Harvesting 田地培育90~180天对成熟羊肚菌进行采收即可。Field cultivation takes 90 to 180 days to harvest mature morels. 2.根据权利要求1所述的羊肚菌的培育方法,其特征在于:所述培养基的原料按质量份计,包括麦粒30~40份,木屑20~30份,竹丝15~25份,玉米粉10~15份,麦麸10~15份,谷氨酸5~10份,5~10份维生素C,1~3份柠檬酸,1~5份石膏,0.1~1.0份磷酸二氢钾,0.1~1.0份磷酸氢二钾,15~25份细沙。2. The cultivation method of hickory chick according to claim 1, is characterized in that: the raw material of described culture medium comprises 30~40 parts of wheat grains, 20~30 parts of sawdust, 15~25 parts of bamboo shreds in parts by mass. 10-15 parts of corn flour, 10-15 parts of wheat bran, 5-10 parts of glutamic acid, 5-10 parts of vitamin C, 1-3 parts of citric acid, 1-5 parts of gypsum, 0.1-1.0 parts of diphosphate Potassium hydrogen, 0.1~1.0 parts of dipotassium hydrogen phosphate, 15~25 parts of fine sand. 3.根据权利要求1所述的羊肚菌的培育方法,其特征在于:所述步骤B中乙醇与水的体积比为1:1~5。3. the cultivation method of hickory chick according to claim 1, is characterized in that: in described step B, the volume ratio of ethanol and water is 1:1~5. 4.根据权利要求1所述的羊肚菌的培育方法,其特征在于:所述正硅酸乙酯与所述乙醇的质量比为1:1~3。4. the cultivation method of hickory chick according to claim 1, is characterized in that: the mass ratio of described ethyl orthosilicate and described ethanol is 1:1~3. 5.根据权利要求1所述的羊肚菌的培育方法,其特征在于:所述步骤B中加热温度为30~40℃。5. the cultivation method of hickory chick according to claim 1, is characterized in that: in described step B, heating temperature is 30~40 ℃. 6.根据权利要求1所述的羊肚菌的培育方法,其特征在于:所述步骤C中所述水的质量为所述粉碎料质量的10~50%。6. The cultivation method of hickory chick according to claim 1, characterized in that: the quality of the water in the step C is 10% to 50% of the quality of the ground material.
CN201711278207.5A 2017-12-06 2017-12-06 Cultivation method of morchella Pending CN107915528A (en)

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108718903A (en) * 2018-04-28 2018-11-02 南安市创培电子科技有限公司 A kind of fast-growth implantation methods of hickory chick
CN108812061A (en) * 2018-07-20 2018-11-16 中国农业科学院麻类研究所 A kind of hickory chick culture medium, preparation method and applications
CN110024619A (en) * 2019-04-19 2019-07-19 铜仁职业技术学院 A kind of high yield Cultivation of Dictyophora compost and its cultural method
CN111758483A (en) * 2020-05-18 2020-10-13 宁晋县坤茂食用菌科技有限公司 High-yield morchella planting method
CN114532149A (en) * 2021-12-28 2022-05-27 中国林业科学研究院亚热带林业研究所 Morchella esculenta external aid nutrition bag and application and use method thereof

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996015659A2 (en) * 1994-11-23 1996-05-30 Hps Biotechnologies, Inc. Process for production of mushroom inoculum
CN103804090A (en) * 2014-02-21 2014-05-21 甘肃省科学院生物研究所 Fermentation stock seed for liquid culture of morchella esculenta, preparation method of fermentation stock seed and method for realizing liquid culture by using stock seed
CN104956922A (en) * 2015-07-10 2015-10-07 青川县智农农业开发有限公司 Method for cultivating toadstools
CN106069185A (en) * 2016-06-15 2016-11-09 铜仁市侗菇菌业发展有限公司 A kind of breeding method of Morchella esculenta (L.) Pers
CN107344899A (en) * 2017-05-19 2017-11-14 天长市金农农业发展有限公司 A kind of red maple composite fertilizer for improving soil

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996015659A2 (en) * 1994-11-23 1996-05-30 Hps Biotechnologies, Inc. Process for production of mushroom inoculum
CN103804090A (en) * 2014-02-21 2014-05-21 甘肃省科学院生物研究所 Fermentation stock seed for liquid culture of morchella esculenta, preparation method of fermentation stock seed and method for realizing liquid culture by using stock seed
CN104956922A (en) * 2015-07-10 2015-10-07 青川县智农农业开发有限公司 Method for cultivating toadstools
CN106069185A (en) * 2016-06-15 2016-11-09 铜仁市侗菇菌业发展有限公司 A kind of breeding method of Morchella esculenta (L.) Pers
CN107344899A (en) * 2017-05-19 2017-11-14 天长市金农农业发展有限公司 A kind of red maple composite fertilizer for improving soil

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
丁湖广 等: "《名贵珍稀菇菌生产技术问答》", 30 June 2011, 金盾出版社 *
严泽湘 等: "《名贵珍稀菇菌栽培新技术丛书 鸡腿蘑 鸡枞菌 羊肚菌》", 30 September 2013, 内蒙古科学技术出版社 *
何培新: "《高级微生物学》", 31 August 2017, 中国轻工业出版社 *
顾克礼: "《自然农法》", 31 March 2016, 中国环境科学出版社 *

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108718903A (en) * 2018-04-28 2018-11-02 南安市创培电子科技有限公司 A kind of fast-growth implantation methods of hickory chick
CN108812061A (en) * 2018-07-20 2018-11-16 中国农业科学院麻类研究所 A kind of hickory chick culture medium, preparation method and applications
CN110024619A (en) * 2019-04-19 2019-07-19 铜仁职业技术学院 A kind of high yield Cultivation of Dictyophora compost and its cultural method
CN111758483A (en) * 2020-05-18 2020-10-13 宁晋县坤茂食用菌科技有限公司 High-yield morchella planting method
CN114532149A (en) * 2021-12-28 2022-05-27 中国林业科学研究院亚热带林业研究所 Morchella esculenta external aid nutrition bag and application and use method thereof

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Application publication date: 20180417