CN108901585A - A kind of front and back of needle mushroom bacterium germination cultural method stage by stage - Google Patents
A kind of front and back of needle mushroom bacterium germination cultural method stage by stage Download PDFInfo
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- CN108901585A CN108901585A CN201710226661.XA CN201710226661A CN108901585A CN 108901585 A CN108901585 A CN 108901585A CN 201710226661 A CN201710226661 A CN 201710226661A CN 108901585 A CN108901585 A CN 108901585A
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Abstract
A kind of front and back of needle mushroom bacterium germination of present invention cultural method stage by stage, includes the following steps:It will be cultivated to the bacterium bottle before hot stage in culturing room's early period after inoculation, indoor environment is by following setting:Temperature is 18 DEG C -20 DEG C, humidity >=64%, gas concentration lwevel/ventilation frequency≤2100ppm;It will be cultivated into the bacterium bottle before hot stage to mycelium stimulation in later period culturing room, indoor environment is arranged as following:Temperature≤20 DEG C, humidity >=80%, gas concentration lwevel/ventilation frequency≤3100ppm, after the present invention can be inoculated with using the method that this front and back phase separately cultivates by independent control the culture link parameter of mycelia Restoration stage and hot stage mycelia rapid growth stage come achieve the purpose that make mycelium growing period shorten and stablize, reduce pollution rate, burn bacterium rate.
Description
Technical field
The present invention relates to the cultural methods of needle mushroom bacterium germination more particularly to a kind of front and back of needle mushroom bacterium germination to cultivate stage by stage
Method.
Background technique
There is the yield and quality of industrialized cultivation for needle mushroom in the bacterium germination stage of needle mushroom particularly important influence.?
Growing state of the control of the factors such as temperature, humidity, gas concentration lwevel in bacterium germination stage culture environment to Flammulina velutipes mycelium
It is most important.
Currently, the golden mushroom plantation of batch production mostly uses unified training method in the bacterium germination stage, that is, to before mycelium stimulation after being inoculated with
Bacterium bottle is placed on same storehouse or space is cultivated.This cultural method is simple for site requirements, but is difficult to difference
The conditions such as temperature needed for the bacterium germination stage, humidity, gas concentration lwevel are targetedly controlled, this also results in cultivation cycle
It is longer and unstable, pollution rate is high, burn bacterium rate it is high the problems such as.For this purpose, a kind of ad hoc front and back for counting needle mushroom bacterium germination is trained stage by stage
The method of supporting.
Summary of the invention
To overcome above-mentioned deficiency, the present invention provides a kind of front and back of needle mushroom bacterium germination cultural methods stage by stage.
The technical solution adopted by the present invention to solve the technical problems is:A kind of front and back of needle mushroom bacterium germination is cultivated stage by stage
Method includes the following steps:
(1) it will be cultivated to the bacterium bottle before hot stage in culturing room's early period after inoculation, indoor environment is by following setting:Temperature is
18 DEG C -20 DEG C, humidity >=64%, gas concentration lwevel/ventilation frequency≤2100ppm;
(2) it will be cultivated into the bacterium bottle before hot stage to mycelium stimulation in later period culturing room, indoor environment is arranged as following:Temperature
≤ 20 DEG C, humidity >=80%, gas concentration lwevel/ventilation frequency≤3100ppm.
The indoor environment of described culturing room's early period by following setting temperature is 20 DEG C, humidity 65%-70%, titanium dioxide
Concentration of carbon/ventilation frequency is 1500ppm-2000ppm.
The indoor environment of the later period culturing room by following setting temperature is 20 DEG C, humidity 80%-85%, titanium dioxide
Concentration of carbon/ventilation frequency is 2000ppm-3000ppm.
The present invention will use independent culturing room's early period by the improvement to existing culture environment during bacterium germination culture
With later period culturing room.Culturing room's early period be used to cultivate inoculation after to before hot stage this stage bacterium bottle, environment temperature is relatively
Height is conducive to mycelia fast-germination, growth;Later period culturing room, which is used to cultivate, will enter hot stage until this stage before mycelium stimulation
Bacterium bottle, environment temperature is relatively low, is conducive to reduce and burns bacterium probability.It can be by only using the method that this front and back phase separately cultivates
The culture link parameter of mycelia Restoration stage and hot stage mycelia rapid growth stage keeps bacterium germination all after vertical control inoculation to reach
The purpose that phase shortens and stablizes, reduces pollution rate, burning bacterium rate.
Specific embodiment:
Below with reference to embodiment to further detailed description of the present invention, embodiments of the present invention are not limited thereto.
A kind of front and back of needle mushroom bacterium germination cultural method stage by stage.
The technical solution adopted by the present invention to solve the technical problems is:A kind of front and back of needle mushroom bacterium germination is cultivated stage by stage
Method includes the following steps:
(1) it will be cultivated to the bacterium bottle before hot stage in culturing room's early period after inoculation, indoor environment is by following setting:Temperature is
18 DEG C -20 DEG C, humidity >=64%, gas concentration lwevel/ventilation frequency≤2100ppm;
(2) it will be cultivated into the bacterium bottle before hot stage to mycelium stimulation in later period culturing room, indoor environment is arranged as following:Temperature
≤ 20 DEG C, humidity >=80%, gas concentration lwevel/ventilation frequency≤3100ppm.
It is preferably 20 DEG C by following setting temperature by the indoor environment of culturing room's early period, humidity 65%-70%, dioxy
Change concentration of carbon/ventilation frequency is 1500ppm-2000ppm.The indoor environment of later period culturing room by following setting temperature is 20 DEG C,
Humidity is 80%-85%, gas concentration lwevel/ventilation frequency is 2000ppm-3000ppm.
Claims (3)
1. a kind of front and back of needle mushroom bacterium germination cultural method stage by stage, it is characterized in that including the following steps:
(1) it will be cultivated to the bacterium bottle before hot stage in culturing room's early period after inoculation, indoor environment is by following setting:Temperature is 18
DEG C -20 DEG C, humidity >=64%, gas concentration lwevel/ventilation frequency≤2100ppm;
(2) it will be cultivated into the bacterium bottle before hot stage to mycelium stimulation in later period culturing room, indoor environment is arranged as following:Temperature≤20
DEG C, humidity >=80%, gas concentration lwevel/ventilation frequency≤3100ppm.
2. a kind of front and back of needle mushroom bacterium germination according to claim 1 cultural method stage by stage, it is characterized in that:Before described
The indoor environment of phase culturing room by following setting temperature is 20 DEG C, humidity 65%-70%, gas concentration lwevel/ventilation frequency
For 1500ppm-2000ppm.
3. a kind of front and back of needle mushroom bacterium germination according to claim 1 cultural method stage by stage, it is characterized in that:After described
The indoor environment of phase culturing room by following setting temperature is 20 DEG C, humidity 80%-85%, gas concentration lwevel/ventilation frequency
For 2000ppm-3000ppm.
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN113575277A (en) * | 2021-08-11 | 2021-11-02 | 江苏华绿生物科技股份有限公司 | Sorghum bran culture medium and application thereof in industrial cultivation of white flammulina velutipes |
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CN103314780A (en) * | 2013-06-09 | 2013-09-25 | 潍坊市林海生物科技有限公司 | Factory-like fungus scratching mushroom generation technology for bag-cultivation needle mushroom |
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CN104303837A (en) * | 2014-10-13 | 2015-01-28 | 上海市农业科学院 | Secondary fungus culture method for mushroom factory production |
CN104885783A (en) * | 2015-06-09 | 2015-09-09 | 广西大学 | Cultivation method for bottle-cultivated needle mushrooms |
CN106063424A (en) * | 2015-12-30 | 2016-11-02 | 长春高榕生物科技有限公司 | A kind of production method increasing Flammulina velutiper (Fr.) Sing rugosity |
CN105684733A (en) * | 2016-01-29 | 2016-06-22 | 辽宁江荟菌业生产有限公司 | Bag-culture needle mushroom culture method |
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CN113575277A (en) * | 2021-08-11 | 2021-11-02 | 江苏华绿生物科技股份有限公司 | Sorghum bran culture medium and application thereof in industrial cultivation of white flammulina velutipes |
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