Patent classifications
A01G18/20
ANTRODIA CINNAMOMEA CULTIVATION METHOD AND POROUS CARRIER FOR CULTIVATING ANTRODIA CINNAMOMEA
An Antrodia cinnamomea cultivation method sequentially comprises the following steps: step 1, obtaining a nutrient solution by mixing in proportion, wherein ingredients of the nutrient solution comprises Cinnamomum kanehirai extracts, carbon sources and nitrogen sources, the nutrient solution is placed in a porous carrier, the porous carrier has a peripheral surface and multiple micropores recessed into the peripheral surface, the nutrient solution is able to infiltrate into the micropores to form a nutrient layer on the peripheral surface and inner peripheries of the micropores; step 2, performing a membrane treatment on the porous carrier to form a membrane on the nutrient layer; step 3, sterilizing the porous carrier; and step 4, growing Antrodia cinnamomea strains on the membrane on the porous carrier, and then placing the porous carrier in a sealed environment for cultivation at constant temperature and humidity.
ANTRODIA CINNAMOMEA CULTIVATION METHOD AND POROUS CARRIER FOR CULTIVATING ANTRODIA CINNAMOMEA
An Antrodia cinnamomea cultivation method sequentially comprises the following steps: step 1, obtaining a nutrient solution by mixing in proportion, wherein ingredients of the nutrient solution comprises Cinnamomum kanehirai extracts, carbon sources and nitrogen sources, the nutrient solution is placed in a porous carrier, the porous carrier has a peripheral surface and multiple micropores recessed into the peripheral surface, the nutrient solution is able to infiltrate into the micropores to form a nutrient layer on the peripheral surface and inner peripheries of the micropores; step 2, performing a membrane treatment on the porous carrier to form a membrane on the nutrient layer; step 3, sterilizing the porous carrier; and step 4, growing Antrodia cinnamomea strains on the membrane on the porous carrier, and then placing the porous carrier in a sealed environment for cultivation at constant temperature and humidity.
Monokaryon mycelial material and related method of production
A monokaryotic mycelium sheet producing system for creating a sheet of monokaryotic mycelial material. The mycelium sheet producing system includes a culture unit, a spore stock unit, a plating unit, a section unit, a sub-plating unit, an expanding unit and a colonization unit. The culture unit prepares a monokaryon culture. The spore stock unit grows a plurality of fruit bodies in sterile laboratory conditions to create a spore stock. The plating unit performs a peroxide-based spore rescue and a plating process. The section unit is adaptable to section robust hyphae. The sub-plating unit sub-plates and expands the robust hyphae onto a spawn grain master. The expanding unit subsequently expands the spawn grain master into appropriate production of spawn volume. The colonization unit is adaptable to perform a subsequent colonization of mycelium substrate thereby creating a substantially defect free sheet of mycelium.
Monokaryon mycelial material and related method of production
A monokaryotic mycelium sheet producing system for creating a sheet of monokaryotic mycelial material. The mycelium sheet producing system includes a culture unit, a spore stock unit, a plating unit, a section unit, a sub-plating unit, an expanding unit and a colonization unit. The culture unit prepares a monokaryon culture. The spore stock unit grows a plurality of fruit bodies in sterile laboratory conditions to create a spore stock. The plating unit performs a peroxide-based spore rescue and a plating process. The section unit is adaptable to section robust hyphae. The sub-plating unit sub-plates and expands the robust hyphae onto a spawn grain master. The expanding unit subsequently expands the spawn grain master into appropriate production of spawn volume. The colonization unit is adaptable to perform a subsequent colonization of mycelium substrate thereby creating a substantially defect free sheet of mycelium.
Mycelium growth bed
A mycelium growth bed for optimal production of pure mycelium or a pure mycelium composite with controlled or predictable properties, the bed comprising a tray, a conveying platform, a permeable membrane, a substrate, and a porous material. The permeable membrane is positioned on the conveying platform within the tray. The substrate is positioned on the permeable membrane and the porous material is positioned on top of the substrate. The system provides a configuration wherein the CO.sub.2 concentration is held above 3%, the relative humidity is held above 40% and the O.sub.2 concentration is held below 20% in steady state conditions to produce leather-like mycelium without fruiting bodies.
Mycelium growth bed
A mycelium growth bed for optimal production of pure mycelium or a pure mycelium composite with controlled or predictable properties, the bed comprising a tray, a conveying platform, a permeable membrane, a substrate, and a porous material. The permeable membrane is positioned on the conveying platform within the tray. The substrate is positioned on the permeable membrane and the porous material is positioned on top of the substrate. The system provides a configuration wherein the CO.sub.2 concentration is held above 3%, the relative humidity is held above 40% and the O.sub.2 concentration is held below 20% in steady state conditions to produce leather-like mycelium without fruiting bodies.
Method for co-culturing <i>Inonotus obliquus, Ganoderma lucidum</i>, and <i>Phellinus linteus </i>mycelia
The present invention relates to a method of co-culturing Inonotus obliquus, Ganoderma lucidum, and Phellinus linteus. The co-cultured mycelia prepared through the method of the present invention have high beta-glucan content and thus can exhibit superior health functionality, and can be used as an additive or a cooking seasoning in various foods. In addition, the use of the co-cultured mycelia in curing raw meat enables easy preparation of a meat-based food product that has a good taste and flavor.
Method for co-culturing <i>Inonotus obliquus, Ganoderma lucidum</i>, and <i>Phellinus linteus </i>mycelia
The present invention relates to a method of co-culturing Inonotus obliquus, Ganoderma lucidum, and Phellinus linteus. The co-cultured mycelia prepared through the method of the present invention have high beta-glucan content and thus can exhibit superior health functionality, and can be used as an additive or a cooking seasoning in various foods. In addition, the use of the co-cultured mycelia in curing raw meat enables easy preparation of a meat-based food product that has a good taste and flavor.
CULTIVATION METHOD OF MORCHELLA WITHOUT NUTRIENT BAG
The present disclosure provides a cultivation method of morels and belongs to the technical field of cultivation of edible fungi. After nutrient contents that can be metabolized and utilized by morel mycelia are scientifically matched, sterilization treatment of exogenous nutrients is eliminated, and the exogenous nutrients are directly compressed for forming. Formed exogenous nutrient blocks and spawn is sowed and covered with soil, so as to realize a potential difference between “rich” and “poor” nutrients in a physical space. When the spawn germinate to form a mycelium network, the mycelia will enter a nutrient-rich exogenous nutrient area, secrete various extracellular enzymes to decompose and utilize these exogenous nutrient blocks, and transport them to a nutrient-poor mycelium network for storage, so as to complete nutrient assimilation and absorption, and reserve energy for later sexual reproduction.
CULTIVATION METHOD OF MORCHELLA WITHOUT NUTRIENT BAG
The present disclosure provides a cultivation method of morels and belongs to the technical field of cultivation of edible fungi. After nutrient contents that can be metabolized and utilized by morel mycelia are scientifically matched, sterilization treatment of exogenous nutrients is eliminated, and the exogenous nutrients are directly compressed for forming. Formed exogenous nutrient blocks and spawn is sowed and covered with soil, so as to realize a potential difference between “rich” and “poor” nutrients in a physical space. When the spawn germinate to form a mycelium network, the mycelia will enter a nutrient-rich exogenous nutrient area, secrete various extracellular enzymes to decompose and utilize these exogenous nutrient blocks, and transport them to a nutrient-poor mycelium network for storage, so as to complete nutrient assimilation and absorption, and reserve energy for later sexual reproduction.