다당류 및 그의 제조방법
    3.
    发明授权
    다당류 및 그의 제조방법 失效
    新POLICACCHARIDE

    公开(公告)号:KR1019920001367B1

    公开(公告)日:1992-02-11

    申请号:KR1019890019931

    申请日:1989-12-28

    Abstract: Anticancer effect having mycelium is prepd. by culturing Phellinus linteus (Berk et Curt). Aoshima in principally dried and powdered sapling of mulberry contg. medium, and collecting mycelium. Pref. glucose is added to the medium other than common components. According to this invention, mass prodn. of anticancer effect having mycelium of Phellinus linteus is possible. By adding glucose to the medium, growth rate of mycelia is accelerated. In an example small pieces of fruit bodies of Phellinus linteus were cultered on agar medium. Mycelia were transplanted to medium at 20-28 deg.C, humidity 70% - 90% for 60 days to obtain mycelia.

    Abstract translation: 具有菌丝体的抗癌作用是制备的。 通过培养桑黄(Berk et Curt)。 Aoshima主要干燥和粉末树苗桑树contg。 中等,收集菌丝体。 县。 将葡萄糖加入除普通组分以外的培养基中。 根据本发明, 具有桑黄菌丝体的抗癌作用是可能的。 通过向培养基中加入葡萄糖,菌丝体的生长速度加快。 在一个例子中,在琼脂培养基上培养一小部分桑皮果实体。 将菌丝体在20-28℃,湿度70%-90%下移植到培养基中60天,得到菌丝体。

    페리누스 린테우스 균사체의 배양방법
    4.
    发明授权
    페리누스 린테우스 균사체의 배양방법 失效
    培养PHELLINUS LINTEUS的方法

    公开(公告)号:KR1019920001194B1

    公开(公告)日:1992-02-06

    申请号:KR1019890019933

    申请日:1989-12-28

    Abstract: Anticancer effect having mycelium is prepd. by culturing Phellinus linteus (Berk et Curt). Aoshima in principally dried and powdered sapling of mulberry contg. medium, and collecting mycelium. Pref. glucose is added to the medium other than common components. According to this invention, mass prodn. of anticancer effect having mycelium of Phellinus linteus is possible. By adding glucose to the medium, growth rate of mycelia is accelerated. In an example small pieces of fruit bodies of Phellinus linteus were cultered on agar medium. Mycelia were transplanted to medium at 20-28 deg.C, humidity 70% - 90% for 60 days to obtain mycelia.

    Abstract translation: 具有菌丝体的抗癌作用是制备的。 通过培养桑黄(Berk et Curt)。 Aoshima主要干燥和粉末树苗桑树contg。 中等,收集菌丝体。 县。 将葡萄糖加入除普通组分以外的培养基中。 根据本发明, 具有桑黄菌丝体的抗癌作用是可能的。 通过向培养基中加入葡萄糖,菌丝体的生长速度加快。 在一个例子中,在琼脂培养基上培养一小部分桑皮果实体。 将菌丝体在20-28℃,湿度70%-90%下移植到培养基中60天,得到菌丝体。

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