首页> 外国专利> CULTURE MEDIUM COMPOSITION FOR CULTURING PHELLINUS LINTEUS MYCELIUM AND CULTURE OF PHELLINUS LINTEUS MYCELIUM USING THE SAME COMPOSITION

CULTURE MEDIUM COMPOSITION FOR CULTURING PHELLINUS LINTEUS MYCELIUM AND CULTURE OF PHELLINUS LINTEUS MYCELIUM USING THE SAME COMPOSITION

机译:用于培养桑白球菌的培养培养基组合物和使用该组合物培养桑白球菌的培养基

摘要

PROBLEM TO BE SOLVED: To provide a culture medium composition for culturing Phellinus linteus mycelium in which the culture of Phellinus linteus mycelium is easily conducted and a special process for extracting mycelium is needless, and to provide a method for producing Phellinus linteus mycelium using the same culture medium. SOLUTION: This method comprises the following steps: preparing a culture medium by formulating 40-60 wt.% of at least one kind selected from the group consisting of brown rice, roasted brown rice, barley (or wheat), its powder, and uncracked and roasted grains of barley with 40-60 wt.% of underground water, by pouring the mixture into a bottle for culturing spawn, by heating them at a steam pressure of 15 lb/cm2 (120-121 deg.C) for 50-60 min to perform high pressure sterilization and by cooling them; separating tissue from carpophore of natural Phellinus linteus, subculturing the tissue in a medium extracted from mulberry trees and then performing seed culture in a similar medium; and inoculating the seed culture solution in the above formulated culture medium, followed by culturing it at 25±10 deg.C for 25-30 days.
机译:解决的问题:提供一种用于培养桑黄菌丝体的培养基组合物,其中容易进行桑黄菌丝体的培养,并且不需要特殊的提取菌丝体的方法,并提供了使用该培养基生产桑黄菌丝体的方法。培养基。解决方案:该方法包括以下步骤:通过配制40-60 wt%的选自糙米,烤糙米,大麦(或小麦),其粉末和未破碎的至少一种来制备培养基通过将混合物倒入用于培养卵的瓶中,并在15 lb / cm2的蒸汽压力(120-121℃)下将其加热50- 60分钟以进行高压灭菌并冷却。从天然桑黄的果树中分离组织,在从桑树中提取的培养基中继代培养组织,然后在相似的培养基中进行种子培养;将种子培养液接种于上述配制的培养基中,然后在25±10℃下培养25-30天。

著录项

  • 公开/公告号JP2001017158A

    专利类型

  • 公开/公告日2001-01-23

    原文格式PDF

  • 申请/专利权人 SOMOKU:KK;

    申请/专利号JP19990181931

  • 发明设计人 CHO SEIJIN;KIN TETSU;

    申请日1999-06-28

  • 分类号C12N1/14;A01G1/04;

  • 国家 JP

  • 入库时间 2022-08-22 01:30:59

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