摘要
选用玻璃纸液体培养基培养的不同菌龄的菌丝体,分别注入用不同渗透稳定剂配制的1.5%溶壁酶进行酶解,释放出原生质体,再经浅层液体培养获得再生菌丝,可用于栽培,比对照形成子实体快,其产量略高于对照。
Fresh mycelium of different ages were selected from liquid medium cultures maintained in glassing and immersed in 1.5% Lywallzyme which were prepared with different osmoticas, round and transparent protoplasts with clear protoplast membrane began to be liberated in great quantity. After 2 day's culture in liquid medium, hypha regeneration was found. Two months later, normal fruiting bodies formed. These fruiting bodies had big pileus, normal color, and increased yield compared with control.
出处
《西南农业大学学报(自然科学版)》
CSCD
1990年第5期483-485,共3页
Journal of Southwest Agricultural University