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Formation manner null of homogeneous polyploids

机译:同质多倍体的形成方式无效

摘要

PURPOSE:To obtain the subject polyploid for producing industrially useful genetic recombinant at high frequency and in a short time without using genetic marker by exposing test cell of conidia or mycelium of fungi to colchicines having polyploid-organization potency in cell division period. CONSTITUTION:Test cell (e.g. Trichoderma reesei QM 9414 strain) of conidia or mycelium of fungi is subjected to shake culture in liquid medium containing colchicine or/and colchicine derivative having polyploid-organization potency (e.g. colcemid) in cell division period of said cell at a temperature of 30 deg.C for 2-3 day and the cell formed many pellet-like aggregates is transplanted on agar-agar medium, then cultured at a temperature of 30 deg.C for 2-3 day to afford the aimed autopolyploid of fungi having increased nuclear size.
机译:目的:通过将分生孢子或真菌菌丝的试验细胞暴露于细胞分裂期具有多倍体组织潜能的秋水仙碱中,从而获得不需使用遗传标记就可在短时间内高频率生产工业有用的基因重组体的多倍体。组成:分生孢子或真菌菌丝的受试细胞(例如里氏木霉QM 9414菌株)在含有秋水仙碱或/和具有多倍体组织潜能的秋水仙碱衍生物(例如秋水仙碱)的液体培养基中于该细胞的细胞分裂期于60℃摇动培养。在30℃的温度下2-3天,将形成许多团状聚集体的细胞移植到琼脂培养基上,然后在30℃的温度下培养2-3天,得到目标的多倍体核大小增加的真菌。

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