首页> 外文期刊>Folia microbiologica >Protoplast isolation from cultured lichen Usnea ghattensis, their fusion with protoplasts of Aspergillus nidulans, fusant regeneration and production of usnic acid
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Protoplast isolation from cultured lichen Usnea ghattensis, their fusion with protoplasts of Aspergillus nidulans, fusant regeneration and production of usnic acid

机译:培养的地衣松萝的原生质体分离,与构巢曲霉的原生质体融合,融合融合再生和松萝酸的产生

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Protoplasts isolated from the mycobiont of a cultured lichen Usnea ghattensis were fused with protoplasts of the fungus Aspergillus nidulans in order to increase the growth rate of the cultured lichen mycobiont in vitro. The maximum protoplast yield (102 x 10(4)/g fresh cell mass) was reached in citrate buffer with 50 mmol/L 2-sulfanylethanol ('2-mercaptoethanol') containing 0.1 % Novozym after 1.5 h at pH 5 and a parts per thousand currency sign25 A degrees C. The increase in the concentration of the above effectors or the addition of others (e.g., MgSO4) as well as increase in time, shaking frequency, etc. caused the lower yield of protoplasts. The fused protoplasts were regenerated after transfer to malt extract-yeast extract medium and produced, after a 45-d cultivation, a fresh cell mass of 0.232 g (from starting 0.3 g) along with the lichen substance usnic acid.
机译:从培养的地衣松萝菌的分枝杆菌的原生质体与真菌构巢曲霉的原生质体融合,以提高培养的地衣真菌分枝杆菌的体外生长速率。在柠檬酸缓冲液中在50 h / h的pH值1.5 h下含有50 mmol / L含0.1%Novozym的2-硫烷基乙醇('2-巯基乙醇')的柠檬酸盐缓冲液中达到最大原生质体产量(102 x 10(4)/ g新鲜细胞质量)每千个货币符号25 A摄氏度。上述效应物的浓度增加或其他效应物(例如MgSO4)的添加以及时间,摇动频率等的增加,导致原生质体的产量降低。融合的原生质体在转移至麦芽提取物-酵母提取物培养基后再生,并在45天培养后产生0.232 g(从0.3 g开始)的新鲜细胞团以及地衣物质松萝酸。

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