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Fermentation Process for Double-Stranded Ribonucleic Acid, an Interferon Inducer

机译:双链核糖核酸的发酵过程,干扰素诱导剂

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Double-stranded ribonucleic acid (ds-RNA) isolated from Escherichia coli infected with bacteriophage MS2 is a potent interferon inducer. High levels of ds-RNA are formed in nonpermissive cells infected with MU9, an amber coat protein mutant of MS2. This mutant has been used to develop a process for large-scale ds-RNA production. Preparation of quantities of MU9 lysate sufficient for ds-RNA production in fermentors is described. Over 300 μg of ds-RNA/ml can be accumulated after MU9 infection of cultures grown to high density in corn steep liquor medium. This is approximately 300 times the amount of ds-RNA made by MS2 infection of cells grown in tryptone medium. Maximum ds-RNA formation requires only 3 hr. The ds-RNA is stable and remains inside nonaerated cells for at least 17 hr.
机译:与噬菌体MS2感染的大肠杆菌中分离的双链核糖核酸(DS-RNA)是有效的干扰素诱导剂。高水平的DS-RNA形成在用MU9感染的非智能细胞中形成,MS 2的琥珀色涂层蛋白突变体。该突变体已被用于开发大规模DS-RNA生产的方法。描述了足以用于发酵罐中的DS-RNA生产的MU9裂解物的量的制备。在玉米陡液介质中生长至高密度的培养物中,可以累积超过300μg的DS-RNA / mL。这约为由在蛋白质培养基中生长的细胞MS2感染的DS-RNA的量的300倍。最大DS-RNA形成只需要3小时。 DS-RNA是稳定的,留在非包裹细胞内至少17小时。

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