Lago B D, Birnbaum J, Demain A L
Appl Microbiol. 1972 Sep;24(3):430-6. doi: 10.1128/am.24.3.430-436.1972.
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 mug 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.
从感染噬菌体MS2的大肠杆菌中分离出的双链核糖核酸(ds-RNA)是一种有效的干扰素诱导剂。在感染了MS2的琥珀型外壳蛋白突变体MU9的非允许细胞中会形成高水平的ds-RNA。该突变体已被用于开发大规模生产ds-RNA的方法。本文描述了制备足以在发酵罐中生产ds-RNA的大量MU9裂解物的方法。在玉米浆培养基中高密度培养的培养物感染MU9后,每毫升可积累超过300微克的ds-RNA。这大约是在胰蛋白胨培养基中生长的细胞感染MS2所产生的ds-RNA量的300倍。ds-RNA的最大形成仅需3小时。ds-RNA很稳定,在未通气的细胞内至少可保留17小时。