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Gene 24-controlled osmotic shock resistance in bacteriophage T4: probable multiple gene functions.

机译:基因24助长的噬菌体T4中的渗透抗冲击性:可能的多基因功能。

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By use of mixed infections with conditional lethal mutations in the head genes and an osmotic shock-resistant mutant we have demonstrated that osmotic shock resistance is controlled by gene 24. Using acrylamide gel electrophoresis combined with the "immune replicate" technique, we confirmed the positions of gene products 24 and 24* (P24 and P24*). In this paper we have still used the notation "P24," etc., for designating the product of gene 23, etc., although we prefer and use in general the designation "gp23" as introduced by Casjens and King (Annu. Rev. Biochem. 44:585, 1975). The reason for using the old notation is because the illustrations were prepared several years ago.) P24 ts showed a significantly slower mobility. Both osmotic shock-resistant and -sensitive mature phages contain 24*. Giants constructed with the Osr phage showed the same surface lattice as normal phage. Through temperature-shift experiments with 24(tsL90) alone and in combinations, we studied the phages which are matured after the shift to permissive temperature in the absence of new protein synthesis. Our results strongly suggest that only a fraction of the total phage complement of gene 24-controlled proteins is involved in determining the phenotype of shock resistance, and the remainder is necessary to mature the head.
机译:通过在头基因和渗透抗冲击突变体中使用有条件的致命突变的混合感染,我们已经证明渗透抗冲击性由基因24控制。使用丙烯酰胺凝胶电泳与“免疫复制”技术合并,我们确认了该位置基因产物24和24 *(P24和P24 *)。在本文中,我们仍然使用了符号“P24”等,用于指定基因23等产品,尽管我们更喜欢Casgens和King引入的指定“GP23”(Annu。Rev. Biochem。44:585,1975)。使用旧符号的原因是因为在几年前准备了插图。)P24 TS显示出显着较慢的流动性。渗透抗冲击性和敏感的成熟噬菌体含有24 *。用OSR噬菌体构建的巨型表现出与正常噬菌体相同的表面晶格。通过单独的24(TSL90)和组合的温度换档实验,我们研究了在没有新的蛋白质合成的情况下在允许温度变化后成熟的噬菌体。我们的结果强烈表明,只有基因24级蛋白的总噬菌体补充的一部分才参与确定抗冲击性表型,并且其余的是成熟头部所必需的。

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