GROMAN N B, SUZUKI G
J Bacteriol. 1963 Aug;86(2):187-94. doi: 10.1128/jb.86.2.187-194.1963.
Groman, Neal B. (University of Washington, Seattle) and Grace Suzuki. Quantitative study of endolysin synthesis during reproduction of lambda phages. J. Bacteriol. 86:187-194. 1963.-Endolysin is presumed to be a phage-induced enzyme participating in lysis through its destructive action on the host cell wall. A method for assaying endolysin is described, which was utilized in studying endolysin synthesis at 37 and 44 C by induced strains of K-12 (lambda), K-12 (lambdatem), and K-12 (lambda112). In all cases, endolysin was detected prior to the appearance of mature, intracellular phage and was detected earlier at 44 C than at 37 C. It was synthesized at a linear rate, as was phage, and both syntheses terminated at the same time. Surprisingly, endolysin also accumulated under conditions in which induced K-12 (lambda112) exhibited lysis inhibition. Under these conditions, endolysin concentration per induced cell was 2 to 2.5 times that produced by normally lysing K-12 (lambda). Since alterations introduced into the lytic process by temperature, mutation, or both correlate well with the timing and rate of endolysin synthesis, the data tend to support the concept that endolysin determines the kinetics of the process. However, the accumulation of endolysin during lysis inhibition suggests the need for alternative hypotheses. One hypothesis is that although endolysin action is the key to lysis some preliminary steps are required to release the enzyme so that it may contact its substrate in the cell wall. A second hypothesis is that basically the lytic process involves an alteration in the permeability barrier of the cell and that lytic enzymes such as endolysin have evolved as an auxillary but dispensable mechanism to this process.
格罗曼,尼尔·B.(华盛顿大学,西雅图)和格雷斯·铃木。λ噬菌体繁殖过程中内溶素合成的定量研究。《细菌学杂志》86:187 - 194。1963年。——内溶素被认为是一种噬菌体诱导的酶,通过对宿主细胞壁的破坏作用参与裂解。描述了一种测定内溶素的方法,该方法用于研究K - 12(λ)、K - 12(λtem)和K - 12(λ112)诱导菌株在37℃和44℃下的内溶素合成。在所有情况下,在成熟的细胞内噬菌体出现之前就检测到了内溶素,并且在44℃比在37℃更早检测到。它与噬菌体一样以线性速率合成,并且两种合成同时终止。令人惊讶的是,在内溶素诱导的K - 12(λ112)表现出裂解抑制的条件下,内溶素也会积累。在这些条件下,每个诱导细胞的内溶素浓度是正常裂解的K - 12(λ)产生浓度的2至2.5倍。由于温度、突变或两者对裂解过程的改变与内溶素合成的时间和速率密切相关,这些数据倾向于支持内溶素决定该过程动力学的概念。然而,在裂解抑制期间内溶素的积累表明需要其他假设。一种假设是,尽管内溶素的作用是裂解的关键,但需要一些初步步骤来释放该酶,以便它可以接触细胞壁中的底物。另一种假设是,基本上裂解过程涉及细胞通透性屏障的改变,并且诸如内溶素之类的裂解酶已经进化成为该过程的一种辅助但非必需的机制。