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噬菌体Mu杀死宿主细胞所涉及的多种因素和过程:表征与定位

Multiple factors and processes involved in host cell killing by bacteriophage Mu: characterization and mapping.

作者信息

Waggoner B T, Marrs C F, Howe M M, Pato M L

出版信息

Virology. 1984 Jul 15;136(1):168-85. doi: 10.1016/0042-6822(84)90257-5.

Abstract

The regions of bacteriophage Mu involved in host cell killing were determined by infection of a lambda-immune host with 12 lambda pMu-transducing phages carrying different amounts of Mu DNA beginning at the left end. Infecting lambda pMu phages containing 5.0 (+/- 0.2) kb or less of the left end of Mu DNA did not kill the lambda-immune host, whereas lambda pMu containing 5.1 kb did kill, thus locating the right end of the kil gene between approximately 5.0 and 5.1 kb. For the Kil+ phages the extent of killing increased as the multiplicity of infection (m.o.i.) increased. In addition, killing was also affected by the presence of at least two other regions of Mu DNA: one, located between 5.1 and 5.8 kb, decreased the extent of killing; the other, located between 6.3 and 7.9 kb, greatly increased host cell killing. Killing was also assayed after lambda pMu infection of a lambda-immune host carrying a mini-Mu deleted for most of the B gene and the middle region of Mu DNA. Complementation of mini-Mu replication by infecting B+ lambda pMu phages resulted in killing of the lambda-immune, mini-Mu-containing host, regardless of the presence or absence of the Mu kil gene. The extent of host cell killing increased as the m.o.i. of the infecting lambda pMu increased, and was further enhanced by both the presence of the kil gene and the region located between 6.3 and 7.9 kb. These distinct processes of kil-mediated killing in the absence of replication and non-kil-mediated killing in the presence of replication were also observed after induction of replication-deficient and kil mutant prophages, respectively.

摘要

通过用12种携带不同长度Mu DNA(从左端开始)的λpMu转导噬菌体感染λ免疫宿主,确定了噬菌体Mu中参与宿主细胞杀伤的区域。感染含有5.0(±0.2)kb或更少Mu DNA左端的λpMu噬菌体不会杀死λ免疫宿主,而含有5.1 kb的λpMu则会杀死宿主,从而将kil基因的右端定位在大约5.0至5.1 kb之间。对于Kil +噬菌体,杀伤程度随着感染复数(m.o.i.)的增加而增加。此外,杀伤作用还受到Mu DNA至少其他两个区域的影响:一个位于5.1至5.8 kb之间,会降低杀伤程度;另一个位于6.3至7.9 kb之间,会大大增加宿主细胞杀伤。在用大部分B基因和Mu DNA中间区域缺失的mini-Mu感染λ免疫宿主后,也检测了λpMu感染后的杀伤情况。用B +λpMu噬菌体感染来补充mini-Mu复制会导致含有mini-Mu的λ免疫宿主被杀死,无论是否存在Mu kil基因。宿主细胞杀伤程度随着感染λpMu的m.o.i.增加而增加,并且通过kil基因的存在以及位于6.3至7.9 kb之间的区域进一步增强。在分别诱导复制缺陷型和kil突变型原噬菌体后,也观察到了在无复制情况下kil介导的杀伤和有复制情况下非kil介导的杀伤这些不同过程。

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