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一种在DNA结合蛋白方面存在缺陷的T7琥珀突变体。

A T7 amber mutant defective in DNA-binding protein.

作者信息

Araki H, Ogawa H

出版信息

Mol Gen Genet. 1981;183(1):66-73. doi: 10.1007/BF00270140.

Abstract

A T7 amber mutant, UP-2, in the gene for T7 DNA-binding protein was isolated from mutants that could not grow on sup+ ssb-1 bacteria but could grow on glnU ssb-1 and sup+ ssb+ bacteria. The mutant phage synthesized a smaller amber polypeptide (28,000 daltons) than T7 wild-type DNA-binding protein (32,000 daltons). DNA synthesis of the UP-2 mutant in sup+ ssb-1 cells was severely inhibited and the first round of replication was found to be repressed. The abilities for genetic recombination and DNA repair were also low even in permissive hosts compared with those of wild-type phage. Moreover, recombination intermediate T7 DNA molecules were not formed in UP-2 infected nonpermissive cells. The gene that codes for DNA-binding protein is referred to as gene 2.5 since the mutation was mapped between gene 2 and gene 3.

摘要

从不能在sup+ ssb-1细菌上生长但能在glnU ssb-1和sup+ ssb+细菌上生长的突变体中分离出T7 DNA结合蛋白基因的一个T7琥珀突变体UP-2。该突变噬菌体合成的琥珀多肽(28,000道尔顿)比T7野生型DNA结合蛋白(32,000道尔顿)小。UP-2突变体在sup+ ssb-1细胞中的DNA合成受到严重抑制,并且发现第一轮复制受到抑制。与野生型噬菌体相比,即使在允许宿主中,其基因重组和DNA修复能力也较低。此外,在UP-2感染的非允许细胞中未形成重组中间T7 DNA分子。由于该突变位于基因2和基因3之间,编码DNA结合蛋白的基因被称为基因2.5。

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