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首页> 外文期刊>Journal of Virology >Polypeptide synthesis directed by bacteriophage phi W-14 and by mutants defective in DNA synthesis.
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Polypeptide synthesis directed by bacteriophage phi W-14 and by mutants defective in DNA synthesis.

机译:通过噬菌体PHI W-14和DNA合成中的突变体的多肽合成。

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摘要

The latent period of bacteriophage phi W-14 is approximately 65 min when the doubling time of its host, Pseudomonas acidovorans, is 85 min. Host protein synthesis is shut off relatively slowly, stopping approximately 25 min after infection. There are several phases of phage-specific polypeptide synthesis during the latent period: early polypeptides appear within 10 min after infection; middle polypeptides start to appear between 10 nd 30 min; late polypeptides appear after 30 min. The lengths of time for which individual polypeptides are synthesized vary widely. Several late polypeptides do not appear in the virion. DNA replication is not required for late gene expression. The hypermodified pyrimidine, alpha-putrescinylthymine, appears not to be required in both strands of the DNA duplex for transcription.
机译:当宿主的倍增时间,假鼠酸维多拉症是85分钟时,噬菌体PHI W-14的潜在时间约为65分钟。宿主蛋白质合成相对缓慢地关闭,感染后约25分钟停止。在潜在的时间内有几个噬菌体特异性多肽合成:早期多肽在感染后10分钟内出现;中间多肽开始出现在10 nd 30分钟之间; 30分钟后晚期多肽出现。单个多肽合成的时间长度很大。几种晚期多肽不会出现在病毒中。晚期基因表达不需要DNA复制。在DNA双链链的两条链中,在转录的两条链中似乎不需要高序嘧啶α-普酰胺胰岛素。

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