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由噬菌体phi W-14及DNA合成缺陷型突变体指导的多肽合成。

Polypeptide synthesis directed by bacteriophage phi W-14 and by mutants defective in DNA synthesis.

作者信息

Miller P B, Gerhard B, Warren R A

出版信息

J Virol. 1984 May;50(2):529-32. doi: 10.1128/JVI.50.2.529-532.1984.

Abstract

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.

摘要

当噬菌体phi W-14的宿主嗜酸假单胞菌的倍增时间为85分钟时,噬菌体phi W-14的潜伏期约为65分钟。宿主蛋白质合成关闭相对较慢,在感染后约25分钟停止。潜伏期内有几个阶段的噬菌体特异性多肽合成:早期多肽在感染后10分钟内出现;中期多肽在10到30分钟之间开始出现;晚期多肽在30分钟后出现。各个多肽合成的时间长度差异很大。几种晚期多肽不出现在病毒粒子中。晚期基因表达不需要DNA复制。超修饰嘧啶α-腐胺基胸腺嘧啶似乎在DNA双链的两条链中都不是转录所必需的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7e2/255663/03ee0cf3bf87/jvirol00134-0252-a.jpg

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