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Gene Expression During the Development of Bacteriophage φ29 III. Analysis of Viral-Specific Protein Synthesis with Suppressible Mutants

机译:噬菌体φ29发育过程中的基因表达具有可抑制突变体的病毒特异性蛋白质合成分析

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摘要

Fifty-four suppressible mutants of bacteriophage φ29 have been isolated with a variety of mutagens and assigned to eight complementation groups. Viral-specific protein synthesis in UV light-irradiated, nonsuppressing Bacillus subtilis 60084 was analyzed with exponential acrylamide gels. Four additional φ29 proteins which were undetected on ordinary acrylamide gels are reported in this paper. Five phage φ29 proteins have been unambiguously assigned to specific cistrons. Two cistrons had pleiotropic effects on viral protein synthesis. Mutants in cistrons I or II were unable to synthesize DNA in nonsuppressing bacteria. Mutants in cistron I were unable to attach viral chromosomes to the host cell membrane, and the protein responsible for this function has been identified. The other viral protein playing a role in phage φ29 DNA synthesis is also identified and assigned to cistron II. Mutants in cistron II can attach viral chromosomes to membrane, but cannot synthesize DNA in nonsuppressing bacteria.
机译:已经分离出具有多种诱变剂的五十四个噬菌体φ29可抑制突变体,并分配给八个互补组。用指数丙烯酰胺凝胶分析了紫外线照射的非抑制枯草芽孢杆菌60084中的病毒特异性蛋白质合成。本文报道了在普通丙烯酰胺凝胶中未检测到的另外四种φ29蛋白。五个噬菌体φ29蛋白已明确分配给特定的顺反子。两个顺反子对病毒蛋白质合成具有多效性作用。顺反子I或II中的突变体不能在非抑制细菌中合成DNA。顺反子I中的突变体无法将病毒染色体附着到宿主细胞膜上,并且已经鉴定出负责此功能的蛋白质。还鉴定了在噬菌体φ29DNA合成中起作用的其他病毒蛋白,并将其分配给顺反子II。顺反子II中的突变体可以将病毒染色体附着在膜上,但不能在非抑制性细菌中合成DNA。

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