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在受感染的微小细胞中合成的噬菌体P1阻遏物和阻遏物旁路(抗阻遏物)多肽的鉴定。

Identification of the repressor and repressor bypass (antirepressor) polypeptides of bacteriophage P1 synthesized in infected minicells.

作者信息

Heilmann H, Reeve J N, Pühler A

出版信息

Mol Gen Genet. 1980 Apr;178(1):149-54. doi: 10.1007/BF00267223.

Abstract

P1 infected minicells synthesize approximately 50 phage-encoded polypeptides. Phage expression is temporally controlled, demonstrating phage polypeptides synthesized both early and late after infection. The P1 repressor, gpcl1 (Mr = 33,000), repressor bypass polypeptide, gpreb A (Mr = 27,500) and cistron 10 product, (gp10) (Mr = 64,000), have been identified by infection of minicells with P1 amber mutants. The beta-lactamase gene product (gpbla) carried by the closely related P7 and the chloramphenicol acetyl-transferase gene product (gpcat) carried by P1 Cm (in Tn9) have been demonstrated. Infection of minicells by P1virs or P1c4 mutants results in increased synthesis of gpreb A and a second polypeptide designated gpreb B (Mr = 40,000). The P1vir11 mutation leads to increased synthesis of a small polypeptide (Mr = 3,500) but does not affect the amount of gpc1 synthesized.

摘要

被P1感染的微小细胞合成大约50种噬菌体编码的多肽。噬菌体的表达受到时间控制,表明在感染后早期和晚期均合成噬菌体多肽。通过用P1琥珀突变体感染微小细胞,已鉴定出P1阻遏蛋白gpcl1(分子量=33,000)、阻遏蛋白旁路多肽gpreb A(分子量=27,500)和顺反子10产物(gp10)(分子量=64,000)。已证实密切相关的P7携带的β-内酰胺酶基因产物(gpbla)和P1 Cm(Tn9中)携带的氯霉素乙酰转移酶基因产物(gpcat)。用P1virs或P1c4突变体感染微小细胞会导致gpreb A和另一种命名为gpreb B(分子量=40,000)的多肽合成增加。P1vir11突变导致一种小多肽(分子量=3,500)合成增加,但不影响gpc1的合成量。

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