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针对通过十二烷基硫酸钠平板凝胶电泳纯化的枯草芽孢杆菌rho因子的抗体。对营养细胞和芽孢形成细胞粗提物中RNA聚合酶转录的影响。

Antibody directed against Bacillus subtilis rho factor purified by sodium dodecyl sulfate slab gel electrophoresis. Effect on transcription by RNA polymerase in crude extracts of vegetative and sporulating cells.

作者信息

Tjian R, Stinchcomb D, Losick R

出版信息

J Biol Chem. 1975 Nov 25;250(22):8824-8.

PMID:810488
Abstract

Antibody directed against rho factor from vegetative Bacillus subtilis was prepared by immunizing a rabbit with denaturated rho polypeptide isolated by electrophoresis of partially purified DNA-dependent RNA polymerase on a sodium dodecyl sulfate-polyacrylamide slab gel. Antiserum to rho reacted specifically with native rho polypeptide but not with core RNA polymerase as judged by complement fixation and by an immunodiffusion assay. Anti-rho antibody also inhibited the ability of rho to stimulate transcription of phage phie DNA but failed to inhibit transcription of poly(dA-dT) by core enzyme. Specific antibody was also raised against a mixture of the beta and beta' subunits of RNA polymerase purified by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. The effect of the anti-rho gamma-globulin on the transcription of phage phie DNA by RNA polymerase in crude extracts of vegetative and sporulating cells was examined. Anti-rho antibody markedly inhibited the transcription of phage DNA by RNA polymerase partially purified from vegetative bacteria by ammonium sulfate fractionation but had little effect on transcription of the phage DNA template by enzyme from sporulating cells. Addition of purified rho to a vegetative extract that had been depleted of rho by treatment with the anti-rho antibody restored active transcription of phage DNA. However, addition of purified rho to an antibody-treated extract of sporulating cells had little effect on phie RNA synthesis. These findings suggest that sporulating cells contain a component that interferes with the activity of the rho subunit of RNA polymerase.

摘要

通过用在十二烷基硫酸钠-聚丙烯酰胺平板凝胶上对部分纯化的依赖DNA的RNA聚合酶进行电泳分离得到的变性rho多肽免疫兔子,制备了针对枯草芽孢杆菌营养细胞rho因子的抗体。通过补体结合和免疫扩散试验判断,rho抗血清与天然rho多肽特异性反应,但与核心RNA聚合酶不反应。抗rho抗体也抑制rho刺激噬菌体phie DNA转录的能力,但不能抑制核心酶对聚(dA-dT)的转录。还针对通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳纯化的RNA聚合酶的β和β'亚基混合物产生了特异性抗体。研究了抗rhoγ球蛋白对营养细胞和芽孢形成细胞粗提物中RNA聚合酶转录噬菌体phie DNA的影响。抗rho抗体显著抑制了通过硫酸铵分级分离从营养细菌中部分纯化的RNA聚合酶对噬菌体DNA的转录,但对芽孢形成细胞中的酶对噬菌体DNA模板的转录影响很小。向用抗rho抗体处理而耗尽rho的营养提取物中添加纯化的rho可恢复噬菌体DNA的活性转录。然而,向经抗体处理的芽孢形成细胞提取物中添加纯化的rho对phie RNA合成影响很小。这些发现表明,芽孢形成细胞含有一种干扰RNA聚合酶rho亚基活性的成分。

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