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蚕豆分生组织根细胞多核糖体及多聚腺苷酸化多核糖体RNA的分离与鉴定

Isolation and characterization of polysomes and polyadenylated polysomal RNA from Vicia faba meristematic root cells.

作者信息

Tessier L, Esnault R

出版信息

Mol Cell Biochem. 1980 Feb 28;29(3):173-81. doi: 10.1007/BF00420288.

Abstract

Undegraded Vicia faba polysomes from meristematic root cells were obtained after homogenization in a medium of low ionic strength provided that the pH was equal to 9.0. By minimizing the shearing forces during the homogenization step, polysomes were obtained free of mitochondrial and nuclear contaminants, measured by differential spectrophotometry and CsCl gradient centrifugation respectively. Poly(A)-containing RNA was obtained by poly(U)-Sepharose chromatography and shown to be virtually free of rRNA and its average size was 13-15 S. Approximately 9% of the purified preparation was annealed by [3H]-poly(U). Sucrose gradient analysis under denaturing conditions showed that the poly(A)-CONtaining RNA were non-degraded. This RNA was used to direct the synthesis of proteins in a heterologous cell-free system from wheat germ.

摘要

只要pH值等于9.0,在低离子强度的介质中匀浆后,就能从分生组织根细胞中获得未降解的蚕豆多核糖体。通过在匀浆步骤中尽量减少剪切力,获得了不含线粒体和核污染物的多核糖体,分别通过差示分光光度法和CsCl梯度离心法测定。通过聚(U)-琼脂糖凝胶柱层析获得了含聚(A)的RNA,结果表明其几乎不含rRNA,平均大小为13 - 15S。约9%的纯化制剂能与[³H]-聚(U)退火。变性条件下的蔗糖梯度分析表明,含聚(A)的RNA未降解。这种RNA被用于在来自小麦胚芽的异源无细胞系统中指导蛋白质的合成。

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