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从萌发的蓖麻胚乳中分离和无细胞翻译总信使 RNA。

Isolation and Cell-free Translation of Total Messenger RNA from Germinating Castor Bean Endosperm.

机构信息

Department of Biochemistry, University of Leeds, Yorkshire, England.

出版信息

Plant Physiol. 1979 Apr;63(4):769-73. doi: 10.1104/pp.63.4.769.

Abstract

Polyadenylated RNA was isolated from the total RNA fraction extracted from the endosperm tissue of 3-day-old castor bean seedlings by affinity chromatography on oligo(dT)-cellulose. This polyadenylated RNA was efficiently translated into protein when added to a messenger RNA-dependent cell-free system derived from rabbit reticulocytes. Characterization of the translational products by electrophoresis followed by autoradiography established that numerous discrete polypeptides were formed with molecular weights ranging from 10,000 to over 100,000. Immunoprecipitation in the presence of antiserum raised in rabbits against the total glyoxysomal matrix proteins showed that these proteins accounted for 15 to 20% of the total translational products.Attempts to reconstitute rough endoplasmic reticulum by the addition of washed castor bean microsomal membranes to the translational system were unsuccessful, these membranes severely inhibiting protein synthesis. Canine pancreatic microsomes could be added to endosperm messenger RNA-dependent reticulocyte lysates at relatively high concentrations while still allowing significant protein synthesis.

摘要

多聚腺苷酸 RNA 是从 3 天大的蓖麻种子胚乳组织的总 RNA 部分通过寡聚(dT)-纤维素亲和层析分离出来的。将该多聚腺苷酸 RNA 添加到来自兔网织红细胞的信使 RNA 依赖性无细胞系统中,可有效地将其翻译为蛋白质。通过电泳后放射自显影对翻译产物进行的特征分析表明,形成了许多离散的多肽,分子量范围从 10000 到超过 100000。在针对总乙醛酸体基质蛋白的兔抗血清存在的情况下进行免疫沉淀表明,这些蛋白占总翻译产物的 15%至 20%。通过向翻译系统中添加已洗涤的蓖麻微粒体膜来重新构成粗糙内质网的尝试均未成功,这些膜严重抑制了蛋白质合成。犬胰腺微粒体可以在相对较高的浓度下添加到胚乳信使 RNA 依赖性网织红细胞裂解物中,同时仍允许大量蛋白质合成。

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