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成熟番茄中 1-氨基环丙烷-1-羧酸合成酶的体外翻译产物与体内标记蛋白的比较。

A comparison of 1-aminocyclopropane-1-carboxylate synthase in vitro translation product and in-vivo-labeled protein in ripening tomatoes.

机构信息

MSU-DOE Plant Research Laboratory, Michigan State University, East Lansing, 48824-1312, MI, USA.

出版信息

Planta. 1990 Nov;182(4):635-8. doi: 10.1007/BF02341042.

Abstract

We determined the time course of increases in 1-aminocyclopropane-1-carboxylate (ACC) synthase activity in ripening tomato (Lycopersicon esculentum (L.) Mill.) pericarp discs following wounding and treatment with 75 mM LiCl. Over the course of 24 h, we detected oscillations in the amount of enzyme activity from an initial peak at 6 h to a subsequent, even higher level at 18 h. In-vitro translation products derived from poly(A)(+) RNAs isolated at various times of treatment and in-vivo-labeled proteins were immunoprecipitated using antibodies specific for ACC synthase. Analysis by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and fluorography showed that wounding and treatment with LiCl induced an accumulation of translatable ACC-synthase-specific mRNAs. In addition, single, prominent bands were apparent for both in-vivo and in-vitro samples but their molecular masses differed. It appears that the in-vitro translation product is a polypeptide of 56 kDa while the in-vivo-labeled enzyme has a molecular mass of 47 kDa.

摘要

我们测定了成熟番茄(Lycopersicon esculentum (L.) Mill.)果皮圆片在受伤和用 75mM LiCl 处理后 1-氨基环丙烷-1-羧酸合酶(ACC 合酶)活性增加的时间过程。在 24 小时的过程中,我们检测到酶活性量的波动,从最初的 6 小时峰值到 18 小时的后续更高水平。从在不同处理时间分离的 poly(A)(+) RNA 中获得的体外翻译产物和体内标记的蛋白质使用针对 ACC 合酶的特异性抗体进行免疫沉淀。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳和荧光分析表明,受伤和 LiCl 处理诱导了可翻译的 ACC 合酶特异性 mRNA 的积累。此外,体内和体外样品均出现单一明显的条带,但它们的分子量不同。体外翻译产物似乎是 56kDa 的多肽,而体内标记的酶的分子量为 47kDa。

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