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芝麻种子中硫胺素结合蛋白编码cDNA的克隆与序列分析。

Cloning and sequence analysis of cDNA encoding thiamin-binding proteins from sesame seeds.

作者信息

Watanabe Katsumi, Takahashi Hideyuki, Mitsunaga Toshio

机构信息

Department of Food and Nutrition, Faculty of Agriculture, Kinki University, 3327-204 Nakamachi, Nara 631-8505, Japan.

出版信息

Physiol Plant. 2001 Aug;112(4):546-551. doi: 10.1034/j.1399-3054.2001.1120412.x.

Abstract

The amino acid sequences of the large polypeptides of thiamin-binding proteins (TBPs) from sesame (Sesamum indicum L.) seeds (STBP-I, -II and -III) were analyzed. The large polypeptides of STBP-I, -II and -III had the same amino acid sequences as did their small polypeptides. The peptide sequence information obtained from STBPs was used to synthesize DNA primers for amplification of the gene(s) encoding STBPs. A 200-bp fragment was amplified from cDNA synthesized from RNA from sesame seeds 4 weeks after flowering. The 200-bp fragment was used to clone full-length cDNA(s) encoding STBP(s) with RACE techniques. A 644-bp fragment was amplified, cloned and sequenced. The cDNA was a full-length clone encoding STBP(s). It contained an open reading frame, which defined a 143-residue polypeptide. The identified small and large polypeptide sequences of STBPs exactly matched the sequence encoded within the cDNA clone. These results indicated that the small and large polypeptides of STBPs were encoded on the mRNA as a single large proprotein precursor and that the final mature forms were generated by post-translational processing in the same manner as the other 2S albumins of plant seeds.

摘要

对芝麻(Sesamum indicum L.)种子中硫胺素结合蛋白(TBPs)的大分子量多肽(STBP-I、-II和-III)的氨基酸序列进行了分析。STBP-I、-II和-III的大分子量多肽与其小分子量多肽具有相同的氨基酸序列。从STBPs获得的肽序列信息用于合成DNA引物,以扩增编码STBPs的基因。从开花后4周的芝麻种子RNA合成的cDNA中扩增出一个200 bp的片段。该200 bp的片段用于通过RACE技术克隆编码STBP的全长cDNA。扩增、克隆并测序了一个644 bp的片段。该cDNA是编码STBP的全长克隆。它包含一个开放阅读框,该开放阅读框定义了一个143个残基的多肽。所鉴定的STBPs的小分子量和大分子量多肽序列与cDNA克隆中编码的序列完全匹配。这些结果表明,STBPs的小分子量和大分子量多肽在mRNA上作为单一的大前体蛋白进行编码,并且最终的成熟形式是通过与植物种子的其他2S白蛋白相同的方式进行翻译后加工产生的。

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