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cDNA Cloning and Sequence Analysis of Rice Sbe1 and Sbe3 Genes

机译:水稻Sbe1和Sbe3基因的cDNA克隆和序列分析

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摘要

Two starch-branching enzyme (SBE) in rice, is known to be a key enzyme in amylopectin biosynthesis. The cDNA of two SBE(starch-branching enzyme) genes Sbe1 and Sbe3 encoding SBE Ⅰ and SBE Ⅲ (two major isoforms in rice) were cloned by an improved RT-PCR technique, from a template cDNA library derived from the total mRNAs extracted from the immature seeds of a japonica rice Wuyunjing 7. DNA sequence analysis showed that the size of the cloned Sbe1 and Sbe3 cDNAs were 2490 and 2481 bp long, respectively, including their entire coding sequences. Comparison analysis indicated that the nucleotide sequence of Sbe3 was the same as that of sbe3 (Genbank Accession No. D16201) as reported previously. There were only four base-pairs difference, which resulted in changes of two deduced amino acids between the cloned Sbe1 cDNA and the reported sbe1 (Genbank Accession No. D11082). The cloned Sbe1 and Sbe3 cDNAs make it possible to improve rice starch quality through genetic engineering.
机译:水稻中的两种淀粉分支酶(SBE)是支链淀粉生物合成中的关键酶。通过改进的RT-PCR技术,从模板cDNA文库中克隆了编码SBEⅠ和SBEⅢ(水稻的两个主要亚型)的两个SBE(淀粉分支酶)基因Sbe1和Sbe3的cDNA。 DNA序列分析表明,克隆的Sbe1和Sbe3 cDNA的大小分别为2490和2481 bp,包括其全部编码序列。比较分析表明,Sbe3的核苷酸序列与先前报道的sbe3的核苷酸序列(Genbank登录号D16201)相同。只有四个碱基对的差异,导致克隆的Sbe1 cDNA与报道的sbe1(Genbank登录号D11082)之间两个推导的氨基酸发生变化。克隆的Sbe1和Sbe3 cDNA使通过基因工程提高稻米淀粉质量成为可能。

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