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通过转录后沉默分支酶基因生产超高直链玉米淀粉。

Production of very-high-amylose cassava by post-transcriptional silencing of branching enzyme genes.

机构信息

National Key Laboratory of Plant Molecular Genetics, CAS Center for Excellence in Molecular Plant Sciences, Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, the Chinese Academy of Sciences, Shanghai, 200032, China.

Shanghai Key Laboratory of Plant Functional Genomics and Resources, Shanghai Chenshan Plant Science Research Center, Shanghai Chenshan Botanical Garden, the Chinese Academy of Sciences, Shanghai, 201602, China.

出版信息

J Integr Plant Biol. 2020 Jun;62(6):832-846. doi: 10.1111/jipb.12848. Epub 2019 Sep 24.

Abstract

High amylose starch can be produced by plants deficient in the function of branching enzymes (BEs). Here we report the production of transgenic cassava (Manihot esculenta Crantz) with starches containing up to 50% amylose due to the constitutive expression of hair-pin dsRNAs targeting the BE1 or BE2 genes. All BE1-RNAi plant lines (BE1i) and BE2-RNAi plant lines (BE2i) were grown up in the field, but with reduced total biomass production. Considerably high amylose content in the storage roots of BE2i plant lines was achieved. Storage starch granules of BE1i and BE2i plants had similar morphology as wild type (WT), however, the size of BE1i starch granules were bigger than that of WT. Comparisons of amylograms and thermograms of all three sources of storage starches revealed dramatic changes to the pasting properties and a higher melting temperature for BE2i starches. Glucan chain length distribution analysis showed a slight increase in chains of DP>36 in BE1i lines and a dramatic increase in glucan chains between DP 10-20 and DP>40 in BE2i lines. Furthermore, BE2i starches displayed a B-type X-ray diffraction pattern instead of the A-type pattern found in BE1i and WT starches. Therefore, cassava BE1 and BE2 function differently in storage root starch biosynthesis.

摘要

高直链淀粉淀粉可以由缺乏分支酶(BE)功能的植物产生。在这里,我们报告了由于针对 BE1 或 BE2 基因的发夹 dsRNA 的组成型表达,导致转基因木薯(Manihot esculenta Crantz)产生含有高达 50%直链淀粉的淀粉。所有 BE1-RNAi 植物系(BE1i)和 BE2-RNAi 植物系(BE2i)都在田间生长,但总生物量产量降低。BE2i 植物系中贮藏根的直链淀粉含量相当高。BE1i 和 BE2i 植物的贮藏淀粉粒具有与野生型(WT)相似的形态,但是 BE1i 淀粉粒的大小大于 WT。对三种贮藏淀粉的糊化特性和热特性的比较表明,BE2i 淀粉的糊化特性发生了剧烈变化,其熔融温度更高。葡聚糖链长分布分析表明,BE1i 系中 DP>36 的链略有增加,而 BE2i 系中 DP10-20 和 DP>40 之间的葡聚糖链则急剧增加。此外,BE2i 淀粉显示出 B 型 X 射线衍射图案,而不是在 BE1i 和 WT 淀粉中发现的 A 型图案。因此,木薯的 BE1 和 BE2 在贮藏根淀粉生物合成中具有不同的功能。

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