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lpa1-5525:通过一种新型非破坏筛选方法在诱变群体中分离出的一种新的lpa1突变体。

lpa1-5525: A New lpa1 Mutant Isolated in a Mutagenized Population by a Novel Non-Disrupting Screening Method.

作者信息

Borlini Giulia, Rovera Cesare, Landoni Michela, Cassani Elena, Pilu Roberto

机构信息

Department of Agricultural and Environmental Sciences-Production, Landscape, Agroenergy-Università degli Studi di Milano, Via Celoria 2, 20133 Milan, Italy.

Department of Biosciences-Università degli Studi di Milano, Via Celoria 26, 20133 Milan, Italy.

出版信息

Plants (Basel). 2019 Jul 6;8(7):209. doi: 10.3390/plants8070209.

Abstract

Phytic acid, or myo-inositol 1,2,3,4,5,6-hexakisphosphate, is the main storage form of phosphorus in plants. It is localized in seeds, deposited as mixed salts of mineral cations in protein storage vacuoles; during germination, it is hydrolyzed by phytases to make available P together with all the other cations needed for seed germination. When seeds are used as food or feed, phytic acid and the bound cations are poorly bioavailable for human and monogastric livestock due to their lack of phytase activity. Therefore, reducing the amount of phytic acid is one strategy in breeding programs aimed to improve the nutritional properties of major crops. In this work, we present data on the isolation of a new maize ( L.) low phytic acid 1 (lpa1) mutant allele obtained by transposon tagging mutagenesis with the element. We describe the generation of the mutagenized population and the screening to isolate new lpa1 mutants. In particular, we developed a fast, cheap and non-disrupting screening method based on the different density of lpa1 seed compared to the wild type. This assay allowed the isolation of the lpa1-5525 mutant characterized by a new mutation in the locus associated with a lower amount of phytic phosphorus in the seeds in comparison with the wild type.

摘要

植酸,即肌醇1,2,3,4,5,6 - 六磷酸,是植物中磷的主要储存形式。它存在于种子中,以矿物阳离子的混合盐形式沉积在蛋白质储存液泡中;在种子萌发过程中,它被植酸酶水解,从而使磷以及种子萌发所需的所有其他阳离子得以利用。当种子用作食物或饲料时,由于人和单胃家畜缺乏植酸酶活性,植酸和结合的阳离子的生物利用率很低。因此,减少植酸含量是旨在改善主要作物营养特性的育种计划中的一种策略。在这项工作中,我们展示了通过用 元件进行转座子标签诱变获得的一个新的玉米(L.)低植酸1(lpa1)突变等位基因的分离数据。我们描述了诱变群体的产生以及分离新lpa1突变体的筛选过程。特别是,我们基于lpa1种子与野生型相比的不同密度,开发了一种快速、廉价且无干扰的筛选方法。该分析方法使得能够分离出lpa1 - 5525突变体,其特征是在 位点发生了新的突变,与野生型相比,种子中的植酸磷含量较低。

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