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利用 CRISPR/Cas9 技术对马铃薯品种‘Yukon Gold’中的颗粒结合型淀粉合成酶基因进行突变,以获得不含直链淀粉的块茎淀粉。

CRISPR/Cas9-Mediated Mutagenesis of the Granule-Bound Starch Synthase Gene in the Potato Variety Yukon Gold to Obtain Amylose-Free Starch in Tubers.

机构信息

Department of Soil & Crop Sciences, Texas A&M University, College Station, TX 77843-2474, USA.

Department of Horticultural Sciences, Texas A&M University, College Station, TX 77843-2133, USA.

出版信息

Int J Mol Sci. 2022 Apr 22;23(9):4640. doi: 10.3390/ijms23094640.

DOI:10.3390/ijms23094640
PMID:35563030
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9101600/
Abstract

Potato ( L.) is the third most important food crop after rice and wheat. Its tubers are a rich source of dietary carbohydrates in the form of starch, which has many industrial applications. Starch is composed of two polysaccharides, amylose and amylopectin, and their ratios determine different properties and functionalities. Potato varieties with higher amylopectin have many food processing and industrial applications. Using -mediated transformation, we delivered Clustered regularly interspaced short palindromic repeats and CRISPR-associated protein 9 (CRISPR/Cas9) reagents to potato (variety Yukon Gold) cells to disrupt the granule-bound starch synthase () gene with the aim of eliminating the amylose component of starch. Lugol-Iodine staining of the tubers showed a reduction or complete elimination of amylose in some of the edited events. These results were further confirmed by the perchloric acid and enzymatic methods. One event (T2-7) showed mutations in all four alleles and total elimination of amylose from the tubers. Viscosity profiles of the tuber starch from six different knockout events were determined using a Rapid Visco Analyzer (RVA), and the values reflected the amylopectin/amylose ratio. Follow-up studies will focus on eliminating the CRISPR components from the events and on evaluating the potential of clones with various amylose/amylopectin ratios for food processing and other industrial applications.

摘要

马铃薯(L.)是继水稻和小麦之后的第三大重要粮食作物。其块茎是膳食碳水化合物的丰富来源,形式为淀粉,具有许多工业应用。淀粉由两种多糖组成,直链淀粉和支链淀粉,它们的比例决定了不同的性质和功能。支链淀粉比例较高的马铃薯品种有许多食品加工和工业应用。我们使用介导的转化,将簇状规律间隔短回文重复序列和 CRISPR 相关蛋白 9(CRISPR/Cas9)试剂递送到马铃薯(品种育空金)细胞中,以破坏颗粒结合淀粉合成酶()基因,目的是消除淀粉中的直链淀粉成分。块茎的卢戈碘染色显示,一些编辑事件中直链淀粉的减少或完全消除。这些结果通过高氯酸和酶法进一步得到证实。一个事件(T2-7)显示四个 等位基因的突变和块茎中直链淀粉的完全消除。使用快速粘度分析仪(RVA)测定来自六个不同敲除事件的块茎淀粉的粘度曲线,值反映了支链淀粉/直链淀粉的比例。后续研究将集中于从事件中消除 CRISPR 成分,并评估具有不同支链淀粉/直链淀粉比例的克隆在食品加工和其他工业应用中的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6343/9101600/cbe95e91eeaa/ijms-23-04640-g006.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6343/9101600/1999edc03fe4/ijms-23-04640-g002.jpg
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