Creating saponin‐free yellow pea seeds by CRISPR/Cas9‐enabled mutagenesis on β‐amyrin synthase

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-01-01 DOI:10.1002/pld3.563
Connor L Hodgins, Eman M. Salama, Rahul Kumar, Yang Zhao, Susan A. Roth, Irene Z. Cheung, Jieyu Chen, Gene C. Arganosa, Tom Warkentin, Pankaj Bhowmik, Byung‐Kook Ham, Dae-Kyun Ro
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Abstract

Abstract Dry pea ( Pisum sativum ) seeds are valuable sources of plant protein, dietary fiber, and starch, but their uses in food products are restricted to some extent due to several off‐flavor compounds. Saponins are glycosylated triterpenoids and are a major source of bitter, astringent, and metallic off‐flavors in pea products. β‐amyrin synthase (BAS) is the entry point enzyme for saponin biosynthesis in pea and therefore is an ideal target for knock‐out using CRISPR/Cas9 genome editing to produce saponin deficient pea varieties. Here, in an elite yellow pea cultivar (CDC Inca), LC/MS analysis identified embryo tissue, not seed coat, as the main location of saponin storage in pea seeds. Differential expression analysis determined that PsBAS1 was preferentially expressed in embryo tissue relative to seed coat and was selected for CRISPR/Cas9 genome editing. The efficiency of CRISPR/Cas9 genome editing of PsBAS1 was systematically optimized in pea hairy roots. From these optimization procedures, the AtU6‐26 promoter was found to be superior to the CaMV35S promoter for gRNA expression, and the use of 37°C was determined to increase the efficiency of CRISPR/Cas9 genome editing. These promoter and culture conditions were then applied to stable transformations. As a result, a bi‐allelic mutation (deletion and inversion mutations) was generated in the PsBAS1 coding sequence in a T1 plant, and the segregated psbas1 plants from the T2 population showed a 99.8% reduction of saponins in their seeds. Interestingly, a small but statistically significant increase (~12%) in protein content with a slight decrease (~5%) in starch content was observed in the psbas1 mutants under phytotron growth conditions. This work demonstrated that flavor‐improved traits can be readily introduced in any pea cultivar of interest using CRISPR/Cas9. Further field trials and sensory tests for improved flavor are necessary to assess the practical implications of the saponin‐free pea seeds in food applications.
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通过对 β-amyrin 合成酶进行 CRISPR/Cas9 诱变,培育出不含皂素的黄豌豆种子
摘要 干豌豆(Pisum sativum)种子是植物蛋白、膳食纤维和淀粉的重要来源,但由于含有多种异味化合物,其在食品中的应用受到一定限制。皂素是糖基化的三萜类化合物,是豌豆产品中苦味、涩味和金属异味的主要来源。β-amyrin合成酶(BAS)是豌豆中皂素生物合成的入口酶,因此是利用CRISPR/Cas9基因组编辑技术敲除以培育皂素缺乏豌豆品种的理想目标。在本文中,通过对黄豌豆精英栽培品种(CDC Inca)进行 LC/MS 分析,确定胚组织(而非种皮)是豌豆种子中储存皂素的主要部位。差异表达分析确定,相对于种皮,PsBAS1 在胚组织中优先表达,并被选中进行 CRISPR/Cas9 基因组编辑。在豌豆毛根中对 PsBAS1 的 CRISPR/Cas9 基因组编辑效率进行了系统优化。通过这些优化程序,发现AtU6-26启动子比CaMV35S启动子更适合表达gRNA,并确定使用37°C的温度可提高CRISPR/Cas9基因组编辑的效率。这些启动子和培养条件随后被应用于稳定转化。结果,在一株 T1 植物的 PsBAS1 编码序列中产生了一个双等位突变(缺失突变和反转突变),从 T2 群体中分离出的 psbas1 植物种子中的皂苷含量减少了 99.8%。有趣的是,在植物生长条件下,psbas1 突变体的蛋白质含量略有增加(约 12%),而淀粉含量则略有减少(约 5%),这在统计学上具有显著意义。这项研究表明,利用 CRISPR/Cas9 技术可以很容易地在任何感兴趣的豌豆栽培品种中引入改善风味的性状。要评估无皂苷豌豆种子在食品应用中的实际意义,还需要进一步的田间试验和风味改良感官测试。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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