Division of Plant Science and Technology, University of Missouri, Columbia, MO 65211, USA.
Plant Genetics Research Unit, US Department of Agriculture-Agricultural Research Service, Columbia, MO 65211, USA.
Int J Mol Sci. 2024 May 21;25(11):5578. doi: 10.3390/ijms25115578.
Despite the high quality of soybean protein, raw soybeans and soybean meal cannot be directly included in animal feed mixtures due to the presence of Kunitz (KTi) and Bowman-Birk protease inhibitors (BBis), which reduces animal productivity. Heat treatment can substantially inactivate trypsin and chymotrypsin inhibitors (BBis), but such treatment is energy-intensive, adds expense, and negatively impacts the quality of seed proteins. As an alternative approach, we have employed CRISPR/Cas9 gene editing to create mutations in genes to drastically lower the protease inhibitor content in soybean seed. Agrobacterium-mediated transformation was used to generate several stable transgenic soybean events. These independent CRISPR/Cas9 events were examined in comparison to wild-type plants using Sanger sequencing, proteomic analysis, trypsin/chymotrypsin inhibitor activity assays, and qRT-PCR. Collectively, our results demonstrate the creation of an allelic series of loss-of-function mutations affecting the major gene in soybean. Mutations in two of the highly expressed seed-specific genes lead to substantial reductions in both trypsin and chymotrypsin inhibitor activities.
尽管大豆蛋白质量很高,但由于存在 Kunitz(KTi)和 Bowman-Birk 蛋白酶抑制剂(BBis),生大豆和大豆粉不能直接添加到动物饲料混合物中,因为这会降低动物的生产力。热处理可以大大使胰蛋白酶和糜蛋白酶抑制剂(BBis)失活,但这种处理方法耗能大、成本高,并且会对种子蛋白的质量产生负面影响。作为一种替代方法,我们利用 CRISPR/Cas9 基因编辑技术在基因中创建突变,从而大幅降低大豆种子中蛋白酶抑制剂的含量。我们使用农杆菌介导的转化生成了多个稳定的转基因大豆事件。通过 Sanger 测序、蛋白质组分析、胰蛋白酶/糜蛋白酶抑制剂活性测定和 qRT-PCR 等方法,将这些独立的 CRISPR/Cas9 事件与野生型植物进行了比较。总的来说,我们的结果证明了在大豆中创建了一系列影响主要基因的功能丧失突变等位基因。两个高表达的种子特异性基因中的突变导致胰蛋白酶和糜蛋白酶抑制剂活性显著降低。