Kim Won-Seok, Krishnan Hari B
Department of Agronomy, University of Missouri, Columbia, MO 65211, USA.
Plant Biotechnol J. 2004 May;2(3):199-210. doi: 10.1111/j.1467-7652.2004.00063.x.
Soybean (Glycine max (L.) Merr.) is an important protein source in human diets and animal feeds. The sulphur content of soybean seed proteins, however, is not optimal for ration formulations. Thus, increasing the methionine and cysteine content of soybean seed proteins would enhance the nutritional quality of this widely utilized legume. We have earlier reported the isolation of an 11 kDa delta-zein protein rich in methionine from the endosperm of the maize (Zea mays L.) inbred line W23a1 [Kim, W.-S. and Krishnan, H.B. (2003) Allelic variation and differential expression of methionine-rich-delta-zeins in maize inbred lines B73 and W23a1. Planta, 217, 66-74]. Using Agrobacterium-mediated transformation, a construct consisting of the coding region of the cloned delta-zein gene under regulation of the beta-conglycinin alpha'-promoter was introduced into the soybean genome. The 11 kDa delta-zein gene was expressed in the seeds of transgenic soybeans, although low-level expression was also detected in the leaves. In situ hybridization indicated that the 11 kDa delta-zein mRNA was expressed predominantly in transitional cells located between the vascular tissue and storage parenchyma cells. Immunohistochemistry of developing transgenic soybeans revealed that the accumulation of the 11 kDa delta-zein occurred primarily in these transitional cells. Expression of the 11 kDa delta-zein gene in transgenic soybean resulted in the formation of two endoplasmic reticulum-derived protein bodies that were designated as either spherical or complex. Immunocytochemical localization demonstrated that both the spherical and complex protein bodies accumulated the 11 kDa delta-zein. Although expression of the 11 kDa delta-zein gene elevated the methionine content of the alcohol-soluble protein fraction 1.5-1.7-fold above that of the non-transgenic line, the overall methionine content of seed flour was not increased. Our results suggest that the confined expression of the 11 kDa delta-zein gene in transitional cells could be limiting the increase in methionine content in transgenic soybean seeds.
大豆(Glycine max (L.) Merr.)是人类饮食和动物饲料中的重要蛋白质来源。然而,大豆种子蛋白的硫含量对于日粮配方而言并不理想。因此,提高大豆种子蛋白中的蛋氨酸和半胱氨酸含量将提升这种广泛使用的豆类的营养品质。我们之前报道过从玉米(Zea mays L.)自交系W23a1的胚乳中分离出一种富含蛋氨酸的11 kDa δ-玉米醇溶蛋白[Kim, W.-S. 和 Krishnan, H.B.(2003年)玉米自交系B73和W23a1中富含蛋氨酸的δ-玉米醇溶蛋白的等位基因变异和差异表达。《植物》,217卷,66 - 74页]。利用农杆菌介导的转化,将一个由克隆的δ-玉米醇溶蛋白基因的编码区在β-伴大豆球蛋白α'-启动子调控下组成的构建体导入大豆基因组。11 kDa δ-玉米醇溶蛋白基因在转基因大豆种子中表达,不过在叶片中也检测到了低水平表达。原位杂交表明11 kDa δ-玉米醇溶蛋白mRNA主要在位于维管组织和贮藏薄壁细胞之间的过渡细胞中表达。对发育中的转基因大豆进行免疫组织化学分析显示,11 kDa δ-玉米醇溶蛋白的积累主要发生在这些过渡细胞中。11 kDa δ-玉米醇溶蛋白基因在转基因大豆中的表达导致形成了两种源自内质网的蛋白体,分别被命名为球形蛋白体或复合蛋白体。免疫细胞化学定位表明球形和复合蛋白体都积累了11 kDa δ-玉米醇溶蛋白。尽管11 kDa δ-玉米醇溶蛋白基因的表达使醇溶蛋白组分中的蛋氨酸含量比非转基因品系提高了1.5 - 1.7倍,但种子粉的总体蛋氨酸含量并未增加。我们的结果表明,11 kDa δ-玉米醇溶蛋白基因在过渡细胞中的局限性表达可能限制了转基因大豆种子中蛋氨酸含量的增加。