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转基因大豆中大肠杆菌K99菌毛主要抗原亚基FanC的叶绿体靶向

Chloroplast targeting of FanC, the major antigenic subunit of Escherichia coli K99 fimbriae, in transgenic soybean.

作者信息

Garg Renu, Tolbert Melanie, Oakes Judy L, Clemente Thomas E, Bost Kenneth L, Piller Kenneth J

机构信息

Department of Biology, University of North Carolina-Charlotte, 9201 University City Boulevard, Charlotte, NC 28223, USA.

出版信息

Plant Cell Rep. 2007 Jul;26(7):1011-23. doi: 10.1007/s00299-007-0322-y. Epub 2007 Mar 1.

Abstract

Enterotoxigenic Escherichia coli (ETEC) strains are a major cause of enteric diseases affecting livestock and humans. Edible transgenic plants producing E. coli fimbrial subunit proteins have the potential to vaccinate against these diseases, but have not reached their full potential as a renewable source of oral vaccines due in part to insufficient levels of recombinant protein accumulation. Previously, we reported that cytosol targeting of the E. coli K99 fimbrial subunit antigen resulted in FanC accumulation to approximately 0.4% of total soluble protein in soybean leaves (Piller et al. in Planta 222:6-18, 2005). In this study, we report on the subcellular targeting of FanC to chloroplasts. Twenty-two transgenic T1 progeny derived from seven individual T0 transformation events were characterized, and 17 accumulated transgenic FanC. All of the characterized events displayed relatively low T-DNA complexity, and all exhibited proper targeting of FanC to the chloroplast. Accumulation of chloroplast-targeted FanC was approximately 0.08% of total soluble leaf protein, or approximately 5-fold less than cytosol-targeted FanC. Protein analysis of leaves at various stages of maturity suggested stability of chloroplast-targeted FanC throughout leaf maturation. Furthermore, mice immunized intraperitoneally with protein extract derived from transgenic leaves expressing chloroplast-targeted FanC developed significant antibody titers against FanC. This is the first report of subcellular targeting of a vaccine subunit antigen in soybean.

摘要

产肠毒素大肠杆菌(ETEC)菌株是影响家畜和人类的肠道疾病的主要病因。生产大肠杆菌菌毛亚基蛋白的可食用转基因植物有针对这些疾病进行疫苗接种的潜力,但作为口服疫苗的可再生来源尚未发挥其全部潜力,部分原因是重组蛋白积累水平不足。此前,我们报道了将大肠杆菌K99菌毛亚基抗原靶向细胞质可使FanC在大豆叶片中积累至约占总可溶性蛋白的0.4%(Piller等人,《植物》222:6 - 18,2005年)。在本研究中,我们报道了FanC靶向叶绿体的情况。对来自7个独立T0转化事件的22个转基因T1后代进行了表征,其中17个积累了转基因FanC。所有表征的事件显示出相对较低的T - DNA复杂性,并且所有事件都表现出FanC正确靶向叶绿体。靶向叶绿体的FanC积累量约占叶片总可溶性蛋白的0.08%,比靶向细胞质的FanC少约5倍。对不同成熟阶段叶片的蛋白质分析表明,靶向叶绿体的FanC在叶片整个成熟过程中具有稳定性。此外,用表达靶向叶绿体的FanC的转基因叶片的蛋白提取物腹腔注射免疫的小鼠产生了针对FanC的显著抗体滴度。这是大豆中疫苗亚基抗原亚细胞靶向的首次报道。

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