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RSS FeedsIJMS, Vol. 18, Pages 2458: Cellular Localization of Wheat High Molecular Weight Glutenin Subunits in Transgenic Rice Grain (International Journal of Molecular Sciences)

 
 

18 november 2017 11:35:58

 
IJMS, Vol. 18, Pages 2458: Cellular Localization of Wheat High Molecular Weight Glutenin Subunits in Transgenic Rice Grain (International Journal of Molecular Sciences)
 


Rice (Oryza sativa L.) is a primary global food cereal. However, when compared to wheat, rice has poor food processing qualities. Dough that is made from rice flour has low viscoelasticity because rice seed lacks storage proteins that are comparable to gluten protein from wheat. Thus, current research efforts aim to improve rice flour processing qualities through the transgenic expression of viscoelastic proteins in rice seeds. In this study, we characterized the transgenic expression of wheat glutenin subunits in rice seeds. The two genes 1Dx5_KK and 1Dy10_JK, which both encode wheat high-molecular-weight glutenin subunits that confer high dough elasticity, were cloned from Korean wheat cultivars KeumKang and JoKyung, respectively. These genes were inserted into binary vectors under the control of the rice endosperm-specific Glu-B1 promoter and were expressed in the high-amylose Korean rice cultivar Koami (Oryza sativa L.). Individual expression of both glutenin subunits was confirmed by SDS-PAGE and immunoblot analyses performed using T3 generation of transgenic rice seeds. The subcellular localization of 1Dx5_KK and 1Dy10_JK in the rice seed endosperm was confirmed by immunofluorescence analysis, indicating that the wheat glutenin subunits accumulate in protein body-II and novel protein body types in the rice seed. These results contribute to our understanding of engineered seed storage proteins in rice.


 
112 viewsCategory: Biochemistry, Biophysics, Molecular Biology
 
IJMS, Vol. 18, Pages 2450: New Insights into the Microbiota of Moth Pests (International Journal of Molecular Sciences)
IJMS, Vol. 18, Pages 2455: Identification of Physiological Substrates and Binding Partners of the Plant Mitochondrial Protease FTSH4 by the Trapping Approach (International Journal of Molecular Sciences)
 
 
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