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Deletion of high-molecular-weight glutenin subunits in wheat significantly reduced dough strength and bread-baking quality

机译:缺失小麦的高分子量谷蛋白亚基显着降低了面团强度和面包烘烤质量

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摘要

Abstract Background High-molecular-weight glutenin subunits (HMW-GS) play important roles in the elasticity of dough made from wheat. The HMW-GS null line is useful for studying the contribution of HMW-GS to the end-use quality of wheat. Methods In a previous work, we cloned the Glu-1E b x gene from Thinopyrum bessarabicum and introduced it into the wheat cultivar, Bobwhite. In addition to lines expressing the Glu-1E b x gene, we also obtained a transgenic line (LH-11) with all the HMW-GS genes silenced. The HMW-GS deletion was stably inherited as a dominant and conformed to Mendel’s laws. Expression levels of HMW-GS were determined by RT-PCR and epigenetic changes in methylation patterns and small RNAs were analyzed. Glutenins and gliadins were separated and quantitated by reversed-phase ultra-performance liquid chromatography. Measurement of glutenin macropolymer, and analysis of agronomic traits and end-use quality were also performed. Results DNA methylation and the presence of small double-stranded RNA may be the causes of post-transcriptional gene silencing in LH-11. The accumulation rate and final content of glutenin macropolymer (GMP) in LH-11 were significantly lower than in wild-type (WT) Bobwhite. The total protein content was not significantly affected as the total gliadin content increased in LH-11 compared to WT. Deletion of HMW-GS also changed the content of different gliadin fractions. The ratio of ω-gliadin increased, whereas α/β- and γ-gliadins declined in LH-11. The wet gluten content, sedimentation value, development time and stability time of LH-11 were remarkably lower than that of Bobwhite. Bread cannot be made using the flour of LH-11. Conclusions Post-transcriptional gene silencing through epigenetic changes and RNA inhibition appear to be the causes for the gene expression deficiency in the transgenic line LH-11. The silencing of HMW-GW in LH-11 significantly reduced the dough properties, GMP content, wet gluten content, sedimentation value, development time and stability time of flour made from this wheat cultivar. The HMW-GS null line may provide a potential material for biscuit-making because of its low dough strength.
机译:摘要背景高分子量谷蛋白亚基(HMW-GS)在小麦制成的面团弹性中起重要作用。 HMW-GS空线对于研究HMW-GS对小麦的最终使用质量的贡献有用。方法在先前的工作中,我们将Glu-1E B X基因克隆到薄孔Bessarabicum,并将其引入小麦品种,鲍勃特。除了表达Glu-1E B X基因的线外,还通过沉默的所有HMW-GS基因获得转基因系(LH-11)。 HMW-GS删除稳定地遗传为占主导地位,并符合孟德尔的法律。通过RT-PCR测定HMW-GS的表达水平,分析甲基化图案中的表观遗传变化和小RNA。通过反相超高效液相色谱法分离并定量谷蛋白和胶质苷。还进行了谷蛋白大聚合物的测量,以及农艺性状分析和农艺性状和最终用途质量。结果DNA甲基化和小双链RNA的存在可能是LH-11中转录后基因沉默的原因。 LH-11中谷蛋白大聚合物(GMP)的累积率和最终含量显着低于野生型(WT)鲍勃特。与wt相比,随着LH-11的总胶质蛋白含量增加,蛋白质含量没有显着影响。 HMW-GS的缺失也改变了不同的胶林蛋白分数的含量。 ω-gliadin的比例增加,而α/β-和γ-胶质剂在LH-11中下降。 LH-11的湿筋含量,沉积值,发育时间和稳定时间显着低于鲍勃特。面包不能使用LH-11的面粉进行。结论转录后基因通过表观遗传变化和RNA抑制似乎是转基因系LH-11中基因表达缺乏的原因。 LH-11中HMW-GW的沉默显着降低了面粉的面团特性,GMP含量,湿麸质含量,沉降价值,开发时间和稳定时间由这种小麦品种制成的面粉。由于其低的面团强度,HMW-GS空线可以提供用于饼干的潜在材料。

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