首页> 外文期刊>Journal of Bioscience and Bioengineering >Carbohydrate profiling in seeds and seedlings of transgenic triticale modified in the expression of sucrose:sucwse-l-fructosyltransferase (1-SST) and sucrose:fructan-6-fructosyltransferase (6-SFT)
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Carbohydrate profiling in seeds and seedlings of transgenic triticale modified in the expression of sucrose:sucwse-l-fructosyltransferase (1-SST) and sucrose:fructan-6-fructosyltransferase (6-SFT)

机译:在蔗糖:蔗糖-1-果糖基转移酶(1-SST)和蔗糖:果聚糖-6-果糖基转移酶(6-SFT)的表达中修饰的转基因小黑麦种子和幼苗中的碳水化合物分布

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摘要

Constructs with sucrose-sucrose 1-fructosyItransferase (1-SST) from rye and or sucrose-fructan 6-fructosyltransferase (6-SFT) from wheat were placed under the control of wheat aleurone-specific promoter and expressed in triticale using biolistic and microspore transformation. Transgenic lines expressing one or both the 1-SST and the 6-SFT accumulated 50% less starch and 10-20 times more fructan, particularly 6-kestose, in the dry seed compared to the untransformed wild-type (WT) triticale; other fructans ranged in size from DP 4 to DP 15. During germination from 1 to 4 days after imbibition (dai), fructans were rapidly metabolized and only in transgenic lines expressing both 1-SST and 6-SFT were fructan contents significantly higher than in the untransformed controls after 4 days. In situ hybridization confirmed expression of 6-SFT in the aleurone layer in imbibed seeds of transformed plants. When transgenic lines were subjected to a cold stress of 4°C for 2 days, synthesis of fructan increased compared to untransformed controls during low-temperature germination. The increase of fructan in dry seed and germinating seedling was generally associated with transcript expression levels in transformed plants but total gene expression was not necessarily correlated with the time course accumulation of fructan during germination. This is the first report of transgenic modification of cereals to achieve production of fructans in cereal seeds and during seed germination.
机译:将来自黑麦的蔗糖-蔗糖1-果糖I转移酶(1-SST)和来自小麦的蔗糖-果糖6-果糖基转移酶(6-SFT)的构建体置于小麦糊粉蛋白特异性启动子的控制下,并使用生物弹和小孢子转化法在黑小麦中表达。与未转化的野生型黑小麦相比,表达1-SST和6-SFT之一或二者的转基因品系在干燥种子中积累的淀粉少50%,果聚糖,特别是6-果糖多10-20倍;其他果聚糖的大小从DP 4到DP 15不等。在吸收(dai)后1到4天的发芽过程中,果聚糖迅速代谢,仅在表达1-SST和6-SFT的转基因品系中,果聚糖的含量明显高于4天后未转化的对照。原位杂交证实了6-SFT在转化植物吸收种子的糊粉层中表达。当转基因品系受到4°C的冷胁迫2天时,低温萌发期间果聚糖的合成与未转化的对照相比增加。干果和发芽幼苗中果聚糖的增加通常与转化植物中转录本的表达水平相关,但总基因表达不一定与果聚糖在发芽过程中的时间过程积累相关。这是对谷物进行转基因修饰以实现谷物种子中和种子发芽过程中果聚糖产量的首次报道。

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