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Transgenic expression of phytase and acid phosphatase genes in alfalfa (Medicagosativa) leads to improved phosphate uptake in natural soils

机译:紫花苜蓿(Medicagosativa)中植酸酶和酸性磷酸酶基因的转基因表达可改善天然土壤中的磷酸盐吸收

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摘要

Alfalfa (Medicagosativa L.) is one of the most widely grown crops in the USA. Phosphate (P) deficiency is common in areas where forage crops are grown. To improve the use of organic phosphate by alfalfa, two Medicagotruncatula genes, phytase (MtPHY1) and purple acid phosphatase (MtPAP1), were overexpressed in alfalfa under the control of the constitutive CaMV35S promoter or the root-specific MtPT1 promoter. Root enzyme activity analyses revealed that although both genes lead to similar levels of acid phosphatase activities, overexpression of the MtPHY1 gene usually results in a higher level of phytase activity than overexpression of the MtPAP1 gene. The MtPT1 promoter was more effective than the CaMV35S promoter in regulating gene expression and extracellular secretion under P-deficient conditions. Measurement of growth performance of the transgenic lines further proved that the best promoter–gene combination is the MtPHY1 gene driven by the MtPT1 promoter. Compared to the control, the plants with high levels of transgene expression showed improved growth. The biomass of several transgenic lines was three times that of the control when plants were grown in sand supplied with phytate as the sole P source. When the plants were grown in natural soils without additional P supplement, the best performing transgenic lines produced double the amount of biomass after 12 weeks (two cuts) of growth. Transgene effects were more obvious in soil with lower pH and lower natural P reserves than in soil with neutral pH and relatively higher P storage. The total P concentration in leaf tissues of the high-expressing transgenic lines was significantly higher than that of the control. The transgenes have great potential for improving plant P acquisition and biomass yield in P-deficient agricultural soils.Electronic supplementary materialThe online version of this article (doi:10.1007/s11032-011-9628-0) contains supplementary material, which is available to authorized users.
机译:苜蓿(Medicagosativa L.)是美国种植最广泛的农作物之一。缺乏草饲料的地区普遍存在磷缺乏症。为了改善苜蓿对有机磷酸盐的利用,在组成型CaMV35S启动子或根特异性MtPT1启动子的控制下,苜蓿中有两个Medicagotruncatula基因植酸酶(MtPHY1)和紫色酸性磷酸酶(MtPAP1)过表达。根酶活性分析表明,尽管两个基因都导致相似水平的酸性磷酸酶活性,但MtPHY1基因的过表达通常会导致植酸酶活性的水平高于MtPAP1基因的过表达。在缺磷条件下,MtPT1启动子比CaMV35S启动子更有效地调节基因表达和细胞外分泌。测量转基因品系的生长性能进一步证明,最佳的启动子-基因组合是由MtPT1启动子驱动的MtPHY1基因。与对照相比,具有高水平转基因表达的植物显示出改善的生长。当植物在提供植酸作为唯一磷源的沙中生长时,几种转基因品系的生物量是对照的三倍。当植物生长在不含其他磷补充剂的天然土壤中时,表现最佳的转基因品系在生长12周(两次切割)后产生的生物量增加了一倍。 pH值较低和天然P储量较低的土壤中的转基因效应比pH值中性和P相对较高的土壤中的转基因效应更为明显。高表达转基因株系叶片组织中的总磷浓度显着高于对照。转基因具有改善缺磷农业土壤中植物P的获取和生物量产量的巨大潜力。电子补充材料本文的在线版本(doi:10.1007 / s11032-011-9628-0)包含补充材料,可授权使用用户。

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