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首页> 外文期刊>Journal of Inorganic Biochemistry: An Interdisciplinary Journal >A proteomic approach to the mechanisms underlying activation of aluminium resistance in roots of Urochloa decumbens
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A proteomic approach to the mechanisms underlying activation of aluminium resistance in roots of Urochloa decumbens

机译:一种蛋白质组学方法,其含铝耐铝耐铝耐铝抗性的抗性

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The mechanisms of extreme Al-resistance in Urochloa decumbens are not established. Full resistance expression requires a lag time of 72-96 h and is preceded by a sensitive phase (24-48 h) with Al-induced root growth inhibition. The aim here was to identify key processes of the activation phase of Al-resistance analysing both root exudates and comparative root proteome. Samples were taken after 0, 24 and 96 h exposure to 0 or 200 mu M Al. Al-induced stimulation of citrate and oxalate efflux was limited to the sensitive phase. Only 11 proteins revealed Al-induced abundance differences; six were identified. After 24 h, phenylalanine ammonium lyase (PAL), methionine synthase (MS), and deoxymugineic acid synthase (DMAS) decreased, while acid phosphatase (APase) abundance increased. Coincident with growth recovering, PAL and MS, but not DMAS, returned to initial levels. After 96 h, gamma-carbonic anhydrase (gamma-CA) and adenylate kinase (AK) along with two unidentified proteins were more abundant. In conclusion, few protein changes characterize the initial response to Al in signalgrass. During the alarm phase, changes are related to P-mobilization, downregulation of Fe-acquisition, reduction of phenolic biosynthesis, and small stimulation of organic acid exudation. After recovering (resistant phase), biosynthesis of phenolics and methionine, but not Fe-mobilization are re-established. Full expression of Al-resistance is characterized by enhanced gamma-CA mediating mitochondrial complex I assembly and increased AK abundance indicating higher root respiration and better provision of ADP and Mg2+ to ATP synthase, respectively. The unidentified proteins and the specific role of gamma-CA in Al resistance of U. decumbens will centre future research.
机译:不建立Urochloa Depumbens的极端抗性的机制。全抗性表达需要72-96小时的滞后时间,并且在敏感相(24-48h)之前,具有Al诱导的根生长抑制。这里的目的是识别抗性分析的抗性阶段的关键过程分析根部渗出物和对比根蛋白质。在0,24和96小时暴露于0或200μm,得到样品。 Al诱导的柠檬酸盐和草酸异化的刺激限于敏感阶段。只有11个蛋白质揭示了Al诱导的丰富差异;六次被确定。 24小时后,苯丙氨酸氨酶(PAL),甲硫氨酸合酶(MS)和脱氧氨酰酸合酶(DMA)降低,而酸性磷酸酶(APase)丰度增加。与生长恢复,PAL和MS相一致,但不是DMA,返回初始层面。在96小时后,γ-碳酸酐酶(Gamma-Ca)和腺苷酸激酶(Ak)以及两个未识别的蛋白质更丰富。总之,很少有蛋白质变化表征对信号的初始反应。在报警阶段期间,变化与P-Mobilization有关,下调Fe-获取,减少酚类生物合成,以及对有机酸渗出的小刺激。恢复(抗阶段)后,重新建立酚类和蛋氨酸的生物合成,但不是Fe-Mobilization。通过增强的γ-Ca介导的线粒体复合物I组装和增加A10呼吸和更好地提供ADP和MG2 +至ATP合酶的AK丰度,表达了抗性的γ-CA的性能。未识别的蛋白质和γ-CA在U. Depumbens中的γ-CA在U. Depumbens中的特定作用。

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