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Ammonium stress and supplemental calcium influence growth of in vitro cultured blueberry plantlets

机译:铵胁迫和补充钙对体外培养的蓝莓植物生长

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Background of the study - Salt damage has recently become a serious problem worldwide. Though ammonium-N is widely used as the main N source for growth of blueberry, few studies on ammonium damage to blueberry were reported. Objectives - The current research aimed to explore the effects of ammonium stress and supplemental calcium on blueberry growth using an in vitro model. Methods - In vitro cultured blueberry plantlets subjected to 1/4 MS itself containing 0.005M NH4+, 1/4 MS containing 0.01M NH4+, 1/4 MS containing 0.02M NH4+, 1/4 MS containing 0.02M NH4+ plus 0.01M Ca2+. Plant biomass, nutrient compositions and anti-oxidants in plantlets were analyzed. Results - Ammonium stress induced by 0.02M NH4+ significantly inhibited growth of in vitro cultured blueberry. Plants under ammonium stress showed the highest contents of N and Fe, and lowest contents of K, Ca, Mg and Mn. Ammonium stress also significantly inhibited contents of proline (Pro), Methane Dicarboxylic Aldehyde (MDA), soluble protein (SP) and the activity of superoxide dismutase (SOD), and promoted the activities of catalase (CAT), peroxidase (POD) and glutamine synthetase (GS). 0.01M supplemental Ca2+ proved to enhance the growth of blueberry plantlets exposed to ammonium stress with the obviously increased contents of K, Ca, Mg and Mn, Pro, MDA, SP and the increased activity of SOD. Close correlations were observed among plant biomass, nutrient compositions and anti-oxidants in blueberry plantlets. Conclusions - Ammonium stress affects growth of blueberry plantlets by regulating the allocation of nutrient composition and the anti-oxidant activity, which closely correlate with calcium signaling pathways. Supplemental Ca2+ could prevent ammonium damage. In vitro culture used as a model provides an effective and promising approach for study of plant stress, and a powerful technical support for field management of Vaccinium plants.
机译:研究的背景 - 盐损伤最近在全球范围内成为一个严重的问题。虽然氨基-N被广泛用作蓝莓生长的主要N个来源,但据报道少数关于蓝莓损害的研究。目的 - 目前的研究旨在探讨使用体外模型对蓝莓生长的铵胁迫和补充钙的影响。方法 - 体外培养的蓝莓植株对含有0.01m NH 4 +,1/4 Ms的0.005m NH 4 +,1 / 4ms含有0.02m NH 4 +,1/4 Ms的0.01M NH 4 +,1/4 MS的0.02M NH 4 +加0.01M Ca2 +。分析了植物生物质,营养物质组合物和植物中的抗氧化剂。结果 - 由0.02M NH 4 +诱导的铵胁迫显着抑制体外培养的蓝莓生长。铵胁迫下的植物显示出N和Fe的最高含量,以及K,Ca,Mg和Mn的最低含量。铵胁迫也显着抑制脯氨酸(Pro),甲烷二羧酸醛(MDA),可溶性蛋白质(SP)和超氧化物歧化酶(SOD)的活性,并促进过氧化氢酶(猫),过氧化物酶(POD)和谷氨酰胺的活性合成酶(GS)。 0.01M补充Ca2 +证明增强了暴露于铵胁迫的蓝莓植物的生长,随着K,Ca,Mg和Mn,Pro,MDA,Sp的显然增加,Ca,MDA,Sp和SOD活性的显着增加。在蓝莓植物中的植物生物质,营养成分和抗氧化剂中观察到紧密相关性。结论 - 铵胁迫通过调节营养成分和抗氧化活性的分配来影响蓝莓植物的生长,与钙信号通路密切相关。补充Ca2 +可以防止铵损伤。用作模型的体外培养提供了一种有效和有希望的植物压力研究的方法,以及用于疫苗植物的现场管理的强大技术支持。

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