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1.
盐生植物是研究植物耐盐分子机制和分离耐盐基因的良好材料,可以反映植物对盐胁迫的适应策略。综述盐生植物响应盐胁迫的转录因子、渗透平衡调节、离子平衡调节、氧化还原平衡调节、光合作用调节及代谢变化,反映盐生植物在多个方面适应盐胁迫的策略。此外,还对盐生植物耐盐分子机制的研究前景作了展望。  相似文献   

2.
植物抗盐分子机制及作物遗传改良耐盐性的研究进展   总被引:2,自引:0,他引:2  
盐胁迫是全球农业生产上的一个主要逆境因子。解析耐盐分子机制有助于培育耐盐能力提高的作物新品种。我们综述了植物对盐胁迫的感应及信号传导、主要Na^+运输体、盐胁迫下的解毒途径以及耐盐途径中涉及到的表观遗传研究。此外,我们还讨论了利用遗传改良手段提高作物耐盐性的研究进展。  相似文献   

3.
藜科盐生植物的形态特征与耐盐分子机理研究进展   总被引:1,自引:0,他引:1  
在非生物环境胁迫因子中,盐胁迫是造成农作物减产的主要因素之一.从藜科植物耐盐的形态生理学机制和分子生物学角度入手,讨论了藜科植物耐盐基因工程的新进展,探讨藜科盐生植物的盐胁迫机理,为利用基因工程手段培育耐盐植物奠定基础.  相似文献   

4.
盐腺是泌盐盐生植物抵御盐胁迫的重要表皮结构,泌盐盐生植物可以通过盐腺将体内多余的盐离子排出体外,从而避免盐胁迫。盐腺作为泌盐盐生植物实现高效抗盐的重要结构,在逆境生理、发育和进化等领域都引起了关注和讨论,集中在盐腺的超微结构、生理功能、泌盐机制以及发育模式等不同层面已有广泛的研究报道。本文综述了盐腺结构、分泌机制、盐腺发育的研究进展,总结了盐腺泌盐的可能途径以及盐腺发育的调控方式和关键基因,对未来盐腺泌盐和发育的研究提出了相关见解,讨论了盐腺这一独特形态学结构对于植物耐盐性的作用,并对提高植物耐盐性、培育耐盐品种提出了理论依据和建议,有利于深入解析植物耐盐适应演化、培育抗盐作物和高效利用盐碱地。  相似文献   

5.
植物耐盐性机理研究进展   总被引:56,自引:6,他引:50  
廖岩  彭友贵  陈桂珠 《生态学报》2007,27(5):2077-2089
在盐胁迫下环境中某些植物会在发生一些变化。从生理学、生物化学、盐胁迫分子学机制的角度对植物对盐胁迫的反应研究进行了回顾,并提供了一些目前知识水平上能增加植物盐耐性的方法。解释了在盐胁迫下植物的离子吸收、相溶性物质、抗氧化酶、植物激素、光合作用等方面的变化规律,其中也有耐盐植物功能调节的研究,这有助于从多学科研究的角度评估盐胁迫的生态重要性。  相似文献   

6.
以较耐盐花生品种‘花育25’、‘鲁花12’和盐敏感品种‘海花1’、‘花育20’为材料,采用盆栽试验,设置0、1.0、2.0、3.0 g/kg土壤NaCl胁迫浓度梯度,测定其净光合速率、表观量子效率、气孔导度等光合特性,以及抗氧化酶活性和渗透调节物质含量等指标,明确NaCl胁迫条件下不同耐盐性花生品种光合和生理生化特性的适应特征。结果表明:(1)NaCl胁迫明显抑制各品种花生叶片光合作用,净光合速率随盐胁迫浓度的升高呈明显降低的趋势。(2)各品种花生叶片净光合速率均先随光照强度的增强而升高,当光强达到一定数值时趋于平稳;光补偿点和光饱点因品种和盐胁迫浓度差异较大,较高的盐胁迫浓度使叶片光补偿点升高,盐敏感品种的光饱和点降低。(3)盐胁迫条件下,各品种叶片表观量子效率和最大净光合速率均随盐胁迫强度的增加呈显著降低趋势,盐敏感品种利用弱光的能力在低盐胁迫下强于耐盐品种,其最大净光合速率在较高盐胁迫浓度(3.0 g/kg)下明显低于耐盐品种,但两类品种的叶片表观量子效率降幅相近(78.65%~88.00%)。(4)在NaCl胁迫下,耐盐品种叶片自由水含量显著高于盐敏感品种;在2.0~3.0 g/kg NaCl胁迫下,耐盐品种叶片SOD、CAT、POD活性和MDA含量的升降幅度均低于盐敏感品种;耐盐品种在NaCl浓度低于2.0 g/kg时的抗氧化能力明显高于盐敏感品种。研究发现,盐胁迫下花生品种抗盐耐逆的主要生理响应特征是提高光补偿点和最大净光合速率,增强叶片持水能力和物质代谢能力,以及提升抗氧化和渗透调节能力。  相似文献   

7.
高粱不同器官生长对NaCl胁迫的响应及其耐盐阈值   总被引:3,自引:0,他引:3  
用砂基培养研究高粱不同器官生长对NaCl胁迫的响应及其耐盐阈值。NaCl胁迫下,独角虎和糖高粱均表现为生长叶叶鞘鲜重下降最大,其次是生长叶叶片、成熟叶叶鞘和叶片变化最小。长期胁迫单株叶片数及叶面积也明显下降。相同胁迫情况下,糖高梁的生长抑制明显大于独角虎。独角虎和糖高粱耐盐阈值分别为135和82mmol/LNaCI。以上结果表明独角虎耐盐能力明显大于糖高粱。讨论了不同器官生长抑制的机制。  相似文献   

8.
盐逆境下转基因耐盐小麦与其受体呼吸途径的动态变化   总被引:4,自引:0,他引:4  
以转基因耐盐品种89122和其受体陇春13号两种小麦为实验材料,研究科幼苗在不同盐浓度胁迫下呼吸途径动态变化。结果表明,89122出现盐呼吸明显迟于其受体;两听Valt与ρValt变化并不同步,且Valt均受高盐浓度的抑制,但低盐浓度能诱导其受体的Valt;两品种的ρValt与ρ′Vcyt彼此协同调节适应盐境,且ρ′Vcyt仍是盐胁迫过程中线粒体电子传递的主要途径。同时讨论了盐逆境下抗氰呼吸的一些  相似文献   

9.
植物响应盐胁迫组学研究进展   总被引:3,自引:0,他引:3  
盐胁迫对植物生长的影响主要表现在离子毒害、渗透胁迫以及次级氧化胁迫等,植物遭受盐胁迫时迅速启动相关基因,进行转录调控,进而合成相应蛋白质来控制代谢物合成和离子转运以调节渗透平衡。随着现代分子生物学迅速发展,对植物耐盐机理研究也深入到了转录组、蛋白质组、代谢组及离子组等水平,"组学"研究为耐盐基因鉴定及标志性代谢物的挖掘等提供了有力手段。该文对近年来国内外有关转录组学、蛋白质组学、代谢组学、离子组学的主要研究方法及在盐胁迫中的应用研究进展进行综述,以揭示植物耐盐机理,为优良耐盐碱植物的筛选与培育提供支持。  相似文献   

10.
植物盐胁迫应答蛋白质组学分析   总被引:3,自引:0,他引:3  
张恒  郑宝江  宋保华  王思宁  戴绍军 《生态学报》2011,31(22):6936-6946
土壤盐渍化是限制植物生长和分布的关键因素之一,揭示植物盐胁迫应答的分子机理是借助分子生物学手段提高植物耐盐性的基础.近年来,人们利用高通量蛋白质组学技术分析了拟南芥、水稻等19种植物的盐胁迫应答蛋白质表达图谱.从植物类群(盐生植物和甜土植物)、组织器官(根、地上部分/茎、胚根和胚轴、叶片、花序和配子体)、细胞(悬浮培养细胞、愈伤组织细胞和单细胞生物)和亚细胞结构(叶绿体、质膜和质外体)几方面整合分析了植物盐胁迫应答蛋白质组表达模式特征,主要特征包括:(1)盐生植物通过全面调节细胞骨架重塑、离子转运和区隔化、渗透平衡、活性氧(ROS)清除、信号转导、光合作用和能量代谢等信号与代谢网络体系,获得相对较高的抗/耐盐能力;(2)植物地上部分(叶片、茎、配子体)或光合组织细胞(悬浮培养细胞、愈伤组织细胞和单细胞盐藻)通过调节参与光合作用、碳和能量代谢、ROS清除过程蛋白质的表达模式应对盐胁迫环境;(3)植物地下部分(根、胚根)通过调控信号转导和离子转运相关蛋白质感知/传递盐胁迫信号并维持离子平衡;(4)花序中参与渗透调节、转录调控、蛋白质加工和ROS清除的蛋白质在盐胁迫条件下变化显著;(5)叶绿体通过调控参与光合作用、蛋白质加工和周转,以及氧化还原系统平衡等过程应对盐胁迫;(6)质外体中参与细胞壁代谢、胁迫防御和信号转导过程的蛋白质受盐胁迫影响明显;(7)细胞膜中参与维持膜结构稳定、物质/离子运输和信号转导过程的蛋白质对植物盐胁迫应答具有重要作用.这些分析为深入研究植物耐盐的分子机制提供了重要信息.  相似文献   

11.
榄仁树的生态分布与耐盐性研究   总被引:2,自引:0,他引:2  
调查了榄仁树(Terminalia catappa)在海南岛沿海地区的分布情况,并就基质盐度对温室中人工培育的榄仁幼苗的影响进行研究。结果表明,榄仁具有较强的耐盐能力,在盐度高达17.09‰条件下仍可正常生长,温室里幼苗可在10‰左右的盐度下存活。结果还表明,10‰盐度能增加幼苗叶片叶绿素含量,20‰~30‰则下降;盐胁迫下叶片光合速率呈下降趋势,而叶片可溶性糖含量则随盐度增加呈上升趋势。  相似文献   

12.

Key message

The role of transporters in imparting salt tolerance to mangroves is not yet understood. Identification of the role of transporters in halophytes is promising, as far as the development of genetically engineered salt tolerant crops is concerned.

Abstract

Mangroves are models for stress tolerance and they provide a reservoir for some of the novel genes and proteins, involved in salt tolerance. Biochemical or physiological mechanisms contribute to salt tolerance depending on variations in the environment. A great deal of research on salinity tolerance of plants, probes into water relations, photosynthesis, and accumulation of various in-organic ions and organic metabolites. The ability of the plant to react to high salinity depends on the genes that are expressed during stress. The mechanism of salinity tolerance becomes complicated when the responses of plants varies with salinity and environmental conditions. During the onset and development of salt stress within a plant, major processes such as photosynthesis, protein synthesis and lipid metabolisms are affected. The present review attempts to dissect out the role of transporters in salt tolerance of mangroves.  相似文献   

13.
Halophyte species demonstrate differing levels of salt tolerance. Understanding interspecific variation to salinity levels is of value from both the scientific perspective, which includes the identification of traits associated with salinity tolerance, as well as from an applied perspective, which includes identifying plant species for specific salinity restoration and remediation projects. This paper investigates the effects of salinity on germination of 12 Australian species of the plant genus Frankenia L. (Frankeniaceae). We use saline solutions that corresponded to the average soil–water salinity concentrations in the arid zones of inland Australia. These solutions consisted of 10 mM calcium chloride, 30 mM magnesium sulphate, and 450 mM sodium chloride. The aims of our study were: (1) to investigate the germination (germination rates, germination success) of Frankenia seeds to four salinity levels (0%, 10%, 20%, 30%), (2) to test for possible interaction effects between seed mass, germination, and salinity, and (3) to examine the effect of salinity levels on the inhibition of germination and/or seed damage. Species varied in their salt tolerance for germination rates and success. Species with larger seeds had higher germination rates and germination success for high salinity levels. Several species did not germinate well at any salinity level. Finally, no seeds were adversely affected by exposure to high salinity levels pre-germination. There is potential for including some Frankenia species in remediation and revegetation projects in areas affected by salinity, and also as garden plants in saline regions.  相似文献   

14.
Salinity reduces substrate water potential, thereby restricting water and nutrient uptake by plants; salinity may also cause ionic imbalance and toxicity. Because substrate salinity fluctuates through the growing season, a plant may be exposed to different salinity levels, at various stages of development, with potentially significant consequences on population dynamics. Here, we present the results of a study of the effect of substrate salinity on seed germination, seedling emergence, and growth of Aster laurentianus, an annual marsh plant, endemic to the Gulf of St. Lawrence and potentially threatened. Seed germination was reduced in low salt concentration (10 g sea salt/L) and completely inhibited by salinity levels >/=20 g sea salt/L. However, this inhibiting effect was reversible: seeds from the salt treatments germinated readily after being washed in distilled water. Though seedling emergence was diminished at low salinity levels, postemergence survival was little affected. Plant growth was reduced, but net carbon assimilation rate was not affected by high salinity levels. Increased root respiration and respiratory costs associated with salt tolerance might have contributed to lower C accumulation at higher salinity levels. All developmental processes considered are thus negatively affected by substrate salinity, with potentially significant consequences on population abundance and distribution in salt marshes. Yet, the tolerance of this species to high salinity levels after seedling emergence is remarkable. Seed germination represents a major bottleneck in the species life cycle, potentially controlling local distribution and abundance in the natural habitat.  相似文献   

15.
High densities of Tylenchulus semipenetrans and slow decline symptoms are dominant in citrus-producing areas with high salinity. Currently, no commercial citrus rootstock is both nematode-resistant and salt-tolerant. Interaction effects of citrus rootstocks, salinity and T. semipenetrans were evaluated for the partitioning of salinity ions (Cl and Na) and K in microplots. Treatments comprised six citrus rootstocks with wide ranges of salt tolerance, 0 and 3 mols NaCl + 0.25 mols CaCl2 l−1 water and 0 and 856 300 nematodes. At harvest, eight months after salinity treatments, the three–factor interaction was significant (P=0.05) for the alteration in the partitioning of salinity ions and K. Nematodes generally increased salinity ions in leaves and reduced salinity ions in roots and K in both leaves and roots. Thus, management of nematodes is critical in areas with salinity problems.  相似文献   

16.
盐胁迫下不同水稻种质形态指标与耐盐性的相关分析   总被引:22,自引:4,他引:18  
选用中国、韩国和国际水稻研究所(IRRI)不同耐盐能力的籼、粳、爪哇稻16份为材料进行芽期和苗期试验。随着NaCl浓度增加,种子开始发芽的时间推迟、发芽过程延长、发芽率降低;品种的发芽率能有效地指示其芽期耐盐能力。NaCl浓度对许多苗期形态指标有显影响,其中叶片盐害指数能反映品种的苗期耐盐能力;随着NaCl处理时间的增长,叶片盐害指数与NaCl浓度间的相关性越来越大。同一品种在芽期的耐盐能力和苗期表现不一致,两的相关系数很低。  相似文献   

17.
Pruthi  Rajat  Puram  Venkata Ramana Rao  Ontoy  John  Subudhi  Prasant K. 《Genetica》2022,150(5):273-288
Genetica - Rice is highly vulnerable to salt stress at both seedling and flowering stage. While research efforts largely focused on seedling stage salinity tolerance, flowering stage salt tolerance...  相似文献   

18.
High soil salinity negatively influences plant growth and yield. Some taxa have evolved mechanisms for avoiding or tolerating elevated soil salinity, which can be modulated by the environment experienced by parents or offspring. We tested the contribution of the parental and offspring environments on salinity adaptation and their potential underlying mechanisms. In a two-generation greenhouse experiment, we factorially manipulated salinity concentrations for genotypes of Medicago truncatula that were originally collected from natural populations that differed in soil salinity. To compare population level adaptation to soil salinity and to test the potential mechanisms involved we measured two aspects of plant performance, reproduction and vegetative biomass, and phenological and physiological traits associated with salinity avoidance and tolerance. Saline-origin populations had greater biomass and reproduction under saline conditions than non-saline populations, consistent with local adaptation to saline soils. Additionally, parental environmental exposure to salt increased this difference in performance. In terms of environmental effects on mechanisms of salinity adaptation, parental exposure to salt spurred phenological differences that facilitated salt avoidance, while offspring exposure to salt resulted in traits associated with greater salt tolerance. Non-saline origin populations expressed traits associated with greater growth in the absence of salt while, for saline adapted populations, the ability to maintain greater performance in saline environments was also associated with lower growth potential in the absence of salt. Plastic responses induced by parental and offspring environments in phenology, leaf traits, and gas exchange contribute to salinity adaptation in M. truncatula. The ability of plants to tolerate environmental stress, such as high soil salinity, is likely modulated by a combination of parental effects and within-generation phenotypic plasticity, which are likely to vary in populations from contrasting environments.  相似文献   

19.
Saline or alkaline soils present a strong stress on plants that together may be even more deleterious than alone. Australia''s soils are old and contain large, sometimes overlapping, areas of high salt and alkalinity. Acacia and other Australian plant lineages have evolved in this stressful soil environment and present an opportunity to understand the evolution of salt and alkalinity tolerance. We investigate this evolution by predicting the average soil salinity and pH for 503 Acacia species and mapping the response onto a maximum-likelihood phylogeny. We find that salinity and alkalinity tolerance have evolved repeatedly and often together over 25 Ma of the Acacia radiation in Australia. Geographically restricted species are often tolerant of extreme conditions. Distantly related species are sympatric in the most extreme soil environments, suggesting lack of niche saturation. There is strong evidence that many Acacia have distributions affected by salinity and alkalinity and that preference is lineage specific.  相似文献   

20.
Breeding for salt tolerance in crop plants is envisaged as one way to combat a worldwide problem of increasing soil salinity in agricultural land. Tissue culture techniques may prove valuable as a means of achieving this goal. In this review, reports of the selection and characterization of plant cell cultures tolerant to excess salt are assessed, in the context of variability from tissue culture and the significance of cellular physiological adaptation to salinity. The examples of plant regeneration from salt grown cell cultures are also outlined, with emphasis on correlation to the effect of salt on cell cultures, genetic variability for salt tolerance in vitro, and the value of regenerates in the development of salt tolerant plants.  相似文献   

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