毛白杨幼苗叶片生长及其光合参数和硼转运蛋白基因对高硼胁迫的响应

该研究采用毛白杨(Populus tomentosa)为试验材料,分析了温室条件下沙培幼苗对短期高硼胁迫(1、5、10 mmol/L硼酸)下的叶片生长、光合参数和硼转运蛋白的响应特征。结果显示:(1)与对照(0.05 mmol/L硼酸)相比,1 mmol/L硼酸处理导致毛白杨幼苗叶片叶绿素荧光参数上调,活性氧含量上升,树苗基部叶片出现少量黑色坏死斑;5 mmol/L硼酸胁迫下,叶片净光合速率、气孔导度和蒸腾速率下调,胞间二氧化碳浓度上升,叶绿素荧光参数和过氧化氢含量进一步上调,超氧阴离子含量较1 mmol/L硼酸胁迫时下调但仍然高于对照,除顶部叶片之外的其他叶片上出现大量坏死斑;10 mmol/L硼酸胁迫下,气体交换参数、叶绿素荧光参数和活性氧含量与5 mmol/L硼酸胁迫时相似,所有叶片均在平行于次级叶脉的方向出现呈带状分布的坏死斑。(2)毛白杨幼苗根和茎硼含量在硼胁迫条件下与对照相比变化幅度较小,而叶片硼含量在5 mmol/L和10 mmol/L硼酸胁迫下比对照显著上升,此时硼转移系数和生物富集系数均维持较高的水平。(3)硼转运蛋白(BOR)基因家族成员中PtoBOR4和PtoBOR8在根中的表达水平随着外界硼浓度的增加呈先上升后下降的趋势;在茎中,PtoBOR3基因下调表达,PtoBOR5上调表达;在叶片中,PtoBOR4表达先上升后下降,而PtoBOR7和PtoBOR8上调表达。研究表明,毛白杨幼苗叶片叶绿素荧光参数、活性氧、气体交换参数及硼转运蛋白基因家族表达对高硼胁迫较为敏感,硼胁迫症状在较短的时间内在叶片上以坏死斑的形式出现,可能与其较强的控制根系硼浓度的能力和向地上部分迅速运输硼的能力有关。     

Oryza sativa Lysine‐Histidine‐type Transporter 1 functions in root uptake and root‐to‐shoot allocation of amino acids in rice

In agricultural soils, amino acids can represent vital nitrogen (N) sources for crop growth and yield. However, the molecular mechanisms underlying amino acid uptake and allocation are poorly understood in crop plants. This study shows that rice (Oryza sativa L.) roots can acquire aspartate at soil concentration, and that japonica subspecies take up this acidic amino acid 1.5‐fold more efficiently than indica subspecies. Genetic association analyses with 68 representative japonica or indica germplasms identified rice Lysine‐Histidine‐type Transporter 1 (OsLHT1) as a candidate gene associated with the aspartate uptake trait. When expressed in yeast, OsLHT1 supported cell growth on a broad spectrum of amino acids, and effectively transported aspartate, asparagine and glutamate. OsLHT1 is localized throughout the rice root, including root hairs, epidermis, cortex and stele, and to the leaf vasculature. Knockout of OsLHT1 in japonica resulted in reduced root uptake of amino acids. Furthermore, in ¹⁵N‐amino acid‐fed mutants versus wild‐type, a higher percentage of ¹⁵N remained in roots instead of being allocated to the shoot. ¹⁵N‐ammonium uptake and subsequently the delivery of root‐synthesized amino acids to Oslht1 shoots were also significantly decreased, which was accompanied by reduced shoot growth. These results together provide evidence that OsLHT1 functions in both root uptake and root to shoot allocation of a broad spectrum of amino acids in rice.     

The aromatic/arginine selectivity filter of NIP aquaporins plays a critical role in substrate selectivity for silicon, boron, and arsenic

Nodulin-26-like intrinsic proteins (NIPs) of the aquaporin family are involved in the transport of diverse solutes, but the mechanisms controlling the selectivity of transport substrates are poorly understood. The purpose of this study was to investigate how the aromatic/arginine (ar/R) selectivity filter influences the substrate selectivity of two NIP aquaporins; the silicic acid (Si) transporter OsLsi1 (OsNIP2;1) from rice and the boric acid (B) transporter AtNIP5;1 from Arabidopsis; both proteins are also permeable to arsenite. Native and site-directed mutagenized variants of the two genes were expressed in Xenopus oocytes and the transport activities for Si, B, arsenite, and water were assayed. Substitution of the amino acid at the ar/R second helix (H2) position of OsLsi1 did not affect the transport activities for Si, B, and arsenite, but that at the H5 position resulted in a total loss of Si and B transport activities and a partial loss of arsenite transport activity. Conversely, changes of the AtNIP5;1 ar/R selectivity filter and the NPA motifs to the OsLsi1 type did not result in a gain of Si transport activity. B transport activity was partially lost in the H5 mutant but unaffected in the H2 mutant of AtNIP5;1. In contrast, both the single and double mutations at the H2 and/or H5 positions of AtNIP5;1 did not affect arsenite transport activity. The results reveal that the residue at the H5 position of the ar/R filter of both OsLsi1 and AtNIP5;1 plays a key role in the permeability to Si and B, but there is a relatively low selectivity for arsenite.     

植物对硼元素的吸收转运机制

硼是植物生长发育所必需的微量元素,但是在世界范围内,土壤中硼含量过高或者过低都会对植物生长产生影响,是农业生产上的主要问题.近来人们对硼的吸收转运机制的研究取得了突破性进展,鉴定了一些硼的转运通道和转运蛋白,例如：NIP5;1、NIP6;1、BOR1和BOR4,并对它们的转运机制有了一些了解.植物在硼缺少的情况下首先通过转运通道NIP5;1把硼吸收到共质体,然后通过转运蛋白BOR1运入中柱;在高硼毒害时,通过转运蛋白BOR4把过多的硼转出植物体,同时在植物中增加糖醇的含量,过表达BOR1或BOR4都能改变植物对硼含量变化的耐受性.因此,对植物中硼吸收转运机制的研究将有利于人们通过生物学手段提高作物对土壤中硼过高或过低的抗性.     

Arabidopsis thaliana NIP7;1: an anther-specific boric acid transporter of the aquaporin superfamily regulated by an unusual tyrosine in helix 2 of the transport pore

Plant nodulin-26 intrinsic proteins (NIPs) are members of the aquaporin superfamily that serve as multifunctional transporters of uncharged metabolites. In Arabidopsis thaliana, a specific NIP pore subclass, known as the NIP II proteins, is represented by AtNIP5;1 and AtNIP6;1, which encode channel proteins expressed in roots and leaf nodes, respectively, that participate in the transport of the critical cell wall nutrient boric acid. Modeling of the protein encoded by the AtNIP7;1 gene shows that it is a third member of the NIP II pore subclass in Arabidopsis. However, unlike AtNIP5;1 and AtNIP6;1 proteins, which form constitutive boric acid channels, AtNIP7;1 forms a channel with an extremely low intrinsic boric acid transport activity. Molecular modeling and molecular dynamics simulations of AtNIP7;1 suggest that a conserved tyrosine residue (Tyr81) located in transmembrane helix 2 adjacent to the aromatic arginine (ar/R) pore selectivity region stabilizes a closed pore conformation through interaction with the canonical Arg220 in ar/R region. Substitution of Tyr81 with a Cys residue, characteristic of established NIP boric acid channels, results in opening of the AtNIP7;1 pore that acquires a robust, transport activity for boric acid as well as other NIP II test solutes (glycerol and urea). Substitution of a Phe for Tyr81 also opens the channel, supporting the prediction from MD simulations that hydrogen bond interaction between the Tyr81 phenol group and the ar/R Arg may contribute to the stabilization of a closed pore state. Expression analyses show that AtNIP7;1 is selectively expressed in developing anther tissues of young floral buds of A. thaliana, principally in developing pollen grains of stage 9-11 anthers. Because boric acid is both an essential nutrient as well as a toxic compound at high concentrations, it is proposed that Tyr81 modulates transport and may provide an additional level of regulation for this transporter in male gametophyte development.     

俄罗斯杨水培苗对硼胁迫的生长和生理响应

该研究采用水培试验,分析了俄罗斯杨(Populus russkii)对短期硼胁迫(1、5、10mmol/L硼酸)的生长和生理响应特征,探明其对硼胁迫的耐受范围,初步揭示其耐硼的生理基础。结果显示:(1)与对照相比,1mmol/L硼酸处理俄罗斯杨水培苗的生长情况更优,叶片光合色素含量和净光合速率显著上升,SOD和APX活性及抗坏血酸含量显著上调。(2)5mmol/L硼酸处理幼苗有轻微胁迫受害症状,叶片褪绿变黄,叶绿素b含量比对照显著上升,而Chla/Chlb比值显著下降,其SOD和APX活性显著上调。(3)10mmol/L硼酸处理幼苗表现出严重毒害症状,叶片发黄、茎尖和根尖生长受抑制;叶片PSⅡ原初光能转换效率(F_v/F_m)和Chla/Chlb比值比对照显著下降;其叶片MDA含量、POD活性、抗坏血酸含量以及游离脯氨酸和可溶性糖含量均比对照显著上升。研究表明,在不同浓度硼酸短期胁迫下,俄罗斯杨水培苗能通过上调抗氧化酶活性和抗氧化物质、渗透调节物质含量来有效清除体内胁迫产生的活性氧,减轻膜脂过氧化伤害,使其在低于5mmol/L硼酸胁迫环境下正常生长,表现出较强的耐硼性。     

Boric acid increases the expression levels of human anion exchanger genes SLC4A2 and SLC4A3

Boron is an important micronutrient in plants and animals. The role of boron in living systems includes coordinated regulation of gene expression, growth and proliferation of higher plants and animals. There are several well-defined genes associated with boron transportation and tolerance in plants and these genes show close homology with human anion exchanger genes. Mutation of these genes also characterizes some genetic disorders. We investigated the toxic effects of boric acid on HEK293 cells and mRNA expression of anion exchanger (SLC4A1, SLC4A2 and SLC4A3) genes. Cytotoxicity of boric acid at different concentrations was tested by using the methylthiazolyldiphenyl-tetrazolium bromide assay. Gene expression profiles were examined using quantitative real-time PCR. In the HEK293 cells, the nontoxic upper concentration of boric acid was 250 μM; more than 500 μM caused cytotoxicity. The 250 μM boric acid concentration increased gene expression level of SLC4A2 up to 8.6-fold and SLC4A3 up to 2.6-fold, after 36-h incubation. There was no significant effect of boric acid on SLC4A1 mRNA expression levels.     

Permeability and channel-mediated transport of boric acid across membrane vesicles isolated from squash roots

Boron is an essential micronutrient for plant growth and the boron content of plants differs greatly, but the mechanism(s) of its uptake into cells is not known. Boron is present in the soil solution as boric acid and it is in this form that it enters the roots. We determined the boron permeability coefficient of purified plasma membrane vesicles obtained from squash (Cucurbita pepo) roots and found it to be 3 x 10(-7) +/-1.4 x 10(-8) cm s(-1), six times higher than the permeability of microsomal vesicles. Boric acid permeation of the plasma membrane vesicles was partially inhibited (30%-39%) by mercuric chloride and phloretin, a non-specific channel blocker. The inhibition by mercuric chloride was readily reversible by 2-mercaptoethanol. The energy of activation for boron transport into the plasma membrane vesicles was 10.2 kcal mol(-1). Together these data indicate that boron enters plant cells in part by passive diffusion through the lipid bilayer of the plasma membrane and in part through proteinaceous channels. Expression of the major intrinsic protein (MIP) PIP1 in Xenopus laevis oocytes resulted in a 30% increase in the boron permeability of the oocytes. Other MIPs tested (PIP3, MLM1, and GlpF) did not have this effect. We postulate that certain MIPs, like those that have recently been shown to transport small neutral solutes, may also be the channels through which boron enters plant cells.     

Distribution of Foliar-applied Boron Measured by Spark-source Mass Spectrometry and Laser-probe Mass Spectrography

The distribution of foliar-applied boron ([¹⁰B]boric acid) in radish (Raphanus sativus L.) was studied using for analysis of the stable isotopes a technique allowing a high sensitivity: spark-source mass spectrometry. Boron was recovered in the nontreated aerial parts and in the roots; however, the greatest fraction was in the treated leaf. It was possible with a laser-probe mass spectrograph to show that boron was not superficially located in the treated area but was present in tissues at all levels of depth considered.     

The role of boron in plant response to mycorrhizal infection

Summary In a Morrison sandy loam marginal in boron, fertilization with 1.1 ppm boron increased the shoot dry weight of mycorrhizal red clover (Trifolium pratense L.) an average of 16%, but did not affect nonmycorrhizal clover weight. Root colonization and foliar phosphorus concentrations were not significantly affected by B deficiency. With alfalfa (Medicago sativa L.) and Morrison soil in which B deficiency had been intensified by the addition of 100 ppm nitrogen as NH₄NO₃, inadequate B reduced the shoot dry weight of mycorrhizal plants 71%vs a reduction of 35% for nonmycorrhizal plants. Boron deficiency was more severe in the earlier cuttings and delayed the onset of mycorrhizal infection and the subsequent spread of mycorrhizal fungi within the roots. This delay may contribute to the lower concentrations of P and Cu seen by others during early developmental stages of B-deficient alfalfa.     

Infection Process of Burkholderia glumae Before Booting Stage of Rice

Burkholderia glumae is a well‐known pathogen for causing bacterial panicle blight of rice. In this study, the infection process of B. glumae in rice plants at different growing stages was tracked by means of real‐time fluorescence quantitative PCR. Burkholderia glumae tended to colonize at the growing point of rice plants, and the biomass of population was 10⁴ to 10⁸ CFU/g. The most intensive colonization was detected in the upmost leaf in the two‐leaf period. However, after the two‐leaf period, the population of pathogens decreased significantly, and they successfully recovered in the booting stage and broke out in panicles. We also illustrated the incubation location of B. glumae by presenting the infection pattern in the seedling and tillering stage of rice. Under fluorescent microscopy, the gfp‐labelled pathogens were first found in the vascular bundle of lateral roots, taproots and injured cells, then they were observed in the root hairs, epidermal cells and main root cap. The pathogens in the vascular bundle laterally dispersed towards the epidermal cells. By spray application of a bacterial suspension, the pathogens landed on the leaf sheaths and leaves, colonized in the epidermal hairs and leaf hairs, or invaded into the cells through the stomas. At the same time, the pathogens from the vascular bundle of the roots spread into the vascular bundle of leaf sheaths and leaves, which caused the leaves to curl and wilt, beginning from the tip.     

Plant regeneration,origin, and development of shoot buds from root segments of <Emphasis Type="Italic">Melia azedarach</Emphasis> L. (<Emphasis Type="Italic">Meliaceae</Emphasis>) seedlings

Summary In vitro regeneration of plants from root culture of Melia azedarach seedlings was obtained. The origin and mode of development of the regenerated shoot buds were studied by means of histological analysis and scanning electron microscopy (SEM). Maximum shoot bud regeneration was achieved when root segments were cultured on Murashige and Skoog (MS) medium at quarter strength with 3% sucrose and 0.44 μM benzyladenine (BA) and kept under light (116 μmol m⁻² s⁻¹). Shoot bud elongation was achieved on MS with 0.44 μM BA, 0.46 μM kinetin (KIN), and 3.26 μM adenine sulphate (AD). Regenerated shoots were rooted on MS with 12.26 μM indole-3-butyric acid (IBA) for 4 d and subsequently in MS lacking plant growth regulators for 26 d. Plants were established in a potting substrate. Histological analysis of roots from intact seedlings (without treatment) demonstrated that during the early life of the roots, M. azedarach lacks preformed buds. In contrast, when the roots were excised and cultured in vitro, the histology and SEM observations revealed that buds originated from meristematic groups of cells, which had been formed from the pericycle and several layers beneath. These meristematic groups of cells grew towards the periphery of the cortex by crushing the outer layer of cortical cells. Further develoment led to the differentiation of leaf primordia and a shoot apical meristem.     

Boron uptake by ectomycorrhizas of silver birch

Boron (B) is an essential micronutrient for plants but it is thought not to be essential for fungi. We studied whether the extraradical mycelia of Paxillus involutus in symbiosis with silver birch (Betula pendula) take up B and transport it to the host plant. We grew mycorrhizal plants in flat microcosms with a partitioning wall, below which there was only extraradical mycelium. A boric acid solution enriched in ¹⁰B was applied to these mycelia. Increased ¹⁰B/¹¹B isotope ratios were subsequently measured in birch leaves, stems, and roots plus mycorrhizas in the upper compartment. Boron was therefore taken up by the mycorrhizal mycelia and transported to the host plant in this species combination.     

Ascending Migration of Endophytic Rhizobia, from Roots to Leaves, inside Rice Plants and Assessment of Benefits to Rice Growth Physiology

Rhizobia, the root-nodule endosymbionts of leguminous plants, also form natural endophytic associations with roots of important cereal plants. Despite its widespread occurrence, much remains unknown about colonization of cereals by rhizobia. We examined the infection, dissemination, and colonization of healthy rice plant tissues by four species of gfp-tagged rhizobia and their influence on the growth physiology of rice. The results indicated a dynamic infection process beginning with surface colonization of the rhizoplane (especially at lateral root emergence), followed by endophytic colonization within roots, and then ascending endophytic migration into the stem base, leaf sheath, and leaves where they developed high populations. In situ CMEIAS image analysis indicated local endophytic population densities reaching as high as 9 × 10¹⁰ rhizobia per cm³ of infected host tissues, whereas plating experiments indicated rapid, transient or persistent growth depending on the rhizobial strain and rice tissue examined. Rice plants inoculated with certain test strains of gfp-tagged rhizobia produced significantly higher root and shoot biomass; increased their photosynthetic rate, stomatal conductance, transpiration velocity, water utilization efficiency, and flag leaf area (considered to possess the highest photosynthetic activity); and accumulated higher levels of indoleacetic acid and gibberellin growth-regulating phytohormones. Considered collectively, the results indicate that this endophytic plant-bacterium association is far more inclusive, invasive, and dynamic than previously thought, including dissemination in both below-ground and above-ground tissues and enhancement of growth physiology by several rhizobial species, therefore heightening its interest and potential value as a biofertilizer strategy for sustainable agriculture to produce the world's most important cereal crops.     

Improving rice tolerance to potassium deficiency by enhancing OsHAK16p:WOX11‐controlled root development

Potassium (K) deficiency in plants confines root growth and decreases root‐to‐shoot ratio, thus limiting root K acquisition in culture medium. A WUSCHEL‐related homeobox (WOX) gene, WOX11, has been reported as an integrator of auxin and cytokinin signalling that regulates root cell proliferation. Here, we report that ectopic expression of WOX11 gene driven by the promoter of OsHAK16 encoding a low‐K‐enhanced K transporter led to an extensive root system and adventitious roots and more effective tiller numbers in rice. The WOX11‐regulated root and shoot phenotypes in the OsHAK16p:WOX11 transgenic lines were supported by K‐deficiency‐enhanced expression of several RR genes encoding type‐A cytokinin‐responsive regulators, PIN genes encoding auxin transporters and Aux/IAA genes. In comparison with WT, the transgenic lines showed increases in root biomass, root activity and K concentrations in the whole plants, and higher soluble sugar concentrations in roots particularly under low K supply condition. The improvement of sugar partitioning to the roots by the expression of OsHAK16p:WOX11 was further indicated by increasing the expression of OsSUT1 and OsSUT4 genes in leaf blades and several OsMSTs genes in roots. Expression of OsHAK16p:WOX11 in the rice grown in moderate K‐deficient soil increased total K uptake by 72% and grain yield by 24%–32%. The results suggest that enlarging root growth and development by the expression of WOX11 in roots could provide a useful option for increasing K acquisition efficiency and cereal crop productivity in low K soil.