硝酸根调控植物开花和产量分子机制的研究进展

选育早熟高产的新品种是作物遗传育种研究的重要方向。氮素是植物生长发育不可或缺的大量元素,也是调控植物开花时间和种子产量最为重要的营养元素。硝酸根(NO3-)是植物获取氮素的主要来源。其作为营养物质和信号分子,通过转运、代谢和信号转导等多种方式参与调控植物开花和产量。对模式植物拟南芥、水稻和其他主要农作物中硝酸根调控植物早熟高产的分子机制进行了较为全面的概括和阐述,以期为合理利用氮肥、提高氮素利用效率和培育早熟高产作物新品种提供理论参考。     

拟南芥无机氮素转运蛋白及其磷酸化调控研究进展

氮元素是植物必需的营养元素之一, 氮素供需失衡会严重影响植物的生长发育。无机氮(硝酸根NO₃^-和铵根NH₄⁺)是植物体内氮素的主要来源, 对其有效吸收和利用依赖于多种类型转运蛋白的协同作用。其中, 部分无机氮素转运蛋白的活性受到可逆磷酸化作用的精准调控。该文将对模式植物拟南芥(Arabidopsis thaliana)中硝酸根和铵根转运蛋白的分类、结构、定位和功能特点等进行总结, 并重点对可逆磷酸化调控转运蛋白的分子机制加以阐述。     

生物固氮及在可持续农业中的应用

氮是限制农业生产的重要营养元素.生物固氮指某些原核生物能利用体内的固氮酶将空气中的氮气还原为氨,为植物生长提供氮素.自然界中存在多种具有固氮能力的微生物,依据其固氮方式分为自生固氮、共生固氮和联合固氮三种类型.联合固氮茵通过趋化定殖在植物根表,并生长、固氮.     

植物氮素吸收与转运的研究进展

氮素是植物生长发育所必须的基本营养元素,在植物生长发育和形态建成中起着重要作用.土壤中植物所利用的主要氮素形式是铵态氮和硝态氮,在进化过程中植物形成不同的吸收和转运铵态氮和硝态氮的分子机制.该文对植物吸收与转运氮素的生理学特征、分子机制及涉及的相关基因等研究进行概括性综述,为研究水稻中氮素吸收、转运相关基因提供理论基础...     

土壤-植物-大气连续体系中氮的研究进展

氮素是植物最需要的重要养分元素之一.近年来,土壤-植物-大气这一连续体系(SPAC)中的氮循环成为研究的热点之一.大气中的氮素可以通过生物固定和N沉降等作用进入土壤和植物内,同时土壤和植物内的氮素又会以氨挥发和氮氧化物等方式排放到大气中.氮素通过生物固持和植物吸收等方式进入植物体内,植物器官脱落使植物损失一部分的氮素,另外雨水的淋洗和植物溢出液也会造成植物的N损失.植物氮素在植物体内的积累和分布随着生长时期和各营养器官而有所不同.另外,植物吸收氮素的过程又受到大气状况和土壤状况的制约.土壤中氮素经过矿化作用、硝化作用和反硝化作用进行转化,一部分把氮素转化成植物能吸收的营养形态,另一部分则从土壤中损失.凋落物的分解和N沉降能补充土壤中的氮素,而植物吸收、微生物固持、水文流失和N溢出等方式使氮素从土壤中损失出去.另外,凋落物的分解和根际土壤、CO2浓度和臭氧对氮素循环有着重要的作用.N污染、N沉降、碳氮循环的耦合作用是今后研究的热点问题.     

高等植物体内铁运输机制研究进展

铁是植物所必需的微量矿质元素,在光合作用、呼吸作用等过程中发挥着重要的作用。虽然铁在地壳中含量丰富,但生物有效获取率非常低。因此,探索高等植物铁吸收及运输机制一直是植物铁营养领域研究的热点问题。近几年来,人们对于高等植物体内铁运输,尤其是细胞内铁运输又有了新的认识。本文主要对高等植物体内长距离铁运输(木质部,韧皮部)和细胞内的铁运输(液泡,叶绿体和线粒体)两方面的运输机制进行了综述,这将帮助我们进一步了解植物铁代谢机制,对我们培育高铁含量作物和提高植物抗逆性有着重要意义。     

CO_2 倍增对长白赤松幼苗根 土界面水分运输过程的影响(英文)

用具有非破坏性的电导率方法测定土壤水分的廓线 ,与挖掘法 (或打孔法 )获取的根系分布对比 ,研究CO2倍增条件下一年生的长白赤松 (PinussylvestrisLinn .var.sylvestriformis (Takenouchi)ChengetC .D .Chu)幼苗根 土界面的水分运输状态。结果表明 :(1)土壤水分廓线由植物的活性所调制 ,根系分布密集的土层其水分含量也高。(2 )CO2 倍增 ,根系 土壤水分运输的活跃层及根系分布都将向土壤深处位移。研究证明 ,电导率方法能够指示发生于根 土界面上的水分运输状态 ,方法简单 ,且对土壤无破坏     

大豆根瘤菌

最近報紙上登着中國科學院東北分院將研究大豆根瘤菌來增加東北大豆產量的新聞。大豆根瘤菌究竟是什麽東西呢?现在我來簡單的介紹一下,我們知道植物的生活是離不開蛋白質的。蛋白質是含有氮素的化合物,所以當植物製造蛋白質時就必定要從外界環境裏吸取氮素為原料。氮氣在植物的周圍很多,空氣中有五分之四是氮氣,但是空氣中的氮,綠色植物都不能直接利用它作養分。綠色植物的氮素原料乃是依賴土壤中肥料內所產生的硝酸鹽等來供給。大豆根瘸菌是一種生長在大豆的根上而使松生瘤的細菌,我們挖出一株大豆時,根上有許多圓球就是瘤(如圖),細     

丛枝菌根利用氮素研究进展

氮素是植物需求量最大的元素,丛枝菌根真菌与植物形成共生体后能从土壤中获取无机氮、简单的氨基酸,还能利用一些复杂的有机态氮.考虑到NH+4在土壤中的移动性低及丛枝菌根真菌的专性共生菌的特点,丛枝菌根真菌吸收NH+4对植物的贡献较大.近年来的研究发现丛枝菌根真菌内存在与氮素代谢有关的鸟氨酸循环,而精氨酸则是菌丝内氮素转移的主要形式.综述最近的AMF对氮素的吸收、转运、同化、交换等方面的文献,旨在揭示丛枝菌根真菌氮素利用特点,阐明丛枝菌根真菌在氮循环系统中的重要作用.     

陆地生态系统植物的氮源及氮素吸收

氮是植物生长发育所必需的营养元素,也是其主要的限制因子之一.陆地生态系统植物所需氮的来源及植物对氮素的吸收利用均受控于其种类和生长环境.环境条件的改变,一方面可能改变植物生长区原有氮的形态、浓度、赋存方式等,从而改变氮对植物的供给状况;另一方面可能引起植物生长区土壤质量、水分利用状况、光照等的改变,从而产生耦合现象,直接影响植物的生理生态特性,使植物对氮素的吸收利用发生改变,导致植物生长区的种群类型及物种多样性发生改变,并直接影响到生态系统的功能及演替.本文主要对陆地生态系统中高等植物生长发育所需氮素的来源及植物对氮素吸收利用过程中的影响因素进行了综述和讨论,并结合国内外在该领域的研究现状对其研究前景进行了展望.     

Uptake, allocation and signaling of nitrate

Plants need to acquire nitrogen (N) efficiently from the soil for growth. Nitrate is one of the major N sources for higher plants. Therefore, nitrate uptake and allocation are key factors in efficient N utilization. Membrane-bound transporters are required for nitrate uptake from the soil and for the inter- and intracellular movement of nitrate inside the plants. Four gene families, nitrate transporter 1/peptide transporter (NRT1/PTR), NRT2, chloride channel (CLC), and slow anion channel-associated 1 homolog 3 (SLAC1/SLAH), are involved in nitrate uptake, allocation, and storage in higher plants. Recent studies of these transporters or channels have provided new insights into the molecular mechanisms of nitrate uptake and allocation. Interestingly, several of these transporters also play versatile roles in nitrate sensing, plant development, pathogen defense, and/or stress response.     

AtPTR1 and AtPTR5 transport dipeptides in planta

Transporters for di- and tripeptides belong to the large and poorly characterized PTR/NRT1 (peptide transporter/nitrate transporter 1) family. A new member of this gene family, AtPTR5, was isolated from Arabidopsis (Arabidopsis thaliana). Expression of AtPTR5 was analyzed and compared with tissue specificity of the closely related AtPTR1 to discern their roles in planta. Both transporters facilitate transport of dipeptides with high affinity and are localized at the plasma membrane. Mutants, double mutants, and overexpressing lines were exposed to several dipeptides, including toxic peptides, to analyze how the modified transporter expression affects pollen germination, growth of pollen tubes, root, and shoot. Analysis of atptr5 mutants and AtPTR5-overexpressing lines showed that AtPTR5 facilitates peptide transport into germinating pollen and possibly into maturating pollen, ovules, and seeds. In contrast, AtPTR1 plays a role in uptake of peptides by roots indicated by reduced nitrogen (N) levels and reduced growth of atptr1 mutants on medium with dipeptides as the sole N source. Furthermore, overexpression of AtPTR5 resulted in enhanced shoot growth and increased N content. The function in peptide uptake was further confirmed with toxic peptides, which inhibited growth. The results show that closely related members of the PTR/NRT1 family have different functions in planta. This study also provides evidence that the use of organic N is not restricted to amino acids, but that dipeptides should be considered as a N source and transport form in plants.     

Altered expression of the PTR/NRT1 homologue OsPTR9 affects nitrogen utilization efficiency,growth and grain yield in rice

The plant PTR/NRT1 (peptide transporter/nitrate transporter 1) gene family comprises di/tripeptide and low‐affinity nitrate transporters; some members also recognize other substrates such as carboxylates, phytohormones (auxin and abscisic acid), or defence compounds (glucosinolates). Little is known about the members of this gene family in rice (Oryza sativa L.). Here, we report the influence of altered OsPTR9 expression on nitrogen utilization efficiency, growth, and grain yield. OsPTR9 expression is regulated by exogenous nitrogen and by the day‐night cycle. Elevated expression of OsPTR9 in transgenic rice plants resulted in enhanced ammonium uptake, promotion of lateral root formation and increased grain yield. On the other hand, down‐regulation of OsPTR9 in a T‐DNA insertion line (osptr9) and in OsPTR9‐RNAi rice plants had the opposite effect. These results suggest that OsPTR9 might hold potential for improving nitrogen utilization efficiency and grain yield in rice breeding.     

Cloning and functional characterization of a constitutively expressed nitrate transporter gene, OsNRT1, from rice

Elucidating how rice (Oryza sativa) takes up nitrate at the molecular level could help improve the low recovery rate (<50%) of nitrogen fertilizer in rice paddies. As a first step toward that goal, we have cloned a nitrate transporter gene from rice called OsNRT1. OsNRT1 is a new member of a growing transporter family called PTR, which consists not only of nitrate transporters from higher plants that are homologs of the Arabidopsis CHL1 (AtNRT1) protein, but also peptide transporters from a wide variety of genera including animals, plants, fungi, and bacteria. However, despite the fact that OsNRT1 shares a higher degree of sequence identity with the two peptide transporters from plants (approximately 50%) than with the nitrate transporters (approximately 40%) of the PTR family, no peptide transport activity was observed when OsNRT1 was expressed in either Xenopus oocytes or yeast. Furthermore, contrasting the dual-affinity nitrate transport activity of CHL1, OsNRT1 displayed only low-affinity nitrate transport activity in Xenopus oocytes, with a K(m) value of approximately 9 mM. Northern-blot and in situ hybridization analysis indicated that OsNRT1 is constitutively expressed in the most external layer of the root, epidermis and root hair. These data strongly indicate that OsNRT1 encodes a constitutive component of a low-affinity nitrate uptake system for rice.     

Nitrate transporters and peptide transporters

In higher plants, two types of nitrate transporters, NRT1 and NRT2, have been identified. In Arabidopsis, there are 53 NRT1 genes and 7 NRT2 genes. NRT2 are high-affinity nitrate transporters, while most members of the NRT1 family are low-affinity nitrate transporters. The exception is CHL1 (AtNRT1.1), which is a dual-affinity nitrate transporter, its mode of action being switched by phosphorylation and dephosphorylation of threonine 101. Two of the NRT1 genes, CHL1 and AtNRT1.2, and two of the NRT2 genes, AtNRT2.1 and AtNRT2.2, are known to be involved in nitrate uptake. In addition, AtNRT1.4 is required for petiole nitrate storage. On the other hand, some members of the NRT1 family are dipeptide transporters, called PTRs, which transport a broad spectrum of di/tripeptides. In barley, HvPTR1, expressed in the plasma membrane of scutellar epithelial cells, is involved in mobilizing peptides, produced by hydrolysis of endosperm storage protein, to the developing embryo. In higher plants, there is another family of peptide transporters, called oligopeptide transporters (OPTs), which transport tetra/pentapeptides. In addition, some OPTs transport GSH, GSSH, GSH conjugates, phytochelatins, and metals.     

Potential transceptor AtNRT1.13 modulates shoot architecture and flowering time in a nitrate-dependent manner

Compared with root development regulated by external nutrients, less is known about how internal nutrients are monitored to control plasticity of shoot development. In this study, we characterize an Arabidopsis thaliana transceptor, NRT1.13 (NPF4.4), of the NRT1/PTR/NPF family. Different from most NRT1 transporters, NRT1.13 does not have the conserved proline residue between transmembrane domains 10 and 11; an essential residue for nitrate transport activity in CHL1/NRT1.1/NPF6.3. As expected, when expressed in oocytes, NRT1.13 showed no nitrate transport activity. However, when Ser 487 at the corresponding position was converted back to proline, NRT1.13 S487P regained nitrate uptake activity, suggesting that wild-type NRT1.13 cannot transport nitrate but can bind it. Subcellular localization and β-glucuronidase reporter analyses indicated that NRT1.13 is a plasma membrane protein expressed at the parenchyma cells next to xylem in the petioles and the stem nodes. When plants were grown with a normal concentration of nitrate, nrt1.13 showed no severe growth phenotype. However, when grown under low-nitrate conditions, nrt1.13 showed delayed flowering, increased node number, retarded branch outgrowth, and reduced lateral nitrate allocation to nodes. Our results suggest that NRT1.13 is required for low-nitrate acclimation and that internal nitrate is monitored near the xylem by NRT1.13 to regulate shoot architecture and flowering time.

Nitrate transporter/transceptor NRT1.13 monitors xylem 12 nitrate level to regulate shoot architecture and flowering time.     

Determinants for Arabidopsis peptide transporter targeting to the tonoplast or plasma membrane

Di- and tripeptide transporters of the PTR/NRT1 (peptide transporter/nitrate transporter1)-family are localized either at the tonoplast (TP) or plasma membrane (PM). As limited information is available on structural determinants required for targeting of plant membrane proteins, we performed gene shuffling and domain swapping experiments of Arabidopsis PTRs. A 7 amino acid fragment of the hydrophilic N-terminal region of PTR2, PTR4 and PTR6 was required for TP localization and sufficient to redirect not only PM-localized PTR1 or PTR5, but also sucrose transporter SUC2 to the TP. Alanine scanning mutagenesis identified L(11) and I(12) of PTR2 to be essential for TP targeting, while only one acidic amino acid at position 5, 6 or 7 was required, revealing a dileucine (LL or LI) motif with at least one upstream acidic residue. Similar dileucine motifs could be identified in other plant TP transporters, indicating a broader role of this targeting motif in plants. Targeting to the PM required the loop between transmembrane domain 6 and 7 of PTR1 or PTR5. Deletion of either PM or TP targeting signals resulted in retention in internal membranes, indicating that PTR trafficking to these destination membranes requires distinct signals and is in both cases not by default.     

Cloning of a cDNA for a constitutive NRT1 transporter from soybean and comparison of gene expression of soybean NRT1 transporters

We have isolated a cDNA for a putative transporter, named GmNRT1-3, in the NRT1 family from soybean. It was predicted to have a similar topological structure not only to both GmNRT1-1 and GmNRT1-2 reported previously, but also to other members of the family. Two other cDNAs isolated have parts of the sequence for putative NRT1 transporters, GmNRT1-4 and GmNRT1-5, suggesting that at least five NRT1 transporters occur in soybean. These GmNRT1 genes and the GmNRT2 gene, encoding a soybean NRT2 nitrate transporter, showed different expression patterns to each other under various nitrogen conditions. Specifically, GmNRT1-3 was constitutively expressed in both roots and leaves, while GmNRT1-2 was gradually expressed as the roots developed in the presence of ammonium as a nitrogen source, but not in the presence of both ammonium and nitrate. Based on these results, we discussed the possible regulation in the expression and role of these transporters in nitrate uptake.