RESUMEN
In the past 50 years, the application of synthetic nitrogen (N) fertilizer to farmland resulted in a dramatic increase in crop yields but with considerable negative impacts on the environment. New solutions are therefore needed to simultaneously increase yields while maintaining, or preferably decreasing, applied N to maximize the nitrogen use efficiency (NUE) of crops. In this review, we outline the definition of NUE, the selection and development of NUE crops, and the factors that interact with NUE. In particular, we emphasize the challenges of developing crop plants with enhanced NUE, using more classical genetic approaches based on utilizing existing allelic variation for NUE traits. The challenges of phenotyping, mapping quantitative trait loci (QTLs), and selecting candidate genes for NUE improvement are described. In addition, we highlight the importance of different factors that lead to changes in the NUE components of nitrogen uptake efficiency (NUpE) and nitrogen utilization efficiency (NUtE).
Asunto(s)
Productos Agrícolas/genética , Productos Agrícolas/metabolismo , Nitrógeno/metabolismo , Fertilizantes , Variación Genética , Hordeum/genética , Hordeum/metabolismo , Nitrógeno/farmacocinética , Sitios de Carácter Cuantitativo , Triticum/genética , Triticum/metabolismo , Zea mays/genética , Zea mays/metabolismoRESUMEN
Plant aluminum-activated malate transporters (ALMTs) are currently classified as anion channels; they are also known to be regulated by diverse signals, leading to a range of physiological responses. Gamma-aminobutyric acid (GABA) regulation of anion flux through ALMT proteins requires a specific amino acid motif in ALMTs that shares similarity with a GABA binding site in mammalian GABAA receptors. Here, we explore why TaALMT1 activation leads to a negative correlation between malate efflux and endogenous GABA concentrations ([GABA]i) in both wheat (Triticum aestivum) root tips and in heterologous expression systems. We show that TaALMT1 activation reduces [GABA]i because TaALMT1 facilitates GABA efflux but GABA does not complex Al3+ TaALMT1 also leads to GABA transport into cells, demonstrated by a yeast complementation assay and via 14C-GABA uptake into TaALMT1-expressing Xenopus laevis oocytes; this was found to be a general feature of all ALMTs we examined. Mutation of the GABA motif (TaALMT1F213C) prevented both GABA influx and efflux, and resulted in no correlation between malate efflux and [GABA]i We conclude that ALMTs are likely to act as both GABA and anion transporters in planta. GABA and malate appear to interact with ALMTs in a complex manner to regulate each other's transport, suggestive of a role for ALMTs in communicating metabolic status.
Asunto(s)
Aluminio/metabolismo , Malatos/metabolismo , Proteínas de Plantas/metabolismo , Triticum/metabolismo , Ácido gamma-Aminobutírico/metabolismo , Transporte Biológico/fisiología , Transporte Iónico/fisiologíaRESUMEN
On average less than half of the applied N is captured by crops, thus there is scope and need to improve N uptake in cereals. With nitrate (NO3-) being the main form of N available to cereal crops there has been a significant global research effort to understand plant NO3- uptake. Despite this, our knowledge of the NO3- uptake system is not sufficient to easily target ways to improve NO3- uptake. Based on this there is an identified need to better understand the NO3- uptake system and the signalling molecules that modulate it. With strong transcriptional control governing the NO3- uptake system, we also need new leads for modulating transcription of NO3- transporter genes.
Asunto(s)
Grano Comestible/metabolismo , Nitratos/metabolismo , Nitrógeno/metabolismo , Transporte Biológico , Grano Comestible/genéticaRESUMEN
KEY MESSAGE: Degradation of nitrogen-rich purines is tightly and oppositely regulated under drought and low nitrogen supply in bread wheat. Allantoin is a key target metabolite for improving nitrogen homeostasis under stress. The metabolite allantoin is an intermediate of the catabolism of purines (components of nucleotides) and is known for its housekeeping role in nitrogen (N) recycling and also for its function in N transport and storage in nodulated legumes. Allantoin was also shown to differentially accumulate upon abiotic stress in a range of plant species but little is known about its role in cereals. To address this, purine catabolic pathway genes were identified in hexaploid bread wheat and their chromosomal location was experimentally validated. A comparative study of two Australian bread wheat genotypes revealed a highly significant increase of allantoin (up to 29-fold) under drought. In contrast, allantoin significantly decreased (up to 22-fold) in response to N deficiency. The observed changes were accompanied by transcriptional adjustment of key purine catabolic genes, suggesting that the recycling of purine-derived N is tightly regulated under stress. We propose opposite fates of allantoin in plants under stress: the accumulation of allantoin under drought circumvents its degradation to ammonium (NH4+) thereby preventing N losses. On the other hand, under N deficiency, increasing the NH4+ liberated via allantoin catabolism contributes towards the maintenance of N homeostasis.
Asunto(s)
Alantoína/metabolismo , Nitrógeno/metabolismo , Purinas/metabolismo , Triticum/metabolismo , Agua , Alantoína/genética , Mapeo Cromosómico , Cromosomas de las Plantas , Sequías , Regulación de la Expresión Génica de las Plantas , Genes de Plantas/genética , Homeostasis , Metaboloma , Estrés Fisiológico , Sintenía/genética , Triticum/genéticaRESUMEN
Glycine max symbiotic ammonium transporter 1 was first documented as a putative ammonium (NH4(+)) channel localized to the symbiosome membrane of soybean root nodules. We show that Glycine max symbiotic ammonium transporter 1 is actually a membrane-localized basic helix-loop-helix (bHLH) DNA-binding transcription factor now renamed Glycine max bHLH membrane 1 (GmbHLHm1). In yeast, GmbHLHm1 enters the nucleus and transcriptionally activates a unique plasma membrane NH4(+) channel Saccharomyces cerevisiae ammonium facilitator 1. Ammonium facilitator 1 homologs are present in soybean and other plant species, where they often share chromosomal microsynteny with bHLHm1 loci. GmbHLHm1 is important to the soybean rhizobium symbiosis because loss of activity results in a reduction of nodule fitness and growth. Transcriptional changes in nodules highlight downstream signaling pathways involving circadian clock regulation, nutrient transport, hormone signaling, and cell wall modification. Collectively, these results show that GmbHLHm1 influences nodule development and activity and is linked to a novel mechanism for NH4(+) transport common to both yeast and plants.
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Compuestos de Amonio/metabolismo , Factores de Transcripción Básicos con Cremalleras de Leucinas y Motivos Hélice-Asa-Hélice/metabolismo , Proteínas de Transporte de Catión/metabolismo , Glycine max/crecimiento & desarrollo , Glycine max/metabolismo , Nódulos de las Raíces de las Plantas/crecimiento & desarrollo , Nódulos de las Raíces de las Plantas/metabolismo , Proteínas de Soja/metabolismo , Transporte Biológico , Membrana Celular/metabolismo , ADN de Plantas/metabolismo , Regulación de la Expresión Génica de las Plantas , Unión Proteica , Nódulos de las Raíces de las Plantas/citología , Nódulos de las Raíces de las Plantas/ultraestructura , Saccharomyces cerevisiae/metabolismo , Glycine max/genética , Glycine max/ultraestructuraRESUMEN
⢠Despite the great agricultural and ecological importance of efficient use of urea-containing nitrogen fertilizers by crops, molecular and physiological identities of urea transport in higher plants have been investigated only in Arabidopsis. ⢠We performed short-time urea-influx assays which have identified a low-affinity and high-affinity (K(m) of 7.55 µM) transport system for urea-uptake by rice roots (Oryza sativa). ⢠A high-affinity urea transporter OsDUR3 from rice was functionally characterized here for the first time among crops. OsDUR3 encodes an integral membrane-protein with 721 amino acid residues and 15 predicted transmembrane domains. Heterologous expression demonstrated that OsDUR3 restored yeast dur3-mutant growth on urea and facilitated urea import with a K(m) of c. 10 µM in Xenopus oocytes. ⢠Quantitative reverse-transcription polymerase chain reaction (qPCR) analysis revealed upregulation of OsDUR3 in rice roots under nitrogen-deficiency and urea-resupply after nitrogen-starvation. Importantly, overexpression of OsDUR3 complemented the Arabidopsis atdur3-1 mutant, improving growth on low urea and increasing root urea-uptake markedly. Together with its plasma membrane localization detected by green fluorescent protein (GFP)-tagging and with findings that disruption of OsDUR3 by T-DNA reduces rice growth on urea and urea uptake, we suggest that OsDUR3 is an active urea transporter that plays a significant role in effective urea acquisition and utilisation in rice.
Asunto(s)
Arabidopsis/genética , Proteínas de Plantas/metabolismo , Urea/metabolismo , Animales , Arabidopsis/efectos de los fármacos , Arabidopsis/crecimiento & desarrollo , Transporte Biológico/efectos de los fármacos , Membrana Celular/efectos de los fármacos , Membrana Celular/metabolismo , Perfilación de la Expresión Génica , Regulación de la Expresión Génica de las Plantas/efectos de los fármacos , Prueba de Complementación Genética , Proteínas Fluorescentes Verdes/metabolismo , Proteínas de Transporte de Membrana/genética , Proteínas de Transporte de Membrana/metabolismo , Mutación/genética , Nitrógeno/metabolismo , Oocitos/efectos de los fármacos , Oocitos/metabolismo , Oryza/efectos de los fármacos , Oryza/genética , Oryza/crecimiento & desarrollo , Oryza/metabolismo , Proteínas de Plantas/genética , Raíces de Plantas/efectos de los fármacos , Raíces de Plantas/metabolismo , Plantas Modificadas Genéticamente , ARN Mensajero/genética , ARN Mensajero/metabolismo , Proteínas Recombinantes de Fusión/metabolismo , Saccharomyces cerevisiae/efectos de los fármacos , Saccharomyces cerevisiae/genética , Homología de Secuencia de Aminoácido , Fracciones Subcelulares/efectos de los fármacos , Fracciones Subcelulares/metabolismo , Urea/farmacología , Xenopus laevis , Transportadores de UreaRESUMEN
Predictions for wheat grown under future climate conditions indicate a decline in grain protein concentration accompanied with an increase in yield due to increasing carbon dioxide concentrations. Currently, there is a lack of understanding as to the complete mechanism that governs the response of grain protein concentration (GPC) to elevated carbon dioxide (e[CO2]). We investigated the GPC of 18 wheat genotypes from a doubled haploid wheat population and the two parental genotypes, Kukri and RAC0875. In addition, other nitrogen and biomass related traits were analysed to further elucidate which traits are connected with the decline in GPC. Wheat was grown under ambient and elevated [CO2] in an environmentally controlled glasshouse. Plant nitrogen and biomass accumulation were measured at anthesis and maturity. We found that GPC declined under e[CO2] and that the response of GPC to e[CO2] was negatively correlated with nitrogen utilisation efficiency and harvest index. The extent that total biomass (anthesis), harvest index, photosynthesis, nitrogen utilisation and remobilisation efficiency, total nitrogen remobilisation and post-anthesis nitrogen uptake impacted GPC in response to e[CO2] varied across genotype, suggesting that multiple mechanisms are responsible for GPC decline at e[CO2] and that these mechanisms are effected differentially across genotypes.
RESUMEN
Global use of nitrogen (N) fertilizers has increased sevenfold from 1960 to 1995 but much of the N applied is lost to the environment. Modifying the temporal and spatial distribution of organic N within the plant can lead to improved grain yield and/or grain protein content for the same or reduced N fertilizer inputs. Biotechnological approaches to modify whole plant distribution of amino acids and ureides has proven successful in several crop species. Manipulating selective autophagy pathways in crops has also improved N remobilization efficiency to sink tissues whilst the contribution of ribophagy, RNA and purine catabolism to N recycling in crops is still too early to foretell. Improved recycling and remobilization of N must exploit N-stress responsive transcriptional regulators, N-sensing or phloem-localized promotors and genetic variation for N-responsive traits.
Asunto(s)
Fertilizantes , Nitrógeno , Productos Agrícolas/genética , Productos Agrícolas/metabolismo , Grano Comestible/metabolismo , Nitrógeno/metabolismoRESUMEN
The non-protein amino acid γ-aminobutyric acid (GABA) has been proposed to be an ancient messenger for cellular communication conserved across biological kingdoms. GABA has well-defined signalling roles in animals; however, whilst GABA accumulates in plants under stress it has not been determined if, how, where and when GABA acts as an endogenous plant signalling molecule. Here, we establish endogenous GABA as a bona fide plant signal, acting via a mechanism not found in animals. Using Arabidopsis thaliana, we show guard cell GABA production is necessary and sufficient to reduce stomatal opening and transpirational water loss, which improves water use efficiency and drought tolerance, via negative regulation of a stomatal guard cell tonoplast-localised anion transporter. We find GABA modulation of stomata occurs in multiple plants, including dicot and monocot crops. This study highlights a role for GABA metabolism in fine tuning physiology and opens alternative avenues for improving plant stress resilience.
Asunto(s)
Proteínas de Arabidopsis/genética , Arabidopsis/metabolismo , Canales de Cloruro/genética , Glutamato Descarboxilasa/genética , Estomas de Plantas/metabolismo , Transpiración de Plantas/genética , Agua/metabolismo , Ácido gamma-Aminobutírico/metabolismo , Ácido Abscísico/metabolismo , Ácido Abscísico/farmacología , Adaptación Fisiológica/genética , Arabidopsis/genética , Proteínas de Arabidopsis/metabolismo , Canales de Cloruro/metabolismo , Sequías , Regulación de la Expresión Génica de las Plantas , Glutamato Descarboxilasa/metabolismo , Proteínas Fluorescentes Verdes/genética , Proteínas Fluorescentes Verdes/metabolismo , Hordeum/genética , Hordeum/metabolismo , Isoenzimas/genética , Isoenzimas/metabolismo , Hojas de la Planta/genética , Hojas de la Planta/metabolismo , Estomas de Plantas/efectos de los fármacos , Estomas de Plantas/genética , Transpiración de Plantas/efectos de los fármacos , Proteínas Recombinantes de Fusión/genética , Proteínas Recombinantes de Fusión/metabolismo , Transducción de Señal , Glycine max/genética , Glycine max/metabolismo , Estrés Fisiológico , Nicotiana/genética , Nicotiana/metabolismo , Vicia faba/genética , Vicia faba/metabolismoRESUMEN
Nitrogen is an essential nutrient for plants, but crop plants are inefficient in the acquisition and utilization of applied nitrogen. This often results in producers over applying nitrogen fertilizers, which can negatively impact the environment. The development of crop plants with more efficient nitrogen usage is, therefore, an important research goal in achieving greater agricultural sustainability. We utilized genetically modified rice lines over-expressing a barley alanine aminotransferase (HvAlaAT) to help characterize pathways which lead to more efficient use of nitrogen. Under the control of a stress-inducible promoter OsAnt1, OsAnt1:HvAlaAT lines have increased above-ground biomass with little change to both nitrate and ammonium uptake rates. Based on metabolic profiles, carbon metabolites, particularly those involved in glycolysis and the tricarboxylic acid (TCA) cycle, were significantly altered in roots of OsAnt1:HvAlaAT lines, suggesting higher metabolic turnover. Moreover, transcriptomic data revealed that genes involved in glycolysis and TCA cycle were upregulated. These observations suggest that higher activity of these two processes could result in higher energy production, driving higher nitrogen assimilation, consequently increasing biomass production. Other potential mechanisms contributing to a nitrogen-use efficient phenotype include involvements of phytohormonal responses and an alteration in secondary metabolism. We also conducted basic growth studies to evaluate the effect of the OsAnt1:HvAlaAT transgene in barley and wheat, which the transgenic crop plants increased seed production under controlled environmental conditions. This study provides comprehensive profiling of genetic and metabolic responses to the over-expression of AlaAT and unravels several components and pathways which contribute to its nitrogen-use efficient phenotype.
RESUMEN
The unidirectional motion of a camphor boat along an annular water channel is observable. When camphor boats are placed in a water channel, both homogeneous and inhomogeneous states occur as collective motions, depending on the number of boats. The inhomogeneous state is a type of congestion, that is, the velocities of the boats change with temporal oscillation, and the shock wave appears along the line of travel of the boats. The unidirectional motion of a single camphor boat and the homogeneous state can be represented by traveling wave solutions in a mathematical model. Because the experimental results described here are thought of as a type of bifurcation phenomenon, the destabilization of traveling wave solutions may indicate the emergence of congestion. We previously attempted to study a linearized eigenvalue problem associated with a traveling wave solution. However, the problem is too difficult to analyze rigorously, even for just two camphor boats. Therefore we developed a center manifold theory and derived a reduced model in our previous work. In the present paper, we study the reduced model and show that the original model and our reduced model qualitatively exhibit the same properties by applying numerical techniques. Moreover, we demonstrate that the numerical results obtained in our models for camphor boats are quite similar to those in a car-following model, the OV model, but there are some different features between our reduced model and a typical OV model.
RESUMEN
Turn-over of RNA and catabolism of nucleotides releases one to four ammonia molecules; the released nutrients being reassimilated into primary metabolism. Preliminary evidence indicates that monocots store high levels of free nucleotides and nucleosides but their potential as a source of internal organic nitrogen for use and remobilization is uncharted. Early tillering wheat plants were therefore starved of N over a 5-day time-course with examination of nucleic acid yields in whole shoots, young and old leaves and roots. Nucleic acids constituted â¼4% of the total N pool of N starved wheat plants, which was comparable with the N available from nitrate (NO3 -) and greater than that available from the sum of 20 proteinogenic amino acids. Methods were optimized to detect nucleotide (purine and pyrimidine) metabolites, and wheat orthologs of RNA degradation (TaRNS), nucleoside transport (TaENT1, TaENT3) and salvage (TaADK) were identified. It was found that N starved wheat roots actively catabolised RNA and specific purines but accumulated pyrimidines. Reduced levels of RNA corresponded with induction of TaRNS2, TaENT1, TaENT3, and TaADK in the roots. Reduced levels of GMP, guanine, xanthine, allantoin, allantoate and glyoxylate in N starved roots correlated with accumulation of allantoate and glyoxylate in the oldest leaf, suggesting translocation of allantoin. Furthermore, N starved wheat plants exogenously supplied with N in the form of purine catabolites grew and photosynthesized as well as those plants re-supplied with NO3 -. These results support the hypothesis that the nitrogen and carbon recovered from purine metabolism can support wheat growth.
RESUMEN
There are many reports of an arginine-dependent nitric oxide synthase activity in plants; however, the gene(s) or protein(s) responsible for this activity have yet to be convincingly identified. To measure nitric oxide synthase activity, many studies have relied on a citrulline-based assay that measures the formation of L-citrulline from L-arginine using ion exchange chromatography. In this article, we report that when such assays are used with protein extracts from Arabidopsis, an arginine-dependent activity was observed, but it produced a product other than citrulline. TLC analysis identified the product as argininosuccinate. The reaction was stimulated by fumarate (> 500 microM), implicating the urea cycle enzyme argininosuccinate lyase (EC 4.3.2.1), which reversibly converts arginine and fumarate to argininosuccinate. These results indicate that caution is needed when using standard citrulline-based assays to measure nitric oxide synthase activity in plant extracts, and highlight the importance of verifying the identity of the product as citrulline.
Asunto(s)
Proteínas de Arabidopsis/metabolismo , Arabidopsis/metabolismo , Argininosuccinatoliasa/metabolismo , Citrulina/metabolismo , Óxido Nítrico Sintasa/metabolismo , Arabidopsis/enzimología , Arginina/metabolismo , Ácido Argininosuccínico/metabolismo , Bioensayo/métodos , Catálisis/efectos de los fármacos , Cromatografía por Intercambio Iónico , Cromatografía en Capa Delgada , Fumaratos/metabolismo , Fumaratos/farmacología , Cinética , Extractos Vegetales/metabolismoRESUMEN
BACKGROUND: The spike of a cereal plant is the grain-bearing organ whose physical characteristics are proxy measures of grain yield. The ability to detect and characterise spikes from 2D images of cereal plants, such as wheat, therefore provides vital information on tiller number and yield potential. RESULTS: We have developed a novel spike detection method for wheat plants involving, firstly, an improved colour index method for plant segmentation and, secondly, a neural network-based method using Laws texture energy for spike detection. The spike detection step was further improved by removing noise using an area and height threshold. The evaluation results showed an accuracy of over 80% in identification of spikes. In the proposed method we also measure the area of individual spikes as well as all spikes of individual plants under different experimental conditions. The correlation between the final average grain yield and spike area is also discussed in this paper. CONCLUSIONS: Our highly accurate yield trait phenotyping method for spike number counting and spike area estimation, is useful and reliable not only for grain yield estimation but also for detecting and quantifying subtle phenotypic variations arising from genetic or environmental differences.
RESUMEN
Genetic variation has been observed in both protein concentration in wheat grain and total protein content (protein yield). Here we describe the genetic analysis of variation for grain protein in response to nitrogen (N) supply and locate significant genomic regions controlling grain protein components in a spring wheat population. In total, six N use efficiency (NUE) field trials were carried out for the target traits in a sub-population of doubled haploid lines derived from a cross between two Australian varieties, RAC875 and Kukri, in Southern and Western Australia from 2011 to 2013. Twenty-four putative Quantitative Trait Loci (QTL) for protein-related traits were identified at high and low N supply and ten QTL were identified for the response to N for the traits studied. These loci accounted for a significant proportion of the overall effect of N supply. Several of the regions were co-localised with grain yield QTL and are promising targets for further investigation and selection in breeding programs.
Asunto(s)
Mapeo Cromosómico , Nitrógeno/farmacología , Semillas/genética , Triticum/genética , Australia , Clima , Cruzamientos Genéticos , Grano Comestible/genética , Haploidia , Fenotipo , Proteínas de Plantas/metabolismo , Sitios de Carácter Cuantitativo/genética , Carácter Cuantitativo Heredable , Semillas/efectos de los fármacos , Suelo/química , Triticum/efectos de los fármacosRESUMEN
Leaf senescence, an indicator of plant age and ill health, is an important phenotypic trait for the assessment of a plant's response to stress. Manual inspection of senescence, however, is time consuming, inaccurate and subjective. In this paper we propose an objective evaluation of plant senescence by color image analysis for use in a high throughput plant phenotyping pipeline. As high throughput phenotyping platforms are designed to capture whole-of-plant features, camera lenses and camera settings are inappropriate for the capture of fine detail. Specifically, plant colors in images may not represent true plant colors, leading to errors in senescence estimation. Our algorithm features a color distortion correction and image restoration step prior to a senescence analysis. We apply our algorithm to two time series of images of wheat and chickpea plants to quantify the onset and progression of senescence. We compare our results with senescence scores resulting from manual inspection. We demonstrate that our procedure is able to process images in an automated way for an accurate estimation of plant senescence even from color distorted and blurred images obtained under high throughput conditions.
Asunto(s)
Algoritmos , Imagen Óptica/métodos , Desarrollo de la Planta , Cicer/crecimiento & desarrollo , Color , Ensayos Analíticos de Alto Rendimiento/métodos , Imagen Óptica/instrumentación , Triticum/crecimiento & desarrolloRESUMEN
Nitrogen (N) is a major nutrient needed to attain optimal grain yield (GY) in all environments. Nitrogen fertilisers represent a significant production cost, in both monetary and environmental terms. Developing genotypes capable of taking up N early during development while limiting biomass production after establishment and showing high N-use efficiency (NUE) would be economically beneficial. Genetic variation in NUE has been shown previously. Here we describe the genetic characterisation of NUE and identify genetic loci underlying N response under different N fertiliser regimes in a bread wheat population of doubled-haploid lines derived from a cross between two Australian genotypes (RAC875 × Kukri) bred for a similar production environment. NUE field trials were carried out at four sites in South Australia and two in Western Australia across three seasons. There was genotype-by-environment-by-treatment interaction across the sites and also good transgressive segregation for yield under different N supply in the population. We detected some significant Quantitative Trait Loci (QTL) associated with NUE and N response at different rates of N application across the sites and years. It was also possible to identify lines showing positive N response based on the rankings of their Best Linear Unbiased Predictions (BLUPs) within a trial. Dissecting the complexity of the N effect on yield through QTL analysis is a key step towards elucidating the molecular and physiological basis of NUE in wheat.
Asunto(s)
Estudios de Asociación Genética , Nitrógeno/metabolismo , Sitios de Carácter Cuantitativo , Carácter Cuantitativo Heredable , Triticum/genética , Triticum/metabolismo , Biomasa , Cruzamiento , Mapeo Cromosómico , Cruzamientos Genéticos , Grano Comestible , Ambiente , Fertilizantes , Ligamiento Genético , Genotipo , Triticum/crecimiento & desarrolloRESUMEN
Over 100million tonnes of nitrogen (N) fertiliser are applied globally each year to maintain high yields in agricultural crops. The rising price of N fertilisers has made them a major cost for farmers. Inefficient use of N fertiliser leads to substantial environmental problems through contamination of air and water resources and can be a significant economic cost. Consequently, there is considerable need to improve the way N fertiliser is used in farming systems. The efficiency with which crops use applied N fertiliser - the nitrogen-use efficiency (NUE) - is currently quite low for cereals. This is the case in both high yielding environments and lower yielding environments characteristic of cereal growing regions of Australia. Multiple studies have attempted to identify the genetic basis of NUE, but the utility of the results is limited because of the complex nature of the trait and the magnitude of genotype by environment interaction. Transgenic approaches have been applied to improve plant NUE but with limited success, due, in part, to a combination of the complexity of the trait but also due to lack of accurate phenotyping methods. This review documents these two approaches and suggests future directions in improving cereal NUE with a focus on the Australian cereal industry.
RESUMEN
Our continuing survey of phototoxins from higher plants has led to the isolation and identification from the common rush, Juncus effusus L., of the phenanthrene, dehydroeffusol (1), and the dihydrophenanthrene, juncusol (2), compounds that display enhanced antimicrobial activities in light. The antimicrobial activities (minimum inhibitory concentrations) for these compounds against methicillin-resistant and -sensitive Staphylococcus aureus and Candida albicans were increased 16- and two-fold, respectively, by irradiation with ultraviolet A (UVA). Photosensitized DNA-binding activities (as possible covalent bond formation) of these compounds were determined by using restriction enzymes and a specially prepared 1.5 kb DNA fragment. Under UVA irradiation, dehydroeffusol strongly inhibited all the restriction enzymes (KpnI, XbaI, PmeI, DraI, PacI and BciVI) that have at least one 5'-TpA sequence in their recognition sites. Weak inhibitions were found for the restriction enzymes EcoRI, SacI, BamHI, SalI, PstI and HindIII, which do not possess a 5'-TpA sequence at their restriction sites and the restriction site sequences of which consist of all bases, A, T, G and C. Trace or no inhibition was found for AscI and SmaI, the restriction site sequences of which are composed of only C and G. The results indicate the necessity of thymine (adenine) for the photosensitized DNA-binding activity of dehydroeffusol. A strong inhibition against SphI, which does not have a 5'-TpA sequence in the restriction sequence, indicates that there are possibly other binding sequence(s) for dehydroeffusol. With juncusol and UVA, strong inhibitions for KpnI and BciVI and trace inhibitions for PacI, XbaI, PmeI and DraI were found. This result also showed a preference of juncusol for 5'-TpA, but the preference could be more selective than that of dehydroeffusol depending on the surrounding sequences of 5'-TpA in the respective restriction sites. A strong inhibition of SphI by juncusol with UVA also indicated the existence of an unknown binding sequence for this compound. Generally, the DNA-binding activity of this compound was weaker than that of dehydroeffusol.