130 research outputs found

    Propagation of Grevillea

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    Grevillea (Proteaceae) is a native Australian genus with high commercial value as landscape ornamentals, and they are known to be difficult to root. There has been only limited research into the propagation of Grevillea. The effect of indole-3-butyric acid (IBA) on the rooting G. 'Poorinda Royal Mantle' in winter, spring and summer was evaluated at UQ Gatton, southern Queensland in order to determine the rooting ability of this species in different seasons. The effect of cutting type, i.e. tip and stem cuttings, and method of auxin application, i.e. top and basal application, were also tested on G. 'Poorinda Royal Mantle' and G. 'Coastal Dawn'. G. 'Poorinda Royal Mantle' demonstrated a seasonal rooting and was more responsive than G. 'Coastal Dawn' to the applied IBA. Stem cuttings had a higher survival than tip cuttings, but tip cuttings had a higher capacity to root. Top application of auxin at low concentration (1 g L-1) in G. 'Poorinda Royal Mantle' in spring resulted in a significantly higher rooting percentage than basal application at the same concentration. These findings could be useful for setting up a practical propagation protocol on Grevillea

    Sucrose interacts with auxin in the burst of axillary buds

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    Research focus. Branching is an important process for productivity (number of productive branches) and for visual quality of ornamental plants (branches spatial arrangement). But branching behaviour is difficult to predict due to the lack of knowledge on the all mechanisms regulating the plasticity of the burst of axillary buds. Auxin has an inhibitory action on bud burst and interacts with cytokinins (CKs) and strigolactones (SLs) [1]. Our study focuses on understanding and modelling how a newly - identified player, sugars [2,3], interact with the hormonal network to control bud burst . Methods. Experiments consisted in cultivating nodal stem segments of rosebush in vitro with different sucrose and auxin levels, and in quantifying bud elongation, CK level, and the expression of genes involve in SL biosynthesis and signalling. From these data, we designed and calibrated a computational model accounting for sucrose modulation of bud inhibition by auxin. Results. We observed that increasing sucrose level decreased the inhibition of bud elongation by auxin, so that buds fed with high sucrose level were less inhibited by a given amount of auxin than those fed with low sucrose level. In accordance with literature, auxin repressed CKs and stimulated the expression of SLs biosynthesis genes. We demonstrate that the main effect of sucrose was to repress SL signalling. The model developed from these results reproduced the combined action of sucrose and auxin on bud burst. We validated it for its capacity to predict the effect of external CK supply for different sucrose levels. Conclusions. Our study proposes for the first time a physiological model of the effect of sucrose on bud regulation by auxin at the scale of the bud. Initially observed for rosebush, our results were also validated in pea, demonstrating model genericity. Next step is to understand the role of sugars, together with hormones, in the spatio-temporal regulation of bud burst at the scale of the plant. For that, we will use the computational tool, by coupling our bud model to models simulating sugar and hormone fluxes within a plant architecture. (Texte intégral

    Strigolactones positively regulate chilling tolerance in pea and in Arabidopsis

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    Strigolactones (SL) fulfil important roles in plant development and stress tolerance. Here, we characterized the role of SL in the dark chilling tolerance of pea and Arabidopsis by analysis of mutants that are defective in either SL synthesis or signalling. Pea mutants (rms3, rms4, and rms5) had significantly greater shoot branching with higher leaf chlorophyll a/b ratios and carotenoid contents than the wild type. Exposure to dark chilling significantly decreased shoot fresh weights but increased leaf numbers in all lines. Moreover, dark chilling treatments decreased biomass (dry weight) accumulation only in rms3 and rms5 shoots. Unlike the wild type plants, chilling‐induced inhibition of photosynthetic carbon assimilation was observed in the rms lines and also in the Arabidopsis max3‐9, max4‐1, and max2‐1 mutants that are defective in SL synthesis or signalling. When grown on agar plates, the max mutant rosettes accumulated less biomass than the wild type. The synthetic SL, GR24, decreased leaf area in the wild type, max3‐9, and max4‐1 mutants but not in max2‐1 in the absence of stress. In addition, a chilling‐induced decrease in leaf area was observed in all the lines in the presence of GR24. We conclude that SL plays an important role in the control of dark chilling tolerance.BBSRC, Grant/Award Number: BB/K501839/1https://wileyonlinelibrary.com/journal/pce2019-06-01hj2018Forestry and Agricultural Biotechnology Institute (FABI)Plant Production and Soil Scienc

    Lipidomics analysis of juveniles' blue mussels (Mytilus edulis L. 1758), a key economic and ecological species

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    Blue mussels (Mytilus edulis L. 1758) are important components of coastal ecosystems and in the economy of rural and coastal areas. The understanding of their physiological processes at key life stages is important both within food production systems and in the management of wild populations. Lipids are crucial molecules for bivalve growth, but their diversity and roles have not been fully characterized. In this study, traditional lipid profiling techniques, such as fatty acid (FA) and lipid class analysis, are combined to un-targeted lipidomics to elucidate the lipid metabolism in newly settled spat fed on a range of diets. The evaluated diets included single strains treatments (Cylindrotheca fusiformis CCAP 1017/2 –CYL, Isochrysis galbana CCAP 927/1– ISO, Monodopsis subterranean CCAP 848/1 –MONO, Nannochloropsis oceanica CCAP 849/10– NANNO) and a commercial algae paste (SP). Spat growth was influenced by the diets, which, according to their efficacy were ranked as follows: ISO>NANNO/CYL>SP>MONO. A higher triacylglycerols (TG) content, ranging from 4.23±0.82 μg mgashfree Dry weight (DW)-1 at the beginning of the trial (T0) to 51±15.3 μg mgashfreeDW-1 in ISO, characterised significant growth in the spat, whereas, a reduction of TG (0.3±0.08 μg mgashfreeDW-1 in MONO), mono unsaturated FA–MUFA (from 8.52±1.02 μg mgFAashfreeDW-1 at T0 to 2.81±1.02 μg mgFAashfreeDW-1 in MONO) and polyunsaturated FA–PUFA (from 17.57±2.24 μg mgFAashfreeDW-1 at T0 to 6.19±2.49 μg mgFAashfreeDW-1 in MONO) content characterised poor performing groups. Untargeted lipidomics evidenced how the availability of dietary essential PUFA did not influence only neutral lipids but also the membrane lipids, with changes in lipid molecular species in relation to the essential PUFA provided via the diet. Such changes have the potential to affect spat production cycle and their ability to respond to the surrounding environment. This study evidenced the advantages of coupling different lipid analysis techniques, as each technique disclosed relevant information on nutritional requirements of M. edulis juveniles, expanding the existing knowledge on the physiology of this important species

    Sucrose interacts with auxin in the burst of axillary buds

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    National audienceResearch focus. Branching is an important process for productivity (number of productive branches) and for visual quality of ornamental plants (branches spatial arrangement). But branching behaviour is difficult to predict due to the lack of knowledge on the all mechanisms regulating the plasticity of the burst of axillary buds. Auxin has an inhibitory action on bud burst and interacts with cytokinins (CKs) and strigolactones (SLs) [1]. Our study focuses on understanding and modelling how a newly-identified player, sugars [2,3], interact with the hormonal network to control bud burst. Methods. Experiments consisted in cultivating nodal stem segments of rosebush in vitro with different sucrose and auxin levels, and in quantifying bud elongation, CK level, and the expression of genes involve in SL biosynthesis and signalling. From these data, we designed and calibrated a computational model accounting for sucrose modulation of bud inhibition by auxin. Results. We observed that increasing sucrose level decreased the inhibition of bud elongation by auxin, so that buds fed with high sucrose level were less inhibited by a given amount of auxin than those fed with low sucrose level. In accordance with literature, auxin repressed CKs and stimulated the expression of SLs biosynthesis genes. We demonstrate that the main effect of sucrose was to repress SL signalling. The model developed from these results reproduced the combined action of sucrose and auxin on bud burst. We validated it for its capacity to predict the effect of external CK supply for different sucrose levels. Conclusions. Our study proposes for the first time a physiological model of the effect of sucrose on bud regulation by auxin at the scale of the bud. Initially observed for rosebush, our results were also validated in pea, demonstrating model genericity. Next step is to understand the role of sugars, together with hormones, in the spatio-temporal regulation of bud burst at the scale of the plant. For that, we will use the computational tool, by coupling our bud model to models simulating sugar and hormone fluxes within a plant architecture

    LATERAL BRANCHING OXIDOREDUCTASE acts in the final stages of strigolactone biosynthesis inArabidopsis

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    Strigolactones are a group of plant compounds of diverse but related chemical structures. They have similar bioactivity across a broad range of plant species, act to optimize plant growth and development, and promote soil microbe interactions. Carlactone, a common precursor to strigolactones, is produced by conserved enzymes found in a number of diverse species. Versions of the MORE AXILLARY GROWTH1 (MAX1) cytochrome P450 from rice and Arabidopsis thaliana make specific subsets of strigolactones from carlactone. However, the diversity of natural strigolactones suggests that additional enzymes are involved and remain to be discovered. Here, we use an innovative method that has revealed a missing enzyme involved in strigolactone metabolism. By using a transcriptomics approach involving a range of treatments that modify strigolactone biosynthesis gene expression coupled with reverse genetics, we identified LATERAL BRANCHING OXIDOREDUCTASE (LBO), a gene encoding an oxidoreductase-like enzyme of the 2-oxoglutarate and Fe(II)-dependent dioxygenase superfamily. Arabidopsis lbo mutants exhibited increased shoot branching, but the lbo mutation did not enhance the max mutant phenotype. Grafting indicated that LBO is required for a graft-transmissible signal that, in turn, requires a product of MAX1. Mutant lbo backgrounds showed reduced responses to carlactone, the substrate of MAX1, and methyl carlactonoate (MeCLA), a product downstream of MAX1. Furthermore, lbo mutants contained increased amounts of these compounds, and the LBO protein specifically converts MeCLA to an unidentified strigolactone-like compound. Thus, LBO function may be important in the later steps of strigolactone biosynthesis to inhibit shoot branching in Arabidopsis and other seed plants

    Molecular dissection of the pea shoot apical meristem*

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    The shoot apical meristem (SAM) is responsible for the development of all the above-ground parts of a plant. Our understanding of the SAM at the molecular level is incomplete. This study investigates the gene expression repertoire of SAMs in the garden pea (Pisum sativum). To this end, 10 346 EST sequences representing 7610 unique genes were generated from SAM cDNA libraries. These sequences, together with previously reported pea ESTs, were used to construct a 12K oligonucleotide array to identify genes with differential SAM expression, as compared to axillary meristems, root apical meristems, or non-meristematic tissues. A number of genes were identified, predominantly expressed in specific cell layers or domains of the SAM and thus are likely components of the gene networks involved in stem cell maintenance or the initiation of lateral organs. Further in situ hybridization analysis confirmed the spatial localization of some of these genes within the SAM. Our data also indicate the diversification of some gene expression patterns and hence functions in legume crop plants. A number of transcripts highly expressed in all three meristems have also been uncovered and these candidates may provide valuable insight into molecular networks that underpin the maintenance of meristematic functionality
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