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See detailFunction and application of plant volatiles in ecological regulation and management of pest.
Zhou, Haibo ULg

(2008, November 02)

Study on the ecological regulation of pests was one of the hotspot in the researches of sustainable agriculture in recent years,and the plant volatiles have been shown to exert important influence on ... [more ▼]

Study on the ecological regulation of pests was one of the hotspot in the researches of sustainable agriculture in recent years,and the plant volatiles have been shown to exert important influence on behaviors of pests. This paper reviewed the effect and mechanism of plant volatiles to pests in host selection, attraction,antifeeding, repellence, growth inhibition, the prospect and application of plant volatiles to agricultural cultivation was further discussed. [less ▲]

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See detailFunction and dysfunction of the lower airways
Lekeux, Pierre ULg; Art, Tatiana ULg

in Proceedings: 9e Congrès de médecine et chirurgie équine (2005)

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See detailTHE FUNCTION OF HMG-BOX TRANSCRIPTION FACTORS Sox4a AND Sox4b IN ZEBRAFISH BONE DEVELOPMENT AND HOMEOSTASIS.
Aceto, Jessica ULg; Motte, Patrick ULg; Martial, Joseph ULg et al

in Journal of Gravitational Physiology : A Journal of the International Society for Gravitational Physiology (2008), 15

In mammals, the Sox4 gene is involved in development of endocardial crests, the brain, the lung, teeth, gonads and lymphocytes. Recently, Sox4 was shown to control bone mass and mineralization in mice. In ... [more ▼]

In mammals, the Sox4 gene is involved in development of endocardial crests, the brain, the lung, teeth, gonads and lymphocytes. Recently, Sox4 was shown to control bone mass and mineralization in mice. In zebrafish, two homologs for the mammalian Sox4 are present, sox4a and sox4b. Here we investigate the function of the sox4a and sox4b genes in cartilage and bone development in zebrafish. Therefore, we focus our attention on the first bone structures to be formed, the head skeleton and more precisely the pharyngeal cartilage. We show that both genes are expressed in the pharyngeal region, albeit at different time points during development. Double in situ hybridization experiments are used to exactly define the particular tissues where they are expressed. Furthermore, microinjection experiments of antisense oligonucleotides are used to block translation of these specific genes and to define their precise function during cartilage and bone development. [less ▲]

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See detailFunction of Penicillin-binding protein 3 in Streptococcus Faecium
Coyette, Jacques; Somzé, Anne; Briquet, Jean-Jacques et al

in Hakenbeck, Regine; Höltje, Joachim-Volker; Labischinski, Harald (Eds.) The Target Penicillin : the Murein Sacculus of Bacterial Cell Walls Architecture and Growth : Proceedings (1983)

Cefotaxime at concns. around the min. inhibitory concn. (MIC, 5 μM) or below (0.1-1.0 μM) causes transformation of the normal S. faecium cells to bacilliform cells whose length increases with increasing ... [more ▼]

Cefotaxime at concns. around the min. inhibitory concn. (MIC, 5 μM) or below (0.1-1.0 μM) causes transformation of the normal S. faecium cells to bacilliform cells whose length increases with increasing duration of treatment. Septa are initiated but never reach completion. Affinity detn. for cefotaxime binding showed that the antibiotic binds preferentially to the 3 highest mol. wt. penicillin-binding proteins (PBP); PBP-2 and PBP-3 are about 100-fold more sensitive to cefotaxime than PBP-1. It appears, therefore, that PbP-2 and PBP-3 are involved in cell septation. This was confirmed by using cefatoxime in subinhibitory concns. (1 μM). From cell samples collected 30 and 60 min after addn. of cefotaxime, membranes were isolated, labeled with satg. [3H]benzylpenicillin and examd. by fluorog. Under these conditions only PBP-2 and PBP-3 were satd. by cefotaxime. At this stage no distinction could be made between the 2 proteins; either both or 1 of them may be involved in cell division. Cefoxitin produced morphol. alteration of a different nature than cefotaxime. The cefoxitin-treated cells had increased diam. and were slightly elongated. The most striking alteration was the frequent presence of conical poles contrasting with round poles obsd. in control cells. The morphol. alteration obsd. in cefoxitin-treated cells could be attributed to the inhibition of the function of PBP-1, PBP-2, or PBP-3. Elongated cells similar to those obtained with cefotaxime were not found with cefoxitin at concns. sufficient to sat. PBP-2. The main difference between cefotaxime- and cefoxitin-treated cells is that PBP-3 is satd. by cefotaxime but not altered at all by cefoxitin. Thus, septation inhibition must be due to the interaction of cefotaxime with PBP-3 [less ▲]

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See detailFunction of the Chloroplast Hydrogenase in the Microalga Chlamydomonas: The Role of Hydrogenase and State Transitions during Photosynthetic Activation in Anaerobiosis
Ghysels, Bart ULg; Godaux, Damien ULg; Matagne, René-Fernand ULg et al

in PLoS ONE (2013), 8(5), 64161

Like a majority of photosynthetic microorganisms, the green unicellular alga Chlamydomonas reinhardtii may encounter O2 deprived conditions on a regular basis. In response to anaerobiosis or in a ... [more ▼]

Like a majority of photosynthetic microorganisms, the green unicellular alga Chlamydomonas reinhardtii may encounter O2 deprived conditions on a regular basis. In response to anaerobiosis or in a respiration defective context, the photosynthetic electron transport chain of Chlamydomonas is remodeled by a state transition process to a conformation that favours the photoproduction of ATP at the expense of reductant synthesis. In some unicellular green algae including Chlamydomonas, anoxia also triggers the induction of a chloroplast-located, oxygen sensitive hydrogenase, which accepts electrons from reduced ferredoxin to convert protons into molecular hydrogen. Although microalgal hydrogen evolution has received much interest for its biotechnological potential, its physiological role remains unclear. By using specific Chlamydomonas mutants, we demonstrate that the state transition ability and the hydrogenase function are both critical for induction of photosynthesis in anoxia. These two processes are thus important for survival of the cells when they are transiently placed in an anaerobic environment. [less ▲]

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See detailFunction of the chloroplastic hydrogenase in the microalga Chlamydomonas reinhardtii: A trvel from dark to light
Godaux, Damien ULg

Doctoral thesis (2014)

The decreasing availability of fossil energy stocks and the eventuality of tragic climate changes caused by greenhouse gases lead to search for alternative renewable energy sources. Biological hydrogen ... [more ▼]

The decreasing availability of fossil energy stocks and the eventuality of tragic climate changes caused by greenhouse gases lead to search for alternative renewable energy sources. Biological hydrogen might be one promising renewable energy carrier. A specific and restricted group of microalgae developed the ability to produce hydrogen based on an oxygen-sensitive hydrogenase enzyme coupled to the photosynthetic pathway, acting as a putative valve for excess electrons in conditions where other electron acceptors are scarce. The unicellular green alga Chlamydomonas reinhardtii is widely regarded as a model organism for various biological processes, especially for photosynthesis. Moreover, the capacity of Chlamydomonas hydrogenase is claimed as the highest recorded in literature. Less than twenty years ago, a group of American scientists designed a new approach for sustained photobiological production of hydrogen, based on a two-stage protocol that temporally separates photosynthetic O2 evolution from the H2 production phase (Melis et al., 2000). The transition occurs upon sulfur deprivation of the culture and leads to an operating continuous production for several days, opening new possibilities in the aim of an economically rentable bioproduction. For these reasons, hydrogen photoproduction in Chlamydomonas reinhardtii has been extensively examined in the last decade as extension of photosynthesis research entailing the understanding of hydrogen metabolism in microalgae (for reviews, see Hankamer et al., 2007; Ghirardi et al., 2009; Ghysels and Franck, 2010). Despite the attractive trait of generating a renewable fuel from nature’s most plentiful resources, i.e. light and water, the physiological significance of such oxygen-sensitive enzyme coupled to oxygenic photosynthesis has been poorly investigated with the exception of some old studies (Kessler, 1973; Schreiber and Vidaver, 1974). In this work, hydrogenase implication in photosynthetic reactivation from dark and anoxic environment is investigated. In the first part of the work, by analyzing several strains affected in hydrogen metabolism (e.g. nda2-RNAi (Jans et al., 2008), pfl1 (Philipps et al., 2011), dum11 (Dorthu et al., 1992)), we show that the PSII–dependent photosynthetic electron flow upon dark to light shift is linearly related to the activity of hydrogenase, both for short and long-terms adaptation (Publication I). In agreement with this conclusion, a hydrogenase-deficient strain for the HydEF maturation factor (hydef, Posewitz et al., 2004) shows peculiar chlorophyll fluorescence induction kinetics after adaptation to dark and anoxia. Based on these findings, a novel imaging screening method is developed, allowing rapid identification of strains impaired in hydrogen metabolism. Compared to existing screens (for review, see Hemschemeier et al., 2009), our protocol is remarkably fast, sensitive and non-invasive. At this stage, application of this new screening method allowed us to isolate several hydrogenase-deficient strains, among which one was impaired for the hydrogenase maturation protein HydG (hydg-2 mutant). Chlamydomonas reinhardtii might frequently encounter period of dark and anoxia in its natural habitat, especially during the night when the microbial community respires the available oxygen. In the second part of my work, the physiological importance of hydrogenase is investigated in the context of photosynthesis induction at the onset of light upon anoxia. In such conditions, the plastoquinone pool is known as being overreduced. This triggers the process of state transitions which is described as allowing the redistribution of light capture between both photosystems to manage the redox poise of the photosynthetic pathway (for review, see Lemeille and Rochaix, 2010). We therefore revisit the impact of both state transitions and hydrogenase activity on the reactivation of photosynthetic electron flow (Publication II). Here we show that, in presence of hydrogenase, photosynthesis reactivation is slightly faster in stt7 mutant locked in state 1 (Depege et al., 2003) compared to wild type which is in state 2. However, photosynthesis reactivation is delayed in hydef stt7-9 double mutant compared to hydef mutant. This indicates that, in a hydrogenase-deficient context, state 2 promotes photosynthesis reactivation. Considered for a long time as being tightly interconnected (Finazzi et al., 1999; Finazzi et al., 2002; Finazzi and Forti, 2004), state transitions and PSI-CEF have recently been revealed as unrelated to each other (Takahashi et al., 2013). Nonetheless, the increasing of PSI antenna size in state 2 could even though enhance the PSI-CEF rate, in an indirect way, by enhancing PSI energy capture (Cardol et al., 2009; Alric, 2014). This reasonably raises the question of a possible involvement of PSI-CEF in photosynthesis induction. This possibility is further studied in the third and last part of the work. Thanks to mutants devoid of PSI-CEF (i.e. pgrl1 mutant (Tolleter et al., 2011)) and hydrogenase activity (i.e. hydg-2 mutant (Publication I)), we investigate the role played by PSI-CEF along with hydrogenase during photosynthesis reactivation during a shift from dark anoxia to light (Publication III). Herein, we demonstrate that Calvin cycle reactivation is proton gradient-dependent, most likely due to ATP requirement for carbon dioxide fixation. By measuring the PSI/PSII efficiency ratio during the re- illumination period, we point out the physiological occurrence of PSI-CEF within the first minutes of ilumination. We therefore propose a schematic model that assesses the electron flow through hydrogenase, PSI-CEF and Calvin cycle in function of the illumination period in all studied strains. Although lack of PSI-CEF does not appear to be essential for cell survival, photosynthesis reactivation is delayed in pgrl1 mutants. We also isolate a pgrl1 hydg-2 double mutant and demonstrate that the combination of both defects prevents any photosynthetic activity and strongly impairs growth. This highlights the importance for algae to keep both pathways in the course of evolution, being critical for the survival of Chlamydomonas reinhardtii in its natural environment. [less ▲]

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See detailFunction of the chloroplastic NAD(P)H dehydrogenase Nda2 for H(2) photoproduction in sulphur-deprived Chlamydomonas reinhardtii.
Mignolet, Emmanuel; Lecler, Renaud; Ghysels, Bart ULg et al

in Journal of biotechnology (2012), 162(1), 81-8

The relative contributions of the PSII-dependent and Nda2-dependent pathways for H(2) photoproduction were investigated in the green microalga Chlamydomonas reinhardtii after suphur-deprivation. For this ... [more ▼]

The relative contributions of the PSII-dependent and Nda2-dependent pathways for H(2) photoproduction were investigated in the green microalga Chlamydomonas reinhardtii after suphur-deprivation. For this purpose, H(2) gas production was compared for wild-type and Nda2-deficient cells with or without DCMU (a PSII-inhibitor) in the same experimental conditions. Nda2-deficiency caused a 30% decrease of the maximal H(2) photoevolution rate observed shortly after the establishment of anoxia, and an acceleration of the decline of H(2) photoevolution rate with time. DCMU addition to Nda2-deficient cells completely inhibited H(2) photoproduction, showing that the PSII-independent H(2) photoproduction relies on the presence of Nda2, which feeds the photosynthetic electron transport chain with electrons derived from oxidative catabolism. Nda2-protein abundance increased as a result of sulphur deprivation and further during the H(2) photoproduction process, resulting in high rates of non-photochemical plastoquinone reduction in control cells. Nda2-deficiency had no significant effect on photosynthetic and respiratory capacities in sulphur-deprived cells, but caused changes in the cell energetic status (ATP and NADPH/NADP+ ratio). The rapid decline of H(2) photoevolution rate with time in Nda2-deficient cells revealed a more pronounced inhibition of H(2) photoproduction by accumulated H(2) in the absence of non-photochemical plastoquinone reduction. Nda2 is therefore important for linking H(2) photoproduction with catabolism of storage carbon compounds, and seems also involved in regulating the redox poise of the photosynthetic electron transport chain during H(2) photoproduction. [less ▲]

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See detailFunction of the chloroplastic NADP(H) dehydrogenase NDA2 for the H2 photoproduction in sulphur-deprived Chlamydomonas reinhardtii
Mignolet, Emmanuel ULg; Lecler, Renaud ULg; Ghysels, Bart ULg et al

in Journal of Biotechnology (2012), 162

The relative contributions of the PSII-dependent and Nda2-dependent pathways for H2 photoproduction were investigated in the green microalga Chlamydomonas reinhardtii after suphur-deprivation. For this ... [more ▼]

The relative contributions of the PSII-dependent and Nda2-dependent pathways for H2 photoproduction were investigated in the green microalga Chlamydomonas reinhardtii after suphur-deprivation. For this purpose, H2 gas production was compared for wild-type and Nda2-deficient cells with or without DCMU (a PSII-inhibitor) in the same experimental conditions. Nda2-deficiency caused a 30 % decrease of the maximal H2 photoevolution rate observed shortly after the establishment of anoxia, and an acceleration of the decline of H2 photoevolution rate with time. DCMU addition to Nda2-deficient cells completely inhibited H2 photoproduction, showing that the PSII-independent H2 photoproduction relies on the presence of Nda2, which feeds the photosynthetic electron transport chain with electrons derived from oxidative catabolism. Nda2-protein abundance increased as a result of sulphur deprivation and further during the H2 photoproduction process, resulting in high rates of non-photochemical plastoquinone reduction in control cells. Nda2-deficiency had no significant effect on photosynthetic and respiratory capacities in sulphur-deprived cells, but caused changes in the cell energetic status (ATP and NADPH/NADP+ ratio). The rapid decline of H2 photoevolution rate with time in Nda2-deficient cells revealed a more pronounced inhibition of H2 photoproduction by accumulated H2 in the absence of non-photochemical plastoquinone reduction. Nda2 is therefore important for linking H2 photoproduction with catabolism of storage carbon compounds, and seems also involved in regulating the redox poise of the photosynthetic electron transport chain during H2 photoproduction. [less ▲]

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See detailThe function of the transcription factor Egr1 in zebrafish cartilage development
Dalcq, Julia ULg; Pasque, Vincent; Ramos, Sonia Davila et al

in Developmental Biology (2007, June 01), 306(1), 439-440

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See detailFunction, diversity and therapeutic potential of the N-terminal domain of human chemokine receptors
Szpakowska, Martyna ULg; Fievez, Virginie; Arumugan, Karthik et al

in Biochemical Pharmacology (2012)

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See detailFunctional adaptations of the bacterial chaperone trigger factor to extreme environmental temperatures
Godin-Roulling, Amandine ULg; Schmidpeter, P.A.M.; Schmid, F.X. et al

in Environmental Microbiology (2015)

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See detailFunctional adaptations of the bacterial chaperone trigger factor to extreme environmental temperatures
Godin, Amandine ULg; Schmidpeter, P.; Schmid, F.X. et al

Poster (2014)

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See detailFunctional amphiphilic and biodegradable copolymers for intravenous vectorization
Van Butsele, Kathy ULg; Jérôme, Robert ULg; Jérôme, Christine ULg

in Polymer (2007), 48

This paper aims at reporting on the design of polymeric drug nanocarriers used in cancer therapy, with a special emphasis on the control of their biodistribution. First, the prominent role of poly ... [more ▼]

This paper aims at reporting on the design of polymeric drug nanocarriers used in cancer therapy, with a special emphasis on the control of their biodistribution. First, the prominent role of poly(ethylene oxide) in the lifetime of nanocarriers circulating in the blood stream is highlighted, and the origin of a passive targeting based on a difference in the anatomy of tumors and normal tissues is discussed. The main body of the review is devoted to the targeting of nanocarriers towards tumors and the underlying concepts. As a rule, either the constitutive polymer is stimuli-responsive and the locus of drug release is where the stimulation occurs, or a ligand endowed with specific recognition is grafted onto the nanocarrier. Finally, the fate of the nanocarrier after drug delivery and the bioelimination of the polymer(s) involved are briefly considered. [less ▲]

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See detailFunctional amphiphilic and degradable copolymers for drug delivery systems
Freichels, Hélène ULg; Pourcelle, Vincent; Plapied, Laurence et al

Poster (2008, December 18)

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See detailFunctional Analysis and the Finite Element Method
Stainier, Laurent; Tossings, Patricia ULg

Learning material (2008)

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See detailFunctional analysis of an FLC-LIKE gene in root chicory
Périlleux, Claire ULg; Pieltain, Alexandra ULg; D'Aloia, Maria ULg et al

in Comparative Biochemistry and Physiology. Part A, Physiology (2009), 153A(2/Suppl.), 198-199

Vernalization is known to promote flowering in Arabidopsis thaliana by inhibiting the expression of a strong repressor: FLOWERING LOCUS C (FLC). The recent cloning of an FLC-LIKE gene in sugar beet (Beta ... [more ▼]

Vernalization is known to promote flowering in Arabidopsis thaliana by inhibiting the expression of a strong repressor: FLOWERING LOCUS C (FLC). The recent cloning of an FLC-LIKE gene in sugar beet (Beta vulgaris; BvFL1) and – here – in root chicory (Cichorium intybus; CiFL1) suggests the conservation of FLC biological function during evolution of eudicots. Hence physiological questions that remain difficult to address in Arabidopsis can be studied in other species. We investigated the correlation between CiFL1 expression and plant-age dependent responsiveness to vernalization. We also studied the effect of post-vernalization growing temperature, which can stabilize or erase the vernalized state. [less ▲]

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