36 research outputs found
Evaluation of the phytochemical composition and antimicrobial properties of two aromatic plants used in the production of sweet wort and tchapalo, two artisanal beverages from CĂŽte d'Ivoire
The search for new antimicrobial molecules from natural sources is an opportunity to preserve food. The objective of this study is to evaluate the phytochemical composition and antimicrobial properties of the leaves of Adansonia digitata (Bombacaceae) and the bark of Grewia venusta (Tilaceae), two aromatic plants used in the production of sweet must and tchapalo. Phytochemical screening from the aqueous, decocted and methanolic extracts of these plants was performed using standard colorimetric methods. Antimicrobial activity was also evaluated on 21 strains using the well diffusion method. Minimum Inhibitory Concentrations (MIC) and Bactericides were determined respectively by the liquid macro-dilution and agar plating methods. Results showed the presence of tannins, triterpenoids, cardiotonic glycosides and saponins in these extracts. All extracts were active on Staphylococcus aureus ATCC25923 with inhibition diameters ranging from 10.33±1 to 20.3±1.5 mm. The methanolic extracts had the lowest MICs (12.5 mg/mL), with bactericidal and/or fungicidal activity on most of the microbial strains tested. These results confirm the antimicrobial activities of the phytochemical compounds of these plants that could play the role of stabilizer and preservative of sweet wort and tchapalo.
La recherche de nouvelles molĂ©cules antimicrobiennes Ă partir de sources naturelles est une opportunitĂ© pour conserver les aliments. Lâobjectif de cette Ă©tude est dâĂ©valuer la composition phytochimique et les propriĂ©tĂ©s antimicrobiennes des feuilles de Adansonia digitata (Bombacaceae) et des Ă©corces de Grewia venusta (Tilaceae), deux plantes aromatiques utilisĂ©es dans la production du moĂ»t sucrĂ© et du tchapalo. Le criblage phytochimiques Ă partir des extraits aqueux, dĂ©coctĂ©s et mĂ©thanoliques de ces plantes a Ă©tĂ© rĂ©alisĂ© selon les mĂ©thodes standards de colorimĂ©tries. LâactivitĂ© antimicrobienne a Ă©tĂ© Ă©galement Ă©valuĂ©e sur 21 souches en utilisant la mĂ©thode de diffusion en puits. Les Concentrations Minimales Inhibitrices (CMI) et BactĂ©ricides ont Ă©tĂ© dĂ©terminĂ©es respectivement par les mĂ©thodes de macro-dilution en milieu liquide et ensemencement sur milieu gĂ©losĂ©. Les rĂ©sultats ont montrĂ© la prĂ©sence de tannins, de triterpĂ©noĂŻdes, de cardiotoniques glycosides et de saponines dans ces extraits. Tous les extraits ont Ă©tĂ© actifs sur Staphylococcus aureus ATCC25923 avec des diamĂštres dâinhibition allant de 10,33±1 Ă 20,3± 1,5 mm. Les extraits mĂ©thanoliques ont prĂ©sentĂ© les CMI les plus faibles (12,5 mg/mL), avec une activitĂ© bactĂ©ricide et/ou fongicide sur la plupart des souches microbiennes testĂ©es. Ces rĂ©sultats confirment les activitĂ©s antimicrobiennes des composĂ©s phytochimiques de ces plantes qui pourraient jouer le rĂŽle de stabilisant et conservateur du moĂ»t sucrĂ© et du tchapalo
The state of the Martian climate
60°N was +2.0°C, relative to the 1981â2010 average value (Fig. 5.1). This marks a new high for the record. The average annual surface air temperature (SAT) anomaly for 2016 for land stations north of starting in 1900, and is a significant increase over the previous highest value of +1.2°C, which was observed in 2007, 2011, and 2015. Average global annual temperatures also showed record values in 2015 and 2016. Currently, the Arctic is warming at more than twice the rate of lower latitudes
Interhemispheric Temperature Gradient and Equatorial Pacific SSTs Drive Sahel Monsoon Uncertainties under Global Warming
International audienceAbstract The Sahel is one of the most vulnerable regions to climate change. Robust estimation of future changes in the Sahel monsoon is therefore essential for effective climate change adaptation. Unfortunately, state-of-the-art climate models show large uncertainties in their projections of Sahel rainfall. In this study, we use 32 models from CMIP6 to identify the sources of this large intermodel spread of Sahel rainfall. By using maximum covariance analysis, we first highlight two new key drivers of this spread during boreal summer: the interhemispheric temperature gradient and equatorial Pacific sea surface temperature (SST) changes. This contrasts with previous studies, which have focused mainly on the Northern Hemisphere rather than the global scale, and in which the Pacific Ocean has been neglected in favor of the Atlantic. Next, we unravel the physical mechanisms behind these statistical relationships. First, the modulation of the interhemispheric temperature gradient across the models leads to varying latitudinal positions of the intertropical convergence zone and, consequently, varying Sahel rainfall intensity. Second, models that exhibit less warming than the multimodel mean in the equatorial Pacific, thereby projecting a less âEl Niñoâlikeâ mean state, simulate enhanced precipitation over the central Sahel in the future through modulations of the Walker circulation, the tropical easterly jet, the meridional tropospheric temperature gradient, and hence regional zonal wind shear. Finally, we show that these two indices collectively explain 62% of Sahel rainfall change uncertainty: 40% due to the interhemispheric temperature gradient and 22% through equatorial Pacific SST
CSAP Acts as a Regulator of TTLL-Mediated Microtubule Glutamylation
Summary: Tubulin glutamylation is a reversible posttranslational modification that accumulates on stable microtubules (MTs). While abnormally high levels of this modification lead to a number of disorders such as male sterility, retinal degeneration, and neurodegeneration, very little is known about the molecular mechanisms underlying the regulation of glutamylase activity. Here, we found that CSAP forms a complex with TTLL5, and we demonstrate that the two proteins regulate their reciprocal abundance. Moreover, we show that CSAP increases TTLL5-mediated glutamylation and identify the TTLL5-interacting domain. Deletion of this domain leads to complete loss of CSAP activating function without impacting its MT binding. Binding of CSAP to TTLL5 promotes relocalization of TTLL5 toward MTs. Finally, we show that CSAP binds and activates all of the remaining autonomously active TTLL glutamylases. As such, we present CSAP as a major regulator of tubulin glutamylation and associated functions. : Bompard et al. describe an activator of tubulin glutamylases that modify the microtubule-based cytoskeleton. They find that CSAP forms a complex with TTLL5, which controls its localization and activity on microtubules. Keywords: posttranslational modification, MAPs, microtubule dynamics, severing, brain, tubulin cod
Direct coupling of detergent purified human mGlu5 receptor to the heterotrimeric G proteins Gq and Gs
The metabotropic glutamate (mGlu) receptors are class C G protein-coupled receptors (GPCRs) that modulate synaptic activity and plasticity throughout the mammalian brain. Signal transduction is initiated by glutamate binding to the venus flytrap domains (VFT), which initiates a conformational change that is transmitted to the conserved heptahelical domains (7TM) and results ultimately in the activation of intracellular G proteins. While both mGlu1 and mGlu5 activate Gαq G-proteins, they also increase intracellular cAMP concentration through an unknown mechanism. To study directly the G protein coupling properties of the human mGlu5 receptor homodimer, we purified the full-length receptor, which required careful optimisation of the expression, N-glycosylation and purification. We successfully purified functional mGlu5 that activated the heterotrimeric G protein Gq. The high-affinity agonist-PAM VU0424465 also activated the purified receptor in the absence of an orthosteric agonist. In addition, it was found that purified mGlu5 was capable of activating the G protein Gs either upon stimulation with VU0424465 or glutamate, although the later induced a much weaker response. Our findings provide important mechanistic insights into mGlu5 G protein-dependent activity and selectivity. © 2018 The Author(s).The authors would like to acknowledge Laurent PrĂ©zeau, Julie Kniazeff, Philippe Rondard and Cyril Goudet for helpful discussion and Chris Tate for a critical reading of the manuscript. We are grateful to Eric Trinquet (Cisbio, France) for providing us the SNAP tag full-length mGlu5 expression plasmid, as well as to Arpege and FFP platforms at the IGF. Karine Rottier was supported by FRM âingenieur de Rechercheâ program and Chady Nasrallah is supported by ATIP grant (2014â2016) and the University of Montpellier, Postodocotral scientist program (2016â2018). Joan Font and Amadeu Llebaria acknowledge MINECO (PCIN-2013â017 C03-01 and CTQ2014-57020-R), the Catalan Government (2014SGR109 and 2014CTP0002) and to ERANET Neuron project âLIGHTPAINâfor support. Guillaume Lebon acknowledges Program ATIP (2013â2016), the CNRS, INSERM and the University of Montpellier for their support.Peer reviewe
Evolutionary Divergence of Enzymatic Mechanisms for Tubulin Detyrosination
International audienceThe two related members of the vasohibin family, VASH1 and VASH2, encode human tubulin detyrosinases. Here we demonstrate that, in contrast to VASH1, which requires binding of small vasohibin binding protein (SVBP), VASH2 has autonomous tubulin detyrosinating activity. Moreover, we demonstrate that SVBP acts as a bona fide activator of both enzymes. Phylogenetic analysis of the vasohibin family revealed that regulatory diversification of VASH-mediated tubulin detyrosination coincided with early vertebrate evolution. Thus, as a model organism for functional analysis, we used Trypanosoma brucei (Tb), an evolutionarily early-branched eukaryote that possesses a single VASH and encodes a terminal tyrosine on both a- and b-tubulin tails, both subject to removal. Remarkably, although detyrosination levels are high in the flagellum, TbVASH knockout parasites did not present any noticeable flagellar abnormalities. In contrast, we observed reduced proliferation associated with profound morphological and mitotic defects, underscoring the importance of tubulin detyrosination in cell division
Pro-apoptotic activity of acylated triterpenoid saponins from the stem bark of Albizia chevalieri harms
International audienceAs a continuation of our interest in apoptosis-inducing triterpenoid saponins from Albizia genus, phytochemical investigation of the stem bark of Albizia chevalieri led to the isolation of three new oleanane-type saponins, named chevalierosides AâC (1â3). Their structures were established on the basis of extensive analysis of 1D and 2D NMR (1H-, 13C NMR, DEPT, COSY, TOCSY, ROESY, HSQC and HMBC) experiments, HRESIMS studies, and by chemical evidence. The pro-apoptotic effect of the three saponins was evaluated on two human cell lines (pancreatic carcinoma AsPC-1 and hematopoietic monocytic THP-1). Cytometric analyses showed that saponins 1â3 induced apoptosis of both human cell lines (AsPC-1 and THP-1) in a dose-dependent manner
Tableau encyclop\ue9dique et m\ue9thodique des trois r\ue8gnes de la nature : Vers, coquilles, mollusques et polypiers
t.1 (1827
The T cell CD6 receptor operates a multitask signalosome with opposite functions in T cell activation
International audienceTo determine the respective contribution of the LAT transmembrane adaptor and CD5 and CD6 transmembrane receptors to early TCR signal propagation, diversification, and termination, we describe a CRISPR/Cas9-based platform that uses primary mouse T cells and permits establishment of the composition of their LAT, CD5, and CD6 signalosomes in only 4 mo using quantitative mass spectrometry. We confirmed that positive and negative functions can be solely assigned to the LAT and CD5 signalosomes, respectively. In contrast, the TCR-inducible CD6 signalosome comprised both positive (SLP-76, ZAP70, VAV1) and negative (UBASH3A/STS-2) regulators of T cell activation. Moreover, CD6 associated independently of TCR engagement to proteins that support its implication in inflammatory pathologies necessitating T cell transendothelial migration. The multifaceted role of CD6 unveiled here accounts for past difficulties in classifying it as a coinhibitor or costimulator. Congruent with our identification of UBASH3A within the CD6 signalosome and the view that CD6 constitutes a promising target for autoimmune disease treatment, single-nucleotide polymorphisms associated with human autoimmune diseases have been found in the Cd6 and Ubash3a genes