However, we could not identify significant differences between the two groups in terms of functional outcomes.”
“Grafting copolymers of polyacrylamide (PAM) with Konjac gum (KGM) have been synthesized using ceric-ion-induced initiation technique. The copolymers were characterized using several instrumental techniques, including infrared (IR) spectroscopy, elementary analysis, scanning electron microscopy (SEM), size exclusion chromatography (SEC) analysis, and intrinsic viscosity to confirm the success of grafting. The flocculation performance of graft copolymers was characterized by two methods. One was to study the relationship
between the flocculants BIX 01294 molecular weight doses in kaolin Suspension and the Supernatant transmittance, and the other is to examine the time dependence of sediment height of kaolin suspensions. It was found that the graft copolymer is better than KGM and pure PAM. Biodegradation behavior was testified
by monitoring the Selleck GSK1210151A decay of relative viscosities, and approved by KGM ether bonds breaking in IR spectra and the molecule weight reduction in SEC analysis. The results indicate that the grafted KGM copolymers have improved both, flocculation performance and better biodegradable properties than the unmodified parent KGM and pure PAM. (c) 2008 Wiley Periodicals, Inc. J Appl Polym Sci 111: 2527-2536, 2009″
“P>The plant hormone auxin (indole-3-acetic acid or IAA) regulates plant development by inducing rapid cellular responses and changes in gene expression. Auxin promotes the degradation of Aux/IAA transcriptional repressors, thereby allowing auxin response factors AZD6738 (ARFs) to activate the transcription of auxin-responsive genes. Auxin enhances the binding of Aux/IAA proteins to the receptor TIR1, which is an F-box
protein that is part of the E3 ubiquitin ligase complex SCFTIR1. Binding of Aux/IAA proteins leads to degradation via the 26S proteasome, but evidence for SCFTIR1-mediated poly-ubiquitination of Aux/IAA proteins is lacking. Here we used an Arabidopsis cell suspension-based protoplast system to find evidence for SCFTIR1-mediated ubiquitination of the Aux/IAA proteins SHY2/IAA3 and BDL/IAA12. Each of these proteins showed a distinct abundance and repressor activity when expressed in this cell system. Moreover, the amount of endogenous TIR1 protein appeared to be rate-limiting for a proper auxin response measured by the co-transfected DR5::GUS reporter construct. Co-transfection with 35S::TIR1 led to auxin-dependent degradation, and excess of 35S::TIR1 even led to degradation of Aux/IAAs in the absence of auxin treatment. Expression of the mutant tir1-1 protein or the related F-box protein COI1, which is involved in jasmonate signaling, had no effect on Aux/IAA degradation.