Controlling the Morphology of Aggregates of an Amphiphilic Synthetic Receptor through Host-Guest Interactions

A new amphiphilic receptor containing a macrocyclic anionic headgroup and a single alkyl chain was prepared through an efficient templated synthesis. The interdependence of the aggregation behavior and the host-guest chemistry was studied. In the absence of any guest the terminus of the alkyl chain of the receptor is included inside the hydrophobic cavity of the macrocycle (as evident from 1H NMR studies) leading to self-assembly into micrometer-long nanotubes (as evident from TEM studies). The alkyl chain can be displaced by an acridizinium bromide guest (as evident from 1H NMR and ITC), which leads to a dramatic change in aggregate size and morphology (as evident from DLS). Studies of the solubilization of Nile red suggest that the resulting aggregates are micelles with a cmc of around 35 µM. These results represent a new addition to the still small number of water-soluble amphiphilic receptors and one of the first examples in which specific host-guest chemistry controls the size and shape of nanoscale aggregates.

Distribution of arabinogalactan protein (AGP) epitopes on the anther derived embryoid cultures of Brassica napus

The anther-derived embryoid cultures of Brassica napus is stably embryogenic and has an extracellular matrix (ECM) layer covering the surface of the developing embryoids. In this study, the distribution of arabinogalactan protein (AGP) epitopes in the ECM layer and the embryogenic tissue of winter oilseed rape were investigated by immuno-labelling with anti-AGP monoclonal antibodies (mAb JIM4, JIM8, and JIM 13). There was no labelling by the JIM4 and JIM8 mAbs in the ECM layer, unlike what was reported in other plant species. JIM 13 epitope is developmentally regulated because it was only present in the ECM layer of the mature embryogenic tissue. These observations indicate a possible variability in the AGP epitopes present in the ECM layer among the different plant species. JIM8 and JIM 13 epitopes were found in some epidermal cells of embryogenic tissue, but not in the non-embryogenic tissue, implying that AGPs might have a specific role in embryogenic competency or determining the cell fate of the B. napus embryogenic cell

Extracellular localization of napin in the embryogenic tissues of Brassica napus spp. oleifera

Napin, a storage protein, has been reported to be transcribed abundantly during the pre-embryogenic stage and associated with the induction of Brassica napus secondary embryogenesis. In this study, we studied the distribution pattern of napin in the winter oilseed rape embryogenic tissue in comparison to that of the non-embryogenic tissue using the indirect immunofluorescence localisation coupled with the ultrastructural immunogold labelling techniques. Immunolocalisation studies revealed that the extracellular matrix layer outside the outer epidermal cell wall of B. napus embryogenic tissues contained napin. This is the first study to report the extracellular localisation of napin. In addition, we have also further characterised the expression pattern of Eg1 that encodes for napin in the B. napus embryogenic tissue

A Technique for Correlative Scanning and Transmission Electron Microscopy of Individual Human Placental Villi: An Example Demonstrating Syncytial Sprouts in Early Gestation

Correlating the surface appearances of certain features with their internal structure is made particularly difficult in the human placenta by the complex three-dimensional branching pattern of the villous tree. This places a possible limitation on the use of the scanning electron microscope in this field, both for basic research purposes and as a tool in pathological diagnosis. To help overcome this problem, a technique for handling individual placental villi has been devised. By attaching single villi to glass pipette tips it has proved possible to scan the villi, embed them in resin and then section them in a known pre-determined orientation. Exact correlations between the surface appearances and the internal structure, as seen with either the light or transmission electron microscope, can then be drawn. This paper describes the technique and, using an example based on syncytial sprouts in early pregnancy, illustrates the precision afforded by the method

With a flick of the lid: a novel trapping mechanism in Nepenthes gracilis pitcher plants.

Carnivorous pitcher plants capture prey with modified leaves (pitchers), using diverse mechanisms such as 'insect aquaplaning' on the wet pitcher rim, slippery wax crystals on the inner pitcher wall, and viscoelastic retentive fluids. Here we describe a new trapping mechanism for Nepenthes gracilis which has evolved a unique, semi-slippery wax crystal surface on the underside of the pitcher lid and utilises the impact of rain drops to 'flick' insects into the trap. Depending on the experimental conditions (simulated 'rain', wet after 'rain', or dry), insects were captured mainly by the lid, the peristome, or the inner pitcher wall, respectively. The application of an anti-slip coating to the lower lid surface reduced prey capture in the field. Compared to sympatric N. rafflesiana, N. gracilis pitchers secreted more nectar under the lid and less on the peristome, thereby directing prey mainly towards the lid. The direct contribution to prey capture represents a novel function of the pitcher lid

A Scanning Electron Microscopic Study of the Chick Chorioallantoic Membrane: Cell Death and the Involvement of Oxygen Free Radicals

Cell death is a normal feature within the chick chorioallantoic membrane, occurring principally between days 10 and 14 of incubation. Samples of chorioallantoic membrane were obtained on days 6, 8, 10, 12 and 14 of incubation, after the creation of artificial air chambers on day 3. These were examined by scanning electron microscopy (SEM), transmission electron microscopy (TEM) after staining for acid phosphatase activity, and by light microscopy after demonstrating oxygen free radicals with nitro blue tetrazolium. On day 6, small defects in the plasmalemma, approximately 200 nm in diameter, could be seen by SEM. A sequence of events leading to complete destruction of the plasmalemma, with exposure of the nucleus and other cytoplasmic organelles, could be traced, and by day 8 the membrane was a mosaic of healthy cells and others in various stages of degeneration. TEM revealed that acid phosphatase activity was confined to the golgi apparatus and associated vesicles even in advanced stages of degeneration. By comparison, oxygen free radicals were demonstrated in individual cells from day 6 onwards. Application of superoxide dismutase and catalase to the epithelium using a nebuliser spray significantly reduced the amount of cell death seen by scanning microscopy on day 12. It is concluded that oxygen free radicals may mediate cell death in the chorioallantoic membrane

Relative efficiency of fishing gears and investigation of resource availability in tropical demersal scalefish fisheries FRDC REPORT – PROJECT 2006/031

This project identified that there is substantial spatial variation in the demersal fish assemblages in the NDSF with some species more abundant in the north of the fishery and others in the south. At finer scales within sites and depths there is spatial variation associated with different habitats (e.g. sand vs sponge gardens or reef)