The native form of FtsA, a septal protein of Escherichia coli, is located in the cytoplasmic membrane.

Antisera able to recognize FtsA, one of the septal proteins of Escherichia coli, have been obtained and used to show that native FtsA, when expressed at levels ranging from physiological to induced from lambda pR, is located in the inner membrane. Experiments of trypsin accessibility to FtsA in membranes, spheroplasts, and vesicles indicated that FtsA is located such that it faces the cytoplasm. This location is consistent with current knowledge about the participation of FtsA in a molecular complex active in cell division called septator.     

Identification of a site in the alpha chain of platelet glycoprotein Ib that participates in von Willebrand factor binding

The binding of von Willebrand factor (vWF) to the platelet receptor glycoprotein (GP) Ib-IX complex is a key event in hemostasis and may participate in the development of thrombotic vascular occlusion. We present here evidence that residues Ser251-Tyr279 in the GP Ib alpha-chain participate in this function. Initial studies suggested that the modality of vWF interaction with GP Ib depended on the conditions used for induction of binding, either in the presence of ristocetin, or botrocetin, or with asialo-vWF. In fact, only the 45-kDa amino-terminal fragment of GP Ib alpha inhibited the vWF-GP Ib interaction under all conditions tested, while the 84-kDa macroglycopeptide was significantly effective only in the presence of ristocetin. Moreover, the 45-kDa fragment with reduced disulfide bonds still inhibited ristocetin-induced binding but had no effect, at the concentrations tested, on botrocetin-mediated or direct asialo-vWF binding. In order to localize in more detail the functional site, the entire sequence of the 45-kDa fragment was reproduced in 27 overlapping synthetic peptides that were then used in inhibition of binding assays. This led to the identification of a linear GP Ib alpha sequence (residues Ser251-Tyr279) that effectively inhibited platelet interaction with vWF mediated by ristocetin and, at higher concentration, also by botrocetin. A shorter peptide overlapping with the longer one (residues Gly271-Glu285) was the second most active inhibitory species. This region of the molecule contains several residues with a high surface probability index, as expected for a site involved in ligand binding. Thus, while native conformation of GP Ib alpha appears to be important for optimal interaction with vWF, the results obtained with short synthetic peptides may help in defining the amino acid residues participating in this essential function.     

Cadmium and zinc biosorption byChlorella homosphaera

Summary Cadmium and zinc biosorption byChlorella homosphaera cells were tested under laboratory conditions, in a range of concentrations from 0.5 to 14.0 mg/l. The results indicated two distinct phases for cadmium biosorption: a rapid phase probably associated with metal adsorption around the cell wall and a slower phase associated with the metal transport into the interior of the cells. For zinc biosorption these phases were not well defined probably due to the metabolic use of this metal by the cells.     

Regulation of urease by urea and its precursors in the lichen Evernia prunmtri

Thallus samples of £. prunastri (L.) Adi, floated on 40 mM urea developed urease (EC 3.5.1.5.) activity which levelled off after 6h. L-Arguiine, L-ornitfaine and patrescine added to the incubation media intitially enhanced the effect of urea, but the urease activity ceased after 4h of incubation in the presence of the latter two compounds or when L-arginine was used; as the sole source of nitrogen. This decline in activity was observed after 6h when L-arginine was added to urea-containing media. The loss of urease activity is thought to result from the synthesis of repressers in the presence of the amino acids, whereas putrescine appears to affect membrane permeability by increasing the uptake of urea by the cells. Declining urease activity in the latter case would then be due to feedback inhibition caused by the excess of ammonia produced in both hydrolysis of urea and oxidation of putrescine.     

Induction of Rat Brain Tubulin Following Ammonium Ingestion

The effect of oral administration of ammonium acetate for 2, 15, 30, and 100 days on protein synthesis in rat brain was investigated. Although protein synthesis changes were modest, i.e., maximal increase of 24%, there was induction of synthesis and accumulation of a protein with an Mr of 55,000. We show, on the basis of its position on two-dimensional electrophoresis and its immunological reactivity, that this protein is tubulin. Its content increased by 33% as determined by isolation of tubulin after 15 days of oral administration of ammonium and to 49% after 100 days as determined by quantitative immunoblotting.     

An amino-proximal domain required for the localization of FtsQ in the cytoplasmic membrane, and for its biological function in Escherichia coli

The location of FtsQ, an Escherichia coli protein essential for cell division, is, under physiological conditions, in the cytoplasmic membrane facing towards the periplasmic space. An amino-proximal hydrophobic domain is required for FtsQ to reach its location and for its activity in the cell. Overexpression of modified forms of FtsQ is deleterious for the cell.     

Influence of hot environments on some blood variables of sheep

Thirty-two Polwarth sheep of ages up to 1 year were observed under temperatures varying from 10.5 to 46.5°C. The following blood cell counts were made: erythrocyte (RBC), leucocyte (WBC), eosinophil (EOS), neutrophil (NEU), lymphocyte (LYM) and monocyte (MON). Other traits measured were: haemoglobin (HB), haematocrit (HT), blood glucose (GLU) and serum protein (PROT). Multivariate analysis of variance was used and the results showed a significant (P<0.001) effect for the interaction of shearing and temperature treatment. Under temperatures >25°C, sheep presented a decrease of RBC, WBC, HB and HT, these differences being greater in the shorn than in the unshorn animals. Unshorn animals presented higher variations in EOS, NEU, LYM, MON and GLU. Blood glucose increased under high temperatures in the shorn animals (from 56.36±0.65 mg/100 ml to 60.52±0.69 mg/100 ml) as in the unshorn animals (from 54.72±0.74 mg/100 ml to 57.56±0.77 mg/100 ml).     

Bioturbation by Nereis sp. and its effects on the phosphate flux across the sediment-water interface in the Palmones River estuary

The effects of Nereis sp. on the flux of dissolved phosphate across the sediment-water interface has been studied in Palmones River estuary using benthic flux-chambers and intact cores. Diffusive fluxes of phosphate were calculated from pore water gradient concentration and compared with those obtained from benthic chambers experiments. The high abundance of Nereis in the upper sediment layers appears to play an important part in the dissolved oxygen profiles in the overlying water, but had no effect on the redox potential. A negative relationship was found between the Nereis abundance and the phosphate gradient; this gradient ranged between 40 µmol 1^–1 cm^–1 with 340 Nereis individuals m^–2 and 20 µmol 1^–1 cm^–1 with 900 Nereis individuals m^–2. The ratio of the in situ flux to the flux gradient concentration for dissolved phosphate increased with the abundance of Nereis (from 1.7 at low abundance to 5.8 at high abundance).     

Protoplasts fromPodospora anserina: Isolation,purification, and transformation

Protoplasts fromPodospora anserina mycelium were produced using the commercially available enzyme Novozym 234. Different parameters involved in protoplast isolation were analyzed in order to establish optimal conditions, and protoplast production was notably increased. For the purification of protoplasts, several techniques based on both centrifugation and filtration were assayed, with filtration yielding the best results. Regeneration of protoplasts was studied on different media and osmostic stabilizers, and about 80% regeneration was obtained. The good physiological condition of the protoplasts produced with this method is demonstrated by the lack of cell wall and high regeneration rate and transformation frequencies.     

Substrate Temperature Effect on Microstructure,Optical, and Glucose Sensing Characteristics of Pulsed Laser Deposited Silver Nanoparticles

This work reports the substrate temperature-influenced change in the structural, morphological, optical, and glucose sensing properties of silver (Ag) nanoparticles (NPs) deposited on p-type Si (100) wafers. AgNP films grown at temperatures ranging from RT to 600 °C clearly show a dependence of orientation texture and surface morphology on substrate temperature (T _s). As T _s increases from RT towards 600 °C, the preferred orientation of AgNP film changes from (111) to (200). The AgNPs size, that is T _s-dependent, reaches the maximum value at T _s = 300 °C. This result is attributed to restructuring of AgNPs texture. Moreover, the AgNP shape also changes from ellipsoid to sphere as T _s increases from RT to 600 °C. Surface plasmon enhancement in photoluminescence intensity is observed with increase in T _s. It is found also that the AgNP film deposited at 300 °C has considerable reflectance reduction relative to the silicon substrate, in wavelength range of 300–800 nm and a progressive red shift of localized surface plasmon resonances caused by the adding of increasing quantities of glucose has been observed. As a proof of concept, we also demonstrate the capability of grown AgNP substrates for glucose detection based on surface enhanced Raman spectroscopy in physiological concentration range with short integration time 10 s, varying with T _s.