Electric birefringence of recombinant spectrin segments 14, 14-15, 14-16, and 14-17 from Drosophila alpha-spectrin

Members of the spectrin protein family can be found in many different cells and organisms. In all cases studied, the major functional role of these proteins is believed to be structural rather than enzymatic. All spectrin proteins are highly elongated and consist mainly of homologous repeats that constitute rigid segments connected in tandem. It is commonly believed that the details of the spectrin function depend critically on the flexibility of the links between the segments. Here we report on a work addressing this question by studying the transient electric birefringence of recombinant spectrin fragments consisting of segments 14, 14-15, 14-16, and 14-17, respectively, from Drosophila alpha-spectrin. Transient electric birefringence depends sharply on both molecular length and flexibility. We found that the birefringence relaxation time of segment 14 measured at 4 degrees C, but scaled to what is expected at 20 degrees C, equals 16 ns (+/-15%) at pH 7.5 and ionic strength 6 mM. This is consistent with this single segment being rigid, 5 nm long and having an axial ratio equal to about two. Under the same conditions, segments 14-15, 14-16 and 14-17 show relaxation times of 45, 39 and 164 ns (all +/-20%), respectively, scaled to what is expected at 20 degrees C. When the temperature is increased to 37 degrees C the main relaxation time for each of these multisegment fragments, scaled to what is expected at 20 degrees C, increased to 46, 80, and 229 ns (all +/-20%), respectively. When the ionic strength and the Debye shielding is low, the dynamics of these short fragments even at physiological temperature is nearly the same as for fully extended weakly bending rods with the same lengths and axial ratios. When the ionic strength is increased to 85 mM, the main relaxation time for each of these multisegment fragments is reduced 20-50% which suggests that at physiological salt and temperature conditions the links in 2-4-segment-long fragments exhibit significant thermally induced flexing. Provided that the recombinant spectrin fragments can serve as a model for native spectrin, this implies that, at physiological conditions, the overall conformational dynamics of a native spectrin protein containing 20-40 segments equals that of a flexible polymer.     

Plant uptake of 14C-EDTA, 14C-Citrate, and 14C-Histidine from chelator-buffered and conventional hydroponic solutions

Chelator-buffered hydroponic solutions provide low and buffered free-metal concentrations and allow the easy calculation of nutrient species expected in these solutions. Some researchers suspect that the solutions allow plant uptake of chelates and that this uptake explains the failure of the free-ion activity model using these solutions. To determine the amount and method of chelate uptake, swiss chard was grown in solution culture in growth chambers for about three wks and then transferred to solutions containing ¹⁴C-EDTA, ¹⁴C-citrate, or ¹⁴C-L-histidine for a 21-hour assay. Much higher root and shoot ¹⁴C were found from treatments containing metabolites histidine (2706097 shoot Bq ¹⁴C) or citrate (2241953 shoot Bq ¹⁴C) than EDTA (280110 shoot Bq ¹⁴C). Passive transpirational flow could explain all of the EDTA uptake, but active uptake would be required to explain most of the citrate and histidine uptake even assuming some adsorption of ligand bound to roots. Swiss chard grown in solutions with the same total EDTA concentrations, but different amounts of Fe bound to EDTA, had 3-fold differences in root and shoot ¹⁴C concentrations. In a second experiment, swiss chard roots removed more EDTA from solutions containing mostly M-EDTA⁰ than M-EDTA^1- or M-EDTA^2- (288140, 245051, and 192559 Bq ¹⁴C, respectively) suggesting plant selectivity for EDTA and a non-apoplastic route of uptake or an effect resulting from root cell-wall adsorption. Results indicated buffering of metals by ligands allowed some ligand uptake with much more uptake occurring with metabolites citrate and histidine than EDTA. A passive or indiscriminate form of uptake does not appear to explain all EDTA uptake with a selectivity by swiss chard for M-EDTA complexes of lower charge.     

Assimilative Pathway of Methanol in Candida sp. Incorporation of 14C-Methanol, 14C-Formaldehyde, 14C-Formate and 14C-Bicarbonate into Cell Constituents

1. The incorporation of ¹⁴C-methanol, ¹⁴C-formaldehyde, ¹⁴C-formate and ¹⁴C-bicarbonate into a methanol-utilizing yeast, Candida N–16, was examined by paper-chromato-graphy and radioautography.

2. At the earliest time period examined, the highest percentage of radioactivity fixed from ¹⁴C-methanol or ¹⁴C-formaIdehyde into methanol-grown cells was found in fructose phosphate. The percentage distribution of radioactivity in fructose phosphate decreased as time elapsed. The radioactivity fixed from these compounds into glucose-grown cells was negligible compared with that fixed into methanol-grown cells.

3. The incorporation of ¹⁴C-formate into methanol-grown cells was extremely low. The highest percentage of radioactivity fixed for short time incubation was found in serine. The incorporation pattern of glucose-grown cells was similar to that of methanol-grown cells.

4. At the earliest time period, over 70% of radioactivity fixed from ¹⁴C-bicarbonate into methanol- or glucose-grown cells was found in aspartate.

5. These results suggest that in Candida N–16 methanol is specifically assimilated by a route with hexose phosphate as a primary stable intermediate.

     

Storage Pools and Turnover Systems in Growing and Non-growing Cells: Experiments with 14C-Sucrose, 14C-Glutamine, and 14C-Asparagine

¹⁴C-labelled sucrose, glutamine, and asparagine have been suppliedto aseptically cultured carrot explants that either grew rapidlyby cell division or, by contrast, only slowly by cell expansion.The radioactive substrates were supplied in a brief ‘pulse’followed by a much longer period during which the tissues weresupplied with ¹²C-substrates. The passage of ¹⁴C through thevarious soluble compounds of the tissue and into the proteinwas followed. Alternatively, the ¹⁴C-labelled compound was suppliedthroughout the entire period of an experiment while the tissuealso received ¹²C-sucrose. The pulse-labelling experiments demonstrateturnover and the fate of the breakdown products, as well asthe emphasis placed on this kind of metabolism by cells at differentlevels of activity in their growth. The long-term labellingexperiments show the different ways in which carbon from varioussources may be used and how these pathways are affected by growth.The amount of ¹⁴C present in the various free (ethanol soluble)and combined (ethanol insoluble, acid-hydrolysable compounds—proteins)was determined, as well as the specific activity of the carbonin each compound. The fate of ¹⁴C supplied as sucrose had muchin common with ¹⁴C supplied as glutamine, with respect to theease with which it entered both the protein being synthesizedand the carbon dioxide evolved, but it was very different from¹⁴C supplied as asparagine. To interpret these data, compartmentsor pools of metabolites are postulated in the organized cell;exogenous ¹⁴C-sucrose and ¹⁴C-glutamine readily furnish carbonfor pools of amino-acids en route to protein, which are protectedfrom both the stored compounds and those which arise after proteinbreakdown. However, exogenous ¹⁴C-asparagine enters, is accumulated,and persists in the pool of stored compounds which also receivethe nitrogen-rich substances that arise from protein breakdown.The kinetic data and the specific activities of the carbon inits various forms require that protein breakdown and re-synthesisoccur concomitantly, that the stimulus to grow, exerted by coconutmilk, accentuates protein synthesis and also the pace of itsturnover, that some respired carbon dioxide arises from protein,and that this moiety of the respiration is increased by thecoconut-milk stimulus as it accentuates the pace of cyclicalturnover. In similar experiments with free cells from differentplants, the same general conclusions apply, but the rates ofturnover of protein are greater in free cells than in tissueexplants. Some specific differences, however, exist. Cells ofArachis, the only legume investigated, permit ¹⁴C-asparagineto contribute, like ¹⁴C-glutamine, to both protein synthesisand respired ¹⁴CO₂; it is not merely segregated in a storagepool. Thus, by virtue of their organization, plant cells maintainthe same substances simultaneously in distinct phases or compartments,where they play distinctive roles, without mingling. Geneticsendows each cell with the information that makes its biochemicalreactions feasible; the organization of the cells determineshow far the feasible becomes practised in cells in any givensituation.     

Preparation of L-tyrosine-ring- 14 C, L-DOPA-ring- 14 C and related metabolites

The reversibility of the tyrosine phenol-lyase reaction has been utilized to develop a simple system in which phenol-¹⁴C is incorporated into l-tyrosine in high yield. By use of mushroom tyrosinase, catechol-¹⁴C can be prepared from phenol-¹⁴C and l-DOPA-¹⁴C from l-tyrosine-¹⁴C. Catechol-¹⁴C can also be incorporated into l-DOPA-¹⁴C by use of tyrosine phenol-lyase, giving the possibility of preparing DOPA with two labeling patterns in the ring when starting with phenol-¹⁴C. Two further tyrosine metabolites, para-coumaric acid and homogentisic acid, have also been enzymatically prepared with ¹⁴C in the ring.     

Volume 14, 1998

World Journal of Microbiology and Biotechnology -     

IC14, an anti-CD14 antibody, inhibits endotoxin-mediated symptoms and inflammatory responses in humans

CD14 is a receptor for cell wall components of Gram-negative and Gram-positive bacteria that has been implicated in the initiation of the inflammatory response to sepsis. To determine the role of CD14 in LPS-induced effects in humans, 16 healthy subjects received an i.v. injection of LPS (4 ng/kg) preceded (-2 h) by i.v. IC14, a recombinant chimeric mAb against human CD14, at a dose of 1 mg/kg over 1 h, or placebo. In subjects receiving IC14, saturation of CD14 on circulating monocytes and granulocytes was >90% at the time of LPS injection. IC14 attenuated LPS-induced clinical symptoms and strongly inhibited LPS-induced proinflammatory cytokine release, while only delaying the release of the anti-inflammatory cytokines soluble TNF receptor type I and IL-1 receptor antagonist. IC14 also inhibited leukocyte activation, but more modestly reduced endothelial cell activation and the acute phase protein response. The capacity of circulating monocytes and granulocytes to phagocytose Escherichia coli was only marginally reduced after infusion of IC14. These data provide the first proof of principle that blockade of CD14 is associated with reduced LPS responsiveness in humans in vivo.     

Index,Volume 14, 2001

Abstract

Companion animal abuse is a universal phenomenon recorded since the earliest times. The lack of standardized definitions concerning companion animal abuse impedes research and reporting on the subject. In order to address this problem a typology of companion animal abuse is proposed for general application to identify the different types of abuse. Analysis of the records of the Society for the Prevention of Cruelty to Animals in South Africa indicated the usefulness of such a typology. Education based on the typology may contribute to the prevention of companion animal abuse.     

Thermophilic Anaerobic Biodegradation of [14C]Lignin, [14C]Cellulose, and [14C]Lignocellulose Preparations

Thermophilic (55°C) anaerobic enrichment cultures were incubated with [¹⁴C-lignin]lignocellulose, [¹⁴C-polysaccharide]lignocellulose, and kraft [¹⁴C]lignin prepared from slash pine, Pinus elliottii, and ¹⁴C-labeled preparations of synthetic lignin and purified cellulose. Significant but low percentages (2 to 4%) of synthetic and natural pine lignin were recovered as labeled methane and carbon dioxide during 60-day incubations, whereas much greater percentages (13 to 23%) of kraft lignin were recovered as gaseous end products. Percentages of label recovered from lignin-labeled substrates as dissolved degradation products were approximately equal to percentages recovered as gaseous end products. High-pressure liquid chromatographic analyses of CuO oxidation products of sound and degraded pine lignin indicated that no substantial chemical modifications of the remaining lignin polymer, such as demethoxylation and dearomatization, occurred during biodegradation. The polysaccharide components of pine lignocellulose and purified cellulose were relatively rapidly mineralized to methane and carbon dioxide; 31 to 37% of the pine polysaccharides and 56 to 63% of the purified cellulose were recovered as labeled gaseous end products. An additional 10 to 20% of the polysaccharide substrates was recovered as dissolved degradation products. Overall, these results indicate that elevated temperatures can greatly enhance rates of anaerobic degradation of lignin and lignified substrates to methane and low-molecular-weight aromatic compounds.