The effect of chlorpromazine on the mechanogram, electrocardiogram and membranopotential of the frog heart]

The action of chloropromazine in concentrations between 10(-6) and 10(-3) M was studied with regard to its effect on contractility, ECG, and membrane potential of the isolated frog heart. In concentrations above 10(-6) a depressive influence on the amplitude of contraction was observed; the speed of contraction was reduced. The heart rate showed negatively chronotropic changes. In the ECG there was a striking expansion of the PQ interval. The membrane potential was reduced under the effect of chloropromazine depending on the concentration used. The negative influence on mechanical and bioelectrical parameters of the myocardium is interpreted to be due to membrane-related factors. A vagus-like effect is discussed, particular importance being attached to the mechanisms of the "slow-channel" system.     

Local production of IgG4 in human colostrum

Total IgG4 levels were determined in 27 colostrum and 27 plasma paired samples by using RIA techniques, and total IgG was determined on the same pairs by using radial immunodiffusion. In colostrum, the mean IgG4 level was 4.6 micrograms/ml (0.6 to 19.0), and in the plasma the mean IgG4 level was 170.5 micrograms/ml (30 to 920). IgG averaged 42.3 micrograms/ml (12 to 240) in colostrum and 7980.9 micrograms/ml (3250 to 16,000) in plasma. Of colostral IgG, 15.3% was IgG4, whereas only 3.5% of plasma IgG was IgG4. Specific IgG4 antibodies to beta-lactoglobulin, bovine serum albumin, bermuda grass, and alpha-gliadin were also assayed. In six patients, strong evidence was found for local mammary production of IgG4-specific antibodies.     

Site of synthesis,metabolism and translocation of senecionine N-oxide in cultured roots of Senecio erucifolius

Root cultures of Senecio erucifolius (Asteraceae) efficiently took up and incorporated [¹⁴C]putrescine and [¹⁴C]arginine into the pyrrolizidine alkaloid (PA) senecionine N-oxide. Pulse-chase experiments covering a growth period of 10 to 19 days revealed the absence of any significant alkaloid turnover. The only metabolic activity was a slow but progressive transformation of senecionine N-oxide into its dehydrogenation product, seneciphylline N-oxide. Tracer experiments with single roots showed that the sites of enhanced PA synthesis coincided with the sites of preferred protein synthesis, i.e. root apices, indicating a close correlation between growth activity and alkaloid synthesis. Long-term pulse-chase experiments (10 to 12 days) with ¹⁴C-labelled arginine, putrescine and senecionine fed to single roots indicated that in spite of its metabolic inertia, senecionine N-oxide is a mobile compound which is translocated into tissues newly grown during the chase.Dedicated to Dr. Friedrich Constabel on the occasion of his 60th birthday     

Depurination As a Yield Decreasing Mechanism in Oligodeoxynucleotide Synthesis

Abstract

The synthesis in our laboratory of very long (80–106 bases) oligodeoxynucleotides using the phosphite method of Matteucci and Caruthers in an automated DNA synthesizer indicates the true efficiency of this multiple step process. The coupling efficiency as measured by trityl cation release i s 99.5–99.8%. However the yield obtained is still below the theoretical yield calculated from the above efficiency. We have attempted t o elucidate yield decreasing mechanisms in long ol igodeoxynucleotide synthesis. Crude reaction mixtures of phosphate-deblocked oligonucleotides which had no 5′-trityl group and which were examined immediately after cleavage from the support show one major species by high resolution PAGE. Harsher hydrolysis generates a new pattern of products superimposed upon the initial ladder representing cleavage at purine residues internal to the full length oligonucleotide. In many cases the cleavage ladder is significantly more intense than the coupling ladder. Hydrolysis a t apurinic sites in ammonium hydroxide at 55° C is apparently quantitative. The implications of this study are that internal depurination does not interfere with chain propagation but directly reduces the isolated yield. The efficiency of the phosphite coupling, oxidation, demethylation, and base deprotection are not the yield limiting steps. Synthesis of even longer fragments may be achievable with a reduction in the depurination o f the propagating chain. More significantly, compounds isolated after proper hydrolysis will not contain any apurinic sites making these compounds suitable for biological use.     

Variation in elemental stoichiometry of the marine diatom Thalassiosira weissflogii (Bacillariophyceae) in response to combined nutrient stress and changes in carbonate chemistry

The combined consequences of the multi‐stressors of pH and nutrient availability upon the growth of a marine diatom were investigated. Thalassiosira weissflogii was grown in N‐ or P‐limited batch culture in sealed systems, with pH commencing at 8.2 (“extant” conditions) or 7.6 (“ocean acidification” [OA] conditions), and then pH was allowed to either drift with growth, or was held fixed. Results indicated that within the pH range tested, the stability of environmental pH rather than its value (i.e., OA vs. extant) fundamentally influenced biomass accumul‐ation and C:N:P stoichiometry. Despite large changes in total alkalinity in the fixed pH systems, final biomass production was consistently greater in these systems than that in drifting pH systems. In drift systems, pH increased to exceed pH 9.5, a level of alkalinity that was inhibitory to growth. No statis‐tically significant differences between pH treatments were measured for N:C, P:C or N:P ratios during nutrient‐replete growth, although the diatom expre‐ssed greater plasticity in P:C and N:P ratios than in N:C during this growth phase. During nutrient‐deplete conditions, the capacity for uncoupled carbon fixa‐tion at fixed pH was considerably greater than that measured in drift pH systems, leading to strong contrasts in C:N:P stoichiometry between these treatments. Whether environmental pH was stable or drifted directly influenced the extent of physiological stress. In contrast, few distinctions could be drawn between “extant” versus “OA” conditions for cell physiology.     

Rugiloricus bacatus sp. nov. (Loricifera ‐Pliciloricidae) and a ghost‐larva with paedogenetic reproduction

Abstract

A new species of Loricifera, Rugiloricus bacatus sp. nov. is described together with the diagnoses of two other Rugiloricus species, Rugiloricus sp. nov. A and B, from the Faroe Bank (North Atlantic). Characteristic for all three species is the presence of a new type of reduced larva, a ghost‐larva. This type of reduced larva was discovered in 1986 by Jeanne Renaud‐Mornant, but it was with the Faroe Bank material that it was first discovered that the ghost‐larvae belonged to the phylum Loricifera. The ghost‐larvae are eitherfound inside late instar Higgins‐larvae, called penultimate Higgins‐larvae, or in the sediment. The three types of Higgins‐larvae from the Faroe Bank can be distinguished by characters such as anterior setae, posterior setae and toes. The adults of Rugiloricus bacatus sp. nov. are characterised by a prominent ruff resembling a pearl necklace; two of the eight clavoscalids are modified in the 1st row; the 2nd row of leg‐shaped scalids are very large and robust, and the 9th row with 30 beak‐like scalids alternating with 30 alternating plates. The postlarvae are free‐living and their scalids on the introvert are reduced to protoscalids. Postlarvae and adult stages have not been found for Rugiloricus sp. nov. A and B and therefore only diagnoses of these two species are presented here.     

Comparison of two methods for designing calorimeters using stirred tank reactors

Calorimetry is a robust method for online monitoring and controlling bioprocesses in stirred tank reactors. Up to now, reactor calorimeters have not been optimally constructed for pilot scale applications. Thus, the objective of this paper is to compare two different ways for designing reactor calorimeters and validate them. The “heat capacity” method based on the mass flow of the cooling liquid in the jacket was compared with the “heat transfer” method based on the heat transfer coefficient continuously measured in the cultivation of Escherichia coli VH33 in a 50 L stirred tank reactor. It was found that the values of the “heat transfer” method agreed very well with the calculated values from the oxygen consumption. By contrast, the curve of the “heat capacity” method deviated from that of the oxygen consumption calculated with the oxycaloric equivalent. In conclusion, the “heat transfer” method has been proven to have a higher degree of validity than the “heat capacity” method. Thus, it is a better and more robust means to measure heat generation of fermentations in stirred tank bioreactors on a pilot scale. Biotechnol. Bioeng. 2013; 110: 180–190. © 2012 Wiley Periodicals, Inc.