Influence of Insect Larvae and Plant Roots on the Host-finding Behaviour of Heterorhabditis megidis

We studied the host-finding and dispersion behaviour of Heterorhabditis megidis (strain NLHE 87.3) in the presence of Galleria mellonella or Otiorhynchus sulcatus larvae and strawberry roots. In large Petri dishes (19 cm diameter) filled with moist sand (8% w/w), and incubated at 15°C over 24 h, infective juveniles (IJs) responded positively to the presence of G. mellonella , to roots of a single strawberry plant and to O. sulcatus larvae in direct contact with roots of a single strawberry plant. A neutral or negative response was observed when IJs were presented with only O. sulcatus larvae or a combination of several strawberry plants with O. sulcatus larvae, either in contact or not in contact with the roots. IJs responded strongly to the combination of plant roots and feeding larvae indicating that the tritrophic interaction formed by IJs - O. sulcatus larvae - strawberry plants may be an infochemical-mediated interaction.     

Methylglyoxal: Enzyme distributions relative to its presence in Douglas-fir needles and absence in Douglas-fir needle callus

Methylglyoxal was isolated as its 2,4-dinitrophenylosazone from an insoluble fraction from Douglas-fir [Pseudotsuga menziesii (Mirb.) Franco] needles but was not observed in a similar Douglas-fir needle callus preparation. This result was consistent with the distribution of enzymes of methylglyoxal metabolism between needles and needle callus. Only catabolic glyoxalases and methylglyoxal reductase could be found in the needle callus, whereas extracts of needles of various ages contained methylglyoxal synthetase and methylglyoxal reductase in a manner suggestive of a function for methylglyoxal in needle development and maturation. While glyoxalases I and II were active in all callus clones tested, activities of these enzymes were not immediately evident in needle extracts. However, it was demonstrated that at least small amounts of glyoxalase I occurred in needle extracts in an inhibited state. From the viewpoint that mature needles and needle callus represent resting and proliferative cellular states, respectively, the data indicate that methylglyoxal may be operating in conifers as a cell division inhibitor as envisioned by Szent-Gyorgyi.     

In vitro confirmation of the quantitative differentiation of liposomal encapsulated and non-encapsulated prednisolone (phosphate) tissue concentrations by murine phosphatases

The quantitative differentiation of liposomal encapsulated and non-encapsulated drug tissue concentrations is desirable, since the efficacy and toxicity are only related to the level of non-encapsulated drug. However, such separate concentration profiles in tissues have still not been reported due to lacking analytical methodology. The encapsulation of prodrugs like prednisolone phosphate (PP) in liposomes offers new, analytical opportunities. Instantaneous dephosphorylation of PP into prednisolone (P) by phosphatases after its release from the liposome in vivo makes it possible to differentiate between the encapsulated and the non-encapsulated drug for such preparations of liposomal PP: PP represents the encapsulated drug, while P represents the non-encapsulated drug. In the here described study, the instantaneous dephosphorylation of PP by murine liver and kidney phosphatases has been verified by incubation of PP in liver and kidney homogenates followed by estimation of the dephosphorylation rate constants k and the dephosphorylation time of the expected maximal in vivo non-encapsulated drug concentrations. In vitro PP has been rapidly converted into P in the presence of homogenate from the excretory organs. The calculated values for k have shown that the liver contains more active sites per gram of tissue than the kidneys. However, the dephosphorylation of PP by these active sites is slower compared with the kidneys. Compared with other pharmacokinetic processes of P, the estimated dephosphorylation times of the expected maximal in vivo non-encapsulated drug concentrations in the liver and the kidneys are considered to be instantaneous. This enables the separate determination of the encapsulated and non-encapsulated drug concentrations in the excretory organs after administration of liposomal PP in mice generating the first pharmacokinetic profile of a liposomal preparation, in which the in vivo encapsulated and free drug tissues concentrations are measured separately. This can also gain important insights into the pharmacokinetics of liposomal formulations in general.     

Insights into the Mechanism of Ligand Binding to Octopine Dehydrogenase from Pecten maximus by NMR and Crystallography

Octopine dehydrogenase (OcDH) from the adductor muscle of the great scallop, Pecten maximus, catalyzes the NADH dependent, reductive condensation of L-arginine and pyruvate to octopine, NAD⁺, and water during escape swimming and/or subsequent recovery. The structure of OcDH was recently solved and a reaction mechanism was proposed which implied an ordered binding of NADH, L-arginine and finally pyruvate. Here, the order of substrate binding as well as the underlying conformational changes were investigated by NMR confirming the model derived from the crystal structures. Furthermore, the crystal structure of the OcDH/NADH/agmatine complex was determined which suggests a key role of the side chain of L-arginine in protein cataylsis. Thus, the order of substrate binding to OcDH as well as the molecular signals involved in octopine formation can now be described in molecular detail.