Inhibition sélective de quelques enzymes respiratoires chezEscherichia coli

Summary It is possible to dissociate the activity of different enzymatic systems of the bacteriumEscherichia coli by the action of high hydrostatic pressures. This activity is studied in the microbes after having been subjected to high hydrostatic pressure. Each enzymatic system is inhibited at different pressures. The enzymes of the bacteria submitted to pressures lower than the inhibiting limit show a residual enzymatic activity; sometimes this activity appears after a phase of lag.     

Die biologische Bedeutung der Vitamine

Summary The vital importance of the vitamins resides in theircoferment function, which enables them to catalyse enzymatic processes in living tissues. The term coferment is used in this connection to designate organic compounds of relatively low molecular weight, which in conjunction with the specific proteinous apoferments bring about the transformation of definite substrates. The vitamins are, however, catabolized like ordinary substrates when they come into contact with enzymatic systems in which they have no coferment function. This explains why normal life cannot be sustained, if the living organisms do not receive asnutritional factors the vitamins which they cannot synthesize. From a biochemical point of view not only exogenous hypo- or avitaminoses but all pathological changes may be regarded as the sequelae of disturbances in one or several enzymatic systems. The vitamins may exert a regulating influence also in these enzymatic disturbances which are not directly caused by vitamin deficiency. In such cases they will act asrèmedies.     

Characterization of cellulase fromHumicola lanuginosa

Summary In a carboxymethylcellulose-yeast extract medium,Humicola lanuginosa synthesized cellulase. The purified enzyme possessed a molecular weight of 71,000 daltons and exhibited optimum enzymatic activity at pH 5.0 and 45°C.     

Comparison of circulating lipoprotein lipase activity in Zuckerfa/fa andFa/-rats

Summary Lipoprotein lipase activity was determined in Zucker rats by assaying VLDL radioactivity. Animals were i.v. injected with³H₂-oleic acid and¹⁴C-glycerol with or without Triton WR 1339. This enzymatic activity was higher infa/fa rats than in non-obeseFa/-rats.     

A hydrogen-bonding network in mammalian sorbitol dehydrogenase stabilizes the tetrameric state and is essential for the catalytic power

Subunit interaction in sorbitol dehydrogenase (SDH) has been studied with in vitro and in silico methods identifying a vital hydrogen-bonding network, which is strictly conserved among mammalian SDH proteins. Mutation of one of the residues in the hydrogen-bonding network, Tyr110Phe, abolished the enzymatic activity and destabilized the protein into tetramers, dimers and monomers as judged from gel filtration experiments at different temperatures compared to only tetramers for the wild-type protein below 307 K. The determined equilibrium constants revealed a large difference in Gibbs energy (8 kJ/mol) for the tetramer stability between wild-type SDH and the mutated form Tyr110Phe SDH. The results focus on a network of coupled hydrogen bonds in wild-type SDH that uphold the protein interface, which is specific and favorable to electrostatic, van der Waals and hydrogen-bond interactions between subunits, interactions that are crucial for the catalytic power of SDH. Received 13 July 2007; received after revision 30 September 2007; accepted 1 October 2007     

Immobilization of chicken liver fructose 1,6-bisphosphatase on CNBr-activated Sepharose

Summary Chicken liver fructose 1,6-bisphosphatase is readily immobilized on CNBr-activated Sepharose. The immobilization alters some enzymatic properties. They include broader pH activity curve, loss of activation by K⁺ or NH ₄ ⁺ , increased resistance to inactivation by trypsin, decreased sensitivity to AMP inhibition, and loss of cooperative interaction among AMP-binding sites. The immobilized enzyme retains about 38% or 19% of the specific activity of the native enzyme when the activity is measured in the absence or presence of K⁺, resepctively.This work was supported by grant RR-8006 from the General Research Branch, Division of Research Resources, NIH (USA).     

Preparation of optically pure juvenile hormone I labelled in the ester methyl group with tritium at very high specific activity

Summary Radiolabelled juvenile hormone I (3) was prepared in an optically pure form by an enzymatic method using the capacity of accessory sex gland homogenates from maleHyalophora cecropia to transfer the methyl group of S-adenosyl-L-methionine to the carboxylic acid function of the (10R, 11S)-enantiomer of racemic presursor2; the specific activity of3 is higher than 53 Ci/mmole (1.96 TBq/mmole).We are indebted to Dr W. Thelfer, Philadelphia, for providing us with diapausing pupae of male Cecropia silk moths, and to Dipl.-Biol. G. Klages, Darmstadt, for preparing racemic JH-Iacid. Financial support by the Deutsche Forschungsgemeinschaft (grant No. Em 14/8) is gratefully acknowledged.     

Immobilization of chicken liver fructose 1,6-bisphosphatase on CNBr-activated Sepharose

Chicken liver fructose 1,6-bisphosphatase is readily immobilized on CNBr-activated Sepharose. The immobilization alters some enzymatic properties. They include broader pH activity curve, loss of activation by K+ or NH+4, increased resistance to inactivation by trypsin, decreased sensitivity to AMP inhibition, and loss of cooperative interaction among AMP-binding sites. The immobilized enzyme retains about 38% or 19% of the specific activity of the native enzyme when the activity is measured in the absence or presence of K+, respectively.     

Peroxidase activity in the sponge,Iotrochota birotulata

Summary The spongeIotrochota birotulata contains a peroxidase which was partially characterized. This is the first report of a peroxidase in Porifera, originally thought to be devoid of such enzymatic activity.This study was supported by grant No. CA 21992 from the National Cancer Institute, DHEW.     

N-Acétylation enzymatique de la tryptamine par des homogénats de cerveaux deLocusta migratoria avant et après intoxication par le chlordimeform ou le lindane

Summary Brain homogenates ofLocusta migratoria are found to possess enzyme capable of catalyzing the N-acetylation of tryptamine. A main product of the enzymatic reaction is isolated and identified as N-acetyltryptamine by chromatography analyse. Both insecticides, chlordimeform and lindane, inhibit enzyme activity. A direct correlation between the degree of intoxication and acetylation of tryptamine is described.     

A cold-active salmon goose-type lysozyme with high heat tolerance

The Atlantic salmon (Salmo salar) goose-type lysozyme gene was isolated and revealed alternative splicing within exon 2 affecting the signal peptide-encoding region. The lysozyme was produced in Escherichia coli, and the recombinant enzyme showed a high specific lytic activity that was stimulated by low or moderate concentrations of mono- or divalent cations. Relative lytic activities of 70 and 100% were measured at 4°C and 22°C, respectively, and there was no detectable activity at 60°C. However, 30% activity was retained after heating the enzyme for 3 h at 90°C. This unique combination of thermal properties was surprising since the salmon goose-type lysozyme contains no cysteines for protein structure stabilization through disulphide bond formation. The results point to a rapid reversal of inactivation, probably due to instant protein refolding. Received 14 August 2007; received after revision 07 September 2007; accepted 12 September 2007     

Histochemical localization of acetylcholinesterase in the glycogen body (sinus rhomboidalis) of common brown dove,Streptopelia senegalensis and house sparrow,Passer domesticus

Summary Acetylcholinesterase (AChE) activity was studied in the glycogen bodies of the spinal cords of 2 birds namelyStreptopelia senegalensis andPasser domesticus. A possible functional significance of AChE in the light of relative enzymatic localization especially in Hoffmann-Kolliker nuclei (motor cell groups), substantia gelatinosa and other regions of gray matter of 2 avian glycogen bodies has been discussed.     

Spezifische Wirkung einiger tierischer und bakterieller Polysaccharide auf Leucocytenin vitro

Summary Different purified polysaccharides, mucopolysaccharides, phosphatides and carbohydrat-sulfonic acids have been investigated for their effect on stimulation of leucocytic migrationin vitro. The bacterial polysaccharides of proteus,S. marcescens, shiga and shiga fullantigen, have been found to be of high specific activity. All other compounds have much less or no activity. Therefore it might be concluded that the type of bacterial polysaccharides which promote leucocytic migration belong to a highly specific group.     

Untersuchungen zur Verdauungsphysiologie vonFormica polyctena Foerst. (Hymenoptera,Formicidae)

Summary In this investigation the spectrum of digestive-acting carbohydrates present inFormica polyctena Foerst. was analysed. The digestive tract of worker ants was dissected and the enzymatic activity tested by incubation with different carbohydrates. The results for crop, midgut, malpighian tubes and hindgut are given in the Table.     

Hairpin RNA: a secondary structure of primary importance

An RNA hairpin is an essential secondary structure of RNA. It can guide RNA folding, determine interactions in a ribozyme, protect messenger RNA (mRNA) from degradation, serve as a recognition motif for RNA binding proteins or act as a substrate for enzymatic reactions. In this review, we have focused on cis-acting RNA hairpins in metazoa, which regulate histone gene expression, mRNA localization and translation. We also review evolution, mechanism of action and experimental use of trans-acting microRNAs, which are coded by short RNA hairpins. Finally, we discuss the existence and effects of long RNA hairpin in animals. We show that several proteins previously recognized to play a role in a specific RNA stem-loop function in cis were also linked to RNA silencing pathways where a different type of hairpin acts in trans. Such overlaps indicate that the relationship between certain mechanisms that recognize different types of RNA hairpins is closer than previously thought. Received 21 November 2005; received after revision 3 January 2006; accepted 11 January 2006     

Superoxide anion scavenging effect and superoxide dismutase activity ofGinkgo biloba extract

Summary Ginkgo biloba extract is known to be efficient in diseases associated with free radical generation. The purpose of this work was to study, under in vitro conditions, the action ofGinkgo biloba extract (Gbe) against superoxide anion ( ), which is directly or indirectly implicated in cell damage.Gbe appears to have both an scavenging effect and also a superoxide dismutase activity. Its antiradical effect was demonstrated by low temperature electron spin resonance and in a non-enzymatic system (phenazine methosulfate-NADH), and its enzymatic activity was shown by polarographic determination.     

Relationship of prodigiosin condensing enzyme activity to the biosynthesis of prodigiosin and its precursors inSerratia marcescens

Summary Prodigiosin condensing enzyme (PCE) activities were present inSerratia marcescens wild type 08, mutants OF, WF and 9-3-3. Their specific activities exhibited different maxima and at different times during the late log phase or the early stationary phase of cell growth. The levels of prodigiosin and its precursors also showed a significant increase at this period. The results support that prodigiosin and/or its precursors are secondary metabolites. The ubiquity of the PCE activity in mutants deficient in prodigiosin biosynthesis suggest that this particular enzyme may also be present in non-pigmented clinical isolates.