The potential of Beauveria bassiana inoculum formulated into a polymeric matrix for a microbial control of spruce bark beetle

Two local strains of Beauveria bassiana originally isolated from naturally infected spruce bark beetles in Slovakia were tested for their virulence to Ips typographus (IT) and for their compatibility with a polymeric matrix composed of low-molecular polyethylene. Conidia could be homogenously immobilized in the low-molecular polyethylene matrix with no adverse effect on their viability and infectivity. At constant temperature (25°C), viability of immobilized conidial decreased only by 1–2% after 7 or 14 days when compared with non-formulated conidia. In field conditions, viability of conidia formulated in the matrix was even significantly higher than non-formulated conidia 35 days after their application in traps. Conidia incorporated into the polymeric matrix were infective to IT adults in laboratory bioassays. Mean values of LC₅₀ for native conidia (0.72–2.05?×?10⁶ conidia?ml^?1) and conidia immobilized in the polymeric matrix (0.64–1.03?×?10⁵ conidia?mm^?2) demonstrated high virulence. The efficacy of the local strains was significantly higher than that of B. bassiana strains from mycoinsecticides (Boverol^®, Botanigard^® ES and Naturalis-L^®). Results showed potential of this polymeric material for its use in microbial control of IT when mixed with conidia of B. bassiana.     

Relationships between bryophyte production and substrate properties in restored milled peatlands

The relationship between the small‐scale distribution pattern of bryophyte biomass on restored milled peatlands and substrate properties (e.g. moisture, pH, nutrients, and their ratios) was studied. Substrate properties may determine the species composition of bryophyte communities that have developed in such areas. Two experimental sites were established in northern Estonia where the moss‐layer‐transfer technique had been used for the revegetation of abandoned peatfields for almost a decade before sampling. Diaspores of Sphagnum species common on bogs were distributed in these sites. After 7 years one site was mainly dominated by Sphagnum whereas true mosses (Polytrichum strictum, Aulacomnium palustre, and Pleurozium schreberi) were abundant in the other site. Three moss groups were distinguished: Sphagnum, P. strictum, and other mosses based on cluster analysis. The biomass of Sphagnum was related to peat moisture and potassium content. For P. strictum the N/K ratio was important, and the production of A. palustre grew with the increase in the N/P ratio of peat. It was concluded that peat properties played an important role in the formation and development of bryophyte communities on revegetated peatfields on a small scale (<0.1 ha).     

Human cytomegalovirus (HCMV) smallest capsid protein identified as product of short open reading frame located between HCMV UL48 and UL49.

The capsid of cytomegalovirus contains an abundant, low-molecular-weight protein whose coding sequence within the viral genome had not been identified. We have used a combination of biochemical and immunological techniques to demonstrate that this protein, called the smallest capsid protein in human cytomegalovirus, is encoded by a previously unidentified 225-bp open reading frame (ORF) located between ORFs UL48 and UL49. This short ORF, called UL48/49, is the positional homolog of herpes simplex virus ORF UL35 (encoding capsid protein VP26) and shows partial amino acid sequence identity to positional homologs in human herpes viruses 6 and 7.     

Ligand orientation and haem electronic structure in ferricytochrome c′′ from Methylophilus methylotrophus studied by 13C NMR

Cytochrome c′′ from Methylophilus methylotrophus contains a single haem with bis-histidine coordination which couples electron and proton transfer by reversible detachment of one of the axial ligands on reduction. ¹³C NMR of the haem substituents is now used to determine the orientations of the two histidine ligands of the ferricytochrome. The relative orientation of the ligands is found to be nearly perpendicular (an angle of 85±2° between the histidine planes was obtained), which is consistent with the near-axial g-tensor determined by EPR. Although the absolute orientation of the axial ligands is not well defined in the presence of near-axial symmetry, ¹³C NMR is found to be a useful complement to EPR for obtaining quantitative information for systems of this type. Received: 13 May 1996 / Accepted: 10 July 1996     

Electron microscopical study of a cytosolic enzyme in unfixed cryostat sections: demonstration of glycogen phosphorylase activity in rat liver and heart tissue

Summary Glycogen phosphorylase activity has been demonstrated at the ultrastructural level in liver and heart tissue of fasted rats. Unfixed cryostat sections were incubated by mounting them on a semipermeable membrane stretched over a gelled incubation medium. The medium contained a high concentration of glucose 1-phosphate which enables indirect detection of glycogen phosphorylase activity on the basis of the synthesis of glycogen. Tissue fixation, dehydration and embedding for electron microscopical study were performed after the incubation had been completed. The ultrastructure of both liver and heart tissue was rather well preserved. Glycogen granules resulting from glycogen phosphorylase activity were found in the cytoplasmic matrix of both hepatocytes and cardiomyocytes; no relationship with membranous structures could be detected. It is concluded that the semipermeable membrane method is well suited for localizing cytosolic enzyme activities at the ultrastructural level without prior tissue fixation; this opens further perspectives for correlations between histochemical and biochemical data.     

Postoligomerization folding of human cytomegalovirus glycoprotein B: identification of folding intermediates and importance of disulfide bonding.

Human cytomegalovirus glycoprotein B (gB or UL55) has been demonstrated to be a disulfide-linked homodimer within the envelope of mature virions. Previously, it has been shown that gB undergoes a rapid dimerization nearly coincident with its synthesis. Following dimerization, the molecule slowly folds into a form which can be transported from the endoplasmic reticulum. In this study we have examined the prolonged folding of gB by using a set of defined gB-reactive murine monoclonal antibodies and gB expressed as a recombinant protein in the absence of other human cytomegalovirus proteins. Our results have documented a folding pathway consistent with the relatively rapid dimerization of the translation product followed by delayed conversion into a fully folded molecule. Assembly of the dominant antigenic domain of gB, AD-1, preceded dimerization and folding of the molecule. The fully folded dimer was heat stable, but its conformation was altered by treatment with 2% sodium dodecyl sulfate (SDS), whereas an oligomeric folding intermediate was both heat and SDS stable. Postoligomerization disulfide bond formation could be demonstrated during folding of gB, suggesting that the formation of these covalent bonds could contribute to the prolonged folding of this glycoprotein.     

SEASONAL VARIATIONS IN PHOTOSYNTHESIS-IRRADIANCE RESPONSES BY BIOFILMS IN MEDITERRANEAN STREAMS

The relationships between primary production and irradiance were analyzed over an annual cycle in natural biofilms of two undisturbed streams: La Solana (LS), an open calcareous stream, and Riera Major (RM), a shaded siliceous stream. In LS, low photosynthetic efficiency (α^chl and α^area) and high values of both the light saturation parameter (I_k) and the carotenoid / chlorophyll ratio indicated adaptation to high light regimes. On the other hand, higher photosynthetic efficiency and lower I_k as well as photoinhibition at high irradiance found in the biofilms of RM indicated shade adaptation. However, the lack of correlation between light availability in nature and the photosynthetic parameters studied in the laboratory suggested that light was not the most important factor in determining seasonal changes in the photosynthetic behavior in this stream. Both in the open and shaded streams, algal patches collected simultaneously exhibited different photosynthesis-irradiance (P-I) curues, showing that community composition influenced the P-I parameters. In the open stream (LS), however, significant negative correlations between α^area and chlorophyll a and between P _max^chl and chlorophyll a ( r = -0.994 , P < 0.001, and r = -0.929 , P < 0.05, respectively) suggested that photosynthesis was affected by self-shading. Due to the absence of photoinhibition in the biofilms of LS, high photosynthetic rates were maintained at the ambient high light environment, thus compensating for low photosynthesis at low irradiance. In the shaded stream (RM), because photosynthesis was saturated at low irradiances, primary production was relatively high given the low light conditions .     

A New Glucose-6-Phosphate Dehydrogenase Variant, G6PD Orissa (44 Ala→Gly), is the Major Polymorphic Variant in Tribal Populations in India

Deficiency of glucose-6-phosphate dehydrogenase (G6PD) is usually found at high frequencies in areas of the world where malaria has been endemic. The frequency and genetic basis of G6PD deficiency have been studied in Africa, around the Mediterranean, and in the Far East, but little such information is available about the situation in India. To determine the extent of heterogeneity of G6PD, we have studied several different Indian populations by screening for G6PD deficiency, followed by molecular analysis of deficient alleles. The frequency of G6PD deficiency varies between 3% and 15% in different tribal and urban groups. Remarkably, a previously unreported deficient variant, G6PD Orissa (44 Ala→Gly), is responsible for most of the G6PD deficiency in tribal Indian populations but is not found in urban populations, where most of the G6PD deficiency is due to the G6PD Mediterranean (188 Ser→Phe) variant. The K of G6PD Orissa is fivefold higher than that of the normal enzyme. This may be due to the fact that the alanine residue that is replaced by glycine is part of a putative coenzyme-binding site.