Mapping of the immunodominant regions of the NAD-dependent formate dehydrogenase

A panel of 4 monoclonal antibodies and 7 polyclonal antisera against NAD-dependent formate dehydrogenase from methylotrophic bacterium Pseudomonas sp. 101 has been obtained. The reactivity of the 37 overlapping proteolytic peptides with the monoclonal antibodies and polyclonal antisera has been studied with ELISA test. The data obtained were interpreted residing on the structural model of the formate dehydrogenase at 3 Å resolution. The immunodominant regions in the formate dehydrogenase molecule and the epitopes for the monoclonal antibodies were elucidated.     

über Nothosauria (Sauropterygia,Reptilia) -ein Diskussionsbeitrag

The publication of K. Tschanz (1989):“Lariosaurus buzzii n. sp. from the Middle Triassic of Monte San Giorgio (Switzerland) with comments on the classification of nothosaurs” is reviewed. The results are as follows:

1. Lariosaurus buzzii n. sp. is not a member of the genusLariosaurus, as Tschanz pretends. Therefore a new genusSilvestrosaurus is proposed.
2. Lariosaurus andCeresiosaurus ar not closely related to each other.Ceresiosaurus is not a member of the Lariosauridae, but it requires a separate family, the Ceresiosauridae.
3. The contribution of Tschanz to the classification of the Nothosauria provides no new insight into this group; on the contrary it culminates in an unacceptable diagnosis of the Lariosauridae.

     

Determination of vitamin K1 in serum using catalytic-reduction liquid chromatography with fluorescence detection

A new method for the liquid chromatographic-fluorescence determination of serum vitamin K₁ is described using reduction of the K-quinone to the fluorescent K-hydroquinone. The reduction reaction occurs “on-line” in the LC system using a catalytic reducer column and an alcohol mobile phase as reductant. A procedure for serum determination utilizes a liquid-liquid serum lipid extraction followed by normal-phase fractionation on a solid-phase extraction cartridge. The final measurement uses a reversed-phase (C₁₈) separation with a ethanol-methanol mobile phase and provides a detection limit of approximately 20 pg/ml.     

Seasonal dynamics of denitrification activity in two water meadows

Seasonal variation in denitrification activity was measured in twoflooded water meadows, one on peaty and one on sandy soil, over a three-yearperiod. Measurements were taken during flooded and drained periods, usingthe acetylene-blockage technique, and the rates were compared to massbalance estimates of nitrate removal in the percolating water.Denitrification activity was higher in sandy soil than in peaty soil. Higherwater infiltration rate and thereby higher nitrate load was considered to bethe cause of the higher denitrification in the sandy soil. Floodingsignificantly increased denitrification, and the rates were higher in autumnand winter than in spring. This was considered to be a result of highernitrogen concentration in inflowing stream water during winter. Annualdenitrification was estimated to 430–460 kg N ha^-1yr^-1 in the sandy soil meadow, and 220 kg N ha^-1yr^-1 in the peaty soil meadow. In the sandy soil there was alarge discrepancy between nitrate removal rates and denitrification rates,which can be explained by nitrification of ammonium released from the soil.In the peaty soil nitrate disappearance and denitrification correspondedfairly well.     

Bacterial and phosphorus dynamics in profundal Lake Erken sediments following the deposition of diatoms: a laboratory study

The benthic microbial response to the deposition of naturalseston and the microbial impact on nutrient dynamics wasstudied in an experimental system using whole sediment coresequipped with flow-through systems for the overlying water. For20 days, changes in sediment bacterial activity, totalmetabolic activity (heat production), bacterial biomass,phosphorus fractions and basic chemistry were followed, as wellas the exchange of nutrients between sediment and water.Microbial activity and biomass increased immediately inresponse to the deposition of seston, peaked after seven daysand then decreased linearly over the remaining time of theexperiment. Co-settled bacteria were suggested to play animportant role in the microbial response. Changes in bacterialbiomass production, bacterial biomass and the NaOH-nrPextractable phosphorus fraction were concurrent in response toseston additions. The sediment acted as a trap for SRP from theoverlying water when bacterial activity was high and as asource when the bacterial activity decreased. Altogether, theresults suggest an important role of bacteria in theregeneration of seston P. Mineralization rates estimated fromsediment heat production showed that ca. 11% of the addedseston carbon was oxidized in the sediments during theexperiment. This revised version was published online in July 2006 with corrections to the Cover Date.     

Role of light in changes in free amino acid and polyamine contents at chilling temperature in maize (Zea mays)

The effect of irradiance on changes in photosynthesis, free amino acids and polyamines was investigated. Two-week-old maize ( Zea mays L.) plants were chilled at 5°C in the light (250 μmol m⁻² s⁻¹ PAR) or dark. The chlorophyll fluorescence ratio, F_v/F_m, decreased in the light by ca 50% but did not change in the dark. Similarly to the F_v/F_m, there was no change in the transpiration rate or the stomatal conductance in the dark, while these parameters decreased by ca 55% in the light. The net photosynthesis rate declined in both cases, but to a far greater extent in the light (73%) than in the dark (40%). The intercellular CO₂ partial pressure increased by ca 50% in all cases. The free amino acid contents increased compared to the control during the cold treatment. In most cases this increase was more pronounced in the light than in the dark. There was a continuous increase in the putrescine level, which was more pronounced in the light than in the dark. The spermidine content increased one and a half times after one day in the light but decreased by 70% in the dark compared to the control values. From the second day a 50% decline in the spermidine content was observed in the light and an 80% decline in the dark. These results suggest that light has an influence not only on the photosynthetic processes during chilling stress but also on other stress markers such as polyamines and free amino acids.     

High-Resolution Linkage Map of Mouse Chromosome 13 in the Vicinity of the Host Resistance LocusLgn1

Natural resistance of inbred mouse strains to infection withLegionella pneumophilais controlled by the expression of a single dominant gene on chromosome 13, designatedLgn1.The genetic difference atLgn1is phenotypically expressed as the presence or absence of intracellular replication ofL. pneumophilain host macrophages. In our effort to identify theLgn1gene by positional cloning, we have generated a high-resolution linkage map of theLgn1chromosomal region. For this, we have carried out extensive segregation analysis in a total of 1270 (A/J × C57BL/6J) × A/J informative backcross mice segregating the resistance allele of C57BL/6J and the susceptibility allele of A/J. Additional segregation analyses were carried out in three preexisting panels of C57BL/6J ×Mus spretusinterspecific backcross mice. A total of 39 DNA markers were mapped within an interval of approximately 30 cM overlapping theLgn1region. Combined pedigree analyses for the 5.4-cM segment overlappingLgn1indicated the locus order and the interlocus distances (in cM):D13Mit128–(1.4)–D13Mit194–(0.1)–D13Mit147–(0.9)–D13Mit36–(0.9)–D13Mit146–(0.2)–Lgn1/D13Mit37–(1.0)–D13Mit70.Additional genetic linkage studies of markers not informative in the A/J × C57BL/6J cross positionedD13Mit30, -72, -195,and-203, D13Gor4, D13Hun35,andMtap5in the immediate vicinity of theLgn1locus. The marker density and resolution of this genetic linkage map should allow the construction of a physical map of the region and the isolation of YAC clones overlapping the gene.