Expression of Embryonic Haemoglobin in ts AEV-Transformed Embryonic Erythroid Cells During Temperature-Induced Differentiation

Cells prepared from 1-day-old chick blastoderms were infected with a temperature-sensitive mutant of avian erythroblastosis virus ( ts AEV). Clonal strains of transformed erythroblasts were isolated from the infected blastoderm cells. By shift to the nonpermissive temperature, these cells could be induced to differentiate into erythrocyte-like cells which expressed embryonic haemoglobins. Embryonic haemoglobins could not be detected in ts AEV-transformed erythroblasts from adult bone marrow when induced to differentiate under the same conditions. In contrast to normal primitive erythrocytes, ts AEV-infected embryonic erythroblasts differentiated in vitro expressed also adult haemoglobin. These results suggest an influence of the haematopoietic environment on the switch from embryonic to adult erythrocytes.     

Use of precision cut human liver slices for studying the metabolism and genotoxic potential of xenobiotics by means of the 32P-postlabelling technique: steps towards method validation using testosterone and 2-aminofluorene

In the present study, a new in vitro model combining the short-term incubation of precision-cut human liver slices with DNA-adduct analysis by the ³²P-postlabelling technique is proposed for investigation of the genotoxic potential of xenobiotics. For method validation, the metabolic turnover of testosterone (TES) and the DNA-adduct inducing potential of 2-aminofluorene (2-AF) were used. Precision-cut human liver slices were prepared from a total of 12 human liver samples which were freshly obtained as parts of resectates from liver surgery. The slices were incubated as submersion cultures with TES and 2-AF for up to 6 h in 12-well tissue culture plates at concentrations of 10-50 and 0.06-28 μM, respectively. Slices recovered from the slicing procedure in the 4 °C cold Krebs-Henseleit buffer as indicated by intracellular potassium concentrations which increased for 2 h and then remained stable until the end of the incubation. TES was extensively metabolized by human liver slices with a similar metabolite pattern as observed in vivo. Almost 90% of the metabolites were conjugates. Major phase-I metabolites were androstendione, 6β-OH-androstendione, 6β-OH-TES, and 15β-OHTES. After incubation with 2-AF, substance related DNA-adducts were detected which increased dose-dependently from 12 to 1146 adducts per 10⁹ nucleotides. The adduct pattern consisted of one major adduct spot, A, representing 80-90% of the total adduct level and up to four minor adduct spots, B-E. In summary, the present data demonstrate that precision-cut liver slices are a valuable alternative in vitro system for DNA-adduct determination to screen chemicals for potential genotoxicity in humans.     

Regulation of Prenyl Chain Synthesis in Etiolated Hordeum Seedlings by Far-Red and White Light

The kinetics of prenyl chain formation (C₂₀ phytyl in chlorophylls, vitamin K_I and α-tocopherol; C₄₀ carotenoids and C₄₅ in plastoquinone-9) in plastids of etiolated Hordeum seedlings was compared in continuous darkness and after far-red and white light treatments:

• 1 Continuous far-red (via phytochrome Pfr) enhances the synthesis rate of all prenyl chains, but does practically not change the dark pattern of prenyl chain accumulation. Free C₂₀ phytyl chains could not be detected by means of thin layer chromatography.
• 2 White light induces a much stronger enhancement of prenyl chain formation than does far-red. It also changes the pattern of prenyl chain synthesis by a particularly strong promotion of the synthesis of phytyl chains, which get bound to chlorophyll a. The rate of chlorophyllide formation seems to determine the rate of enhanced phytyl formation.
• 3 It is assumed that the enzyme, which esterifies chlorophyllide a with the phytyl chain, is formed or activated by far-red treatment, but only starts working in white light, when the protochlorophyllide holochrome is re-arranged to the chlorophyllide holochrome.

     

Control of Light-Induced Carotenoid Synthesis in Raphanus Seedlings by Phytochrome

The effect of short pulses of red and or far-red light on the formation of individual carotenoids was tested in etiolated radish seedlings (Raphanus sativus L.). Red light induces an enhanced synthesis of β-carotene, lutein. violaxanthin and neoxanthin, while the level of antheraxanthin is decreased. Far-red light reverses the red light effects to the level of the far-red light control. The data indicate that in radish seedlings active phytochrome P_fr initiates the light-induced carotenoid synthesis, which is bound to thylakoid formation.     

Linking environmental warming to the fitness of the invasive clam Corbicula fluminea

Climate warming is discussed as a factor that can favour the success of invasive species. In the present study, we analysed potential fitness gains of moderate warming (3 °C above field temperature) on the invasive clam Corbicula fluminea during summer and winter. The experiments were conducted under seminatural conditions in a bypass-system of a large river (Rhine, Germany). We showed that warming in late summer results in a significant decrease in the clams' growth rates (body mass and shell length increase) and an increase in mortality rate. The addition of planktonic food dampens the negative effect of warming on the growth rates. This suggests that the reason for the negative growth effect of temperature increase in late summer is a negative energetic balance caused by an enhanced metabolic rate at limited food levels. Warming during early summer revealed contrasting effects with respect of body mass (no warming effect) and shell length (increased shell growth with warming). This differential control of both parameters further enhances the loss of the relative (size-specific) body mass with warming. In contrast, warming in winter had a consistently positive effect on the clams' growth rate as demonstrated in two independent experiments. Furthermore, the reproduction success (as measured by the average number of larvae per clam) during the main breeding period (April) was strongly enhanced by experimental warming during winter, i.e. by eight times during the relatively cold winter 2005/2006 and by 2.6 times during the relatively warm winter 2007/2008. This strong, positive effect of moderate winter warming on the clams' fitness is probably one reason for the recent invasion success of C. fluminea in the northern hemisphere. However, warm summer events might counteract the positive winter warming effect, which could balance out the fitness gains.     

Production of Diamino propionic acid ammonia lyase by a new strain of Salmonella typhimurium PU011

Background  

Seeds of the legume plant Lathyrus sativus, which is grown in arid and semi arid tropical regions, contain Diamino Propionic acid (DAP). DAP is a neurotoxin, which, when consumed, causes a disease called Lathyrism. Lathryrism may manifest as Neurolathyrism or Osteolathyrism, in which the nervous system, and bone formation respectively, are affected. DAP ammonia lyase is produced by a few microorganisms such as Salmonella typhi, Salmonella typhimurium and Pseudomonas, and is capable of detoxifying DAP.     

Modelling the transition from simple to complex Ca2+oscillations in pancreatic acinar cells

A mathematical model is proposed which systematically investigates complex calcium oscillations in pancreatic acinar cells. This model is based on calcium-induced calcium release via inositol trisphosphate receptors (IPR) and ryanodine receptors (RyR) and includes calcium modulation of inositol (1,4,5) trisphosphate (IP₃) levels through feedback regulation of degradation and production. In our model, the apical and the basal regions are separated by a region containing mitochondria, which is capable of restricting Ca²⁺ responses to the apical region. We were able to reproduce the observed oscillatory patterns, from baseline spikes to sinusoidal oscillations. The model predicts that calcium-dependent production and degradation of IP₃ is a key mechanism for complex calcium oscillations in pancreatic acinar cells. A partial bifurcation analysis is performed which explores the dynamic behaviour of the model in both apical and basal regions.     

Top‐down effects on pelagic heterotrophic nanoflagellates (HNF) in a large river (River Rhine): do losses to the benthos play a role?

1. The abundance, production and control of pelagic heterotrophic nanoflagellates (HNF) in the Lower River Rhine (Germany) were investigated. Field samples (live‐counting technique) were taken at least every 2 weeks at Cologne (km 685) over a period of 20 months. In addition, Lagrangian sampling was carried out 160 km downstream of Cologne (Kalkar–Grieth, km 845) over a period of 12 months. Potential HNF growth rates and loss rates caused by planktonic predators were estimated in the laboratory (size fractionation experiments) and compared with the changes in HNF‐density in a water parcel flowing downstream. 2. Mean abundance (±SD) ranged from 7 ± 6 to 4890 ± 560 individuals mL^–1 and was positively correlated with discharge. Heterotrophic nanoflagellates abundance increased up to 30‐fold during flood events, whereas there were only minor changes in the taxonomic composition. 3. HNF growth rate ranged from 0.16 ± 0.12 to 1.98 ± 0.10 day^–1. Between 0 and 95% (mean: 32%) of the gross production was lost to planktonic predators; a larger portion between 0 and 195% (mean: 64%) of the HNF gross production was lost by other means. 4. There may be an important role for benthic predators in the control of pelagic HNF. First, production of HNF was high and grazing losses to planktonic predators low at times when HNF abundance was low. Secondly, high in situ loss rates (not explicable by planktonic predators), which were positively related to temperature, indicate the importance of biotic interactions. Thirdly, the dependence of HNF abundance on discharge indicated a decrease grazing intensity with rising water levels (increase in water volume/colonised river bed ratio). 5. The impact of discharge on planktonic HNF mediated by the grazing impact of benthic predators was modelled, showing a good fit with the field data.     

Phylogenetic diversification of immunoglobulin genes and the antibody repertoire

Immunoglobulins are encoded by a large multigene system that undergoes somatic rearrangement and additional genetic change during the development of immunoglobulin-producing cells. Inducible antibody and antibody-like responses are found in all vertebrates. However, immunoglobulin possessing disulfide-bonded heavy and light chains and domain-type organization has been described only in representatives of the jawed vertebrates. High degrees of nucleotide and predicted amino acid sequence identity are evident when the segmental elements that constitute the immunoglobulin gene loci in phylogenetically divergent vertebrates are compared. However, the organization of gene loci and the manner in which the independent elements recombine (and diversify) vary markedly among different taxa. One striking pattern of gene organization is the "cluster type" that appears to be restricted to the chondrichthyes (cartilaginous fishes) and limits segmental rearrangement to closely linked elements. This type of gene organization is associated with both heavy- and light-chain gene loci. In some cases, the clusters are "joined" or "partially joined" in the germ line, in effect predetermining or partially predetermining, respectively, the encoded specificities (the assumption being that these are expressed) of the individual loci. By relating the sequences of transcribed gene products to their respective germ-line genes, it is evident that, in some cases, joined-type genes are expressed. This raises a question about the existence and/or nature of allelic exclusion in these species. The extensive variation in gene organization found throughout the vertebrate species may relate directly to the role of intersegmental (V<==>D<==>J) distances in the commitment of the individual antibody-producing cell to a particular genetic specificity. Thus, the evolution of this locus, perhaps more so than that of others, may reflect the interrelationships between genetic organization and function.