Fermentation of waste mechanical fibers from a newsprint mill by the rot fungus Sporotrichum pulverulentum

The growth and protein production of Sporotrichum pulverulentum, formerly called Chrysosporium lignorum, have been studied in submerged cultures using lignin-containing waste fibers from a newsprint mill as the only carbon source. The influence of different nitrogen sources on the growth parameters has been particularly investigated. The regulation of the production of extracellular enzymes and their interaction with the fibers is discussed. Experiments with cellulose of different degrees of polymerization and crystallinities showed that the protein content in the residual substance decreased, particularly when the crystallinity increased. When the highly crystalline powder cellulose was used as carbon source, the protein content in the residual substance was only 6% and with the mechanical waste fibers 14%. The results obtained demonstrate that the more complex the carbon source the more difficult it is to digest and the more enzyme has to be produced for its degradation. This puts a heavy burden on the protein synthesizing mechanism. Utilizing results from other work, where the endo- and exo-l, 4-β-glucanases produced by S. pulverulentum for the degradation of cellulose have been quantitatively purified, it has been calculated that the extracellular enzymes under these conditions can together account for approximately 30% of the protein in the mycelium. The endo- and exo-1,4-β-glucanases account for up to 55% of the extracellular protein. Certain possibilities of producing a final product with a high protein content using complex carbon sources are also mentioned.     

Functional Anatomy of the Hearts of Lungfishes and Amphibians

Lungfishes and amphibians have bimodal gas exchange, but variousspecies employ airbreathing with lungs to different degrees.An increased use of pulmonary breathing is correlated with progressivestructural and functional separation of the pulmonary and systemicvascular circuits. Representatives from all genera of lungfishesand several anurans and urodeles utilizing pulmonary breathing,show a preferential distribution of blood tending to minimizerecirculation to the systemic and pulmonary circuits. The degreeof shunting between the two circuits is variable and may expressnormal shifts in regional blood flow. The most important structural and functional features influencingthe preferential circulation through dipnoan and amphibian heartsinclude: (a) Dynamics of inflow in the pulmonary and systemicveins; (b) The extent and localization of atrial septation;(c) The partial ventricular septum in lungfishes and the massiveventricular trabeculation in both amphibians and lungfishes;(d) A laminar ventricular outflow pattern; (e) Structural guidanceof flow in the partially separated bulbus segment of the heart;(f) Vasomotor reactions in the various outflow vessels fromthe heart.     

Cross‐talk between monocyte invasion and astrocyte proliferation regulates scarring in brain injury

Scar formation after brain injury is still poorly understood. To further elucidate such processes, here, we examine the interplay between astrocyte proliferation taking place predominantly at the vascular interface and monocyte invasion. Using genetic mouse models that decrease or increase reactive astrocyte proliferation, we demonstrate inverse effects on monocyte numbers in the injury site. Conversely, reducing monocyte invasion using CCR2^?/? mice causes a strong increase in astrocyte proliferation, demonstrating an intriguing negative cross‐regulation between these cell types at the vascular interface. CCR2^?/? mice show reduced scar formation with less extracellular matrix deposition, smaller lesion site and increased neuronal coverage. Surprisingly, the GFAP⁺ scar area in these mice is also significantly decreased despite increased astrocyte proliferation. Proteomic analysis at the peak of increased astrocyte proliferation reveals a decrease in extracellular matrix synthesizing enzymes in the injury sites of CCR2^?/? mice, highlighting how early key aspects of scar formation are initiated. Taken together, we provide novel insights into the cross‐regulation of juxtavascular proliferating astrocytes and invading monocytes as a crucial mechanism of scar formation upon brain injury.     

The role of lemming herbivory in the sex ratio and shoot demography of willow populations

We investigated the role of lemming herbivory on the age structure and physical form of a stand of willows ( Salix lanata ) using lemming scars on stems as an indication of past herbivory. Salix lanata had a female-biased sex ratio comparable to that found in other willow species and it has been proposed that such a sex ratio may be due to selective herbivory on male genets. There was, however, no difference in the degree of scarring in male and female plants. Scarring did not appear to change the overall physical structure of the willows including the number of stems, the proportion of dead stems and the degree of branching. However, 72% of scarred 7 mm stems were dead, compared to only 22% of non-scarred stems, suggesting that lemming herbivory may play a role in ramet death. There was a significant positive correlation between stem ages and the lemming cycle as determined by the frequency of scars. With experimental scarring, S. lanata increased its production of new shoots in relation to the degree of scarring. We suggest that this demonstrates a pattern of compensatory growth in willows, whereby they take advantage of a period of relatively low herbivory following the crash of the lemming populations in order to compensate for damage that occurred during the lemming peak.     

New methods to evaluate colocalization of fluorophores in immunocytochemical preparations as exemplified by a study on A2A and D2 receptors in Chinese hamster ovary cells.

An important aspect of the image analysis of immunocytochemical preparations is the evaluation of colocalization of different molecules. The aim of the present study is to introduce image analysis methods to identify double-labeled locations exhibiting the highest association of two fluorophores and to characterize their pattern of distribution. These methods will be applied to the analysis of the cotrafficking of adenosine A2A and dopamine D2 receptors belonging to the G protein-coupled receptor family and visualized by means of fluorescence immunocytochemistry in Chinese hamster ovary cells after agonist treatment. The present procedures for colocalization have the great advantage that they are, to a large extent, insensitive to the need for a balanced staining with the two fluorophores. Thus, these procedures involve image processing, visualization, and analysis of colocalized events, using a covariance method and a multiply method and the evaluation of the identified colocalization patterns. Moreover, the covariance method offers the possibility of detecting and quantitatively characterizing anticorrelated patterns of intensities, whereas the immediate detection of colocalized clusters with a high concentration of labeling is a possibility offered by the multiply method. The present methods offer a new and sensitive approach to detecting and quantitatively characterizing strongly associated fluorescence events, such as those generated by receptor-receptor interaction, and their distribution patterns in dual-color confocal laser microscopy.     

Fleshy fruits – origins, niche shifts, and diversification

We examined shifts in fruit type, fleshy vs non-fleshy, in relation to habitat-related niche shifts, species richness, and historical distribution, in 50 phylogenetically independent plant lineages. Each lineage consisted of a sister-group pair of fleshy vs non-fleshy taxa and their outgroup. Niche shifts were assessed based on plant community characteristics. Two niche dimensions assumed to reflect community dynamics were derived: spatial predictability of disturbances and canopy closure. Phylogenetically independent origins of fleshy fruit types (1) were correlated with changes to habitats characterized by more shaded and spatially more unpredictable disturbances, (2) had an opposite effect on species richness in woody and herbaceous clades, enhancing species richness in woody clades, and (3) were continuously distributed over a period covering the last 70 million years. These results support the hypothesis that fleshy fruit evolution is driven by vegetation dynamics, and suggest that the strength of frugivore mediated selection on fleshy fruits increases when recruitment sites are spatially unpredictable and/or characterized by low light conditions.     

ECL cells of the rat stomach: development of lipofuscin in response to sustained gastrin stimulation

Ageing cells, especially post-mitotic cells, are known to accumulate pigments, i.e. highly electron-dense material, referred to as ceroid or lipofuscin. This material is formed as a consequence of autophagocytosis and peroxidation of the products undergoing degradation. The present study describes the development of lipofuscin in the ECL cells of the rat stomach. These cells produce and secrete histamine in response to gastrin. They are rich in secretory vesicles, which fuse to form vacuoles in hypergastrinaemic rats. Hypergastrinaemia was induced by continuous infusion of human Leu¹⁵-gastrin-17 for 6 days or by daily treatment with omeprazole for 10 weeks. Either treatment caused both vacuoles and lipofuscin bodies to appear in large numbers; the vacuoles disappeared promptly after interruption of the hypergastrinaemia, whereas the lipofuscin bodies remained. Antrectomy-evoked hypogastrinaemia was associated with a reduced number and volume density of lipofuscin bodies. Treatment with α-fluoromethylhistidine, an irreversible inhibitor of the histamine-forming enzyme, resulted in depletion of ECL-cell histamine and was found to prevent the omeprazole-evoked formation of vacuoles and lipofuscin. The numbers of both vacuoles and lipofuscin bodies were well-correlated with the serum gastrin concentration, suggesting that gastrin stimulates the development not only of vacuoles but also of lipofuscin, perhaps through enhanced autophagocytosis and/or oxidative stress. Thus, lipofuscin bodies may develop from vacuoles, and both vacuoles and lipofuscin bodies may reflect the efforts of overstimulated ECL cells to cope with the excessive formation of secretory products.     

7 Alpha-hydroxylation of cholesterol by reconstituted systems from rat liver microsomes

A reconstituted system from rat liver microsomes, consisting of partially purified fractions of cytochrome P-450 and NADPH-cytochrome P-450 reductase was shown to catalyze 7α-hydroxylation of cholesterol in the presence of NADPH and a synthetic phosphatidylcholine. The rate of 7α-hydroxylation of added [4-¹⁴C] cholesterol was linear with the concentration of cytochrome P-450 and increased with the concentration of NADPH-cytochrome P-450 reductase up to a certain level and then remained constant. Omission of phosphatidylcholine resulted only in a 20% decrease in cholesterol 7α-hydroxylase activity of the system. The rate of 7α-hydroxylation was 2–3 times higher in reconstituted systems with cytochrome P-450 from cholestyramine-treated rats than in those with cytochrome P-450 from untreated rats.     

12alpha-hydroxylation of 7alpha-hydroxy-4-cholesten-3-one by a reconstituted system from rat liver microsomes

A preparation of partially purified cytochrome P-450 from rat liver microsomes was found to catalyze 12α-hydroxylation of 7α-hydroxy-4-cholesten-3-one in the presence of NADPH and phosphatidyl choline. The reaction was stimulated two- to four-fold by addition of a preparation of cytochrome P-450 reductase. The reaction was inhibited by carbon monoxide to a considerably less extent than other hydroxylations catalyzed by the reconstituted system. In the presence of optimal concentrations of cytochrome P-450 reductase, cytochrome P-450 prepared from livers of starved rats catalyzed the 12α-hydroxylation more efficiently than cytochrome P-450 prepared from livers of normal rats or rats treated with phenobarbital.