Evolution of Volatile Sulfur Compounds during Laboratory-Scale Incubations and Indoor Preparation of Compost Used as a Substrate in Mushroom Cultivation

Volatile sulfur compounds are known to be produced during the preparation of compost used as a substrate in mushroom cultivation. Because they cause odor problems, attempts have been made to reduce the production of these compounds. The influences of temperature and various additions on the production of volatile sulfur compounds from composting material were tested on laboratory-scale preparations. The production of H₂S, COS, CH₃SH, and (CH₃)₂S was proven to be a biological process with an optimal temperature that coincides with the optimal temperature for biological activity. The formation of CS₂ and (CH₃)₂S₂ was shown to be a nonbiological process. The emission of volatile sulfur compounds during the indoor preparation of mushroom compost appeared to be remarkably reduced (about 90%) as compared with the emission during the conventional outdoor process. Introduction of this indoor composting process would result in a significant reduction in environmental pollution.     

Neue Aspekte zur zugzeitlichen Frugivorie der Gartengrasmücke (Sylvia borin)

Zusammenfassung Freilandbeobachtungen und frühere Laboruntersuchungen (Berthold 1976) führten bisher zu einer widersprüchlichen Bewertung der zugzeitlichen Frugivorie bei der Gartengrasmücke. Deshalb wurden das Wahlverhalten gegenüber verschiedenen Beeren und Früchten in deren natürlichem Gehänge in einer Voliere geprüft sowie die Auswirkung unterschiedlich frugivorer Ernährung auf Körpermasse und tägliche Nahrungsaufnahme unter kontrollierten Laborbedingungen untersucht. Zwischen dem Präferenzverhalten gegenüber bestimmten Beeren und Früchten und deren Profitabilität bzw. Nährstoffgehalt bestand kein eindeutiger Zusammenhang. Demnach ist die Wahl zwischen verschiedenen Vegetabilien nicht einfach abhängig von ihrer Größe oder dem Nährstoffgehalt. Erhebliche Unterschiede zwischen den getesteten Beeren und Früchten zeigten sich bei der täglichen Aufnahmerate und den Auswirkungen auf die Körpermasse. Während bestimmte Beeren nur als Zusatzfutter zu einem immer, wenn auch geringfügig notwendigen, animalischen Standardfutter verabreicht werden konnten, waren die Gartengrasmücken mit Schwarzem Holunder und Feige auch bei ausschließlicher Gabe nicht nur in der Lage, ihre Körpermasse zu halten, sondern konnten dabei sogar normale Fettdeposition vollziehen. Offensichtlich sind bestimmte Vegetabilien für die Gartengrasmücke wesentlich bedeutsamer als bisher angenommen. Die Ergebnisse stimmen somit mit Beobachtungen aus dem Freiland überein. Die beobachteten qualitativen Unterschiede zwischen den Früchten und deren Wirkung auf die Körpermasse der Versuchsvögel ließen sich nicht allein mit dem Nährstoffgehalt der Beeren erklären. Vermutlich spielen die spezifische Qualität der Nährstoffe (z. B. Fettsäurezusammensetzung) und möglicherweise auch sekundäre Pflanzenstoffe eine wichtige Rolle.

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The significance of seasonal frugivory in migratory Garden WarblersSylvia borin

Summary In contrast to field observation, exhibiting an important role of seasonal frugivory,Berthold (1976) concluded that fruits are only a supplementary food, and he rejected the hypothesis that songbirds shift to a fruit diet during migration in order to render or to accelerate fat deposition.We investigated the preference of Garden Warblers upon various berries and pulpy fruits in an outdoor aviary. Furthermore, the effects of frugivory on body mass and food intake is measured in caged specimens under controlled laboratory conditions.In almost all feeding trials a significant selection between the two alternative fruit diets are obvious. However, no clearcut relationship between profitability or nutritive content of the various fruits and food choice is evident.In the experiments under controlled laboratory conditions the effects of varying extends of frugivory on body mass and food intake of captive Garden Warblers reveal a considerable difference between various berries and fruits. In some berries, the birds were not able to compensate for a reduction of the standard animal food by increasing frugivory. With Black Elder berries or figs, however, they did not only compensate for to maintain body mass rather they were able to gain mass during migratory fat deposition, even kept on an exclusive fruit diet.These results clearly exhibit a significant role of fruit diets in migrating Garden Warblers, with particular regards to Black Elder berries and figs, respectively.The observed differences between the various fruit diets do not correspond to the crude nutritive content of the pulp. Presumably, the specific quality of nutrients (for instance, fatty acid composition) or even secondary plant compounds have to be considered.The experimental results agree with field observations, indicating the importance of frugivory for the Garden Warbler, and they contradict Berthold's suggestion that fruits are only a least important supplementary food to an always necessary animal food.

     

Preparation and application of a photoreactive thrombin analogue: binding to human platelets

alpha-Thrombin has previously been shown to bind to specific, saturable glycoproteins on the platelet surface. Modification of the thrombin active site with tosyllysyl chloromethyl ketone (TosLysCH2Cl) does not alter thrombin's binding characteristics. Interaction of alpha-thrombin with high-affinity binding sites (KD = 10(-9) M) initiates the platelet response which involves proteolytic hydrolysis of this glycoprotein. Although TosLysCH2Cl--thrombin binds to and competes for the same sites as alpha-thrombin, it cannot induce platelet stimulation because it is enzymatically inactive. In this study, we describe the preparation and application of photoreactive tritium-labeled thrombin analogues. The alpha-thrombin derivative retains its platelet-stimulating and enzymatic activities and, upon photoactivation, covalently binds to specific platelet membrane components. When freshly washed human platelets are exposed to less than saturation doses (less than or equal to 2 nM) of the thrombin derivatives in the dark and photoactivated, a single labeled complex is detected. The same experiment with greater than saturating doses (greater than or equal to 20 nM) of the thrombin derivative yields a similar complex as well as two additional ones. Molecular weight estimates of these thrombin-bound complexes were obtained by gel filtration and NaDodSO4--polyacrylamide gel electrophoresis. The low dose (high affinity) complex with TosLysCH2Cl--thrombin has an approximate molecular weight of 200 000, while that with active alpha-thrombin is smaller, approximately 120 000, due to enzymatic cleavage. The additional complexes detected with the high thrombin dose had estimated molecular weights of 400 000 and 46 000, respectively, and appeared to be the same for TosLysCH2Cl--thrombin and for the alpha-thrombin coupled platelets. These isolated complexes appear to correspond to the two previously detected populations of thrombin binding sites on the platelet.     

Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia

Autism spectrum disorders (ASD) and schizophrenia are neurodevelopmental disorders for which recent evidence indicates an important etiologic role for rare copy number variants (CNVs) and suggests common genetic mechanisms. We performed cytogenomic array analysis in a discovery sample of patients with neurodevelopmental disorders referred for clinical testing. We detected a recurrent 1.4 Mb deletion at 17q12, which harbors HNF1B, the gene responsible for renal cysts and diabetes syndrome (RCAD), in 18/15,749 patients, including several with ASD, but 0/4,519 controls. We identified additional shared phenotypic features among nine patients available for clinical assessment, including macrocephaly, characteristic facial features, renal anomalies, and neurocognitive impairments. In a large follow-up sample, the same deletion was identified in 2/1,182 ASD/neurocognitive impairment and in 4/6,340 schizophrenia patients, but in 0/47,929 controls (corrected p = 7.37 × 10⁻⁵). These data demonstrate that deletion 17q12 is a recurrent, pathogenic CNV that confers a very high risk for ASD and schizophrenia and show that one or more of the 15 genes in the deleted interval is dosage sensitive and essential for normal brain development and function. In addition, the phenotypic features of patients with this CNV are consistent with a contiguous gene syndrome that extends beyond RCAD, which is caused by HNF1B mutations only.     

Intact T cell receptor signaling by CD4+ T cells cultured in the rotating wall‐vessel bioreactor

T lymphocytes fail to proliferate or secrete cytokines in response to T cell receptor (TCR) agonists during culture in spaceflight or ground‐based microgravity analogs such as rotating wall‐vessel (RWV) bioreactors. In RWVs, these responses can be rescued by co‐stimulation with sub‐mitogenic doses of the diacyl glycerol (DAG) mimetic phorbol myristate acetate. Based on this result we hypothesized that TCR activation is abrogated in the RWV due to impaired DAG signaling downstream of the TCR. To test this hypothesis we compared TCR‐induced signal transduction by primary, human, CD4⁺ T cells in RWV, and static culture. Surprisingly, we found little evidence of impaired DAG signaling in the RWV. Upstream of DAG, the tyrosine phosphorylation of several key components of the TCR‐proximal signal was not affected by culture in the RWV. Similarly, the phosphorylation and compartmentalization of ERK and the degradation of IκB were unchanged by culture in the RWV indicating that RAS‐ and PKC‐mediated signaling downstream of DAG are also unaffected by simulated microgravity. We conclude from these data that TCR signaling through DAG remains intact during culture in the RWV, and that the loss of functional T cell activation in this venue derives from the affect of simulated microgravity on cellular processes that are independent of the canonical TCR pathway. J. Cell. Biochem. 109: 1201–1209, 2010. © 2010 Wiley‐Liss, Inc.     

Cleavage of syndecan-4 by ADAMTS1 provokes defects in adhesion

Syndecan-4 is a membrane-bound heparan sulfate proteoglycan that participates in cell-cell and cell-matrix interactions and modulates adhesion and migration of many cell types. Through its extracellular domain, syndecan-4 cooperates with adhesion molecules and binds matrix components relevant for cell migration. Importantly, syndecan-4 is a substrate of extracellular proteases, however the biological significance of this cleavage has not been elucidated. Here, we show that the secreted metalloprotease ADAMTS1, involved in angiogenesis and inflammatory processes, cleaves the ectodomain of syndecan-4. We further showed that this cleavage results in altered distribution of cytoskeleton components, functional loss of adhesion, and gain of migratory capacities. Using syndecan-4 null cells, we observed that ADAMTS1 proteolytic action mimics the outcome of genetic deletion of this proteoglycan with regards to focal adhesion. Our findings suggest that the shedding of syndecan-4 by ADAMTS1 disrupts cell adhesion and promotes cell migration.     

Pharmacological removal of serum amyloid P component from intracerebral plaques and cerebrovascular Aβ amyloid deposits in vivo

Human amyloid deposits always contain the normal plasma protein serum amyloid P component (SAP), owing to its avid but reversible binding to all amyloid fibrils, including the amyloid β (Aβ) fibrils in the cerebral parenchyma plaques and cerebrovascular amyloid deposits of Alzheimer''s disease (AD) and cerebral amyloid angiopathy (CAA). SAP promotes amyloid fibril formation in vitro, contributes to persistence of amyloid in vivo and is also itself directly toxic to cerebral neurons. We therefore developed (R)-1-[6-[(R)-2-carboxy-pyrrolidin-1-yl]-6-oxo-hexanoyl]pyrrolidine-2-carboxylic acid (CPHPC), a drug that removes SAP from the blood, and thereby also from the cerebrospinal fluid (CSF), in patients with AD. Here we report that, after introduction of transgenic human SAP expression in the TASTPM double transgenic mouse model of AD, all the amyloid deposits contained human SAP. Depletion of circulating human SAP by CPHPC administration in these mice removed all detectable human SAP from both the intracerebral and cerebrovascular amyloid. The demonstration that removal of SAP from the blood and CSF also removes it from these amyloid deposits crucially validates the strategy of the forthcoming ‘Depletion of serum amyloid P component in Alzheimer''s disease (DESPIAD)’ clinical trial of CPHPC. The results also strongly support clinical testing of CPHPC in patients with CAA.