cDNA cloning and sequencing of tarantula hemocyanin subunits

Summary Tarantula heart cDNA libraries were screened with synthetic oligonucleotide probes deduced from the highly conserved amino acid sequences of the two copper-binding sites, copper A and copper B, found in chelicerate hemocyanins. Positive cDNA clones could be obtained and four different cDNA types were characterized.     

Zur Feinstruktur der Maxillarnephridien von Scutigerella immaculata Newport (Symphyla,Myriapoda)

Zusammenfassung Die Feinstruktur der Maxillarnephridien von Scutigerella immaculata Newport mit ihren drei Abschnitten Sacculus, Tubulus und Ausführgang wurde untersucht. Die Zellen des Sacculus sind typische Podocyten, an denen eine Ultrafiltration ablaufen kann. Möglicherweise wird die Filtration durch einen den Sacculus umgebenden Muskel unterstützt. Die Zellen des Tubulus zeigen basale Einfaltungen und im proximalen Teil auch Mikrovilli. Sowohl im Tubulus als auch im Ausführgang, dessen Zellen ebenfalls basale Einfaltungen aufweisen, werden Reabsorptionsprozesse vermutet.

---

The fine structure of the maxillary kidney of the garden centipede, Scutigerella immaculata Newport (Symphyla, Myriapoda)

Summary The fine structure of the maxillary kidney of Scutigerella immaculata Newport (Symphyla) has been investigated. It may be compared with segmental organs of other Arthropoda having an end-sac which forms a primary urine by ultrafiltration. The filtration may be supported by a muscle surrounding the end-sac. The tubular part of the nephridium and the efferent duct show structures which may be involved in reabsorption.

     

Beitrag zur Kenntnis der Sinnesorgane von Symphylen (Myriapoda)

Zusammenfassung Am Präanalsegment von Scutigerella befindet sich ein Paar Trichobothrien, das komplizierter gebaut ist als entsprechende Sinnesorgane anderer Arthropoden. Die distalen Fortsätze von sechzehn Sinneszellen stehen mit der Gelenkmembran des nach allen Seiten beweglichen Sinneshaares in Verbindung. Aus ihrer Anordnung kann geschlossen werden, daß Scutigerella mit Hilfe des Trichobothriums mindestens acht verschiedene Richtungen unterscheiden kann. Der adäquate Reiz für die Trichobothrien dürften Luftbewegungen sein.

---

Sense organs of symphyla (Myriapoda)I. Ultrastructure of the trichobothrium of Scutigerella immaculata newport

Summary One pair of trichobothria is situated on the lateral portions of the preanal segment of Scutigerella. They are rather complicated compared to similar organs of other Arthroods. The distal portions of 16 sense cells are connected to the elastic membrane of the sense hair which can be turned in every direction. From the arrangement of the distal parts of the sense cells it may be concluded that Scutigerella can distinguish at least eight different directions. Probably movements of the air are the adequate stimulus for the trichobothrium.

Für technische Mitarbeit danke ich Frl. M. Genehr und Fr. G. Schröer, für die Anfertigung der Zeichnung Fr. C. St. Friedemann.     

The human 5-HT1A receptor expressed in HeLa cells stimulates sodium-dependent phosphate uptake via protein kinase C

Regulation of phosphate uptake was studied in HeLa cell lines after transfection with DNA encoding the human 5-HT1A receptor. Phosphate uptake was saturable and greater than 90% sodium-dependent, with Vmax approximately 30-35% without changing Km. Treatment with 5-HT or the 5-HT1A-specific agonist 8-OH-2-(di-n-propylamino)1,2,3,4-tetrahydronaphthalene increased Vmax approximately 40% without affecting Km. This effect was blocked by pretreatment with the 5-HT1 antagonists, methiothepine and spiperone, or pertussis toxin. Surprisingly, the stimulation was not secondary to an inhibition of adenylyl cyclase because 5-HT stimulated phosphate uptake approximately 20% in the presence of 1 mM 8-Br-cAMP. Rather, the primary pathway linked to the stimulation of phosphate uptake involved activation of protein kinase C because (i) 5-HT measurably activated protein kinase C in these cells, (ii) activators of protein kinase C (phorbol esters and diacylglycerol analogues) stimulated phosphate uptake in these cells (iii) the half-maximal doses for 5-HT-induced phosphatidylinositol hydrolysis and stimulation of phosphate uptake were virtually equivalent, and both effects were equally sensitive to pertussis toxin, and (iv) the stimulation was markedly attenuated in cells made deficient in protein kinase C. These results demonstrate that the stimulation of phosphatidylinositol hydrolysis by the 5-HT1A receptor can generate physiologically measurable effects on cellular transport and suggest that such accessory pathways may play a prominent role in signal transduction.     

Combining industrial ecology tools to assess potential greenhouse gas reductions of a circular economy: Method development and application to Switzerland

Industrial ecology (IE) methodologies, such as input/output or material flow analysis and life cycle assessment (LCA), are often used for the environmental evaluation of circular economy strategies. Up to now, an approach that utilizes these methods in a systematic, integrated framework for a holistic assessment of a geographic region's sustainable circular economy potential has been lacking. The approach developed in this study (IE4CE approach) combines IE methodologies to determine the environmental impact mitigation potential of circular economy strategies for a defined geographic region. The approach foresees five steps. First, input/output analysis helps identify sectors with high environmental impacts. Second, a refined analysis is conducted using material flow and LCA. In step 3, circular strategies are used for scenario design and evaluated in step 4. In step 5, the assessment results are compiled and compared across sectors. The approach was applied to a case study of Switzerland, analyzing 8 sectors and more than 30 scenarios in depth. Carbon capture and storage (CCS) from waste incineration, biogas and cement production, food waste prevention in households, hospitality and production, and the increased recycling of plastics had the highest mitigation potential. Most of the scenarios do not influence each other. One exception is the CCS scenarios: waste avoidance scenarios decrease the reduction potential of CCS. A combination of scenarios from different sectors, including their impact on the CCS scenario potential, led to an environmental impact mitigation potential of 11.9 Mt CO₂-eq for 2050, which equals 14% of Switzerland's current consumption-based impacts.     

Radioimmunoassay of 2-hydroxyestrone

Under the protection of ascorbic acid a 2-hydroxyestrone bovine serum albumin conjugate was prepared containing intact 2-hydroxyestrone as determined by gas chromatographymass spectrometry. Using this antigen highly specific antibodies were raised in rabbits. Cross-reactivity for 2-hydroxyestradiol and 2-hydroxyestriol was 26 and 4.5%, respectively. An assay procedure of 2-hydroxyestrone in human plasma is described. Using special precautions the assay allows the determination of 2-hydroxyestrone in plasma samples of women (50–95 pg/ml), pregnant women (105–220 pg/ml), men (45–65 pg/ml) and children (20–40 pg/ml).     

Characteristics of the F52 protein, a MARCKS homologue.

A recently cloned mouse cDNA designated F52 encodes a putative protein with striking sequence similarity to the MARCKS protein, a major cellular substrate for protein kinase C (PKC). Major regions of sequence similarity include the amino-terminal myristoylation consensus sequence and the central calmodulin-binding/PKC phosphorylation site domain. The F52 protein was expressed in Escherichia coli with apparent M(r) 50,000; it was a substrate for PKC and comigrated on two-dimensional electrophoresis with a myristoylated protein whose phosphorylation was stimulated by phorbol 12-myristate 13-acetate in mouse neuroblastoma cells. The F52 protein also was myristoylated in E. coli by co-expression with N-myristoyltransferase. A 24-amino acid peptide derived from the protein's phosphorylation site domain was a good substrate for PKC; like the cognate MARCKS peptide, it was phosphorylated with high affinity (S0.5 = 173 nM) and positive cooperativity (KH = 5.4). The F52 peptide also bound calmodulin with high affinity (Kd = less than 3 nM); this binding could be disrupted by phosphorylation of the peptide with PKC, with a half-time of 8 min. The F52 protein is clearly a member of the MARCKS family as defined by primary sequence; in addition, the two proteins share several key attributes that may be functionally important.