Deductive biology—Some cautious steps

For certain environments, the Darwinian model allows unique prediction of a function that any surviving system adapted to such an environment has to perform. This is the case for those environments that determine a “survival functional” of position in space-time of known shape. Purely temporal survival functionals can be distinguished from spatial and mixed ones. In each case, there exists an optimum path in combined physical and (reduced) metabolic space. Dependent on the admissible error, approximate solutions of different complexity are sufficient. All solutions possess an afferent, a central, and an efferent part. Within this general frame, specific, “probably simplest”, solutions are proposed for adaptive chemotaxis, insect locomotion, lower vertebrates locomotion, higher vertebrates locomotion, chronobiological systems, and immune systems, respectively—or rather, for the underlying functionals. Presented at the Society for Mathematical Biology Meeting, University of Pennsylvania, Philadelphia, August 19–21, 1976.     

The mechanism of energy conservation and transduction by mitochondrial cytochrome c oxidase

Oxidation of ferrocytochrome c by molecular oxygen catalysed by cytochrome c oxidase (cytochrome aa₃) is coupled to translocation of H⁺ ions across the mitochondrial membrane. The proton pump is an intrinsic property of the cytochrome c oxidase complex as revealed by studies with phospholipid vesicles inlayed with the purified enzyme. As the conformation of cytochrome aa₃ is specifically sensitive to the electrochemical proton gradient across the mitochondrial membrane, it is likely that redox energy is primarily conserved as a conformational “strain” in the cytochrome aa₃ complex, followed by relaxation linked to proton translocation. Similar principles of energy conservation and transduction may apply on other respiratory chain complexes and on mitochondrial ATP synthase.     

Target cells for the activity of a synthetic adjuvant: muramyl dipeptide.

Muramyl dipeptide (MDP), a synthetic adjuvant, increased the primary response of CBA mice to sheep red blood cells (SRBC). In reconstituted irradiated recipients, cooperation between T and B lymphocytes was required for the expression of adjuvant activity and MDP increased the efficiency of SRBC-educated T cells. The role of T-derived lymphocytes in mediating the MDP adjuvant activity was also demonstrated in irradiated mice and in mice reconstituted with various splenic cellular types of donors which had received SRBC and MDP 24 hr earlier. In our experiments, the macrophage did not seem to be involved, since MDP did not increase the phagocytic capacity of peritoneal exudate cells and MDP- and SRBC-pretreated macrophages had no increased ability to induce an anti-SRBC immune response. These results demonstrate the importance of T lymphocytes as mediators of the adjuvant activity of MDP.     

A heme-nonapeptide tracer for electron microscopy

Summary A heme-nonapeptide (H-9-P)¹, applicable to electron microscopic cytochemistry via peroxidase-like activity, was prepared by passing horse heart cytochrome c through a column with Sepharose and covalently attached trypsin. After purification by column chromatography (Sephadex G50 Superfine, Biogel P-2) a maximal yield of 50% and purity of >99% was achieved. A concise schedule allows for inexpensive preparation of H-9-P with standard laboratory equipment. H-9-P has the following properties: Its structure is (14) Cys-Ala-Gln-Cys-His-Thr-Val-Glu-Lys (22) with heme attached to Cys (14) and (17). MW=1630, pI=4.95, _E(max) ^{pH 7} = 397.5 nm, _{22 °C, pH 7} ^{397.5 nm} = 1.11 × 10⁵ [Liter/Mole x cm]. With the use of a diaminobenzidine-H₂O₂-medium — as applied for cytochemistry — we determined spectrophotometrically a pH_opt=12.5 and an apparent K₅ = 3.14 × 10^{– 3} [M]. Glutardialdehyde leads to considerable de-activation and, according to SDS-polyacrylamide-gel-electrophoresis, to diffuse crosslinking accompanied by a shift of the active pH-region towards neutral pH values. An attempt was made to optimize the cytochemical assay. The peroxidase-like activity of H-9-P is well comparable to that of other heme-tracers; only horseradish peroxidase has a higher turnover number. When injected to mice or added to cell suspensions, even high concentrations of H-9-P did not entail any signs of toxicity.Abbreviations AAA amino acid analysis - AHC ammoniumhydrogencarbonate - BSA bovine serum albumin - Cyt c cytochrome c - DAB 5,3-diaminobenzidine - GA glutardialdehyde - H-8-P heme-octapeptide - H-9-P heme-nonapeptide - H-11-P heme-undecapeptide - HR-POX horseradish peroxidase - MW molecular weight - PAGE polyacrylamid-gel-electrophoresis - pI isoelectric point - SDS sodiumdodecylsulphate - SG-TLC silicagel-thin-layer-chromatography This work was supported by the Österreichische Forschungsfonds     

Die Wirkung von Kernpolyedern (Baculovirus spec.) ausMamestra brassicae aufTrichogramma cacoeciae [Hym.: Trichogrammatidae] undChrysopa carnea [Neur.: Chrysopidae]

Zusammenfassung Kernpolyeder vonMamestra brassicae (L.) wurden auf Nebenwirkungen an zwei Entomophagen-Arten in der Basis- Konzentration (LC₁₀₀ für den natürlichen Wirt) sowie der 5- und 10 fachen Konzentration geprüft. Schadwirkung durch Kontakt mit frisch angetrocknetem Belag bzw. durch Verfüttern eines kontaminierten N?hrsubstrates auf den EiparasitenTrichogramma cacoeciae Marchal konnte nicht nachgewiesen werden. Ebenso wurde die Entwicklung vonT. cacoeciae in parasitierten Wirtseiern durch eine Tauchbehandlung mit der Kernpolyeder-Suspension in verschiedenen Intervallen nach der Parasitierung nicht gest?rt. Im Wahl- und Nichtwahlversuch konnte keine Repellentwirkung von Wirtseiern festgstellt werden, die in eine Kernpolyeder-Suspension getaucht worden waren. Die r?uberischen Larven vonChrysopa carnea Steph. waren gegenüber der 10fachen Basiskonzentration bei direktem Bespritzen der Larven, Kontakt mit einem frisch angetrockneten sprit zbelag sowie bei peroraler Aufnahme unempfindlich, wie die Frassleistung der Larven, die Fekundit?t der Imagines sowie die Schlüpfrate der Eier zeigte. Bei praktischen Eins?tzen von Kernpolyeder-Pr?paraten zur Bek?mpfung der Kohleule sind im Gegensatz zu den üblichen Anwendungen von Phosphors?ureestern keine direkten Nebenwirkungen auf die untersuchten Nutzinsekten zu erwarten.

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Summary The side effect of a water suspension of polyhedral inclusion bodies of nuclnear polyhedrosis virus (NPV) fromMamestra brassicae (L.) in a concentration of 1-, 5-, and 10-fold of the LC₁₀₀ for the natural host was tested on two beneficial insects. No reduction in the parasitization capacity ofTrichogramma cacoeciae Marchal (Hym.: Trichogrammatidae) was recorded when adults were exposed to a fresh dry film, or fed on contaminated honey-agar. The development of the parasite inSitotroga cerealella Oliv. host eggs was not affected when these were dipped in a suspension of the NPV at different time intervals after parasitization. In additional tests, it was shown that deposit of the NPV suspension had no repellent effect onTrichogramma. The feeding capacity of the predatory larve ofChrysopa carnea Steph., fecundity of the adults as well as viability of the eggs were not affected when the larvae were directly sprayed with the highest tested concentration of the suspension, exposed to fresh dry film or fed on contaminated diet. These experiments indicate that, in contrast to the use of the conventional organophosphorus insecticides, no hazard to the tested beneficial insects should be expected when the preparation of the polyhedral inclusion bodies will be used in the field.

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Nr. 2 der Serie: Wirkung von Insektenpathogenen auf Entomophagen. Als Nr. 1 gilt:S. Hassan & A. Krieg: über die schonende Wirkung vonBacillus thuringiensis-Pr?paraten auf den ParasitenTrichogramma cacoeciae (Hym.: Trichogrammatidae). — Z. Pfl. Krankh. Pfl. Schutz, 82, 515–521, 1975.     

Comparative Studies on Enrichment And Selective Media for Isolation of Salmonellae from Faecal Specimens

Enrichment media (tetrathionate, selenite and Rapp ap ort broths) and selective media (desoxycholate citrate agar and brilliant green agar) were tested in different combinations to ascertain their capacity for isolation of salmonella bacteria. The material consisted of 299 samples of cattle faeces from two herds infected with salmonella (Table 1), and of 111 artificially contaminated samples of pig faeces (Table 3). The tetrathionate and selenite broths were equally useful for the material as a whole, whereas the results varied between different species of salmonella which is of great practical interest. The number of salmonella isolations was much lower when enrichment with Rappaport broth was used. The rate of salmonella isolations can often be increased by parallel enrichments with two different media. Of the selective agar media tested, brilliant green agar was superior to desoxycholate citrate agar.     

Isolation and characterization of the dut gene of Escherichia coli. II. Restriction enzyme mapping and analysis of polypeptide products

Restriction endonuclease mapping of previously constructed dut plasmids has been carried out using the enzymes PvuI, PvuII and SacI. Various dut plasmids were also tested in the "maxicell" protein-synthesizing system. They all show two protein bands in common, one of Mr 16000 in agreement with the size previously reported for the purified dUTPase subunit (Shlomai and Kornberg, 1978). With the information obtained the structural gene for dUTPase can be assigned to a 950-bp SacI-PvuII fragment of the E. coli genome. Studies, described in the preceding paper, on the overproduction of dUTPase by bacterial strains carrying different dut plasmids strongly suggest that the dut gene is transcribed in the direction from the SacI site towards the PvuII site and that the SacI site is located within the dut control region. The second protein band observed in the "maxicell" experiments has an Mr of 23500. Its identity is unknown but it may represent a precursor of dUTPase or the product of a separate gene located between dut and pyrE.