Beitrag zur Kenntnis der österreichischen Sippen desValeriana officinalis-Aggregats und ihrer Chromosomenzahlen

Zusammenfassung Die vonWalther im wesentlichen für Deutschland ausgearbeitete Gliederung vonValeriana officinalis agg. ist in ihren Grundzügen auch in Österreich anwendbar. Die Chromosomenzahlen der Sippen sind in diesem Land die gleichen wie auch in anderen Teilen Europas.Valeriana officinalis L. s. str. — die in Österreich häufigste Art — ist mit 2n=14 diploid,V. collina Wallr. mit 2n=28 tetraploid. Ob die beiden in Österreich weniger häufigen, einander sehr ähnlichen oktoploiden Sippen mit 2n=56 —V. sambucifolia Mikan fil. undV. procurrens Wallr. — wirklich Artrang verdienen, ist zu diskutieren.V. procurrens wächst in Österreich unter anderem in den Nordtiroler Alpen.

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Summary The subdivision ofValeriana officinalis agg. established byWalther especially for Germany is found to be practicable in its main features in Austria too. The chromosome numbers of the taxa are the same in Austria as in other parts of Europe.Valeriana officinalis L. s. str. is a diploid (2n=14),V. collina Wallr. is a tetraploid species (2n=28). As to the nearly related octoploid taxaV. sambucifolia Mikan fil. andV. procurrens Wallr. (2n=56) it is still to be discussed, if they should be recognized as species or not.

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Herrn Professor Dr. L.Geitler zum 70. Geburtstag gewidmet.     

Cytocatalytic evolution in plants

Low fertility and vigor, and requirements of ecological niches distinct from diploids are not universal characteristics of autoploids. InClaytonia, Hedyotis, Oldenlandia, and other genera, occurrence and frequency of both polyploids and aneuploids within species populations suggest a greater role of such mutations in the evolution of vascular plants than heretofore presumed.     

The flow of a viscous liquid in a converging tube

The problem of the viscous flow of an incompressible Newtonian liquid in a converging tapered tube has been solved in spherical polar coordinates. The method of the solution involves the Stokes' stream function and a technique introduced by Stokes in the study of a sphere oscillating in a fluid. The theory for the flow in a rigid tube includes: (1) the pulsatile flow with both radial and angular velocity components; (2) the steady state flow with both radial and angular velocity components and (3) the very slow steady state flow with only a radial velocity component present. For a tapered elastic tube, the velocity of the propagated pulse wave is determined. The solution given is in terms of the elastic constants of the system and the coordinates for this type of geometry. The pulse velocity is then related to the velocity in an elastic cylindrical tube with the necessary correction terms to account for the tapered tube. Supported in part by the American Heart Association (No. 62F4EG). This work was done during the tenure of an Established Investigatorship of the American Heart Association.     

Distribution,properties, and functions of midgut carboxypeptidases and dipeptidases from Musca domestica larvae

Dipeptidase and carboxypeptidase A activities were determined in cells and luminal contents of the fore-, mid-, and hind-midgut of Musca domestica larvae. Dipeptidase activity was found mainly in hind-midgut cells, whereas carboxy-peptidase activity was recovered in major amounts in both cells and in luminal contents of hind-midguts. The subcellular distribution of dipeptidase and part of the carboxypeptidase A activities is similar to that of a plasma membrane enzyme marker (aminopeptidase), suggesting that these activities are bound to the microvillar membranes. Soluble carboxypeptidase A seems to occur both bound to secretory vesicles and trapped in the cell glycocalyx. Based on density-gradient ultracentrifugation and thermal inactivation, there seems to be only one molecular species of each of the following enzymes (soluble in water or solubilized in Triton X-100): membrane-bound dipeptidase (pH optimum 8.0; Km 3.7 mM GlyLeu, M_r 111,000), soluble carboxypeptidase (pH optimum 8.0; Km 1.22 mM N-carbobenzoxy-glycyl-L-phenylalanine (ZGlyPhe), M_r45,000) and membrane-bound carboxypeptidase (pH optimum 7.5, Km 2.3 mM ZGlyPhe, M_r58,000). The results suggest that protein digestion is accomplished sequentially by luminal trypsin and luminal carboxypeptidase, by membrane-bound carboxypeptidase and aminopeptidase, and finally by membrane-bound dipeptidase.     

Evaluation of a method to measure conjugal transfer of recombinant DNA in soil slurries

Release of recombinant microbes into the environment necessitates an evaluation of their ability to transfer genetic material. The present report evaluates a method to detect conjugal DNA plasmid transfer in soil slurries under various environmental conditions. DonorPseudomonas cepacia containing pR388::Tn1721 andP. cepacia recipient cultures were coincubated in soil slurries containing autoclaved or natural soil and treated with one or more of 14 experimental conditions. Conjugal mating frequency (transconjugants per initial donor) ranged from 4.8×10^–1 to 1.9×10^–7. Highest numbers of transconjugants, 1.5×10⁷ colony forming units/ml soil slurry, were observed following incubation at 35°C with an enriched nutrient supplement added to the soil. Low numbers of transconjugants, 10³ colony forming units/ml soil slurry, were observed when mating pairs were subjected to low nutrient or pH stress even though initial donor and recipient populations were maintained at high levels. This test system provides a simple way to estimate effects of changing environmental factors on plasmid transfer rates and on the survival of recombinant microorganisms. By use of soil collected from sites proposed to receive genetically engineered microorganisms, preliminary risk assessments can be obtained regarding the potential for gene transfer and microorganism survival with this soil slurry test system.     

Evidence for a two-step mechanism involved in assembly of functional signal recognition particle receptor

The signal recognition particle (SRP) and SRP receptor act sequentially to target nascent secretory proteins to the membrane of the ER. The SRP receptor consists of two subunits, SR alpha and SR beta, both tightly associated with the ER membrane. To examine the biogenesis of the SRP receptor we have developed a cell-free assay system that reconstitutes SR alpha membrane assembly and permits both anchoring and functional properties to be assayed independently. Our experiments reveal a mechanism involving at least two distinct steps, targeting to the ER and anchoring of the targeted molecule on the cytoplasmic face of the membrane. Both steps can be reconstituted in vitro to restore translocation activity to ER microsomes inactivated by alkylation with N-ethyl-maleimide. The characteristics elucidated for this pathway distinguish it from SRP-dependent targeting of secretory proteins, SRP-independent ER translocation of proteins such as prepromellitin, and direct insertion mechanisms of the type exemplified by cytochrome b5.