Frequency of Buddleja davidii Franch. (Buddlejaceae) in Germany along ecological gradients

In Central Europe as in most other temperate regions of the world, Buddleja davidii has become a very successful invader. A thorough observation, documentation and analysis of the spread of invasive species is the precondition for the understanding of invasion processes. Therefore, I documented the occurrence of the species along a west–east transect as well as an altitudinal transect, and I tried to reconstruct the spread of the species in the course of the last decades along railroad areas, which have proved to be the most favorized habitats for colonization of Buddleja. Additionally, a literature review is given on its general spread and distribution in Germany. Based on the investigation of 52 stations, the results show that the species, in Germany, has its optimum in the Rhein-Ruhr- and the Rhein-Main-area, that its abundance significantly decreases from west to east and with increasing altitude. A literature review combined with own investigations shows, that it was very successful in Germany on ruins of World War II but decreased and sometimes totally disappeared in cities of East Germany and of the altitudinal higher regions of Germany, i.e. also in many towns of South Germany. In West Germany, the recent spread started about three decades ago and is still in process. As cold winters seem to be the limiting factor for the spread of Buddleja, even an accelerated spread of this species and perhaps a loss of its ruderal character can be expected, considering the progress of climate change.     

Construction of a 42 base pair double stranded DNA microcircle.

A procedure for the construction of double stranded DNA microcircles is described that overcomes the natural limits of established circularization procedures. Starting with two synthetic oligonucleotides which are able to form dumbbell shaped structures, two subsequent ligation reactions yield a microcircle of double stranded DNA of 42 base pairs. This is by far the smallest circle of double stranded DNA yet described. These microcircles can be constructed in quantities required for high resolution structural analyses such as X-ray crystallography and NMR spectroscopy.     

Covalent immobilization of the multienzyme enniatin synthetase

Summary The multienzyme enniatin synthetase was covalently immobilized to N-hydroxysuccinimide activated agarose. The stability of the immobilized enzyme at 25°C was enhanced compared to the soluble enzyme. Immobilization experiments also indicated that the enniatins are synthesized by a single molecule and thus do not require interactions of several enzyme molecules.     

Isolation of oligonucleosomes from active chromatin using HMG17-specific monoclonal antibodies.

We report the preparation of HMG17-containing oligonucleosomes from chicken embryos and from liver and oviduct of laying hens. Monoclonal antibodies against HMG17 were used for their isolation. An unusual size distribution with respect to their repeat number was observed. The oligonucleosomes of repeat number up to N6 were highly enriched for DNA of the vitellogenin II gene (liver) and for DNA of the ovalbumin and lysozyme genes (oviduct).     

Ethanol transport in Zymomonas mobilis measured by using in vivo nuclear magnetic resonance spin transfer.

For the first time, unidirectional rate constants of ethanol diffusion through the lipid membrane of a microorganism, the bacterium Zymomonas mobilis, were determined, thus replacing indirect inferences with direct kinetic data. The rate constants k1 (in to out) were 6.8 +/- 0.4s(-1) at 29 degrees C and 2.7 +/- 0.3s(-1) at 20 degrees C. They were determined by using 1H selective nuclear magnetic resonance spin magnetization transfer. The measurements were done on l-ml cell suspensions. No addition of radiotracers, withdrawing of aliquots, physical separation methods, or chemical manipulations were required. Until now, the rate constants of ethanol transport in microorganisms have been unknown because ethanol diffuses through the cytoplasmic membrane too quickly for radiolabel approaches. Net velocities of ethanol exchange were calculated from unidirectional rate constants and cytoplasmic volume, which was also determined with the same nuclear magnetic resonance experiments. The results (i) confirmed that ethanol would not be rate limiting during the conversion of glucose by Z. mobilis and (ii) indicated that ethanol can serve as an in vivo marker of cytoplasmic volume changes. This was verified by monitoring for the first time the changes of both cytoplasmic volume and extracytoplasmic and cytoplasmic concentrations of alpha and beta anomers of D-glucose in cell suspensions of a microorganism. These findings may open up new possibilities for kinetic studies of ethanol and sugar transport in Z. mobilis and other organisms.     

Selective synthesis of depsipeptides by the immobilized multienzyme enniatin synthetase

Summary The multifunctional enzyme enniatin synthetase was immobilized by adsorption to propyl agarose. The immobilized multienzyme retained 45% of the activity of the free enzyme; an operational half-life of about 15 h was estimated. Selective synthesis of several different enniatin homologues was achieved with propyl agarose-bound enniatin synthetase. In addition to enniatin A, B, and C formation, a selective synthesis of non-naturally occurring depsipeptides, containing norvaline, norleucine, or -aminobutyric acid as sole amino acid moieties, was observed.     

Stabilization of R loop structures by photochemical crosslinking with 4,5',8-trimethylpsoralen: application to gene enrichment and molecular cloning

R loops formed between nucleosomal DNA and tRNA can be photochemically crosslinked with 4,5′,8-trimethylpsoralen directly in the R loop formation buffer. When biotin is coupled to the tRNA 3′-terminus via a diaminohexan linker and the modified tRNA employed for R loop hybridization the crosslinked R loops can be efficiently purified by affinity chromatography on avidin-glass columns. Following tRNA hydrolysis the partially crosslinked double stranded DNA, highly enriched for tRNA genes can be cloned in E. coli χ¹⁷⁷⁶.     

KINETIC-MICROARCHITECTURAL CORRELATIONS IN THE BONE MARROW OF THE MOUSE

Transverse histologic sections of bone marrow obtained from mice that were sacrificed by perfusion fixation at intervals following tritiated thymidine injection were studied by means of radioautography. A kinetic gradient was demonstrated across the marrow section, with the highest proliferative rate in the subendosteal region. Megakaryocytes were shown to originate from the rapidly proliferating subendosteal cells. The immediate proliferating precursors of mature granulocytes were slowly proliferating cells found predominantly in the central region of the marrow. It was concluded that in the steady state there must be a migration of cells from the subendosteal region to the central region with concomitant growth retardation of the migrating cells.