The isolation of IS1 and IS2 DNA

Summary DNA of the IS-elements IS1 and IS2 was prepared by digestion of appropriate heteroduplex molecules with endonuclease S1, followed by sucrose gradient centrifugation or gel electrophoresis. The material obtained is homogeneous with regard to size. The length of IS1 DNA is 820±65 nucleotides, the length of IS2 DNA is 1.350±70 nucleotides. IS1 DNA is not cleaved by the restriction endonucleases Eco R1, Hind II or Hind III. IS2 DNA is cleaved once by each of the two latter enzymes. The buoyant density determined by equilibrium centrifugation of Hg-complexes in Cs₂SO₄ corresponds to a GC content of approximately 50%. Labelling with polynucleotide kinase indicates that both IS DNA's have a guanosyl residue at both of their 5-termini.     

Einbau von 14C-mevalonsäurelacton in hopfenbitterstoffe

Labeled mevalonate is incorporated into terpenes and hop bitter compounds by Humulus lupulus. The role of mevalonate as a precursor for the prenyl (3-methyl-but-2-enyl) side chain of the hop bitter compounds is discussed.     

Introduction

The only concrete basis for the discontinuous and hierarchical organization of extant organisms lies in their genealogical (i. e. germ line) relationships. Individuals and populations of common descent are called sib or stirps. Ideally, systematic classification is based on the formulas: (1) sib + taxonomic category + name = taxon, and (2) divergent genealogy of sibs + hierarchy of taxonomic categories + names = taxonomic system (Fig. 1).Presented at the symposium Speciation and the Species Concept during the XIIth International Botanical Congress, Leningrad, July 8, 1975.     

Chromosome numbers and differentiation of centrospermous families

The patterns of variation of chromosome numbers in theCentrospermae suggest a common ancestry of centrospermous anthocyanin and betalain families. Phylogenetic divergence in the order may have originated with progenitors similar to extantMolluginaceae, Aizoaceae orPhytolaccaceae taxa with x = 9. Evolutionary radiation and advancement in several lines then seems to have been paralleled by trends for increasing chromosome base numbers through dysploidy and polyploidy, e.g. towardsCaryophyllaceae, Portulacaceae-Basellaceae, Hectorellaceae, Cactaceae, Didieraceae, Nyctaginaceae andChenopodiaceae-Amaranthaceae. Presented in the Symposium Evolution of Centrospermous Families, during the XIIth International Botanical Congress, Leningrad, July 8, 1975.     

Purification and properties of chorismate mutase-prephenate dehydratase and prephenate dehydrogenase from Alcaligenes eutrophus.

Chorismate mutase and prephenate dehydratase from Alcaligenes autophus H16 were purified 470-fold with a yield of 24%. During the course of purification, including chromatography on diethylaminoethyl (DEAE)-cellulose, phenylalanine-substituted Sepharose, Sephadex G-200 and hydrogyapatite, both enzymes appeared in association. The ratio of their specific activities remained almost constant. The molecular weight of chorismate mutase-prephenast dehydratase varied from 144,000 to 187,000 due to the three different determination methods used. Treatment of electrophoretically homogeneous mutase-dehydratase with sodium dodecyl sulfate dissociated the enzyme into a single component of molecular weight 47,000, indicating a tetramer of identical subunits. The isoelectric point of the bifunctional enzyme was 5.8. Prephenate dehydrogenase was not associated with other enzyme activities; it was separated from mutasedehydratase by DEAE-cellulose chromatgraphy. Chromatography on DEAE Sephadex, Sephadex G-200, and hydroxyapatite resulted in a 740-fold purification with a yield of 10%. The molecular weight of the enzyme was 55,000 as determined by sucrose gradient centrifugation and 65,000 as determined by gel filtration or electrophoresis. Its isoelectric point was pH 6.6. In the overall conversion of chorismate to phenylpyruvate, free prephenate was formed which accumulated in the reaction mixture. The dissociation of prephenate allowed prephenate dehydrogenase to compete with prephenate dehydratase for the substrate.     

Galium procurrens,a new diploid relic species of theG. sylvaticum-group from the Balkan Peninsula

Galium procurrens is described as a new diploid relic species from Montenegro/N. Albania and SW. Bulgaria. It is related to the tetraploidG. laevigatum and other diploid and polyploid taxa of theG. sylvaticum-group inhabiting European deciduous forests.     

Zur Kenntnis der Wirkung von Gallensalzen auf die Zelle

Zusammenfassung Schon sehr kleine Mengen von Gallensalzen, wie desoxycholsaures und apocholsaures Natrium lassen aus Zellen Stoffe austreten, ohne da\ die Zellen tot sind. Die ausgetretenen Stoffe können mit der Schüttelprobe (Oberflächenspannung), mit der Ninhydrinprobe (Eiwei\bruchstücke), und mit der Silbernitratprobe erfa\t werden.Auch kleine Mengen von Quecksilberchlorid veranlassen Austritt von Stoffen aus der Zelle. Dabei sind die Zellen nicht tot. Bei den Gallensalzproben ist eine untere Grenze der Wirksamkeit schwer anzugeben. Wenn nicht gerade (bei Kartoffelversuchen) Randstücke oder Siebteile mit viel Eiwei\ vorliegen, ist eine Normalgrenze der Wirkung etwa bei 1 75000 bis 1 100000 erreicht, soweit die Ninhydrinprobe in Frage kommt. Bei Gegenwart eiwei\reicher Kartoffelzellen bzw. Siebteile ist die Grenze der mit Ninhydrin zu erfassenden Wirkung viel tiefer anzusetzen, etwa 1 1000000. Durch die physiologischen oder anatomisch-topographischen Sondereigenschaften (viel Eiwei\, viel Siebteile in einzelnen Proben) erhält die Gallensalzmethode bis zu einem gewissen Grad etwas Subjektives. Trotzdem steht unter Umständen der Gallensalzeinflu\ 1 1000000 au\er jedem Zweifel! Die Methodik setzt eben eine gewisse Erfahrung voraus.Bei höheren Pflanzen kann mit der Neutralsalz-Gallensalzbehandlung der Unterschied zwischen Epidermiszellen und Spaltöffnungsapparat ungemein scharf vordemonstriert werden. Bei geeigneter Behandlung lösen sich Zellkerne schrittweise in Neutralsalz-Gallensalz auf, die Kerne der Spaltöffnungszellen sind resistenter.