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  • Articles  (4)
  • Organic Chemistry  (2)
  • Chromosome  (1)
  • Enzymes, extracellular  (1)
  • Membranes, bacterial  (1)
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  • Articles  (4)
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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 116 (1978), S. 259-268 
    ISSN: 1432-072X
    Keywords: Serratia marcescens ; Antibiotics, hypersensitivity to ; Membranes, bacterial ; Enzymes, extracellular ; Lipase, extracellular ; Mutation, pleiotropic ; Proteins, outer membrane ; Detergents, lysis by ; Pectin ; Glycogen
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Various mutants (oxa s ) were isolated from Serratia marcescens SM-6 by selecting for hypersensitivity towards oxacillin. All mutants found are highly pleiotropic and able to yield spontaneous revertants which behave like the wild-type. Mutant W 1421 mostly studied shows the following phenotypic properties not found in the wild-type: (1) The growth is hypersensitive to various antibiotics, detergents and dyes which differ remarkably in their chemical structure and antibacterial action-mechanism, (2) the cells can be easily solubilized by 0.05% Sodium-dodecylsulfate, (3) the cells allow the adsorption of the roughmutant specific Salmonella phage 6SR, (4) strong cellular binding of crystal violet, (5) agglutination of the cells in 0.3% auramin solution and (6) reduced formation of red pigment. Strain W 1421 is assumed to be a lipopolysaccharide-defective mutant. The outer membrane of mutant W 1421 analyzed by Sodiumdodecylsulfate-polyacrylamide gel electrophoresis possesses a single protein less than that of the wild-type. Mutant W 1421 is further characterized by its low exolipase activity; exoprotease and exonuclease activities are as in the wild-type. This specific exoenzyme deficiency can be overcome either by backmutation to oxacillin-resistance or by growing mutant W 1421 in a medium supplemented with certain non-metabolizable polysaccharides, e.g. glycogen or pectin B. Both polysaccharides increase the exolipase activity of the wild-type too.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 252 (1996), S. 342-345 
    ISSN: 1617-4623
    Keywords: Barley ; Arabidopsis thaliana ; Telo-mere ; Chromosome
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Telomeres of most eucaryotes terminate in long stretches of short, guanine-rich repeats. Telomerase, a specialized enzyme with reverse transcriptase-like activity, has been shown to synthesize these repeats in many lower eucaryotes and several animal species. Although a sequence (TTTAGGG)n that matches the eucaryotic consensus sequence Tx(A)Gy is present in several plant species, the activity and expression patterns of plant telomerase have not been reported. Here we document the presence of telomerase activity in plant tissues using a modification of the human Telomeric Repeat Amplification Protocol (TRAP) assay. Telomerase activity was detected in barley embryo, anther and carpel tissues and in immature seeds ofArabidopsis thaliana, but not in barley leaf tissue.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 32 (1966), S. 112-112 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die MICHAEL-Addition von Methylvinylketon an 1-Acetyl-2-benzyl-3-carbomethoxy-4-piperidon verläuft vollständig stereoselektiv und liefert in zwei Reaktionsstufen praktisch ausschließlich eines von vier möglichen Enantiomerenpaaren des 1-Benzyl-2-acetyl-6-keto-9-carbomethoxy-10-hydroxy-decahydroisochinolins (IIIa), wie aus der quantitativ gelungenen Trennung der Säure (IIIb) in die optischen Antipoden hervorgeht. Aus der Rotationsdispersion ergibt sich eine cis-Verknüpfung der beiden Ringe, die außerdem chemisch bewiesen wird.Die Reduktion der 6-Ketogruppe nach MEERWEIN-PONNDORF-VERLEY bzw. durch katalytische Hydrierung an RANEY-Nickel führt überwiegend zum entsprechenden axialen Alkohol, während die Reduktion mit Natriumborhydrid ein Gemisch von äquatorialem und axialem Alkohol (etwa 2:1) liefert. Durch Überführung des äquatorialen Alkohols in das Lacton wird bewiesen, daß von den beiden denkbaren cis-Konformationen diejenige mit (in bezug auf den Cyclohexanring) axialer 9-Carboxylgruppe entstanden ist. Das steht auch in Übereinstimmung mit den Verseifungsgeschwindigkeiten von IIIa und anderen Estern dieses Systems und den Ergebnissen der NMR-Spektroskopie.Die Konformation der Benzylgruppe ließ sich mit Hilfe der IR- und der NMR-Spektroskopie ermitteln.Die Ergebnisse erlauben es, die absolute Konfiguration der Verbindung IIIa festzulegen.Die Gründe für den gefundenen sterischen Verlauf der MICHAEL-Addition werden erörtert und einige allgemeinere Folgerungen daraus abgeleitet.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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