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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Current genetics 14 (1988), S. 171-176 
    ISSN: 1432-0983
    Keywords: Pelargonium ; Plastome mutants ; Plastid RNA ; Northern analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Several plastome mutants ofPelargonium zonale hort. are characterized by either plastid ribosome deficiencies of specific defects in their photosystems. Southern analyses of plastid DNA fragments containing both the rDNA region and therbcL gene revealed no differences between wild-type and mutant leaves. Northern analyses of mutants with plastid ribosome deficiencies indicate lower levels of plastid ribosomal RNA and mRNA coding for the large subunit (LS) of ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) in mutant leaves relative to green leaves. The data presented in this paper indicate a defect at the transcriptional level in the plastid ribosome deficient plants. We suggest that a RNA polymerase defect affects transcriptional efficiency in these mutants.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Current genetics 5 (1982), S. 245-249 
    ISSN: 1432-0983
    Keywords: Hybrid variegation ; Pelargonium ; Extranuclear inheritance ; Plastid DNA ; Restriction patterns
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary. 1) The genetical and cytological analysis of crosses between the wild-type form ‘Roseum’ of Pelargonium zonale (L.) L 'Herit. ex Ait. and the hybrid species Pelargonium zonale hort. ‘Stadt Bern’' revealed the occurrence of hybrid variegation in the genus Pelargonium 2) The plastids in the green-white variegated plants were sorted out in the quick apical way characteristic for Pelargonium chimera. Six types of periclinal chimeras could be observed. 3) The DNAs of the two different plastomes can be distinguished by restriction endonuclease analysis with EcoRl and BamHI. 4) The differences in the cleavage patterns allowed a detailed description of the process of sorting out of the two parental plastids types within the variegated hybrids on the level of their plastid DNA. In all cases observed the cleavage pattern of ‘Roseum’ plastid DNA was found in the green tissue and the pattern of ‘Stadt Bern’ plastid DNA in the white tissue. 5) From these results we draw the conclusion that there is a disharmony between the F1-hybrid nucleus and the plastome of Stadt Bern', which blocks the normal differentiation of ‘Stadt Bern’ plastids.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical and applied genetics 60 (1981), S. 37-41 
    ISSN: 1432-2242
    Keywords: Pelargonium ; Inter- and intra-specific chloroplast DNA variation ; Restriction patterns ; Biparental plastid inheritance
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The comparison of EcoRI patterns of chloroplast DNAs (ctDNAs) from five species of the genus Pelargonium and from 16 cultivars and varieties of Pelargonium zonale hort. demonstrates a remarkable inter- and intraspecific ctDNA (plastome) variation. The plastome of the P. zonale varieties could be differentiated into groups I, II and III. Reasons for this variation seem to be: occurrence of numerous spontaneous plastome mutations, intense hybridisation by gardeners and breeders, and biparental plastid inheritance. Crosses of P. zonale varieties with different ctDNA types lead to the direct evidence on the molecular level of biparental plastid inheritance and plastid sorting-out in F1-hybrids.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 207 (1987), S. 514-516 
    ISSN: 1617-4623
    Keywords: Pelargonium ; Plastid 5S rDNA ; Sequence ; Minicells ; Not transcribed
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The sequence of the plastid 5S rDNA of Pelargonium zonale hort. “Roseum” is presented. In the 5′ region of this gene there is almost no homology to the Escherichia coli promoter consensus sequences. In an E. coli minicell system we have demonstrated that the plastid promoter of the 16S rDNA is active in E. coli but no separate transcript of the cloned 5S rDNA can be detected. These results provide new evidence that the plastid 5S rDNA of P. zonale and probably also of other higher plants is not transcribed as a separate unit.
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  • 5
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Homopolymers of 2-, 3- and 4-trifluoromethylstyrene, 4-perfluoroisopropylstyrene, 3,5-bis-trifluoromethyl-styrene and a 1 : 1 copolymer of 2,4- and 2,5-bis-trifluoromethyl-styrene have been synthesized and the refractive indices nD, Abbe-numbers νD and glass transition temperatures of the polymers have been determined.With regard to optical applications poly-2-trifluoromethyl-styrene is particularly interesting since its optical properties are in a region of the n-ν-diagram that has not been reached by thermoplastic polymers or inorganic glasses before.The most important mechanical and thermal properties of this polymer are reported. Reactivity ratios of the binary copolymerisation of 2-trifluoromethyl-styrene with styrene, methyl-methacrylate and n-butyl-acrylate are listed as well as optical data and glass transition temperatures of some copolymers of 2-trifluoromethyl-styrene.
    Notes: Homopolymerisate aus 2-, 3- und 4-Trifluormethylstyrol, 4-Perfluorisopropylstyrol, 3,5-Bis-trifluormethylstyrol und ein 1 : 1 Copolymerisat aus 2,4- und 2,5-Bis-trifluormethylstyrol wurden hergestellt und Brechungsindices, Abbe-Zahlen sowie Glasübergangstemperaturen der Polymerisate bestimmt.Von diesen Thermoplasten ist das Poly-2-trifluormethylstyrol im Hinblick auf optische Anwendungen besonders interessant, da es in einem weder von anorganischen Gläsern noch von bekannten thermoplastischen Kunststoffen bisher erreichten Gebiet des n-v-Diagrammes liegt.Die wichtigsten mechanischen und thermischen Eigenschaften dieses Polymeren und die Copolymerisationsparameter für die binäre Copolymerisation von 2-Trifluormethylstyrol mit Styrol, Methylmethacrylat und n-Butylacrylat wurden bestimmt. Optische Daten und Glastemperaturen einiger Copolymerisate des 2-Trifluormethylstyrols werden mitgeteilt.
    Additional Material: 2 Ill.
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  • 6
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: [2π+2π]-Photocycloaddition Reactions in Tricyclo[3.2.2.02.4]nonadiene Derivatives. Synthesis of Singly Bridged Tris-σ-homobenzene CompoundsThe direct - not, however the acetone sensitized -excitation (λ 〉 280 nm) of the tricyclo-[3.2.2.02,4]nonadiene diester 6a - c and the bis-trifluoromethyl derivatives 6d, e (Δ 〉 230 nm), resp., yields (60-90%) the pentacycles 7a - e resulting from a [2π + 2π]-cycloaddition reaction. A [2π + 2σ]-addition with participation of the cyclopropane ring (leading to 8a - e) is not observed. With comparable selectivity (〉 90% isolated yield) the [2π + 2π]-cyclisation takes place in the 3-oxa-diester 10 (to 11). The tris-σ-homobenzene compounds 7a - e and 11, resp. are thermally isomerized exclusively in a 2σ → 2π-cleavage to the starting dienes 6a - e and 10, resp. (Ea (7a) = 22 kcal/mole; A = 2.2·1012 S-1-1). As exemplary cases the addition of HCl, CH3OH and H2O to the diester 7a and to the dicarboxylic acid 7g, resp., has been studied; in a rather selective way the adducts 13 and 14 (ratio 9:1) are formed in good yields. With the usual attack upon the nonsubstituted edge of the bishomocyclobutadiene partial structure in 7a being sterically hindered, tetracyanoethylene forms the 1:1 adducts 15 and 16.
    Notes: Die direkte - nicht aber die aceton-sensibilisierte -Lichtanregung (λ 〉 280 nm) der Tricyclo[3.2.2.02,4]nonadien-diester 6a - c bzw. der Bis-trifluormethyl-Derivate 6d,e (λ 〉 230 nm) liefert in 60-80 proz. bzw. 90 proz. Ausbeute die aus einer [2π + 2π]-Cycloaddition resultierenden Pentacyclen 7a - e. Eine [2π + 2σ]-Reaktion unter Beteiligung des Cyclopropanringes (zu 8a - e) ist daneben nicht nachweisbar. Gleichermaßen einheitlich (isolierte Ausbeute 〉 90%) verläuft die [2π + 2π]-Cyclisierung im 3-Oxa-Diester 10 (zu 11). Die Tris-σ-homobenzole 7a - e bzw. 11 werden thermisch ausschließlich unter 2σ → 2π-Spaltung zu den Ausgangsdienen der Photoreaktionen 6a - e bzw. 10 isomerisiert (Ea (7a) = 22 kal/mol; A = 2.2·1012s-1). Am Beispiel des Diesters 7a bzw. der Dicarbonsäure 7g wurde die Addition von HCl und CH3OH bzw. Wasser studiert, wobei selektiv die Addukte 13 und 14 (Verhältnis 9:1) in durchweg guten Ausbeuten gewonnen werden. Bei sterischer Behinderung des üblichen Angriffs auf die unsubstituierte Kante des Bishomocyclobutadien-Partialgerüsts in 7a setzt sich TCÄ zu den 1:1-Addukten 15 und 16 um.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 107 (1974), S. 1957-1970 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: [2π+2π]-Photocycloaddition Reactions in Bicyclo[2.2.2]octadiene DerivativesAs exemplified by the dieser 14a a [2π + 2π]-photocycloaddition in the bicyclo[2.2.2]octadiene skeleton is possible by direct - not, however, by sensitized - excitation. Besides a small fragmentation to dimethylphthalate (and ethylene) no other phototransformation of 14a takes place. With a half-life of ca. 12 min at 19°C the photoproduct 15a is thermally isomerized back to the diene diester 14a. Via a regiospecific addition of HCl, methanol and water to the tetracycles 15a and 15b (H2O) the epimeric products 18, 19 are isolated in a ratio of ca. 9:1. Their structure is elucidated by oxidation of 18c to 21 and 1H-n.m.r. spectroscopic comparison with the isomeric compounds 20 and 22, resp., synthesized by a different route. Towards bishomodienophilic reagents like tetracyanoethylene and dimethyl acetylenedicarboxylate 15a shows the expected reactivity. The addition proceeds at the nonsubstituted edge of the bishomocyclobutadiene unit yielding 24, and 26.
    Notes: Am Beispiel des Diesters 14a wird gezeigt, daß auch im Bicyclo[2.2.2]octadien-Gerüst durch direkte Lichtanregung -nicht jedoch sensibilisiert - eine [2π + 2π]-Cycloaddition möglich ist. Außer einer geringfügigen Fragmentierung zu Phthalsäure-dimethylester (und Äthylen) findet keine konkurrierende Photoumwandlung von 14a statt. Mit einer Halbwertszeit von ca. 12 min bei 19°C isomerisiert sich das Photoprodukt 15a zurück zum Dien-diester 14a. Bei der regiospezifischen Addition von HCl, Methanol und Wasser an die Tetracyclen 15a, 15b (H2O) werden die Epimeren 18, 19 im Verhältnis von ca. 9:1 isoliert. Deren Struktur ist durch Oxidation von 18c zu 21 sowie 1H-NMR-spektrometrischen Vergleich mit den auf anderem Weg synthetisierten Isomeren 20 und 22 gesichert. Auch gegenüber bishomodienophilen Partnern wie Tetracyanäthylen oder Acetylendicarbonsäure-dimethylester besitzt 15a die erwartete Reaktivitat. Die Addition erfolgt stereospezifisch an die nichtsubstituierte Kante des Bishomocyclobutadienteils zu 24 und 26.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 71 (1988), S. 992-999 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The vibrational spectra of some 1,2,4-trioxanes present two characteristic bands at 790 and 880 cm-1. On the basis of 18O-isotopic substitution and comparison with analogous compounds, these bands have been assigned to coupled C—O and O—O stretching modes of the C—O—O element.
    Additional Material: 5 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 77 (1994), S. 1851-1860 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 3,6-substituted 1,2,4-trioxan-5-ones 11-14, on heating to 170-200°, underwent unimolecular thermolysis to generate electronically excited singlet ketones with an efficiency of ca. 0.2%. The chemiluminescence quantum yields (φoSCL) depended on the nature of the 6-substitutents and increased linearly with temperature. The Arrhenius activation energies were obtained by measuring the rate of decay of luminescence and determined as 22.9, 30.4, 35.6, and 34.2 kcal/mol for 11-14, respectively. Step analysis of the chemiluminescence of 14 afforded an average activation energy of 44.3 kcal/mol. This latter result is explicable in terms of two decomposition paths, higher and lower in energy, leading to excited and ‘dark’ products, respectively. The thermolysis of trioxanones 12-14 lacking a H-atom at the 6-position is interpreted as involving successive rupture of the peroxide bond, excision of ketone at the 3-substituted end, and loss of CO2, to finally produce ketone originating from the 6-position (see Scheme 4).
    Additional Material: 4 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 10 (1983), S. 559-566 
    ISSN: 0306-042X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The positive ion and negative ion pyrolysis mass spectra of the herring sperm DNA have been studied using desorption chemical ionization. The positive ion desorption chemical ionization spectra have been produced with CH4, i-C4H10, NH3, HCl and Cl2; the negative ones with N2O/CH4, N2O/i-C4H10, Cl2, CCl4, HCI and via electron capture. These spectra have been compared with the electron impact ionization spectra. We have observed an important increase of sensitivity when negative ionization has replaced the positive ionization mode. The series of diagnostic ions resulting from direct chemical ionization belong to the family of base + reagent ion X [BH + X] and base + X-HX ion [B]. Their abundance has increased considerably compared to the electron impact spectra. The application of these new diagnostic ions in nucleic acid studies is interesting especially for the much higher abundance of the usually weak dG fragment ion obtained in the negative ionization mode. The dG-base segment of the DNA is the most nucleophilic centre of the whole nucleic acid and is implicated in numerous important biochemical reactions involving, for example, proteins.
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