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    ISSN: 0931-1890
    Keywords: Key words Agrobacterium rhizogenes ; Populus tremula ; rol Genes ; Root formation ; Transgenic plants
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract  The potential use of the rol genes from Agrobacterium rhizogenes to improve the root system horticultural characteristics was evaluated in transgenic aspen (Populus tremula) plants, harboring the rol genes under their native promoters. Southern blot and RT-PCR analyses confirmed the presence and expression of A. rhizogenes rolC and rolB genes in four different phenotypically selected transgenic clones. Several of the observed phenotypic modifications were related to rol-gene expression and included, in particular, modified root systems. All in vitro-cultured rol-transgenic plants exhibited extensive root formation in a hormone-free medium, as well as a larger root surface area and mass, as compared to a uidA (β-glucuronidase-encoding)-transgenic aspen line and control (non-transformed) plants. Adventitious root formation in stem segments of rol-transgenic plants exhibited very rapid kinetics, resulting in a much shorter rooting time for rol-transgenic stem segments (e.g. 10 days for 80% rooting in rol-transgenic lines T-26 and T-27, as compared to more than 18 days for control non-transformed or uidA-transgenic aspen plants). rol-Transgenic plants maintained the capacity for 100% rooting throughout the year, versus 70–80% rooting in non-transformed plants during the winter. The four rol-transgenic lines exhibited differences in root development; in two of them enhanced root development was accompanied by increased shoot fresh weight. The root:shoot fresh weight ratio was always higher in rol-transgenic lines than in non-transformed plants. In the T-27 rol-transgenic line, the propagation coefficient of shoot-bud regeneration in liquid root culture was almost three times higher than in non-transformed plants. To the best of our knowledge this is the first report on quantitative phenotypic alterations in rol-transgenic woody plants.
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  • 4
    ISSN: 0931-1890
    Keywords: Key words Transgenic poplar ; Agrobacterium rhizogenes ; Populus tremula ; rol genes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract  Stem and trunk growth, axillary bud break and branching habits are extremely important parameters of wood production in forest trees. The possibility of altering tree form by transformation with genes responsible for hormone biosynthesis and/or activity is most attractive. We examined four different phenotypically selected transgenic clones of a model tree –Populus tremula– expressing rol genes from Agrobacterium rhizogenes under their native promoters. Several of the observed phenotypic modifications were correlated with rol-gene expression, including breaking of stem apical dominance which resulted in the development and branching of up to four axillary buds per explant, as compared to a lack of axillary bud break in a uidA (β-glucuronidase-encoding)-transgenic aspen line and control (non-transformed) plants. rol-Transgenic plants also exhibited a higher cumulative stem length and enhanced growth rate, and hence a higher stem production index. During their first and second years in the greenhouse, rol-transgenic aspen plants exhibited enhanced growth and delayed winter dormancy relative to non-transformed plants. Although initially rol-transgenic plants had smaller, wrinkled leaves, these changes were not observed in the 2-year-old plants, which exhibited a phenotypically true-to-type leaf shape.
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  • 5
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 53 (1997), S. 151-159 
    ISSN: 1399-0047
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The structure of membrane-active antibiotic cyclodecapeptide gramicidin S in the crystals of its complex with urea, C60H92N12010.0.5[(NH2)2CO].7.94H20, has been investigated with three-dimensional X-ray data by the automatic sequential approximation method. The crystals are trigonal, space group P3121, a = 25.80(3), c= 21.49 (2) Å, Mr = 7968, calculated density = 1.088 mg m−3, Z = 1. Conventional R factor: R1 = 0.0943, wR2 = 0.2478 [I〉 2σ(I)]. The molecule possesses an antiparallel twisted β-structure, with turns involving the Phe-Pro peptides. The Orn side chains extend on one side of the sheet, while the non-polar Val and Leu side chains are located on the other face. One of the Orn residues (namely Orn2) is linked by an intermolecular hydrogen bond to the O atom of Phe4 residue, the other is free. The side chains of the Phe residues have trans orientation (χ1 ∼ 180°) and those of the Val, Orn, Leu residues, except those of Orn2, have the preferential gauche orientation with the χ1 angle close to 60. Two side chains show statistical disorder and conformation of the Pro residues is Cs—Cβ-exo. There is half a urea molecule and also 7.94 water molecules distributed on 13 positions for each antibiotic molecule. A partially occupied and poorly ordered alcohol molecule had been identified. The gramicidin S molecules are arranged around the 31 axis in the form of a left-handed double spiral forming suggestive channels. The outer hydrophobic surface of the spiral is made of uncharged side radicals while the inside surface consists of the main-chain atoms, mainly O and N, and of ornithine side chains with N atoms at the ends. By changing the Orn side-chain conformation, the inner diameter of the channels may change from 3.4 to 6.3 Å. Thus, ions and particles of rather large size may pass through the channel. The possibility of the creation of the gramicidin S channels in mitochondrial membranes has been noted by some biochemists. The channel complexes are close-packed in a hexagonal arrangement in the crystal. The CI− ions, present in abundance in the mother solution, are not found ordered in the crystals, which may indicate the absence of the charges in the terminal N atoms of the Orn residues.
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  • 6
    Electronic Resource
    Electronic Resource
    [S.l.] : International Union of Crystallography (IUCr)
    Acta crystallographica 44 (1988), S. 821-827 
    ISSN: 1600-5724
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The potential of high-resolution electron microscopy (HREM) is demonstrated by the investigation of complex oxides with a general formula [UnMmO]- [MpO3p + l], M = (Mo, W). The HREM structure images of β-UMo2O8 agree well with the model derived from X-ray data. It is found that the γ- U3Mo20O64 sample considered earlier as a monophase appears in fact as a set of isostructural phases. The structure of these phases with MoO3 octahedral block width varying within p = 1-7 is derived from electron microscope images. Both regular and irregular substitution of cations and the formation of uranium vacancies in M-O rows are detected in γ-U3Mo20O64. Interstitial sites in the structures are detected, which can be occupied by extra U and W cations. The electron microscope images of vacancy rows give evidence for the finite length of some M-O rows. In this case oxygen dangling bonds at the ends of rows are supposed to be saturated by interstitial tungsten atoms.
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  • 7
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochimica et Biophysica Acta (BBA)/Biomembranes 773 (1984), S. 181-188 
    ISSN: 0005-2736
    Keywords: (Sendai virus) ; Membrane fusion ; Membrane reconstitution ; Virus envelope
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Medicine , Physics
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  • 8
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: To study the biogenesis of the photosynthetic apparatus in corollas, as well as compositional differences between corolla and leaf chloroplasts, the levels of 12 nuclear- and plastid-encoded thylakoid and stromal components were analyzed by western blotting using heterologous antisera. Relative levels of the thylakoid polypeptides analyzed in petunia (Petunia hybrida cv. Hit Parade Rosa) and carnation (Dianthus caryophyllus cv. White Sim) corollas increased, per unit chlorophyll, in parallel to corolla development, peaking at the mature stage in both flower types, with the exception of subunit V of the photosystem I (PSI) core complex, which continued to accumulate even after anthesis. The photosystem II (PSII) major light-harvesting chlorophyll a/b protein accumulated in corollas to a level, per unit chlorophyll, similar to that in leaves in both petunia and carnation plants. Components of the cytochrome b6/f complex were found to accumulate to higher levels in corolla chloroplasts than in leaves. The opposite trend was found for components of the PSI core complex, as well as for the stromally located small and large subunits of ribulose-1,5-bisphosphate carboxylase, which accumulated in corollas to levels ca 2. 5 times lower than their respective levels in leaves. The latter subunits accumulated coordinately in corollas of both plant types during flower development. Data obtained from immunological studies were correlated with those at the mRNA level. Nothern blotting revealed that, in petunia corollas, the steady-state transcript level of genes coding for the small subunit of ribulose-l,5-bisphosphate carboxylase was identical to that of genes coding for the major light-harvesting chlorophyll a/b protein. Levels of both transcripts, as well as those of plastid-encoded genes for the PSII reaction center's Dl and D2, were ca two-thirds of their respective levels in leaves. In contrast, the level of transcript for the large subunit of ribulose-1,5-bisphosphate carboxylase was reduced 5-fold in petunia corollas, as compared to leaves.
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  • 9
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Protoplasts prepared from cultured albinoid cells of petunia do not express photosynthetic genes, such as those coding for chlorophyll a/b-binding (Cab) proteins or ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco). They therefore provide a convenient system for expressing recombinant photosynthetic genes, without background interference. Transfection of petunia protoplasts with vectors bearing the Lhcbl*1 Cab gene under the control of the 35S promoter of cauliflower mosaic virus (CaMV) resulted in the appearance of significant amounts of the specific transcripts, but not of the corresponding polypeptides, as inferred from northern and western blot analysis, respectively. The use of an expression vector carrying the translational enhancer Ω of tobacco mosaic virus (TMV) strongly enhanced the appearance of transfected gene products: western blot analysis of transfected protoplasts clearly revealed the appearance of Lemna gibba Lhcbl*1 and Lhcb2*1, tomato Lhcb2*1 and psaD, and pea rbcS gene products. Molecular weight estimations of the newly synthesized polypeptides indicated that each was promptly processed into its mature-cleaved form within the transfected albinoid protoplasts. This occurred despite a lack of chlorophyll and the absence of a thylakoid network.
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  • 10
    ISSN: 1574-6968
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Two different methods, (i) PEG and (ii) biolistic, were employed to transform protoplasts and conidia of Paecilomyces fumosoroseus using hygromycin resistance as selectable marker. Transformation frequencies varied from 1.9 to 2.5 transformants μg−1 of DNA by the PEG method, and from 33 to 153 transformants μg−1 of DNA by the biolistic procedure.
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