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  • 11
    ISSN: 1432-2048
    Keywords: Auxin (flower bud, dose) ; Cell culture (flower bud formation) ; Flower bud formation ; Nicotiana (flower bud formation)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Short-term applications of very high concentrations of 1-naphthaleneacetic acid (NAA) to expiants from flower stalks of tobacco (Nicotiana tabacum L. cv. Samsun) induced flower-bud regeneration to the same extent as longer or continuous incubation on lower concentrations. The maximum number of flower buds per explant after 15 d of culture was obtained not only by continuous culturing at 1 μmol·l−1 NAA but also by 12 h of culturing at 22 μmol·l−1 or 0.5 h at 220 μmol· l−1, followed by incubation on medium without auxin for the remaining period. Continuous application of such high concentrations resulted in callus formation or caused the death of the explanted tissue. In all experiments in which auxin concentration and time of application were independently varied, the product of concentration and time determined the number of buds formed. Most, but not all, of the NAA taken up by the tissues was converted into conjugates. In expiants which had received a dose which was optimal for regeneration, the internal concentration of free NAA remaining beyond the pulse period was between 1.7 and 6.2 μmol·l−1. Suboptimal applications led to lower values, supraoptimal treatments to much higher internal concentrations. The physiological effect, which depends on the internal hormone concentration, thus manifested itself as dose-dependent with regard to applied hormone.
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  • 12
    Electronic Resource
    Electronic Resource
    Springer
    Plant cell reports 15 (1995), S. 133-137 
    ISSN: 1432-203X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Thiophenes are polyacetylene-related heterocyclic metabolites. Some of these compounds are phototoxic, but the bithiophenes occurring inTagetes mainly accumulate in the root where photo-activation is not likely to occur. A cell-free extract from the fungusFusarium oxysporum induced biosynthesis of hydrophilic thiophenes in root cultures and roots of seedlings ofTagetes patula. The thiophenes formed were partially excreted into the culture medium. The excreted thiophenes inhibited fungal growth in the absence of light and thus may play a role in the biochemical defense against pathogens.
    Type of Medium: Electronic Resource
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  • 13
    ISSN: 1432-2048
    Keywords: Pollen (development) ; Lilium (pollen development) ; mRNA expression (pollen development) ; Microgametophyte ; Microspore ; Nicotiana (pollen development)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Homogeneous populations of developing microspores and pollen from anthers of lily (Lilium longiflorum Thumb.) and tobacco (Nicotiana tabacum L.) show a continuous production of biomass, reaching a maximum in young pollen. The rate of RNA synthesis was 460 fg · h−1 in young binucleate cells, 138 fg · h−1 in late binucleate cells and 56 fg · h−1 in microspores. The mRNA population in developing pollen can be separated into three groups. In the first group, certain types of mRNAs are present at a constant level during all stages of development. A second group is characteristic of young pollen and increases quantitatively until anthesis. A third group is seen transiently; to this belong mRNAs present only before mitosis or at a distinct cell stage after mitosis. Some of the translation products of this latter group of mRNAs showed similarities between lily and tobacco on two-dimensional gels in respect of molecular weight and isolectric point, indicating that those mRNAs and proteins play a role in the regulation of pollen development.
    Type of Medium: Electronic Resource
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  • 14
    ISSN: 1432-2145
    Keywords: In situ hybridization ; Pollen-specific gene expression ; mRNA ; Confocal laser scanning microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The application of confocal laser scanning microscopy together with in situ hybridization experiments in tobacco pollen enabled a detailed localization of a pollen-specific mRNA. The three-dimensional distribution of this specific mRNA over the whole pollen grain was reconstructed by means of optical sections of one specimen.
    Type of Medium: Electronic Resource
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  • 15
    ISSN: 1432-2145
    Keywords: Microsporogenesis ; In-vitro pollen maturation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Immature pollen grains of Nicotiana tabacum L., cv ‘Petit Havana’ were isolated at the mid-binucleate stage and cultured in vitro. During the first 66 h of in-vitro culture the pollen developed the same ability to set seed and germinate as pollen matured in vivo. No fertile pollen was produced when protein synthesis was inhibited temporarily at an early stage of development. In the case of inhibition at day 2 of development a delay in the total time necessary for maturation was observed that was equal to the length of time the inhibitor was applied. Hybridization experiments with a pollen-specific cDNA probe showed that the pattern of gene expression in vitro was similar to that in vivo. However, the model system differs from natural pollen development with respect to the dehydration period, which is absent in the model system, and the synthesis of proteins. Protein synthesis of in-vitro cultured pollen differed significantly from that of pollen developing in vivo, even though pollen maturation in vitro proceeded in the same time as in vivo, and led to fully matured fertile pollen. Pollen development in vitro is thus an ideal model system for studying gene expression in relation to fertility and for experimental manipulation of microsporogenesis.
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  • 16
    ISSN: 1432-2145
    Keywords: Key words Brassica oleracea ; Drought-induced gene expression ; Programmed anther dehydration
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract  Anther physiology is characterized by developmentally controlled dehydration. Screening of an anther cDNA expression library with an antiserum raised against proteins isolated from the surface of Brassica oleracea pollen grains resulted in the isolation of bopc15 and bopc34, sequences similar to water stress-inducible genes. Bopc15 transcripts were exclusively present in pollen. The mRNA of bopc34 was found in various tissues, but not in pollen. The accumulation of both transcripts preceded anther dehydration. Premature anther dehydration induced by imposed drought stress affects gene expression in both the sporophytic and gametophytic portions of the anthers the levels of bopc15 and bopc34 transcripts increased to an extent dependent on developmental stage and duration of treatment. The inducible bopc15 transcript accumulation was reversible by rehydration. Bopc34 transcript levels, on the other hand, do not follow this pattern.
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  • 17
    ISSN: 1573-5028
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Large amounts of pathogenesis-related (PR) proteins were found inNicotiana tabacum crown gall tissue, following transformation of normal tobacco cells withAgrobacterium tumefaciens. In contrast, PR proteins were not detected in leaves of grafted plants that had been recovered from crown gall tissue even though these plants were still transformed as shown by their inability to form roots and ability to produce octopine. No difference was observed in susceptibility to virus infection between untransformed and transformed plants grafted onto identical rootstocks. The results are discussed in relation to physiological factors controlling PR protein induction and virus resistance.
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  • 18
    ISSN: 1573-5028
    Keywords: anther ; in situ hybridization ; microspore development ; microspore-specific gene ; Nicotiana tabacum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The characterization of a gene with a unique microspore-specific expression pattern is reported. Isolated microspores from tobacco were used to synthesize a cDNA library. Clones that did not hybridize to leaf cDNA were further characterized by northern analysis. One clone proved to be a microspore-specific cDNA, representing a transcript of 650 nt. The corresponding gene, NTM19 (Nicotiana tabacum microspore-specific), was isolated and its sequence analysed. The gene encodes a protein of 10.8 kDa with a pI of 6.92 and a putative signal sequence at the N-terminus. A localization study revealed a unique spatial and temporal distribution. The transcript was only detected in the unicellular microspore. No hybridization signals were observed in other pollen developmental stages, nor in the surrounding anther tissues or other vegetative tissues of the plant. Therefore it can be concluded that NTM19 is a gene with a highly microspore-specific character according to both localization and stage of expression. Southern blot analysis demonstrated the presence of a small gene family. The occurrence of TNM19 was investigated in a range of closely and distantly related species and was found to be present in other solanaceous species, including the ancestors of tobacco and in a monocot species.
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  • 19
    ISSN: 1432-2048
    Keywords: Agrobacterium ; Crown-gall ; DNA, transferred ; Nicotiana (T-DNA) ; T-DNA structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Data are provided which show that transferred DNA (T-DNA) present in Nicotiana plumbaginifolia crown-gall lines in most cases was scrambled and not intact. Both wild-type, and ‘rooter’- and ‘shooter’-type mutants of octopine-type Agrobacterium tumefaciens were used to infect N. plumbaginifolia plantlets, cultured in vitro. Resulting tumors were excised from the plantlets and cultured for more than three years. During subculturing the tumor lines were scored for the following phenotypic traits: phytohormone autonomous growth in vitro (Aut+), spontaneous shoot regeneration (Reg+), root deficiency of shoots (Rod+), octopine production (Ocs+) and mannopine and agropine production (Mas+Ags+). An unexpectedly large variety of phenotypes was observed. For instance, two out of three tumor lines induced on haploid plantlets by the rooter mutant LBA4210 regenerated shoots, a phenomenon which is not observed for octopine tobacco tumor lines. Fifty percent of the crown-gall lines studied did not contain octopine. Only one line out of six independent lines analyzed was found to have a ‘regular’ T-DNA structure. Occurrence of aberrant T-DNA structures was not correlated with the ploidy level of infected plantlets, nor with the T-region structure of the inciting bacterial strain. The pattern of TL-DNA transcripts was studied for one line and correlated well with the aberrant T-DNA structure detected. Segments of TR-DNA, having irregular structures as well, were detected in two out of the six lines studied. The scrambled nature of the TR-DNA explained the absence of mannopine and agropine in these two lines. In addition, it was observed that N. plumbaginifolia tissue lines which did not carry T-DNA, became readily phytohormone autotrophic (habituated) at an early stage in tissue culture.
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  • 20
    ISSN: 1432-2048
    Keywords: Agrobacterium ; Crown gall ; Nicotiana (crown gall, T-DNA) ; Transformation (tobacco) ; Transferred DNA
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Grafts from the SR1 tobacco crown-gall lines NT1 (having a deletion eliminating part of the transferred (TL)-DNA auxin locus) and NT2 (having an IS60 insertion in gene 2 of this auxin locus) were cross-pollinated with pollen from nontransformed SR1 tobacco plants. One half of the resulting F1 progeny resembled the female parent (“transformed” NT1-like and NT2-like seedlings respectively) and one half resembled the male parent (“non-transformed” SR1-like seedlings). For three states of differentiation (callus, shoot, graft) all phenotypic markers of the transformed seedlings studied were identical to those of the transformed female parent. Most phenotypic markers of non-transformed seedlings corresponded with markers of the male parent. Unlike the SR1 male parent, however, the SR1-like seedlings showed the maternal traits hyperstyly and male sterility. These two traits were inherited by 100% of the F1 seedlings studied. Ninety percent of the non-transformed F2 seedlings were still male-sterile whereas in as much as 50–100% of the non-transformed F3 progeny, male fertility had been restored. The SR1-like F1 seedlings did not contain any T-DNA. At the level of restriction-fragment analysis the T-DNA structures of all 22 NT1-like seedlings examined were identical to the T-DNA structure of their female parent NT1. The steady-state level of transcripts 4 (cytokinin locus) and 6a/6b relative to transcript 3 (octopine-synthase locus) was less in shoots and grafts than in callus. Observed variation in shoot morphology among the twenty-two NT1-like seedlings was not correlated with T-DNA structure, organization and expression at the level of steady-state mRNA. The T-DNA structure of NT2 and its transformed seedlings deviated from regular border-to-border TL-DNA, in that it extended beyond the left border repeat.
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