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  • Articles  (30)
  • Articles: DFG German National Licenses  (30)
  • Life and Medical Sciences  (20)
  • Plasmodesmata  (5)
  • ethylene  (5)
  • EARTH RESOURCES AND REMOTE SENSING
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  • Articles  (30)
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  • Articles: DFG German National Licenses  (30)
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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 174 (1993), S. 36-44 
    ISSN: 1615-6102
    Keywords: Cell-to-cell communication ; Plasmodesmata ; Setcreasea purpurea ; Transport ; Intercellular
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Diffusion coefficients for FITC-molecular probes in intercellular pores (D) and rate of molecular probe loss into the vacuole (k1) have been obtained for FITC molecular probes in staminal hairs ofSetcreasea purpurea. The kinetic curves of FITC-Gly, -Ala, -Leu,-Ser, -Thr, -Cys, -Met, -Tyr, -Asp, -Glu, -Asn, -Gln, -Lys, -His,-Arg, -(Asp)2, -(Glu)2, -(Lys)2, -(Asp)3, -(Glu)3, -(Gln)2, -(Gln)3, -(Gln)4, and carboxyfluorescein (group I probes) matched the curves calculated for simple diffusion through a chain of cells, while the majority of kinetic curves of FITC-Phe, and -Try (group II probes) did not. None of the kinetic curves for FITC-(Met)2 and -(His)2 (group III probes) matched. Average Ds for group I probes ranged from 0.77× 10−8cm2/s to 3.75× 10−8cm2/s and for group II probes were 0.50× 10−8cm2/s. A meaningful average D for group III probes could not be calculated. Average k1 for group I probes ranged from 1.62× 10−7/μm2/s to 13.21× 10−7/μm2/s, and for group II probes were 5.42 and 11.54× 10−7/μm2/s. Average k1s for group III probes could not be calculated. Symplastic transport occurred by cell-to-cell diffusion for most of the probes (e.g., group I probes) but not always for some (e.g., group II probes) and never for others (group III probes). The rate of cell-to-cell diffusion and loss within the vacuole depended upon the molecule's specific structure, molecular weight and charge. We concluded that plasmodesmata select for molecules that are hydrophilic, small and have a charge of from — 2 to — 4, and against molecules that contain either Phe, Try, Met or His groups.
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Phytochemistry 29 (1990), S. 2407-2409 
    ISSN: 0031-9422
    Keywords: Pyrus communis ; Rosaceae ; ethylene ; mRNA. ; pear fruit ; ripening ; storage
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-5028
    Keywords: ethylene ; ethylene receptor ; signal transduction ; ETR1 ; tomato ; gene expression
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Dominant mutations in the Arabidopsis ETR1 gene block the ethylene signal transduction pathway. The ETR1 gene has been cloned and sequenced. Using the ETR1 cDNA as a probe, we identified a cDNA homologue (eTAE1) from tomato. eTAE1 contains an open reading frame encoding a polypeptide of 754 amino acid residues. The nucleic acid sequence for the coding sequence in eTAE1 is 74% identical to that for ETR1, and the deduced amino acid sequence is 81% identical and 90% similar. Genomic Southern blot analysis indicates that three or more ETR1 homologues exist in tomato. RNA blots show that eTAE1 mRNA is constitutively expressed in all the tissues examined, and its accumulation in leaf abscission zones was unaffected by ethylene, silver ions (an inhibitor of ethylene action) or auxin.
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  • 4
    ISSN: 1573-5028
    Keywords: abscission ; cellulase ; ethylene ; Phaseolus vulgaris ; promoter ; transgenic
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Bean leaf abscission (organ separation) correlates with thede novo accumulation of a pI 9.5 cellulase and its mRNA. Overlapping genomic clones encoding the bean abscission cellulase (BAC) were isolated and partially sequenced. In addition, a genomic clone for a soybean abscission cellulase (SAC) was identified and the sequence compared to the BAC genomic sequence. Two 5′-upstream regions are particularly well conserved in the two sequences. Of special interest here is the region between −1 and −200 in the BAC promoter which is highly conserved in the SAC gene. Particle gun bombardment with a BAC promoter construct containing 210 bp of BAC sequence 5′ to the transcription start site was sufficient to drive abscission-specific and ethylene and auxin-regulated transient expression in bean. In addition to the transient expression assay, expression was examined in stably transformed tomato. A similar −210 bp BAC promoter construct supported a low level of ethylene-inducible reporter gene expression in tomato leaf abscission zones and adjacent petioles but not in ethylene-treated stem tissue or fruit. Expression from the −210 promoter in tomato abscission zones was inhibited by silver thiosulfate, an ethylene action inhibitor, and was partially inhibited by treatment with auxin.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Plant molecular biology 28 (1995), S. 647-656 
    ISSN: 1573-5028
    Keywords: abscission ; gene expression ; polygalacturonase ; ethylene ; auxin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Abscission, organ separation, is accompanied by cell wall breakdown in separation layer cells. In tomato (Lycopersicon esculentum), ethylene-induced abscission is correlated with an increase in polygalacturonase (PG) and endo-β-1,4-D-glucanase (cellulase) activity. We have identified a putative, abscission-specific cDNA clone for PG, pTAPG1. The TAPG1 cDNA has 43% identity at the amino acid level with the tomato fruit PG. Genomic blot analysis suggests that the gene for TAPG1 is a member of a small subfamily of PG genes that is distinct from the tomato fruit PG. The TAPG1 cDNA hybridizes to mRNA expressed during the course of ethylene-induced leaf and flower abscission. A high level of PG transcript accumulation coincides with the occurrence of abscission. Auxin, an abscission inhibitor, and silver thiosulfate, an ethylene action inhibitor, suppressed accumulation of mRNA in leaf abscission zones complementary to the TAPG1 cDNA. Expression of TAPG1 transcripts is several-fold higher in flower abscission zones than in leaf abscission zones. The identification of cDNAs that encode abscission-specific PG provide and additional tool to study the regulation of abscission and cell wall dissolution in separation layer cells.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 113 (1982), S. 193-201 
    ISSN: 1615-6102
    Keywords: Intercellular communication ; Plasmodesmata ; Symplastic transport ; Setcreasea purpurea
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Investigations into plant intercellular communication were initiated through an examination of plasmodesmata and cell-to-cell passage of molecular probes in the staminal hairs ofSetcreasea purpurea. Plasmodesmata connecting staminal hair cells of small buds are filled with an electron-opaque homogenous material. To examine the permeation selectivity of plasmodesmata, molecular probes made up of fluorescein isothiocyanate (FITC) complexed with amino acids and peptides were injected into the staminal hair cells and the spread of these fluorescent molecules through the symplast, was monitored. Molecules composed of FITC complexed to single amino acids with polar and aliphatic R groups travel rapidly, while those which include peptides travel slowly. Dye molecules composed of an amino acid with an aromatic side group do not pass from cell to cell at all. It is hypothesized that the material occluding the plasmodesmata constitutes the diffusion barrier, by presenting a hydrophilic environment which allows passage of molecules with maximum molecular weights of 700–800 daltons, but which retains those with aromatic side groups.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 128 (1985), S. 167-172 
    ISSN: 1615-6102
    Keywords: Intercellular transport ; Plasmodesmata ; Setcreasea purpurea ; Symplastic transport
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Previously reported studies of cell ultrastructure and molecular probe passage in immature staminal hairs were extended to kinetic studies. The rate of transport of carboxyfluorescein into the cytoplasm in individual cells was monitored with a video analyzer and transport coefficients were determined. Carboxyfluorescein was found to traverse 5 cells in less than 5 minutes. The values of transport coefficients differed between cells and this was taken to mean that some cells are more closely coupled than others.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 174 (1993), S. 45-49 
    ISSN: 1615-6102
    Keywords: Cell-to-cell communication ; Plasmodesmata ; Setcreasea purpurea ; Azide
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The effect of azide on the diffusion of fluorescent molecular probes was examined in staminal hairs ofSetcreasea purpurea. Staminal hairs were treated with azide before being microinjected with fluorescent molecular probes of different size, charge, and structure. The cell-to-cell movement of these fluorescent molecules was videotaped, analyzed, and coefficients of diffusion through plasmodesmata (D) and coefficients of diffusion across the tonoplast (k1) were calculated and compared to those of untreated cells. The D was larger and the k1 was smaller for many fluorescent probes in azide treated cells compared to normal, untreated cells. In addition, the cell-to-cell diffusion selectivity based on molecule structure, size and charge no longer existed in azide treated cells. An average D of 3.3×10−8cm2/s and an average k1 of 2.9×10−7/μm2/s was calculated for the molecular probes tested. New size limits for permeation were observed indicating that the plasmodesmata had become enlarged.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Protoplasma 137 (1987), S. 140-144 
    ISSN: 1615-6102
    Keywords: Intercellular transport ; Cell-to-cell communication ; Plasmodesmata ; Cytoplasmic streaming ; Setcreasea purpurea
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The effect of inhibition of cytoplasmic streaming on intercellular passage of carboxyfluorescein (CF) in staminal hairs ofS. purpurea was examined. Tip cells of staminal hairs were microinjected with buffered-CF. Cytoplasmic streaming was then inhibited by addition of KCN or NaN3 to the external bathing solution. In separate experiments, cytoplasmic streaming was inhibited by microinjection of cytochalasin D along with the buffered-CF. CF passage over a 5 minutes treatment period was monitored by video fluorescence microscopy and video intensity analysis. Cytoplasmic streaming ceased within 1 minute of inhibitor agent treatment, however, little change in the kinetics of intercellular passage was noted over the 5 minute experimental period. Th us, cytoplasmic streaming plays no major role in the regulation of intercellular passage of the hydrophilic, negatively charged molecule CF.
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  • 10
    ISSN: 1573-5028
    Keywords: cellulase ; endo-(1–4)-beta-D-glucanase ; cDNA sequence ; avocado ; ethylene ; fruit ripening
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A cDNA library was prepared from ripe avocado fruit (Persea americana Mill. cv. Hass) and screened for clones hybridizing to a 600 bp cDNA clone (pAV5) coding for avocado fruit cellulase. This screening led to the isolation of a clone (pAV363) containing a 2021 nucleotide transcribed sequence and an approximately 150 nucleotide poly(A) tail. Hybridization of pAV363 to a northern blot shows that the length of the homologous message is approximately 2.2 kb. The nucleotide sequence of this putative full-length mRNA clone contains an open reading frame of 1482 nucleotides which codes for a polypeptide of 54.1 kD. The deduced amino acid composition compares favorably with the amino acid composition of native avocado cellulase determined by amino acid analysis. Southern blot analysis of Hind III and Eco RI endonuclease digested genomic DNA indicates a small family of cellulase genes.
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