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  • Lycopersicon esculentum  (4)
  • barley  (4)
  • crystal structure  (4)
  • Springer  (12)
  • American Chemical Society
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  • Springer  (12)
  • American Chemical Society
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  • 1
    Electronic Resource
    Electronic Resource
    Synthesis, characterization, and crystal structure of 1,3,7,9-tetramethylpyrido-[2,3-d∶6,5-d′]-dipyrimidine-2,4,6,8-tetrone (1994)
    Springer
    Journal of chemical crystallography 24 (1994), S. 465-468 
    Details
    ISSN: 1572-8854
    Keywords: Pyrimidine ; uracil ; crystal structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract A new and easy method for the preparation of 1,3,7,9-tetramethylpyrido-[2,3-d∶6,5-d′]-dipyrimidine-2,4,6,8-tetrone is described. The structure of this compound has been solved by means of X-ray diffraction methods. The chemical characterization by spectral (mass, ultraviolet, infrared, and proton nuclear magnetic resonance) and thermal (thermogravimetry and differential scanning calorimetry) method is also reported. The compound is monoclinic, space groupP21/c,a=12.720(5),b=13.688(7),c=8.079(2) Å, β=107.06(4)°,Z=4. The structure consists of discrete tricyclic molecules, stacking playing an important role in crystal packing.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01666096
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  • 2
    Electronic Resource
    Electronic Resource
    The crystal and molecular structure of mercury(II) bis(isopropyl)dithiophosphate, Hg[S2P(OPri)2]2, revisited: new comments about its supramolecular self-organization (1999)
    Springer
    Journal of chemical crystallography 29 (1999), S. 831-836 
    Details
    ISSN: 1572-8854
    Keywords: Hg coordination ; crystal structure ; organomercury derivatives
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The crystal structure of the title compound, Hg[S2P(OPri)2]2, has been determined by single-crystal X-ray diffraction. The compound crystallizes in the centrosymmetric P21/c space group with a = 11.800(1), b = 8.925(2), c = 22.167(2) Å, β = 94.988(7)°, and Z = 4. The same compound has been previously reported but the structure is described there in the space group C2/c. In both cases, one phosphorodithioate moiety acts as a chelating group and the other as a bridging group between neighboring mercury atoms (related to one another by the twofold screw axis), giving rise to an infinite polymer along the direction of the b axis. It turns out that in spite of the difference in space group symmetry, the structures are remarkable similar in that they are formed from infinite polymers of similar geometry. The coordination around the Hg ion shows, however, significant differences, mainly for the bridging Hg—S(4) bond length, which is 0.16 Å smaller than that previously reported.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1023/A:1009508122842
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  • 3
    Electronic Resource
    Electronic Resource
    The crystal and molecular structure of 2-S-methylthiouracil (1999)
    Springer
    Journal of chemical crystallography 29 (1999), S. 725-727 
    Details
    ISSN: 1572-8854
    Keywords: 2-thiouracil derivatives ; crystal structure ; S-methyl-thiouracil ; hydrogen bonding ; structural methylation and metallation effects
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract 2-S-Methylthiouracil crystallizes in the triclinic space group P $${\bar 1}$$ with unit cell dimensions a = 5.508(4), b = 7.175(3), c = 8.522(2) Å, α = 80.83(2), β = 80.43(3), γ = 76.86(3)°, and Z = 2. The molecule exists in the crystal in the lactam form and is essentially planar. The molecular packing consists of molecules linked in centrosymmetric hydrogen-bonded pairs. The effects of methylation and subsequent metallation on the 2-thiouracil structure are discussed.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1023/A:1009588223827
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  • 4
    Electronic Resource
    Electronic Resource
    X-ray crystal structure of tetraaquabis (xanthosinato)nickel(II) hexahydrate (1999)
    Springer
    Journal of chemical crystallography 29 (1999), S. 1009-1013 
    Details
    ISSN: 1572-8854
    Keywords: crystal structure ; nickel complex ; xanthosine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The complex [Ni(XsH−1)2(H2O)4]·6H2O (XsH−1: xanthosinate) was isolated from the reaction of nickel carbonate with xanthosine in aqueous solution. The octahedral coordination is supported by the reflectance measurements. Single-crystal X-ray diffraction studies show that the crystals belong to the triclinic P1 space group, with a = 7.152(1), b = 8.830(1),c = 13.783(1) Å, α = 82.024(1)°, β = 86.155(1)°, γ = 70.900(1)°, and D = 1.643 mg/m3, forZ = 1. Nickel is six coordinate with four water molecules, and two N7 atoms from xanthosinato ligands. A complicated hydrogen-bonding network is present, all possible donors taking part in it.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1023/A:1009568616134
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  • 5
    Electronic Resource
    Electronic Resource
    Molecular characterization of glyoxalase-I from a higher plant; upregulation by stress (1995)
    Springer
    Plant molecular biology 29 (1995), S. 1223-1233 
    Details
    ISSN: 1573-5028
    Keywords: expression pattern ; glyoxalase-I ; Lycopersicon esculentum ; phloem ; sequence ; salt-stress
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A cDNA, GLX1, encoding glyoxalase-I was isolated by differential screening of salt-induced genes in tomato. Glyoxalases-I and-II are ubiquitous enzymes whose functions are not clearly understood. They may serve to detoxify methylglyoxal produced from triosephosphates in all cells. The protein encoded by GLX1 shared 49.4% and 58.5% identity with glyoxalase-I isolated from bacteria and human, respectively. Furthermore, yeast cells expressing GLX1 showed a glyoxalase-I specific activity 20-fold higher than non-transformed cells. Both GLX1 mRNA and glyoxalase-I polypeptide levels increased 2- to 3-fold in roots, stems and leaves of plants treated with either NaCl, mannitol, or abscisic acid. Immunohistochemical localization indicated that glyoxalase-I was expressed in all cell types, with preferential accumulation in phloem sieve elements. This expression pattern was not appreciably altered by salt-stress. We suggest that the increased expression of glyoxalase-I may be linked to a higher demand for ATP generation and to enhanced glycolysis in salt-stressed plants.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00020464
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  • 6
    Electronic Resource
    Electronic Resource
    A major barley allergen associated with baker's asthma disease is a glycosylated monomeric inhibitor of insect α-amylase: cDNA cloning and chromosomal location of the gene (1992)
    Springer
    Plant molecular biology 20 (1992), S. 451-458 
    Details
    ISSN: 1573-5028
    Keywords: α-amylase monomeric inhibitor ; baker's asthma ; barley ; cDNA cloning ; genetic mapping ; glycosylated allergen
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A 14.5 kDa barley endosperm protein that is a major allergen in baker's asthma disease, as previously shown by both in vitro (IgE binding) and in vivo tests, has been identified as a glycosylated monomeric member of the multigene family of inhibitors of α-amylase/trypsin from cereals. A cDNA encoding this allergen (renamed BMAI-1) has been isolated and characterized. The deduced sequence for the mature protein, which is 132 residues long, is identical in its N-terminal end to the 20 amino acid partial sequence previously determined from the purified allergen, and fully confirms that it is a member of the multigene family of cereal inhibitors. Southern-blot analysis of wheat/barley addition lines using the insert in the BMAI-1 cDNA clone as a probe, has led to the location of the allergen gene (Iam1) in barley chromosome 2, while another related member of this protein family, the barley dimeric α-amylase inhibitor BDAI-1 gene (Iad1) has been located in chromosome 6. Iam1 is the first member of this inhibitor family in cereals to be assigned to chromosome group 2, thus extending the dispersion of genes in the family to five out of the seven homology groups of chromosomes in wheat and barley (chromosome 2, 3, 4, 6 and 7).
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00040604
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  • 7
    Electronic Resource
    Electronic Resource
    Mercurialis ambigua and Solanum luteum: Two Newly Discovered Natural Hosts of Tomato Yellow Leaf Curl Geminiviruses (2000)
    Springer
    European journal of plant pathology 106 (2000), S. 391-394 
    Details
    ISSN: 1573-8469
    Keywords: Bemisia tabaci ; Datura stramonium ; epidemiology ; Lycopersicon esculentum ; Solanum nigrum ; TYLCV
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract The yellow leaf curl disease of tomato is caused by a complex of virus species, two of which, tomato yellow leaf curl virus (TYLCV)-Sar and TYLCV-Is, are involved in epidemics of southern Spain. Plants of Mercurialis ambigua and Solanum luteum showing abnormal upward leaf curling and leaf distortion collected in the vicinity of tomato crops were found to be naturally infected with TYLCV-Is and TYLCV-Sar, respectively. These weed species, as well as Datura stramonium and S. nigrum, which had also been found to be naturally infected by TYLCVs in the same region in previous studies, were tested for susceptibility to TYLCV-Sar or TYLCV-Is by Agrobacterium tumefaciens-mediated and by Bemisia tabaci inoculation. Results indicated that both TYLCV-Sar and TYLCV-Is were able to infect D. stramonium and M. ambigua, whereas only TYLCV-Sar infected S. nigrum and S. luteum. Implications for the epidemiology of TYLCV are discussed. This is the first report of M.ambigua and S. luteum as hosts of TYLCV.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1023/A:1008758622582
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  • 8
    Electronic Resource
    Electronic Resource
    Growth and osmotic adjustment of two tomato cultivars during and after saline stress (1994)
    Springer
    Plant and soil 166 (1994), S. 75-82 
    Details
    ISSN: 1573-5036
    Keywords: growth ; osmotic adjustment ; saline stress ; solutes ; Lycopersicon esculentum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract The effect of a short period of saline stress was studied in two phenotypically different cultivars, one of normal fruit-size (L. esculentum cv. New Yorker) and one of cherry fruit-size (L. esculentum var.cerasiforme cv. PE-62). In both cultivars the relative growth rate (RGR) and the leaf area ratio (LAR) decreased following salinisation. The leaf turgor potential (ψp) and the osmotic potential at full turgor (ψos) decreased to the same extent in both cultivars. However, the contributions of organic and inorganic solutes to the osmotic adjustment was different between cultivars. New Yorker achieved the osmotic adjustment by means of the Cl− and Na+ uptake from the substrate, and by synthesis of organic solutes. In the cherry cultivar organic solutes did not contribute to the osmotic adjustment, instead, their contribution decreased after salinisation. After the salt stress was removed, the water stress disappeared, the content of organic solutes decreased in plants of both cultivars and, therefore, their growth was not retarded by the diversion of resources for the synthesis of organic solutes. However, the toxic effects of the Cl− and Na+ did not disappear after removal of the salt stress, and the net assimilation rate (NAR) and the rate of growth (RGR) did not recover.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02185483
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  • 9
    Electronic Resource
    Electronic Resource
    Wheat and Barley Inhibitors Active Towards α-Amylase and Trypsin-like Activities from Spodoptera frugiperda (1997)
    Springer
    Journal of chemical ecology 23 (1997), S. 1729-1741 
    Details
    ISSN: 1573-1561
    Keywords: α-Amylase inhibitors ; trypsin inhibitors ; cereal endosperm ; wheat ; barley ; Spodoptera frugiperda ; digestive enzymes ; midgut proteases
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract The α-amylase activity was determined throughout the larval development of Spodoptera frugiperda. Maximal activities with optimal pH in the range 8.5–9.5 were found in last instars. Protein preparations enriched in heterotetrameric inhibitors from wheat flour were active towards gut amylases from last instars, while those corresponding to homodimeric and monomeric inhibitors showed low inhibition levels. These results were further supported by testing purified members of each inhibitor type and by analyzing the effects of the inhibitors on the amylase isoenzyme pattern from native PAGE. High levels of trypsin-like activity were also found in gut extracts from last instars. Different genetic variants of the major barley trypsin inhibitor were active against this gut enzyme. None of the other larval digestive protease activities (chymotrypsin-like, elastase-like, leucine aminopeptidase-like, and carboxypeptidase A and B-like) were inhibited, indicating that the barley inhibitor is specific towards trypsin-like enzymes.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1023/B:JOEC.0000006447.85514.8d
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  • 10
    Electronic Resource
    Electronic Resource
    A method to quantify N fertilizer requirement (1998)
    Springer
    Nutrient cycling in agroecosystems 51 (1998), S. 155-162 
    Details
    ISSN: 1573-0867
    Keywords: barley ; maximum possible yields ; N demand ; soil N mineralization ; tropical highlands
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract A methodology to quantify N fertilizer requirement for a barley crop is proposed. The method consists of establishing a relationship between barley N demand (DEM) and an index of soil N supply (NS). NS values were obtained adding the inorganic N, i.e, (N-NO- 3 + N-NH+ 4, (Ni), measured just before planting in the soil to an index of soil N mineralization (Nor): NS = Ni + Nor Soil organic matter (SOM) was selected as an index of Nor: Nor = 25.9 + 17.9 (SOM) R2; = 0.89; p 〈 0.01 and Ni was measured in a soil extract obtained with KCl (1N). Ns values were related to both grain yield (Y) and N accumulated in the above ground biomass of barley (AB) grown under greenhouse conditions. The following relationships were obtained: Y = 0.81 + 0.99 (NS) - 0.0002 (NS)2 R2 = 0.77; p 〈 0.01 AB = -0.006 + 0.002 (NS) - 0.000003 (NS)2 R2 = 0.84; p 〈 0.01 A graphic relationship was established between DEM and NS, in order to extrapolate the greenhouse results to field conditions. Using this relationship, AB was converted from g N pot-1 to kg N ha-1, and NS from μg g-1 of N in the soil to kg ha-1.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1023/A:1009714932119
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