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  • Helianthus annuus  (6)
  • Analytical Chemistry and Spectroscopy  (2)
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  • 1
    Electronic Resource
    Electronic Resource
    In vitro oleate desaturase in developing sunflower seeds
    Amsterdam : Elsevier
    Phytochemistry 30 (1991), S. 2127-2130 
    Details
    ISSN: 0031-9422
    Keywords: Compositae ; Helianthus annuus ; high oleic mutant ; microsomes ; oleate desaturase ; seeds ; sunflower ; temperature control.
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://linkinghub.elsevier.com/retrieve/pii/0031-9422(91)83599-G
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  • 2
    Electronic Resource
    Electronic Resource
    Oleate desaturation in seeds of two genotypes of sunflower
    Amsterdam : Elsevier
    Phytochemistry 28 (1989), S. 2593-2595 
    Details
    ISSN: 0031-9422
    Keywords: Compositae ; Helianthus annuus ; high oleic acid mutant. ; oleate desaturation ; sunflower, seeds
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://linkinghub.elsevier.com/retrieve/pii/S0031-9422(00)98046-4
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  • 3
    Electronic Resource
    Electronic Resource
    Lipid characterization in seeds of a high oleic acid sunflower mutant
    Amsterdam : Elsevier
    Phytochemistry 28 (1989), S. 2597-2600 
    Details
    ISSN: 0031-9422
    Keywords: Compositae ; Helianthus annuus ; fatty acid composition ; high oleic acid mutant. ; lipids ; seeds ; sunflower
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://linkinghub.elsevier.com/retrieve/pii/S0031-9422(00)98047-6
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  • 4
    Electronic Resource
    Electronic Resource
    Epistatic interaction among loci controlling the palmitic and the stearic acid levels in the seed oil of sunflower (2000)
    Springer
    Theoretical and applied genetics 100 (2000), S. 105-111 
    Details
    ISSN: 1432-2242
    Keywords: Key words Sunflower ; Helianthus annuus ; High palmitic acid ; High stearic acid ; Epistatic interaction ; Inheritance ; Oil quality
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract  Two sunflower (Helianthus annuus L.) mutants with high concentrations of saturated fatty acids in their seed oil have been identified and studied extensively. The mutant line CAS-5 has high concentrations of palmitic acid (C16:0) (〉25% compared with 7% in standard sunflower seed oil) and low-C18:0 values (3%). CAS-3 is characterized by its high levels of stearic acid (C18:0) (〉22% compared with 4% in standard sunflower seed oil) and a low-C16:0 content (5%). CAS-5 also possesses elevated levels of palmitoleic acid (C16:1) (〉5%), which is absent in standard sunflower seed oil. The objective of this study was to determine the relationships between the loci controlling the high-C16:0 and the high-C18:0 traits in these mutants. Plants of both mutants were reciprocally crossed. Gas chromatographic analyses of fatty acids from the seed oil of F1, F2, F3 and the BC1F1 to CAS-5 generations indicated that the loci controlling the high-C16:0 trait exerted an epistatic effect over the loci responsible for the high-C18:0 character. As a result, the phenotypic combination containing both the high-C16:0 levels of CAS-5 and the high-C18:0 levels of CAS-3 was not possible. However, phenotypes with a saturated fatty acid content of 44% (34.5% C16:0+9.5% C18:0) were identified in the F3 generation. These are the highest saturated (C16:0 and C18:0) levels reported so far in sunflower seed oil. When F3 C16:0 segregating generations in both a high- and a low-C18:0 background were compared, the high-C16:1 levels were not expressed as expected in the high-C18:0 background (CAS-3 background). In this case, the C16:1 content decreased to values below 1.5%, compared with 〉5% in a low-C18:0 background. As the stearoyl-ACP desaturase has been reported to catalyze the desaturation from C16:0-ACP to C16:1-ACP, these results suggested that a decrease in its activity was involved in the accumulation of C18:0 in the high-C18:0 mutant CAS-3.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/s001220050015
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  • 5
    Electronic Resource
    Electronic Resource
    Genetic analysis of the high oleic acid content in cultivated sunflower (Helianthus annuus L.) (1989)
    Springer
    Euphytica 41 (1989), S. 39-51 
    Details
    ISSN: 1573-5060
    Keywords: Helianthus annuus ; sunflower ; oleic acid content ; linoleic acid content ; genetical analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Sunflower lines breeding true for very high oleic acid content in their oil (average levels higher than 85%) were crossed with standard sunflower lines with mean oleic acid levels of 30%. Analysis of the oil of F1 seeds indicated dominance for high oleic levels and control of the genotype of the embryo. Segregating generations were obtained selfing heterozygous high oleic BCnF1 plants from several generations of a backcrossing program to incorporate the high oleic character to standard inbred lines and testcrossing these plants to low oleic material. Analysis of F2 and testcrossed seeds showed three kind of segregations, in both F2 and testcrossed populations, with different proportions of low, intermediate and high oleic types. Genetic analysis of these data supported the hypothesis, that the high oleic character is controlled by three dominant complementary genes OL1, OL2 and OL3. Additional data showing F1 seeds with intermediate oleic content and segregations for high oleic in progenies of intermediate types, suggest the presence of major factors modifying high oleic acid content.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00022409
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  • 6
    Electronic Resource
    Electronic Resource
    Sunflower mutant containing high levels of palmitic acid in high oleic background (1997)
    Springer
    Euphytica 97 (1997), S. 113-116 
    Details
    ISSN: 1573-5060
    Keywords: Helianthus annuus ; fatty acids ; palmitic acid ; X-ray mutagenesis ; seed oil ; sunflower
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract A new sunflower mutant, CAS-12, was obtained, which has both high palmitic (≈30%) and high oleic acid contents, and also a substantial amount of palmitoleic acid (≈7%). The mutant was selected after X-ray irradiation of dry seeds of the inbred line BSD-2-423, which had normal palmitic (≈3%) and high oleic (≈88%) acid levels. The increase of palmitic and palmitoleic acids occurred at the expense of the oleic acid content, which decreased to around 55% in respect to the original line. Linoleic acid content is always under 5%. Palmitic and palmitoleic acid levels were similar to those of the high palmitic mutant CAS-5 obtained in a previous programme from a low oleic line isogenic to BSD-2-423 using a similar mutagenic treatment. In that previous programme we also selected three high stearic acid mutants using chemical mutagenic treatment on the same sunflower line (RDF-1-532). We attempted to obtain mutants in other lines but were unsuccessful. The isolation of similar mutants in isogenic parental lines illustrates the importance of the genetic background in the development of specific mutants with an altered seed oil fatty acid composition. The oil of this mutant will increase the range of potential uses of sunflower oil.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1023/A:1003045726610
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  • 7
    Electronic Resource
    Electronic Resource
    The γ-butyrolactone ring puckering (1989)
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 27 (1989), S. 44-49 
    Details
    ISSN: 0749-1581
    Keywords: γ-Butyrolactone ; 1H NMR analysis ; Conformational analysis ; Molecular mechanics ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 60 and 100 MHz 1H NMR spectra of γ-butyrolactone were analysed in detail. The best set of coupling values (Hz ± 0.03) is 3JABc = 7.86, 3JABt = 6.27, 3JBCc = 9.52, 3JBCt = 6.86, 4JACc + 4JACt = -0.18, 2JA - 2JB = 3.89 and 2JB - 2JC = 4.86 (A, B and C refer to α, β and γ protons, with respect to the ring oxygen, and c and t mean the same and opposite side of the ring, respectively). The 3J values support the conclusion that the molecule is interconverting between two equivalent conformations of near envelope type with the β-carbon out of the mean plane defined by the fragment C—O—CO—C.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/mrc.1260270108
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  • 8
    Electronic Resource
    Electronic Resource
    1H and 13C NMR assignments with coordination-induced shift calculations of carbon σ-bonded ortho-metalated rhodium(III) and iridium(III) complexes (1993)
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 31 (1993), S. 529-536 
    Details
    ISSN: 0749-1581
    Keywords: 2D NMR ; Spin-spin coupling ; Coordination-induced shift ; 1H—13C ; HETCOR ; ortho-Metalation ; Cyclometallation ; Polypyridyl ; 2,2′-Bipyridine ; π-Back-bonding ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Complete 1H and 13C NMR assignments and coordination-induced shift [CIS, δ(complex) - δ(free ligand)] calculations for carbon σ-bonded ortho-metalated rhodium(III) and iridium(III) complexes are described. NMR parameters are used as probes of van der Waals interactions and ring current anisotropy in the ligand's environmental framework and to monitor σ-donation and π-back-bonding within the ligand in this family of ortho-metalated complexes. CIS measurements indicate large charge redistribution within the ligands as a result of ortho-metalation to the rhodium(III) or iridium(III) cationic metal centers. The pulse sequences, attached proton test (APT), 1H—1H homonuclear correlation spectroscopy (COSY), single-frequency off-resonance decoupling (SFORD) and 1H—13C heteronuclear correlation spectroscopy (HETCOR), were utilized to assign all proton and carbon resonances of [Rh(ppy)2Cl]2, [Ir(ppy)2Cl]2, [Ir(ptpy)2Cl]2, [Ir(mppy)2Cl]2, [Rh(ppy)2bpy]+, [Ir(ppy)2bpy]+, [Ir(ptpy)2bpy]+ and [Ir(mppy)2bpy]+, where ppy is 2-phenylpyridine, ptpy is 2-(p-tolyl)pyridine, mppy is 3-methyl-2-phenylpyridine and bpy is 2,2′-bipyridine.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/mrc.1260310603
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