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  • 1
    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
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  • 2
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 27 (1989), S. 44-49 
    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
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