2011
DOI: 10.1002/jsfa.4585
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Expression of modified tocopherol content and profile in sunflower tissues

Abstract: Aufbauen und wieder abreißen: Natürliche Pinnasäure und drei ihrer Stereoisomere wurden aus den in der vorangehenden Zuschrift beschriebenen Aldehyden synthetisiert. Ein Schlüsselschritt bei der Synthese natürlicher Pinnasäure war eine hoch stereoselektive Reduktion des Ketons 1. Die Konfiguration wurde anhand der Untersuchung von Abbaureaktionen des synthetischen Materials bestimmt.

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Cited by 4 publications
(4 citation statements)
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“…Putative modifying genes located at LG 1, 9, 14 and 16 were identified in the present research, being the effect of those on LG 1, 14 and 16 highly significant in the epistatic interaction with the Tph2 locus on LG 8. Studies on expression of Tph2 mutations in plant tissues other than seeds also pointed to differences between T2100 and IAST-1 lines, as the latter showed lower gamma-tocopherol content in leaves, roots, and pollen [22]. …”
Section: Discussionmentioning
confidence: 99%
“…Putative modifying genes located at LG 1, 9, 14 and 16 were identified in the present research, being the effect of those on LG 1, 14 and 16 highly significant in the epistatic interaction with the Tph2 locus on LG 8. Studies on expression of Tph2 mutations in plant tissues other than seeds also pointed to differences between T2100 and IAST-1 lines, as the latter showed lower gamma-tocopherol content in leaves, roots, and pollen [22]. …”
Section: Discussionmentioning
confidence: 99%
“…Exceptions in naturally occurring plants are very scarce, for example in lettuce and spinach, which contain higher proportions of γ-tocopherol in leaves (Szymańska and Kruk, 2008). There are also several examples in which modified tocopherol profiles have been obtained in mutant and transgenic lines of plants, with the modified tocopherol profiles being expressed both in seeds and leaves, for example in Arabidopsis (Cheng et al , 2003; Bergmüller et al , 2003; Kanwischer et al , 2005; Mène-Saffrané et al , 2010), tobacco ( Nicotiana tabacum L.; Abbasi et al , 2007) and sunflower ( Helianthus annuus L.; Del Moral et al , 2012). Line BCT-4 was selected for its low α-/γ-tocopherol ratio in seeds in the course of a conventional breeding programme in which two other lines with similarly low α-/γ-tocopherol ratio in seeds, BCT-2 and BCT-5, were developed (Velasco et al , 2013).…”
Section: Discussionmentioning
confidence: 99%
“…The mutation resulting in high γ-tocopherol accumulation in BCT-4 is expressed in plant tissues other than seeds, whereas those in BCT-2 and BCT-5 are seed-specific, which suggests genetic differences between BCT-4 and both BCT-2 and BCT-5. In sunflower, two lines with increased levels of γ-tocopherol in seeds also showed expression of increased γ-tocopherol levels in other plant tissues, such as roots, leaves and pollen (Del Moral et al , 2012). Similarly, Arabidopsis mutants carrying a functional null mutation of the gene encoding for the γ-TMT showed a drastic reduction of α-tocopherol and a concomitant increase of γ-tocopherol in leaves (Bergmüller et al , 2003).…”
Section: Discussionmentioning
confidence: 99%
“…Modifications of seed tocopherols were also reflected at other plant levels. In particular, increased levels of β -, γ -, and δ -tocopherol in the seeds were paralleled by increased levels of these tocopherol forms in roots, leaves, and pollen grains [ 10 ]. A line with reduced total content of α -tocopherol in seeds also showed a reduced content in roots and pollen grains [ 10 ].…”
Section: Introductionmentioning
confidence: 99%