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  • 1
    ISSN: 1520-6041
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2048
    Keywords: Keywords:β-Glucuronidase ; 3-Hydroxy-3-methylglu- taryl coenzyme A reductase ; Lycopersicon (HMG1 regulation) ; Mevalonic acid ; Transgenic tomato ; Transient gene expression (HMG1)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract. The enzyme 3-hydroxy-3-methylglutaryl coenzyme A reductase (HMGR, EC 1.1.1.34) is encoded by a small multigene family in tomato (Lycopersiconesculentum Mill.) and catalyzes the synthesis of mevalonic acid (MVA), a committed step in the biosynthesis of sterols and isoprenoids. A chimeric HMG1::GUS reporter gene fusion was used to analyze the regulation of HMG1 gene expression in detail. HMG1 promoter 5′ deletion mutants established the boundary of a fully inducible promoter. In HMG1::GUS transgenic tomato plants, histochemical staining with 5-bromo-3-indolyl-glucuronide demonstrated that HMG1 was primarily expressed in shoot and root meristems, and in young tomato fruit. This result was confirmed by both HMG1 in-situ hybridization and RNA gel blot analysis. Tomato suspension cell experiments showed that steady-state HMG1 mRNA accumulated during lag and exponential growth phases, but not during the stationary phase. Transient expression of the HMG1::GUS in tissue culture cells treated with mevinolin indicated that HMG1 expression was subject to feedback regulation by a biosynthetic product derived from MVA. These results suggest that a primary, although not exclusive, role of HMG1 is to supply the MVA demand associated with cell division and growth.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Plant molecular biology 36 (1998), S. 733-739 
    ISSN: 1573-5028
    Keywords: AGAMOUS ; tomato ; ripening ; calyx ; gene expression ; sepals ; in vitro
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract In vitro culture of VFNT Cherry tomato sepals (calyx) at 16–21 °C results in developmental changes that are similar to those that occur in fruit tissue [10]. Sepals become swollen, red, and succulent, produce ethylene, and have increased levels of polygalacturonase RNA. They also produce many flavor volatiles characteristic of ripe tomato fruit and undergo similar changes in sugar content [11]. We examined the expression of the tomato AGAMOUS gene, TAG1, in ripening, in vitro sepal cultures and other tissues from the plant and found that TAG1 RNA accumulates to higher levels than expected from data from other plants. Contrary to reports on the absence of AGAMOUS in sepals, TAG1 RNA levels in green sepals from greenhouse-grown plants is detectable, its concentration increasing with in vitro ripening to levels that were even higher than in red, ripe fruit. Sepals of fruit on transgenic tomato plants that expressed TAG1 ectopically were induced by low temperature to ripen in vivo, producing lycopene and undergoing cell wall softening as is characteristic of pericarpic tissue. We therefore propose that the induction of elevated TAG1 gene expression plays a key role in developmental changes that result in sepal ripening.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 4 (1990), S. 493-501 
    ISSN: 0268-2605
    Keywords: C—H activation ; N—H activation ; (η-C5H5)2Rh2(CO)(CF3C2CF3) ; alkenyl ; carboxamide ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: There is activation of olefinic C—H bonds when (η-C5H5)2Rh2(CO)(CF3C2CF3) is treated with vinyl acetate or allyl cyanide. These reactions are initiated by exposure to sunlight. In the vinyl acetate reaction, each of the three vinylic C—H bonds can be broken, but there is strong preference for cleavage at the substituted carbon. The products formed in these reactions are bisalkenyl complexes of the type (η-C5H5)2Rh2{μ-C(CF3)C(CF3)H}(μ-CR=CR′R″), and all isomers have been thoroughly characterized by NMR analysis. Similar reactions with allylamine and other amines (NH2R, NHMe2) occur in the dark and proceed by N—H bond cleavage. Near-quantitative amounts of the products, (η-C5H5)Rh2{C(CF3)C(CF3)H}(C(O)NRR′) are isolated. Spectroscopic data indicate a bridging carboxamide ligand attached to the Rh—Rh bond from oxygen and nitrogen donor sites. It is proposed that coordination of O or N to rhodium has a strong influence on all of the reactions studied.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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