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1.
Chem Asian J ; 17(4): e202101341, 2022 Feb 14.
Artigo em Inglês | MEDLINE | ID: mdl-34939334

RESUMO

During the self-assembly of π-conjugated molecules, linkers and substituents can potentially add supportive noncovalent intermolecular interactions to π-stacking interactions. Here, we report the self-assembly behavior of thienopyrrole-fused thiadiazole (TPT) fluorescent dyes that possess ester or ether linkers and dodecyloxy side chains in solution and the condensed phase. A comparison of the self-association behavior of the ester- and ether-bridged compounds in solution using detailed UV-vis, fluorescence, and NMR spectroscopic studies revealed that the subtle replacement of the ether linkers by ester linkers leads to a distinct increase in the association constant (ca. 3-4 fold) and the enthalpic contribution (ca. 3 kcal mol-1 ). Theoretical calculations suggest that the ester linkers, which are in close proximity to one another due to the π-stacking interactions, induce attractive electrostatic forces and augment self-association. The self-assembly of TPT dyes into well-defined 1D clusters with high aspect ratios was observed, and their morphologies and crystallinity were investigated using SEM and X-ray diffraction analyses. TPTs with ester linkers exhibit a columnar liquid crystalline mesophase in the condensed phase.


Assuntos
Tiadiazóis , Ésteres , Éter , Éteres , Pirróis , Eletricidade Estática
2.
J Plant Physiol ; 168(16): 1927-33, 2011 Nov 01.
Artigo em Inglês | MEDLINE | ID: mdl-21683470

RESUMO

Tomato (Solanum lycopersicum L.) plants were transformed with an antisense construct of a cDNA encoding tomato telomere-binding protein (LeTBP1) to describe the role of a telomere-binding protein at the whole plant level. Fruit size decreased corresponding to the degree of suppression of LeTBP1 expression. This inhibition of fruit development was likely due to a decrease in the number of seeds in the LeTBP1 antisense plants. Pollen fertility and pollen germination rate decreased in accordance with the degree of suppression of LeTBP1 expression. Ovule viability was also reduced in the LeTBP1 antisense plants. Although plant height was somewhat reduced in the antisense plants compared to the control plants, the number and weight of leaves were unaffected by LeTBP1 suppression. The number and morphology of flowers were also normal in the antisense plants. These indicate that reduced fertility in the antisense plants is not an indirect effect of altered vegetative growth. LeTBP1 expression was sensitive to temperature stress in wild-type plants. We conclude that LeTBP1 plays a critical role in seed and fruit development rather than vegetative growth and flower formation.


Assuntos
Frutas/crescimento & desenvolvimento , Sementes/crescimento & desenvolvimento , Solanum lycopersicum/fisiologia , Supressão Genética/genética , Proteínas de Ligação a Telômeros/genética , Cromossomos de Plantas/genética , DNA Antissenso/genética , DNA Complementar/genética , DNA de Plantas/genética , Flores/genética , Flores/crescimento & desenvolvimento , Flores/fisiologia , Frutas/genética , Frutas/fisiologia , Expressão Gênica/genética , Regulação da Expressão Gênica de Plantas/genética , Solanum lycopersicum/citologia , Solanum lycopersicum/genética , Solanum lycopersicum/crescimento & desenvolvimento , Meristema/citologia , Óvulo Vegetal/fisiologia , Folhas de Planta/genética , Folhas de Planta/metabolismo , Proteínas de Plantas/genética , Proteínas de Plantas/metabolismo , Plantas Geneticamente Modificadas , Pólen/fisiologia , Sementes/genética , Sementes/fisiologia , Estresse Fisiológico , Proteínas de Ligação a Telômeros/metabolismo , Temperatura
3.
Biosci Biotechnol Biochem ; 75(5): 994-6, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-21597170

RESUMO

Plant specific O-glycosylation of proteins includes the attachment of arabinogalactan to hydroxyproline (Hyp) residues. These Hyp residues are generated from peptidyl proline residues by the action of prolyl 4-hydroxylase which requires the ferrous ion. We investigated the effect of the ferrous chelator, 2,2'-dipyridyl on tobacco plants, and found that such treatment reduced the arabinogalactosylation of proteins.


Assuntos
2,2'-Dipiridil/farmacologia , Galactanos/metabolismo , Quelantes de Ferro/farmacologia , Nicotiana/efeitos dos fármacos , Nicotiana/metabolismo , Glicosilação/efeitos dos fármacos , Especificidade da Espécie
4.
Planta ; 232(3): 755-64, 2010 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-20571824

RESUMO

Auxin transport network, which is important in the integration of plant developmental signals, depends on differential expression of the auxin efflux carrier PIN gene family. We cloned three tomato PIN (referred as SlPIN) cDNAs and examined their expression patterns in fruit and other organs. The expression of SlPIN1 and SlPIN2 was highest in very young fruit immediately after anthesis, whereas the expression of SlPIN3 was low at this same stage of fruit development. SlPIN2::GUS was expressed in ovules at anthesis and in young developing seeds at 4 days after anthesis, while SlPIN1::GUS was expressed in whole fruit. The DR5::GUS auxin-responsive reporter gene was expressed in the fruit and peduncle at anthesis and was higher in the peduncle 4 days after anthesis. These studies suggest that auxin is likely transported from young seeds by SlPIN1 and SlPIN2 and accumulated in peduncles where SlPIN gene expression is low in tomato. The possible role of SlPINs in fruit set was discussed.


Assuntos
Proteínas de Transporte/genética , Ácidos Indolacéticos/metabolismo , Solanum lycopersicum/metabolismo , Sequência de Aminoácidos , Sequência de Bases , Proteínas de Transporte/química , Proteínas de Transporte/metabolismo , Clonagem Molecular , Primers do DNA , DNA Complementar , Genes de Plantas , Genes Reporter , Solanum lycopersicum/genética , Solanum lycopersicum/crescimento & desenvolvimento , Dados de Sequência Molecular , Reação em Cadeia da Polimerase , Regiões Promotoras Genéticas , Homologia de Sequência de Aminoácidos
5.
Phytochemistry ; 66(24): 2822-8, 2005 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-16289145

RESUMO

The enzyme NAD-dependent sorbitol dehydrogenase (SDH) is well characterized in the Rosaceae family of fruit trees, which synthesizes sorbitol as a translocatable photosynthate. Expressed sequence tags of SDH-like sequences have also been generated from various non-Rosaceae species that do not synthesize sorbitol as a primary photosynthetic product, but the physiological roles of the encoded proteins in non-Rosaceae plants are unknown. Therefore, we isolated an SDH-like cDNA (SDL) from tomato (Lycopersicon esculentum Mill.). Genomic Southern blot analysis suggested that SDL exists in the tomato genome as a single-copy gene. Northern blot analysis showed that SDL is ubiquitously expressed in tomato plants. Recombinant SDL protein was produced and purified for enzymatic characterization. SDL catalyzed the interconversion of sorbitol and fructose with NAD (H). SDL showed highest activity for sorbitol among the several substrates tested. SDL showed no activity with NADP+. Thus, SDL was identified as a SDH, although the Km values and substrate specificity of SDL were significantly different from those of SDH purified from the Japanese pear (Pyrus pyrifolia), a Rosaceae fruit tree. In addition, tomato was transformed with antisense SDL to evaluate the contribution of SDL to SDH activity in tomato. The transformation decreased SDH activity to approximately 50% on average. Taken together, these results provide molecular evidence of SDH in tomato, and SDL was renamed LeSDH.


Assuntos
L-Iditol 2-Desidrogenase/genética , L-Iditol 2-Desidrogenase/metabolismo , Solanum lycopersicum/enzimologia , Sequência de Aminoácidos , Northern Blotting , Southern Blotting , DNA Antissenso , Frutose/metabolismo , Regulação da Expressão Gênica de Plantas , Solanum lycopersicum/genética , Dados de Sequência Molecular , NAD/metabolismo , Proteínas Recombinantes/genética , Proteínas Recombinantes/metabolismo , Rosaceae/enzimologia , Homologia de Sequência de Aminoácidos , Sorbitol/metabolismo , Especificidade por Substrato , Transformação Genética
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