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1.
Dalton Trans ; 47(27): 8892-8896, 2018 Jul 10.
Artigo em Inglês | MEDLINE | ID: mdl-29774331

RESUMO

A neutral heterobimetallic triple-decker stannole complex was prepared by the reaction of an anionic ruthenocene bearing a stannole dianionic ligand with [Rh(cod)Cl]2 (cod = 1,5-cyclooctadiene), and the resulting Ru-Rh complex exhibits an electronic property different from those of the corresponding Ru-Ru and Rh-Rh complexes. The Ru-Rh complex can be decomposed in ionic liquids to metal nanoparticles.

2.
J Am Chem Soc ; 138(35): 11378-82, 2016 09 07.
Artigo em Inglês | MEDLINE | ID: mdl-27513707

RESUMO

Research on zero-valent p-block elements is a recent hot topic in synthetic and theoretical chemistry because of their novel electronic states having two lone pairs in both the s- and p-orbitals. It is considered that σ-donating ligands bearing large substituents are essential to stabilize these species. Herein, we propose a new approach using butadiene as a 4π-electron donor to stabilize zero-valent group 14 elements. During our study to explore the coordination chemistry of stannacyclopentadienyl ligands, unexpected products, in which the tin atom is coordinated by a butadiene in a η(4)-fashion, were obtained. Because butadiene is a neutral 4π-electron donating ligand, the formal oxidation number of the tin atoms of the products should be zero, which is supported by X-ray diffraction analysis and theoretical calculations. A mechanism for the formation of the products is also described.

3.
Plant Signal Behav ; 5(8): 1045-7, 2010 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-20724838

RESUMO

Cytosolic free Ca(2+) mobilization induced by microbe/pathogen-associated molecular patterns (MAMPs/PAMPs) play key roles in plant innate immunity. However, components involved in Ca(2+) signaling pathways still remain to be identified and possible involvement of the CBL (calcineurin B-like proteins)-CIPK (CBL-interacting protein kinases) system in biotic defense signaling has yet to be clarified. Recently we identified two CIPKs, OsCIPK14 and OsCIPK15, which are rapidly induced by MAMPs, involved in various MAMP-induced immune responses including defense-related gene expression, phytoalexin biosynthesis and hypersensitive cell death. MAMP-induced production of reactive oxygen species as well as cell browning were also suppressed in OsCIPK14/15-RNAi transgenic cell lines. Possible molecular mechanisms and physiological functions of the CIPKs in plant innate immunity are discussed.


Assuntos
Calcineurina/imunologia , Oryza/imunologia , Imunidade Vegetal , Proteínas de Plantas/imunologia , Proteínas Quinases/imunologia , Calcineurina/genética , Morte Celular , Regulação da Expressão Gênica de Plantas , Imunidade Inata , Oryza/genética , Proteínas de Plantas/genética , Plantas Geneticamente Modificadas/genética , Plantas Geneticamente Modificadas/imunologia , Proteínas Quinases/genética , Espécies Reativas de Oxigênio/metabolismo , Sesquiterpenos/metabolismo , Transdução de Sinais , Fitoalexinas
4.
Plant Physiol ; 153(2): 678-92, 2010 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-20357140

RESUMO

Although cytosolic free Ca(2+) mobilization induced by microbe/pathogen-associated molecular patterns is postulated to play a pivotal role in innate immunity in plants, the molecular links between Ca(2+) and downstream defense responses still remain largely unknown. Calcineurin B-like proteins (CBLs) act as Ca(2+) sensors to activate specific protein kinases, CBL-interacting protein kinases (CIPKs). We here identified two CIPKs, OsCIPK14 and OsCIPK15, rapidly induced by microbe-associated molecular patterns, including chitooligosaccharides and xylanase (Trichoderma viride/ethylene-inducing xylanase [TvX/EIX]), in rice (Oryza sativa). Although they are located on different chromosomes, they have over 95% nucleotide sequence identity, including the surrounding genomic region, suggesting that they are duplicated genes. OsCIPK14/15 interacted with several OsCBLs through the FISL/NAF motif in yeast cells and showed the strongest interaction with OsCBL4. The recombinant OsCIPK14/15 proteins showed Mn(2+)-dependent protein kinase activity, which was enhanced both by deletion of their FISL/NAF motifs and by combination with OsCBL4. OsCIPK14/15-RNAi transgenic cell lines showed reduced sensitivity to TvX/EIX for the induction of a wide range of defense responses, including hypersensitive cell death, mitochondrial dysfunction, phytoalexin biosynthesis, and pathogenesis-related gene expression. On the other hand, TvX/EIX-induced cell death was enhanced in OsCIPK15-overexpressing lines. Our results suggest that OsCIPK14/15 play a crucial role in the microbe-associated molecular pattern-induced defense signaling pathway in rice cultured cells.


Assuntos
Morte Celular , Oryza/enzimologia , Proteínas de Plantas/metabolismo , Proteínas Quinases/metabolismo , Sesquiterpenos/metabolismo , Células Cultivadas , DNA Complementar/genética , Regulação da Expressão Gênica de Plantas , Dados de Sequência Molecular , Oryza/genética , Oryza/imunologia , Proteínas de Plantas/genética , Plantas Geneticamente Modificadas/enzimologia , Plantas Geneticamente Modificadas/genética , Plantas Geneticamente Modificadas/imunologia , Proteínas Quinases/genética , RNA de Plantas/genética , Proteínas Recombinantes/genética , Proteínas Recombinantes/metabolismo , Transdução de Sinais , Técnicas do Sistema de Duplo-Híbrido , Fitoalexinas
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