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Palabras contadas: polymers: 9
Scherlis, D.A. - Fattebert, J.-L. - Marzari, N.
J Chem Phys 2006;124(19)
2006

Descripción: The stacking of positively charged (or doped) terthiophene oligomers and quaterthiophene polymers in solution is investigated applying a recently developed unified electrostatic and cavitation model for first-principles calculations in a continuum solvent. The thermodynamic and structural patterns of the dimerization are explored in different solvents, and the distinctive roles of polarity and surface tension are characterized and analyzed. Interestingly, we discover a saturation in the stabilization effect of the dielectric screening that takes place at rather small values of ε0. Moreover, we address the interactions in trimers of terthiophene cations, with the aim of generalizing the results obtained for the dimers to the case of higher-order stacks and nanoaggregates. © 2006 American Institute of Physics.
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Tipo de documento: info:ar-repo/semantics/artículo

Baggio, R. - Garland, M.T. - Perec, M.
Acta Crystallogr Sect C Cryst Struct Commun 2003;59(1):m30-m32
2003

Descripción: A new polymeric phase of zinc(II) oxydiacetate, catena-poly[[[diaquazinc(II)]-μ-oxydiacetato] hydrate], {[Zn(C4H4-O5)(H2O)2] ·H2O}n, isomorphous with the Co homologue [Hatfield, Helms, Rohrs, Singh, Wasson & Weller (1987). Proc. Indian Acad. Sci. Chem. Sci. 98, 23-31], is reported. It presents a chain-like structure, generated by ZnO6 cores which are bridged by carboxylate groups in an anti-anti conformation along the unique crystallographic b axis. The chains are held together through hydrogen-bonding interactions with the three water molecules.
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Tipo de documento: info:ar-repo/semantics/artículo

Barón, M. - Stepto, R.F.T. - Noël, C. - Shibaev, V.P. - Hess, M. - Jenkins, A.D. - Jin, I.-Il. - Sirigu, A. - Work, W.J. - Luckhurst, G.R. - Chandrashekhar, S. - Demus, D. - Goodby, J.W. - Gray, G.W. - Lagerwall, S.T. - Lavrentovich, O.D. - Schadt, M. - Allegra, G. - Bareiss, R.E. - Bikales, N.M. - Hatada, K. - Kahovec, J. - Kratochvíl, P. - Maréchal, E. - Metanomski, W.V. - Mita, I. - Papisov, I.M. - Suter, U.W. - Alemán, J.V. - Matyjaszewski, K. - Penczek, S. - Tripathy, S. - Shi, L.
Pure Appl. Chem. 2002;74(3):493-509
2002

Descripción: The document first gives definitions of basic terms related to liquid-crystalline and mesomorphic states of matter and then terms specific to the classification of liquid-crystal polymers. The terms have been restricted to those most commonly encountered in the structural description of the latter class of materials. The terms have been selected from the recently published comprehensive document "Definitions of basic terms relating to low-molar-mass and polymer liquid crystals" [Pure and Applied Chemistry 73 (5), 845-895 (2001)] and are intended to form a readily usable guide for the reader interested in the structural description of polymer liquid crystals. The more comprehensive document should be used for terminology associated with types of mesophases and the optical and physical characteristics of liquid-crystalline materials. The advice given by representatives of the International Liquid Crystal Society for the preparation of this document is gratefully acknowledged.
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Tipo de documento: info:ar-repo/semantics/artículo

Ruiz, J.A. - López, N.I. - Fernández, R.O. - Méndez, B.S.
Appl. Environ. Microbiol. 2001;67(1):225-230
2001

Descripción: Pseudomonas oleovorans GPo1 and its polyhydroxyalkanoic acid (PHA) depolymerization-minus mutant, GPo500 phaZ, residing in natural water microcosms, were utilized to asses the effect of PHA availability on survival and resistance to stress agents. The wild-type strain showed increased survival compared to the PHA depolymerase-minus strain. The appearance of a round cellular shape, characteristic of bacteria growing under starvation conditions, was delayed in the wild type in comparison to the mutant strain. Percent survival at the end of ethanol and heat challenges was always higher in GPo1 than in GPo500. Based on these results and on early experiments (H. Hippe, Arch. Mikrobiol. 56:248-277, 1967) that suggested an association of PHA utilization with respiration and oxidative phosphorylation, we investigated the association between PHA degradation and nucleotide accumulation. ATP and guanosine tetraphosphate (ppGpp) production was analyzed under culture conditions leading to PHA depolymerization. A rise in the ATP and ppGpp levels appeared concomitant with PHA degradation, while this phenomenon was not observed in the mutant strain unable to degrade the polymer. Complementation of the phaZ mutation restored the wild-type phenotype.
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Tipo de documento: info:ar-repo/semantics/artículo

Pearson, J.L. - Robinson, T.J. - Muñoz, M.J. - Kornblihtt, A.R. - Garcia-Blanco, M.A.
J. Biol. Chem. 2008;283(12):7949-7961
2008

Descripción: The transcription factor TCERG1 (also known as CA150) associates with RNA polymerase II holoenzyme and alters the elongation efficiency of reporter transcripts. TCERG1 is also found as a component of highly purified spliceosomes and has been implicated in splicing. To elucidate the function of TCERG1, we used short interfering RNA-mediated knockdown followed by en masse gene expression analysis to identify its cellular targets. Analysis of data from HEK293 and HeLa cells identified high confidence targets of TCERG1. We found that targets of TCERG1 were enriched in microRNA-binding sites, suggesting the possibility of post-transcriptional regulation. Consistently, reverse transcription-PCR analysis revealed that many of the changes observed upon TCERG1 knockdown were because of differences in alternative mRNA processing of the 3′-untranslated regions. Furthermore, a novel computational approach, which can identify alternatively processed events from conventional microarray data, showed that TCERG1 led to widespread alterations in mRNA processing. These findings provide the strongest support to date for a role of TCERG1 in mRNA processing and are consistent with proposals that TCERG1 couples transcription and processing. © 2008 by The American Society for Biochemistry and Molecular Biology, Inc.
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Tipo de documento: info:ar-repo/semantics/artículo

Nikel, P.I. - Pettinari, M.J. - Galvagno, M.A. - Méndez, B.S.
Appl. Environ. Microbiol. 2006;72(4):2614-2620
2006

Descripción: We assessed the effects of different arcA mutations on poly(3- hydroxybutyrate) (PHB) synthesis in recombinant Escherichia coli strains carrying the pha synthesis genes from Azotobacter sp. strain FA8. The arcA mutations used were an internal deletion and the arcA2 allele, a leaky mutation for some of the characteristics of the Arc phenotype which confers high respiratory capacity. PHB synthesis was not detected in the wild-type strain in shaken flask cultures under low-oxygen conditions, while ArcA mutants gave rise to polymer accumulation of up to 24% of their cell dry weight. When grown under microaerobic conditions in a bioreactor, the arcA deletion mutant reached a PHB content of 27% ± 2%. Under the same conditions, higher biomass and PHB concentrations were observed for the strain bearing the arcA2 allele, resulting in a PHB content of 35% ± 3%. This strain grew in a simple medium at a specific growth rate of 0.69 ± 0.07 h-1, whereas the deletion mutant needed several nutritional additives and snowed a specific growth rate of 0.56 ± 0.06 h-1. The results presented here suggest that arcA mutations could play a role in heterologous PHB synthesis in microaerobiosis. Copyright © 2006, American Society for Microbiology. All Rights Reserved.
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Tipo de documento: info:ar-repo/semantics/artículo

Nikel, P.I. - De Almeida, A. - Melillo, E.C. - Galvagno, M.A. - Pettinari, M.J.
Appl. Environ. Microbiol. 2006;72(6):3949-3954
2006

Descripción: A recombinant E. coli strain (K24K) was constructed and evaluated For poly(3-hydroxybutyrate) (PHB) production from whey and corn steep liquor as main carbon and nitrogen sources. This strain bears the pha biosynthetic genes from Azotobacter sp. strain FA8 expressed from a T5 promoter under the control of the lactose operator. K24K does not produce the lactose repressor, ensuring constitutive expression of genes involved in lactose transport and utilization. PHB was efficiently produced by the recombinant strain grown aerobically in fed-batch cultures in a laboratory scale bioreactor on a semisynthetic medium supplemented with the agroindustrial by-products. After 24 h, cells accumulated PHB to 72.9% of their cell dry weight, reaching a volumetric productivity of 2.13 g PHB per liter per hour. Physical analysis of PHB recovered from the recombinants showed that its molecular weight was similar to that of PHB produced by Azotobacter sp. strain FA8 and higher than that of the polymer from Cupriavidus necator and that its glass transition temperature was approximately 20°C higher than those of PHBs from the natural producer strains. Copyright © 2006, American Society for Microbiology. All Rights Reserved.
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Tipo de documento: info:ar-repo/semantics/artículo

Almeida, A. - Catone, M.V. - Rhodius, V.A. - Gross, C.A. - Pettinari, M.J.
Appl. Environ. Microbiol. 2011;77(18):6622-6629
2011

Descripción: Phasins (PhaP) are proteins normally associated with granules of poly(3-hydroxybutyrate) (PHB), a biodegradable polymer accumulated by many bacteria as a reserve molecule. These proteins enhance growth and polymer production in natural and recombinant PHB producers. It has been shown that the production of PHB causes stress in recombinant Escherichia coli, revealed by an increase in the concentrations of several heat stress proteins. In this work, quantitative reverse transcription (qRT)-PCR analysis was used to study the effect of PHB accumulation, and that of PhaP from Azotobacter sp. strain FA8, on the expression of stress-related genes in PHB-producing E. coli. While PHB accumulation was found to increase the transcription of dnaK and ibpA, the expression of these genes and of groES, groEL, rpoH, dps, and yfiD was reduced, when PhaP was coexpressed, to levels even lower than those detected in the non-PHB-accumulating control. These results demonstrated the protective role of PhaP in PHB-synthesizing E. coli and linked the effects of the protein to the expression of stress-related genes, especially ibpA. The effect of PhaP was also analyzed in non-PHBsynthesizing strains, showing that expression of this heterologous protein has an unexpected protective effect in E. coli, under both normal and stress conditions, resulting in increased growth and higher resistance to both heat shock and superoxide stress by paraquat. In addition, PhaP expression was shown to reduce RpoH protein levels during heat shock, probably by reducing or titrating the levels of misfolded proteins. © 2011, American Society for Microbiology.
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Tipo de documento: info:ar-repo/semantics/artículo