Resolución N° 135 ¿La Cámara de Comercio de Bogotá tiene competencia para decidir sobre las acciones de impugnación de actas?

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Notas estadísticas del departamento de Querétaro, formadas por la Asamblea Constitucional del mismo y remitidas al Supremo Gobierno, en cumplimiento de la parte primera del artículo 135 de lasbases orgánicas.

UANL

Culture and exopolysaccharide production from sugarcane molasses by Gordonia polyisoprenivorans CCT 7137, isolated from contaminated groundwater in Brazil

Gordonia polyisoprenivorans CCT 7137 was isolated from groundwater contaminated with leachate in an old controlled landfill (Sauo Paulo, Brazil), and cultured in GYM medium at different concentrations of sugarcane molasses (2%, 6%, and 10%). The strain growth was analyzed by monitoring the viable cell counts (c.f.u. mL(-1)) and optical density and EPS production was evaluated at the end of the exponential phase and 24 h after it. The analysis of the viable cell counts showed that the medium that most favored bacterial growth was not the one that favored EPS production. The control medium (GYM) was the one that most favored the strain growth, at the maximum specific growth rate of 0.232 h(-1). Differences in bacterial growth when cultured at three different concentrations of molasses were not observed. Production of EPS, in all culture media used, began during the exponential phase and continued during the growth stationary phase. The highest total EPS production, after 24 h of stationary phase, was observed in 6% molasses medium (172.86 g L(-1)) and 10% (139.47 g L(-1)) and the specific total EPS production was higher in 10% molasses medium (39.03 x10(-11)g c.f.u.(-1)). After the exponential phase, in 2%, 6%, and 10% molasses media, a higher percentage of free exopolysaccharides (EPS) was observed, representing 88.4%, 62.4%, and 64.2% of the total, respectively. A different result was observed in pattern medium, which presented EPS made up of higher percentage of capsular EPS (66.4% of the total). This work is the first study on EPS production by G. polyisoprenivorans strain in GYM medium and in medium utilizing sugarcane molasses as the sole nutrient source and suggests its potential use for EPS production by G. polyisoprenivorans CCT 7137 aiming at application in biotechnological processes.

Flora polínica da Reserva do Parque Estadual das Fontes do Ipiranga (São Paulo, Brasil): família: 135-Asclepiadaceae

No presente trabalho, foram estudados os polinários de nove gêneros e 16 espécies de Asclepiadaceae ocorrentes na Reserva do Parque Estadual das Fontes do Ipiranga: Asclepias curassavica L., Blepharodon nitidum (Vell.) J F. Macbr., Ditassa burchellii var. vestita (Malme) Fontella, Ditassa hispida (Vell.) Fontella, Ditassa tomentosa (Decne.) Fontella, Gomphocarpus physocarpus E. Mey., Gonianthela axillaris (Vell.) Fontella & E.A. Schwarz, Matelea glaziovii (E. Fourn.) Morillo, Orthosia urceolata E. Fourn., Oxypetalum appendiculatum Mart., Oxypetalum capitatum subsp. capitatum Mart., Oxypetalum insigne (Decne.) Malme, Oxypetalumpachyglossum Decne., Oxypetalumpedicellatum Decne., Oxypetalum wightianum Hook. & Arn., Tassadia subulata var. subulata (Vell.) Fontella & E.A. Schwarz. São apresentadas descrições e ilustrações para todas as espécies estudadas, bem como chaves para identificação das espécies dos gêneros Ditassa e Oxypetalum tomando como base a morfologia dos polinários.

Morgan Reeves Papers- Accession 249 - M105 (135)

Morgan Reeves (1841-1928) was a Confederate Soldier during the American Civil War in Company I of the 13th South Carolina Regiment. He was also an exchanged prisoner at Camp Lee, near Richmond, VA on March 20, 1865. The Morgan Reeves Papers consist of photocopies of company, hospital, receipt rolls, and a morning report of Company I of the 13th South Carolina Regiment of the Confederate Army. The collection is all photocopies.

A urokinase receptor promoter element (-152/-135) bound with an AP-2-alpha-related protein and SP1 is required for the induction of gene expression by PMA and SRC

The urokinase-type plasminogen activator receptor (u-PAR) promotes extracellular matrix degradation, invasion and metastasis. A first objective of this dissertation was to identify cis-elements and trans-acting factors activating u-PAR gene expression through a previously footprinted (–148/–124) promoter region. Mobility shifting experiments on nuclear extracts of a high u-PAR-expressing colon cancer cell line (RKO) indicated Sp1, Sp3 and a factor similar to, but distinct from, AP-2α bound to an oligonucleotide spanning –152/–135. Mutations preventing the binding of the AP-2α-related factor reduced u-PAR promoter activity. In RKO, the expression of a dominant negative AP-2 (AP-2αB) diminished u-PAR promoter activity, protein and u-PAR mediated laminin degradation. Conversely, u-PAR promoter activity in low u-PAR-expressing GEO cells was increased by AP-2αA expression. PMA treatment, which induces u-PAR expression, caused an increased amount of the AP-2α-related factor-containing complex in GEO, and mutations preventing AP-2α-like and Sp1/Sp3 binding reduced the u-PAR promoter stimulation by PMA. In resected colon cancers, u-PAR protein amounts were related to the amount of the AP-2α-related factor-containing complex. In conclusion, constitutive and PMA- inducible u-PAR gene expression and -proteolysis are mediated partly through transactivation via a promoter sequence (–152/435) bound with an AP-2α-related factor and Sp1/Sp3. ^ A second interest of this dissertation was to determine if a constitutively active Src regulates the transcription of the u-PAR gene, since c-src expression increases invasion in colon cancer. Increased u-PAR protein and laminin degradation paralleling elevated Src activity was evident in SW480 colon cancer cells stably expressing a constitutively active Src (Y- c-src527F). Nuclear run-on experiments indicated that this was due largely to transcriptional activation. While transient transfection of SW480 cells with Y-c-src527F induced a u-PAR-CAT-reporter, mutations preventing Sp1-binding to promoter region –152/435 abolished this induction. Mobility shift assays revealed increased Sp1 binding to region –152/135 with nuclear extracts of Src-transfected SW480 cells. Finally, the amounts of endogenous u-PAR in resected colon cancers significantly correlated with Src-activity. These data suggest that u-PAR gene expression and proteolysis are regulated by Src, this requiring the promoter region (–152/–135) bound with Sp1, thus, demonstrating for the first time that transcription factor Sp1 is a downstream effector of Src. ^