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Fructose 1-Phosphate Is the Preferred Effector of the Metabolic Regulator Cra of Pseudomonas putidaScattering of light by colloidal aluminosilicate particles produces the unusual sky-blue color of Río Celeste (Tenorio volcano complex, Costa Rica)Endogenous stress caused by faulty oxidation reactions fosters evolution of 2,4-dinitrotoluene-degrading bacteriaThe IHF regulon of exponentially growing Pseudomonas putida cells.The interplay of the EIIA(Ntr) component of the nitrogen-related phosphotransferase system (PTS(Ntr)) of Pseudomonas putida with pyruvate dehydrogenase.The Entner-Doudoroff pathway empowers Pseudomonas putida KT2440 with a high tolerance to oxidative stress.Modeling and analysis of flux distributions in the two branches of the phosphotransferase system in Pseudomonas putida.Production of selenium nanoparticles in Pseudomonas putida KT2440.A Metabolic Widget Adjusts the Phosphoenolpyruvate-Dependent Fructose Influx in Pseudomonas putida.From dirt to industrial applications: Pseudomonas putida as a Synthetic Biology chassis for hosting harsh biochemical reactions.Canine Distemper Virus in Wild Felids of Costa Rica.Pristine but metal-rich Río Sucio (Dirty River) is dominated by Gallionella and other iron-sulfur oxidizing microbes.Fructose 1-phosphate is the one and only physiological effector of the Cra (FruR) regulator of Pseudomonas putida.The two paralogue phoN (phosphinothricin acetyl transferase) genes of Pseudomonas putida encode functionally different proteins.Pseudomonas putida KT2440 Strain Metabolizes Glucose through a Cycle Formed by Enzymes of the Entner-Doudoroff, Embden-Meyerhof-Parnas, and Pentose Phosphate PathwaysThe Standard European Vector Architecture (SEVA): a coherent platform for the analysis and deployment of complex prokaryotic phenotypesAccumulation of inorganic polyphosphate enables stress endurance and catalytic vigour in Pseudomonas putida KT2440.Regulatory tasks of the phosphoenolpyruvate-phosphotransferase system of Pseudomonas putida in central carbon metabolism.The metabolic cost of flagellar motion in Pseudomonas putida KT2440.Association of dnt genes of Burkholderia sp. DNT with the substrate-blind regulator DntR draws the evolutionary itinerary of 2,4-dinitrotoluene biodegradation.[Four new compounds from the non-polar extract of the plant Amyris brenesii (Rutaceae) from Costa Rica].A second chromosomal copy of the catA gene endows Pseudomonas putida mt-2 with an enzymatic safety valve for excess of catechol.Interplay of the PtsN (EIIA(Ntr)) protein of Pseudomonas putida with its target sensor kinase KdpD.Cra regulates the cross-talk between the two branches of the phosphoenolpyruvate : phosphotransferase system of Pseudomonas putida.Two new cellulolytic fungal species isolated from a 19th-century art collection.An Electro-optical Device from a Biofilm Structure Created by Bacterial ActivityThe urgent need for microbiology literacy in societyBocaparvovirus, Erythroparvovirus and Tetraparvovirus in New World Primates from Central AmericaThe Bacterial Product Violacein Exerts an Immunostimulatory Effect Via TLR8The imbroglio of the physiological Cra effector clarified at lastArsH protects Pseudomonas putida from oxidative damage caused by exposure to arsenicThermoplasmatales and sulfur-oxidizing bacteria dominate the microbial community at the surface water of a CO2-rich hydrothermal spring located in Tenorio Volcano National Park, Costa RicaPhylogenetic analyses of antibiotic-producing Streptomyces sp. isolates obtained from the stingless-bee Tetragonisca angustula (Apidae: Meliponini)Phenolic variation among Chamaecrista nictitans subspecies and varieties revealed through UPLC-ESI(-)-MS/MS chemical fingerprintingVisualizing the invisible: class excursions to ignite children's enthusiasm for microbes
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P50
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