Gotowe bibliografie tematyczne / HXK2 deletion

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Gotowa bibliografia na temat „HXK2 deletion”

Autor: Grafiati
Data publikacji: 3 czerwca 2025
Data aktualizacji: 31 lipca 2025

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Artykuły w czasopismach na temat "HXK2 deletion"

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Petit, Thomas, Jasper A. Diderich, Arthur L. Kruckeberg, Carlos Gancedo, and Karel Van Dam. "Hexokinase Regulates Kinetics of Glucose Transport and Expression of Genes Encoding Hexose Transporters inSaccharomyces cerevisiae." Journal of Bacteriology 182, no. 23 (2000): 6815–18. http://dx.doi.org/10.1128/jb.182.23.6815-6818.2000.

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ABSTRACT Glucose transport kinetics and mRNA levels of different glucose transporters were determined in Saccharomyces cerevisiaestrains expressing different sugar kinases. During exponential growth on glucose, a hxk2 null strain exhibited high-affinity hexose transport associated with an elevated transcription of the genesHXT2 and HXT7, encoding high-affinity transporters, and a diminished expression of the HXT1 andHXT3 genes, encoding low-affinity transporters. Deletion ofHXT7 revealed that the high-affinity component is mostly due to HXT7; however, a previously unidentified very-high-affini
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Diderich, Jasper A., Léonie M. Raamsdonk, Arthur L. Kruckeberg, Jan A. Berden, and Karel Van Dam. "Physiological Properties of Saccharomyces cerevisiae from Which Hexokinase II Has Been Deleted." Applied and Environmental Microbiology 67, no. 4 (2001): 1587–93. http://dx.doi.org/10.1128/aem.67.4.1587-1593.2001.

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ABSTRACT Hexokinase II is an enzyme central to glucose metabolism and glucose repression in the yeast Saccharomyces cerevisiae. Deletion of HXK2, the gene which encodes hexokinase II, dramatically changed the physiology of S. cerevisiae. The hxk2-null mutant strain displayed fully oxidative growth at high glucose concentrations in early exponential batch cultures, resulting in an initial absence of fermentative products such as ethanol, a postponed and shortened diauxic shift, and higher biomass yields. Several intracellular changes were associated with the deletion of hexokinase II. Thehxk2 m
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Miskovic, Ljubisa, Susanne Alff-Tuomala, Keng Cher Soh, et al. "A design–build–test cycle using modeling and experiments reveals interdependencies between upper glycolysis and xylose uptake in recombinant S. cerevisiae and improves predictive capabilities of large-scale kinetic models." Biotechnology for Biofuels 10, no. 1 (2017): 166. https://doi.org/10.1186/s13068-017-0838-5.

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<strong>Background: </strong>Recent advancements in omics measurement technologies have led to an ever-increasing amount of available experimental data that necessitate systems-oriented methodologies for efficient and systematic integration of data into consistent large-scale kinetic models. These models can help us to uncover new insights into cellular physiology and also to assist in the rational design of bioreactor or fermentation processes. Optimization and Risk Analysis of Complex Living Entities (ORACLE) framework for the construction of large-scale kinetic models can be used as guidanc
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Kümmel, Anne, Jennifer Christina Ewald, Sarah-Maria Fendt, et al. "Differential glucose repression in common yeast strains in response to HXK2 deletion." FEMS Yeast Research 10, no. 3 (2010): 322–32. http://dx.doi.org/10.1111/j.1567-1364.2010.00609.x.

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Amigoni, Loredana, Enzo Martegani, and Sonia Colombo. "Lack ofHXK2Induces Localization of Active Ras in Mitochondria and Triggers Apoptosis in the YeastSaccharomyces cerevisiae." Oxidative Medicine and Cellular Longevity 2013 (2013): 1–10. http://dx.doi.org/10.1155/2013/678473.

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We recently showed that activated Ras proteins are localized to the plasma membrane and in the nucleus in wild-type cells growing exponentially on glucose, while in thehxk2Δ strain they accumulated mainly in mitochondria. An aberrant accumulation of activated Ras in these organelles was previously reported and correlated to mitochondrial dysfunction, accumulation of ROS, and cell death. Here we show that addition of acetic acid to wild-type cells results in a rapid recruitment of Ras-GTP from the nucleus and the plasma membrane to the mitochondria, providing a further proof that Ras proteins m
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Herwig, Christoph, and Urs von Stockar. "Quantitative analysis of the oxidative metabolism in HXK2- and REG1-deletion mutants of Saccharomyces cerevisiae." Enzyme and Microbial Technology 31, no. 5 (2002): 698–710. http://dx.doi.org/10.1016/s0141-0229(02)00164-3.

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Herwig, Christoph, Florentina Chetreanu, Peter Niederberger, Ian Marison, and Urs von Stockar. "Quantitative analysis of the impact of HXK2 and REG1 deletion in Saccharomyces cerevisiae on invertase expression and respiration." Enzyme and Microbial Technology 31, no. 4 (2002): 505–15. http://dx.doi.org/10.1016/s0141-0229(02)00145-x.

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Idnurm, Alexander, Steven S. Giles, John R. Perfect, and Joseph Heitman. "Peroxisome Function Regulates Growth on Glucose in the Basidiomycete Fungus Cryptococcus neoformans." Eukaryotic Cell 6, no. 1 (2006): 60–72. http://dx.doi.org/10.1128/ec.00214-06.

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ABSTRACT The function of the peroxisomes was examined in the pathogenic basidiomycete Cryptococcus neoformans. Recent studies reveal the glyoxylate pathway is required for virulence of diverse microbial pathogens of plants and animals. One exception is C. neoformans, in which isocitrate lyase (encoded by ICL1) was previously shown not to be required for virulence, and here this was extended to exclude also a role for malate synthase (encoded by MLS1). The role of peroxisomes, in which the glyoxylate pathway enzymes are localized in many organisms, was examined by mutation of two genes (PEX1 an
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Bae, Yi-Hyun, Dae-Hyuk Kweon, Yong-Cheol Park, and Jin-Ho Seo. "Deletion of the HXK2 gene in Saccharomyces cerevisiae enables mixed sugar fermentation of glucose and galactose in oxygen-limited conditions." Process Biochemistry 49, no. 4 (2014): 547–53. http://dx.doi.org/10.1016/j.procbio.2014.01.030.

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Van de Velde, Sam, and Johan M. Thevelein. "Cyclic AMP-Protein Kinase A and Snf1 Signaling Mechanisms Underlie the Superior Potency of Sucrose for Induction of Filamentation in Saccharomyces cerevisiae." Eukaryotic Cell 7, no. 2 (2007): 286–93. http://dx.doi.org/10.1128/ec.00276-07.

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ABSTRACT Under specific environmental conditions, the yeast Saccharomyces cerevisiae can undergo a morphological switch to a pseudohyphal growth pattern. Pseudohyphal differentiation is generally studied upon induction by nitrogen limitation in the presence of glucose. It is known to be controlled by several signaling pathways, including mitogen-activated protein kinase, cyclic AMP-protein kinase A (cAMP-PKA), and Snf1 kinase pathways. We show that the alpha-glucoside sugars maltose and maltotriose, and especially sucrose, are more potent inducers of filamentation than glucose. Sucrose even in
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