Academic literature on the topic '2-hydroxyisobutyric acid'

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Journal articles on the topic "2-hydroxyisobutyric acid"

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Rohwerder, Thore, and Roland H. Müller. "Biosynthesis of 2-hydroxyisobutyric acid (2-HIBA) from renewable carbon." Microbial Cell Factories 9, no. 1 (2010): 13. http://dx.doi.org/10.1186/1475-2859-9-13.

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Kikunaga, H., T. Yoshimura, T. Kuribayashi, et al. "Separation of Am(III), Cm(III), and Cf(III) using capillary electrophoresis." Proceedings in Radiochemistry 1, no. 1 (2011): 167–71. http://dx.doi.org/10.1524/rcpr.2011.0031.

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AbstractTrivalent actinides Am(III), Cm(III), and Cf(III) were successfully separated for the first time using capillary electrophoresis in 2-hydroxyisobutyric acid/acetic acid. It was found that the ionic radius was primarily important for separation of trivalent actinides as well as lanthanides in this condition. The stability constants of the Am(III) complexes with 2-hydroxyisobutyrate were estimated using the correlations between the molar fraction ratio of lanthanides and their ionic radii.
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Kim, Sangwon, Jimin Yun, JeongHyun Cho, et al. "Self-catalyzed esterification of 2-hydroxyisobutyric acid: A simple method to produce methyl 2-hydroxyisobutyrate." Molecular Catalysis 532 (November 2022): 112721. http://dx.doi.org/10.1016/j.mcat.2022.112721.

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Mardinoglu, Adil, Silvia Gogg, Luca A. Lotta, et al. "Elevated Plasma Levels of 3-Hydroxyisobutyric Acid Are Associated With Incident Type 2 Diabetes." EBioMedicine 27 (January 2018): 151–55. http://dx.doi.org/10.1016/j.ebiom.2017.12.008.

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Weichler, Maria-Teresa, Nadya Kurteva-Yaneva, Denise Przybylski, et al. "Thermophilic Coenzyme B12-Dependent Acyl Coenzyme A (CoA) Mutase from Kyrpidia tusciae DSM 2912 Preferentially Catalyzes Isomerization of (R)-3-Hydroxybutyryl-CoA and 2-Hydroxyisobutyryl-CoA." Applied and Environmental Microbiology 81, no. 14 (2015): 4564–72. http://dx.doi.org/10.1128/aem.00716-15.

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ABSTRACTThe recent discovery of a coenzyme B12-dependent acyl-coenzyme A (acyl-CoA) mutase isomerizing 3-hydroxybutyryl- and 2-hydroxyisobutyryl-CoA in the mesophilic bacteriumAquincola tertiaricarbonisL108 (N. Yaneva, J. Schuster, F. Schäfer, V. Lede, D. Przybylski, T. Paproth, H. Harms, R. H. Müller, and T. Rohwerder, J Biol Chem 287:15502–15511, 2012,http://dx.doi.org/10.1074/jbc.M111.314690) could pave the way for a complete biosynthesis route to the building block chemical 2-hydroxyisobutyric acid from renewable carbon. However, the enzyme catalyzes only the conversion of the stereoisomer
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Hoefel, Torben, Eva Wittmann, Liv Reinecke, and Dirk Weuster-Botz. "Reaction engineering studies for the production of 2-hydroxyisobutyric acid with recombinant Cupriavidus necator H 16." Applied Microbiology and Biotechnology 88, no. 2 (2010): 477–84. http://dx.doi.org/10.1007/s00253-010-2739-4.

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Deepitha, J., K. C. Pitchaiah, G. Chandrasekhar, and N. Sivaraman. "Solubility studies on 2-hydroxyisobutyric acid in supercritical carbon dioxide: Solubility evaluation and application to actinide extraction." Separation and Purification Technology 283 (January 2022): 120174. http://dx.doi.org/10.1016/j.seppur.2021.120174.

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León, Rosa, Duarte M. F. Prazeres, Francesco Molinari та Joaquim M. S. Cabral. "Microbial Stereoselective Oxidation of 2-methyl-1,3-propanediol to (R)-β-hydroxyisobutyric Acid in Aqueous/organic Biphasic Systems". Biocatalysis and Biotransformation 20, № 3 (2002): 201–7. http://dx.doi.org/10.1080/10242420290020723.

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Zahn, Michael, Nadya Kurteva-Yaneva, Judith Schuster, et al. "Structures of 2-Hydroxyisobutyric Acid-CoA Ligase Reveal Determinants of Substrate Specificity and Describe a Multi-Conformational Catalytic Cycle." Journal of Molecular Biology 431, no. 15 (2019): 2747–61. http://dx.doi.org/10.1016/j.jmb.2019.05.027.

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Leon, R., D. M. F. Prazeres, P. Fernandes, F. Molinari та J. M. S. Cabral. "A Multiphasic Hollow Fiber Reactor for the Whole-Cell Bioconversion of 2-Methyl-1,3-propanediol to (R)-β-Hydroxyisobutyric Acid". Biotechnology Progress 17, № 3 (2001): 468–73. http://dx.doi.org/10.1021/bp010015g.

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Dissertations / Theses on the topic "2-hydroxyisobutyric acid"

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Schuster, Judith Christina. "Analyse funktioneller Gene des Abbaues tertiärer Etherstrukturen in dem Bakterienstamm Aquincola tertiaricarbonis L108 anhand von knock-out Mutanten." Doctoral thesis, Universitätsbibliothek Leipzig, 2014. http://nbn-resolving.de/urn:nbn:de:bsz:15-qucosa-142918.

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The switch to unleaded fuels in the 1970s and the high air pollution in areas of high population density due to traffic particularly since the 1990s required the use of alternative fuel additives to achieve an improvement of the combustion. The utilization of oxygenated hydrocarbons as antiknock additives and so-called oxygenates provided a more complete and efficient combustion with simultaneously less harmful and polluting emissions. These include the synthetic ethers methyl tert-butyl ether (MTBE), ethyl tert-butyl ether (ETBE), tert-amyl methyl ether (TAME) and tert-amyl ethyl ether (TAEE)
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Schuster, Judith Christina. "Analyse funktioneller Gene des Abbaues tertiärer Etherstrukturen in dem Bakterienstamm Aquincola tertiaricarbonis L108 anhand von knock-out Mutanten." Doctoral thesis, Helmholtzzentrum für Umweltforschung GmbH - UFZ, 2013. https://ul.qucosa.de/id/qucosa%3A12452.

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The switch to unleaded fuels in the 1970s and the high air pollution in areas of high population density due to traffic particularly since the 1990s required the use of alternative fuel additives to achieve an improvement of the combustion. The utilization of oxygenated hydrocarbons as antiknock additives and so-called oxygenates provided a more complete and efficient combustion with simultaneously less harmful and polluting emissions. These include the synthetic ethers methyl tert-butyl ether (MTBE), ethyl tert-butyl ether (ETBE), tert-amyl methyl ether (TAME) and tert-amyl ethyl ether (TAEE
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Book chapters on the topic "2-hydroxyisobutyric acid"

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Holowach, L. P., G. W. Swift, S. W. Wolk, and L. Klawiter. "Bacterial Conversion of a Waste Stream Containing Methyl-2-hydroxyisobutyric Acid to Biodegradable Polyhydroxyalkanoate Polymers." In ACS Symposium Series. American Chemical Society, 1994. http://dx.doi.org/10.1021/bk-1994-0575.ch014.

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