Year |
Citation |
Score |
2019 |
Engleder M, Müller M, Kaluzna I, Mink D, Schürmann M, Leitner E, Pichler H, Emmerstorfer-Augustin A. Exploring Linalool (De)hydratase-Isomerase for Enzymatic Hydration of Alkenes. Molecules (Basel, Switzerland). 24. PMID 31159367 DOI: 10.3390/Molecules24112092 |
0.412 |
|
2018 |
Engleder M, Horvat M, Emmerstorfer-Augustin A, Wriessnegger T, Gabriel S, Strohmeier G, Weber H, Müller M, Kaluzna I, Mink D, Schürmann M, Pichler H. Recombinant expression, purification and biochemical characterization of kievitone hydratase from Nectria haematococca. Plos One. 13: e0192653. PMID 29420618 DOI: 10.1371/Journal.Pone.0192653 |
0.375 |
|
2016 |
Brummund J, Müller M, Schmitges T, Kaluzna I, Mink D, Hilterhaus L, Liese A. Process development for oxidations of hydrophobic compounds applying cytochrome P450 monooxygenases in-vitro. Journal of Biotechnology. 233: 143-150. PMID 27396939 DOI: 10.1016/J.Jbiotec.2016.07.002 |
0.354 |
|
2016 |
Duan Y, Ba L, Gao J, Gao X, Zhu D, de Jong RM, Mink D, Kaluzna I, Lin Z. Semi-rational engineering of cytochrome CYP153A from Marinobacter aquaeolei for improved ω-hydroxylation activity towards oleic acid. Applied Microbiology and Biotechnology. PMID 27234138 DOI: 10.1007/S00253-016-7634-1 |
0.332 |
|
2016 |
Wriessnegger T, Moser S, Emmerstorfer-Augustin A, Leitner E, Müller M, Kaluzna I, Schürmann M, Mink D, Pichler H. Enhancing cytochrome P450-mediated conversions in P. pastoris through RAD52 over-expression and optimizing the cultivation conditions. Fungal Genetics and Biology : Fg & B. PMID 26898115 DOI: 10.1016/J.Fgb.2016.02.004 |
0.361 |
|
2015 |
Engleder M, Pavkov-Keller T, Emmerstorfer A, Hromic A, Schrempf S, Steinkellner G, Wriessnegger T, Leitner E, Strohmeier GA, Kaluzna I, Mink D, Schürmann M, Wallner S, Macheroux P, Gruber K, et al. Structure-Based Mechanism of Oleate Hydratase from Elizabethkingia meningoseptica. Chembiochem : a European Journal of Chemical Biology. 16: 1730-4. PMID 26077980 DOI: 10.1002/Cbic.201500269 |
0.37 |
|
2015 |
Emmerstorfer A, Wimmer-Teubenbacher M, Wriessnegger T, Leitner E, Müller M, Kaluzna I, Schürmann M, Mink D, Zellnig G, Schwab H, Pichler H. Over-expression of ICE2 stabilizes cytochrome P450 reductase in Saccharomyces cerevisiae and Pichia pastoris. Biotechnology Journal. 10: 623-35. PMID 25641738 DOI: 10.1002/Biot.201400780 |
0.354 |
|
2014 |
Wriessnegger T, Augustin P, Engleder M, Leitner E, Müller M, Kaluzna I, Schürmann M, Mink D, Zellnig G, Schwab H, Pichler H. Production of the sesquiterpenoid (+)-nootkatone by metabolic engineering of Pichia pastoris. Metabolic Engineering. 24: 18-29. PMID 24747046 DOI: 10.1016/J.Ymben.2014.04.001 |
0.347 |
|
2011 |
Magnus NA, Coffey DS, Debaillie AC, Jones CD, Kaluzna IA, Kambourakis S, Pu YJ, Wang L, Wepsiec JP. Diarylketone ketoreductase screen and synthesis demonstration to access mglu2 receptor potentiators Organic Process Research and Development. 15: 1377-1381. DOI: 10.1021/Op2002479 |
0.391 |
|
2007 |
Padhi SK, Kaluzna IA, Buisson D, Azerad R, Stewart JD. Reductions of cyclic β-keto esters by individual Saccharomyces cerevisiae dehydrogenases and a chemo-enzymatic route to (1R,2S)-2-methyl-1-cyclohexanol Tetrahedron Asymmetry. 18: 2133-2138. DOI: 10.1016/J.Tetasy.2007.08.010 |
0.621 |
|
2006 |
Kaluzna IA, Rozzell JD, Kambourakis S. Corrigendum to "Ketoreductases: stereoselective catalysts for the facile synthesis of chiral alcohols". [Tetrahedron: Asymmetry 16 (2005) 3682] (DOI:10.1016/j.tetasy.2005.10.002) Tetrahedron Asymmetry. 17: 2722. DOI: 10.1016/J.Tetasy.2006.10.003 |
0.377 |
|
2005 |
Feske BD, Kaluzna IA, Stewart JD. Enantiodivergent, biocatalytic routes to both taxol side chain antipodes. The Journal of Organic Chemistry. 70: 9654-7. PMID 16268655 DOI: 10.1021/Jo0516077 |
0.62 |
|
2005 |
Kaluzna IA, Feske BD, Wittayanan W, Ghiviriga I, Stewart JD. Stereoselective, biocatalytic reductions of alpha-chloro-beta-keto esters. The Journal of Organic Chemistry. 70: 342-5. PMID 15624945 DOI: 10.1021/Jo0484981 |
0.624 |
|
2005 |
Kaluzna IA, David Rozzell J, Kambourakis S. Ketoreductases: Stereoselective catalysts for the facile synthesis of chiral alcohols Tetrahedron Asymmetry. 16: 3682-3689. DOI: 10.1016/J.Tetasy.2005.10.002 |
0.497 |
|
2004 |
Kaluzna IA, Matsuda T, Sewell AK, Stewart JD. Systematic investigation of Saccharomyces cerevisiae enzymes catalyzing carbonyl reductions. Journal of the American Chemical Society. 126: 12827-32. PMID 15469278 DOI: 10.1021/Ja0469479 |
0.689 |
|
2004 |
Wolberg M, Kaluzna IA, Müller M, Stewart JD. Regio and enantioselective reduction of t-butyl 6-chloro-3,5-dioxohexanoate with baker's yeast Tetrahedron Asymmetry. 15: 2825-2828. DOI: 10.1016/J.Tetasy.2004.07.045 |
0.631 |
|
2002 |
Kaluzna I, Andrew AA, Bonilla M, Martzen MR, Stewart JD. Enantioselective reductions of ethyl 2-oxo-4-phenylbutyrate by Saccharomyces cerevisiae dehydrogenases Journal of Molecular Catalysis - B Enzymatic. 17: 101-105. DOI: 10.1016/S1381-1177(02)00006-1 |
0.633 |
|
Show low-probability matches. |