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000917508 1001_ $$0P:(DE-Juel1)174185$$aSehl, Torsten$$b0$$eCorresponding author
000917508 245__ $$aEnzymatic (2 R ,4 R )‐Pentanediol Synthesis – “Putting a Bottle on the Table”
000917508 260__ $$aWeinheim$$bWiley-VCH Verl.$$c2023
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000917508 520__ $$a(2R,4R)-Pentanediol is an interesting precursor for the synthesis of chiral ligands. A ketoreductase (KRED) was employed for the asymmetric reduction of acetylacetone to this diol. Biocatalysis often suffers from low concentrations of hydrophobic substrates and low stability of the enzyme in unconventional media. Here, we present an engineered KRED variant applicable in a neat substrate system, including upscaling to the multi-liter scale and downstream processing (DSP). Our engineered KRED applied in a neat substrate system is a powerful technique for the synthesis of chiral diols yielding product concentrations of 208 g L−1.
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000917508 7001_ $$0P:(DE-Juel1)188344$$aSeibt, Lisa$$b1$$ufzj
000917508 7001_ $$0P:(DE-Juel1)179370$$aKappauf, Katrin$$b2
000917508 7001_ $$0P:(DE-HGF)0$$aErgezinger, Pia$$b3
000917508 7001_ $$0P:(DE-Juel1)178052$$aSpöring, Jan-Dirk$$b4
000917508 7001_ $$0P:(DE-HGF)0$$aMielke, Kristina$$b5
000917508 7001_ $$aDoeker, Moritz$$b6
000917508 7001_ $$0P:(DE-HGF)0$$aVerma, Neha$$b7
000917508 7001_ $$0P:(DE-HGF)0$$aBocola, Marco$$b8
000917508 7001_ $$0P:(DE-HGF)0$$aDaußmann, Thomas$$b9
000917508 7001_ $$00000-0003-2589-7347$$aChen, Haibin$$b10
000917508 7001_ $$0P:(DE-HGF)0$$aShi, Shumin$$b11
000917508 7001_ $$0P:(DE-Juel1)194474$$aJupke, Andreas$$b12
000917508 7001_ $$0P:(DE-Juel1)144643$$aRother, Dörte$$b13$$eCorresponding author
000917508 773__ $$0PERI:(DE-600)2035041-7$$a10.1002/cite.202200178$$gp. cite.202200178$$n4$$p557-564$$tChemie - Ingenieur - Technik$$v95$$x0009-286X$$y2023
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