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@ARTICLE{Sehl:917508,
author = {Sehl, Torsten and Seibt, Lisa and Kappauf, Katrin and
Ergezinger, Pia and Spöring, Jan-Dirk and Mielke, Kristina
and Doeker, Moritz and Verma, Neha and Bocola, Marco and
Daußmann, Thomas and Chen, Haibin and Shi, Shumin and
Jupke, Andreas and Rother, Dörte},
title = {{E}nzymatic (2 {R} ,4 {R} )‐{P}entanediol {S}ynthesis –
“{P}utting a {B}ottle on the {T}able”},
journal = {Chemie - Ingenieur - Technik},
volume = {95},
number = {4},
issn = {0009-286X},
address = {Weinheim},
publisher = {Wiley-VCH Verl.},
reportid = {FZJ-2023-00721},
pages = {557-564},
year = {2023},
abstract = {(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.},
cin = {IBG-1},
ddc = {660},
cid = {I:(DE-Juel1)IBG-1-20101118},
pnm = {2172 - Utilization of renewable carbon and energy sources
and engineering of ecosystem functions (POF4-217)},
pid = {G:(DE-HGF)POF4-2172},
typ = {PUB:(DE-HGF)16},
UT = {WOS:000914001400001},
doi = {10.1002/cite.202200178},
url = {https://juser.fz-juelich.de/record/917508},
}