| Literature DB >> 30885322 |
Tong-Biao Li1, Feng-Jiao Zhao2, Zhongchuan Liu3, Yun Jin3, Yan Liu3, Xiao-Qiong Pei3, Zhi-Gang Zhang4, Ganggang Wang5, Zhong-Liu Wu6.
Abstract
ChKRED20 is a robust NADH-dependent ketoreductase identified from the genome of Chryseobacterium sp. CA49 that can use 2-propanol as the ultimate reducing agent. The wild-type can reduce over 100 g/l ketones for some pharmaceutical relevant substrates, exhibiting a remarkable potential for industrial application. In this work, to overcome the limitation of ChKRED20 to aryl ketoesters, we first refined the X-ray crystal structure of ChKRED20/NAD+ complex at a resolution of 1.6 Å, and then performed three rounds of iterative saturation mutagenesis at critical amino acid sites to reshape the active cavity of the enzyme. For methyl 2-oxo-2-phenylacetate and ethyl 3-oxo-3-phenylpropanoate, several gain-of-activity mutants were achieved, and for ethyl 2-oxo-4-phenylbutanoate, improved mutants were achieved with kcat/Km increasing to 196-fold of the wild-type. All three substrates were completely reduced at 100 g/l loading catalyzed with selected ChKRED20 mutants, and deliver the corresponding chiral alcohols with >90% isolated yield and 97 - >99%ee.Entities:
Keywords: Bioreduction; Crystal structure; Iterative saturation mutagenesis; Ketoreductase; Short-chain dehydrogenase/reductase
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Year: 2019 PMID: 30885322 DOI: 10.1016/j.enzmictec.2019.03.001
Source DB: PubMed Journal: Enzyme Microb Technol ISSN: 0141-0229 Impact factor: 3.493