Enhanced diastereoselective synthesis of t‐Butyl 6‐cyano‐(3R,5R)‐dihydroxyhexanoate by using aldo‐keto reductase and glucose dehydrogenase co‐producing engineered Escherichia coli
Abstract:t-Butyl 6-cyano-(3R,5R)-dihydroxyhexanoate ((3R,5R)-2) is a key chiral diol precursor of atorvastatin calcium (Lipitor®). We have constructed a Kluyveromyces lactis aldo-keto reductase mutant KlAKR-Y295W/W296L (KlAKRm) by rational design in previous research, which displayed high activity and excellent diastereoselectivity (de > 99.5%) toward t-butyl 6-cyano-(5R)-hydroxy-3-oxohexanoate ((5R)-1). To realize in situ cofactor regeneration, a robust KlAKRm and Exiguobacterium sibiricum glucose dehydrogenase (EsGDH… Show more
“…65 In contrast, co-expression of the KlAKR-Y295W/W296L variant, derived from site-saturation mutagenesis, in E. coli BL21 (DE3) together with Exiguobacterium sibiricum glucose dehydrogenase (EsGDH), enabled the formation of 2 in 243 kg m −3 . 66 Immobilisation of reconstructed E. coli BL21 cells in Celite-polyethyleneimine (PEI)-glutaraldehyde improved the stability of the biocatalyst which could be reused 7 times giving a total of 17.5 g 2 per gram in d e p > 99.5%. 43 Zheng and Wang and coworkers used a variant of the Km AKR from Kluyveromyces marxianus , obtained following multiple rounds of directed evolution, for the efficient asymmetric reduction of 1 .…”
Section: Scope In the Enantioselective Synthesis Of Chiral Alcoholsmentioning
The use of engineered ketoreductases (KREDS), both as whole microbial cells and isolated enzymes, in the highly enantiospecific reduction of prochiral ketones is reviewed. The homochiral alcohol products are key...
“…65 In contrast, co-expression of the KlAKR-Y295W/W296L variant, derived from site-saturation mutagenesis, in E. coli BL21 (DE3) together with Exiguobacterium sibiricum glucose dehydrogenase (EsGDH), enabled the formation of 2 in 243 kg m −3 . 66 Immobilisation of reconstructed E. coli BL21 cells in Celite-polyethyleneimine (PEI)-glutaraldehyde improved the stability of the biocatalyst which could be reused 7 times giving a total of 17.5 g 2 per gram in d e p > 99.5%. 43 Zheng and Wang and coworkers used a variant of the Km AKR from Kluyveromyces marxianus , obtained following multiple rounds of directed evolution, for the efficient asymmetric reduction of 1 .…”
Section: Scope In the Enantioselective Synthesis Of Chiral Alcoholsmentioning
The use of engineered ketoreductases (KREDS), both as whole microbial cells and isolated enzymes, in the highly enantiospecific reduction of prochiral ketones is reviewed. The homochiral alcohol products are key...
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