Structural insights into alcohol dehydrogenases catalyzing asymmetric reductions

J An, Y Nie, Y Xu - Critical reviews in biotechnology, 2019 - Taylor & Francis
Alcohol dehydrogenases are a group of oxidoreductases that specifically use NAD (P)+ or
NAD (P) H as cofactors for electron acceptance or donation and catalyze interconversion …

Artificial Multienzyme Scaffolds: Pursuing in Vitro Substrate Channeling with an Overview of Current Progress

GA Ellis, WP Klein, G Lasarte-Aragones, M Thakur… - ACS …, 2019 - ACS Publications
Artificial multienzyme scaffolds are being developed for in vitro cascaded biocatalytic activity
and, in particular, accessing substrate channeling. This review covers progress in this field …

Self-assembling protein scaffold system for easy in vitro coimmobilization of biocatalytic cascade enzymes

G Zhang, MB Quin, C Schmidt-Dannert - Acs Catalysis, 2018 - ACS Publications
Biocatalytic cascades represent an attractive approach for the synthesis of valuable
chemicals. To be competitive with chemical synthesis, cascade reactions need to be …

Developing a protein scaffolding system for rapid enzyme immobilization and optimization of enzyme functions for biocatalysis

G Zhang, T Johnston, MB Quin… - ACS Synthetic …, 2019 - ACS Publications
Immobilization of enzymes is required for most biocatalytic processes, but chemistries used
in enzyme immobilization are limited and can be challenging. Genetically encoded protein …

Structure-based mechanisms: On the way to apply alcohol dehydrogenases/reductases to organic-aqueous systems

Y Li, R Zhang, Y Xu - International Journal of Biological Macromolecules, 2021 - Elsevier
Alcohol dehydrogenases/reductases catalyze enantioselective syntheses of versatile chiral
compounds relying on direct hydride transfer from cofactor to substrates, or to an …

Enantiodivergent biosynthesis of β-hydroxy esters by self-sufficient heterogeneous biocatalysts in a continuous flow

D Andrés-Sanz, A Maiz-Iginitz, JM Bolivar… - Green …, 2024 - pubs.rsc.org
β-Hydroxy esters are essential building blocks utilised by the pharmaceutical and food
industries in the synthesis of functional products. The asymmetric reduction of β-keto esters …

Establishing biosynthetic pathway for the production of p-hydroxyacetophenone and its glucoside in Escherichia coli

L Lu, X Wang, L Zhou, Q Liu, G Zhang, B Xue, C Hu… - Metabolic …, 2023 - Elsevier
Abstract p-Hydroxyacetophenone (p-HAP) and its glucoside picein are plant-derived natural
products that have been extensively used in chemical, pharmaceutical and cosmetic …

ANN Architecture Specifications for Modelling of Open‐Cell Aluminum under Compression

M Dudzik, AM Stręk - Mathematical Problems in Engineering, 2020 - Wiley Online Library
The knowledge on strength properties of porous metals in compression is essential in
tailored application design, as well as in elaboration of general material models. In this …

Biocatalytic asymmetric reduction of γ‐keto esters to access optically active γ‐Aryl‐γ‐butyrolactones

P Borowiecki, N Telatycka, M Tataruch… - Advanced Synthesis …, 2020 - Wiley Online Library
An efficient stereoselective syntheses of a series of functionalized optically active γ‐aryl‐γ‐
butyrolactones is achieved by enzymatic asymmetric reduction of the corresponding …

Extreme halophilic alcohol dehydrogenase mediated highly efficient syntheses of enantiopure aromatic alcohols

D Alsafadi, S Alsalman, F Paradisi - Organic & Biomolecular Chemistry, 2017 - pubs.rsc.org
Enzymatic synthesis of enantiopure aromatic secondary alcohols (including substituted,
hetero-aromatic and bicyclic structures) was carried out using halophilic alcohol …