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Palabras clave – provistas por la editorial

E. coli; recombinant horseradish peroxidase; site-directed mutagenesis; periplasm; glycosylation sites; Aspergillus niger; quercetin; rutin; rutinose; rutinosidase; “solid-state biocatalysis”; hyaluronic acid; in vitro synthesis; one-pot multi-enzyme; optimization; enzyme cascade; Basidiomycota; Agaricomycotina; nitrilase; cyanide hydratase; nitrile; substrate specificity; overproduction; homology modeling; substrate docking; phylogenetic distribution; indigo; MISO library; flavin; monooxygenase; FMO; β-N-acetylhexosaminidases; transglycosylation; Glide docking; Talaromyces flavus; muramic acid; non-reducing carbohydrate; glucose oxidase; direct electron transfer; amine-reactive phenazine ethosulfate; glucose sensor; glycemic level monitoring; Pseudomonas putida MnB1; biogenic manganese oxides; abiotic manganese oxides; α-Hydroxy-β-keto esters; whole-cell biocatalysis; surface display; cell wall anchor; Lactobacillus plantarum; whole-cell biocatalyst; n/a; Fe(II)/2-ketoglutarate-dependent dioxygenase; 2-ketoglutarate generation; regio- and stereo-selective synthesis; hydroxy amino acids; sequential cascade reaction