Quantitative enzymatic production of sialylated galactooligosaccharides with an engineered sialidase from Trypanosoma rangeli

Enzyme and Microbial Technology

Volumn 82, Issue , 2016, Pages 42-50

  Zeuner, Birgitte ^a   Holck, Jesper ^a   Perna, Valentina ^a   Mikkelsen, Jørn Dalgaard ^a   Meyer, Anne S ^a  

^a TECHNICAL UNIVERSITY OF DENMARK   (Denmark)

Author keywords

Enzymatic membrane reactor; Sialylated galactooligosaccharides; Transsialylation; Trypanosoma rangeli

Indexed keywords

BIOREACTORS; CATALYSIS; ENZYMES; MOLECULES; SACCHARIFICATION;

CASEIN GLYCOMACROPEPTIDE; DEGREE OF POLYMERIZATION; ENZYMATIC MEMBRANE REACTORS; ENZYMATIC PRODUCTION; GALACTO-OLIGOSACCHARIDES; HUMAN MILK OLIGOSACCHARIDES; TRANSSIALYLATION; TRYPANOSOMA;

MEMBRANES;

CYCLIC GMP; GALACTOSE OLIGOSACCHARIDE; GLYCOPROTEIN; OLIGOSACCHARIDE; SIALIDASE; BIOPOLYMER; CASEIN; GALACTOSE; GLYCOPEPTIDE; HYBRID PROTEIN; KAPPA-CASEIN GLYCOMACROPEPTIDE; N ACETYLNEURAMINIC ACID; PROTOZOAL PROTEIN;

ARTICLE; CATALYSIS; CHEESE; MEMBRANE REACTOR; MILK; MUTANT; POLYMERIZATION; SIALYLATION; TRYPANOSOMA CRUZI; TRYPANOSOMA RANGELI; AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; BIOCATALYSIS; BIOREACTOR; CHEMISTRY; CONFORMATION; ENZYME SPECIFICITY; ENZYMOLOGY; GENETICS; HYDROLYSIS; ISOLATION AND PURIFICATION; METABOLIC ENGINEERING; METABOLISM; MICROBIOLOGY; MOLECULAR GENETICS; PH; PICHIA; PROCEDURES; PROTEIN STABILITY; SITE DIRECTED MUTAGENESIS; TEMPERATURE;

AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; BIOCATALYSIS; BIOPOLYMERS; BIOREACTORS; CARBOHYDRATE CONFORMATION; CASEINS; GALACTOSE; GLYCOPEPTIDES; HYDROGEN-ION CONCENTRATION; HYDROLYSIS; INDUSTRIAL MICROBIOLOGY; METABOLIC ENGINEERING; MOLECULAR SEQUENCE DATA; MUTAGENESIS, SITE-DIRECTED; N-ACETYLNEURAMINIC ACID; NEURAMINIDASE; OLIGOSACCHARIDES; PICHIA; PROTEIN STABILITY; PROTOZOAN PROTEINS; RECOMBINANT FUSION PROTEINS; SUBSTRATE SPECIFICITY; TEMPERATURE; TRYPANOSOMA RANGELI;

EID: 84962675291     PISSN: 01410229     EISSN: 18790909     Source Type: Journal    
DOI: 10.1016/j.enzmictec.2015.08.010     Document Type: Article

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