Cloning, expression, characterization, and high cell-density production of recombinant endo-1,4-β-xylanase from Aspergillus niger in Pichia pastoris

Enzyme and Microbial Technology

Volumn 41, Issue 1-2, 2007, Pages 19-25

  Ruanglek, Vasimon ^a   Sriprang, Rutchadaporn ^a   Ratanaphan, Nakul ^a   Tirawongsaroj, Pacawadee ^b   Chantasigh, Duriya ^a   Tanapongpipat, Sutipa ^a   Pootanakit, Kusol ^b   Eurwilaichitr, Lily ^a  

^a NATIONAL SCIENCE AND TECHNOLOGY DEVELOPMENT AGENCY   (Thailand)

^b MAHIDOL UNIVERSITY   (Thailand)

Author keywords

Aspergillus niger; Fed batch; In vitro digestibility; Pichia pastoris; Productivity; Xylanase

Indexed keywords

CLONING; FOOD ADDITIVES; FUNGI; PH EFFECTS; PRODUCTIVITY;

IN VITRO DIGESTIBILITY; PICHIA PASTORIS; RECOMBINANT ENZYME; XYLANASE;

ENZYME ACTIVITY;

DRUG ADDITIVE; ENDO 1,4 BETA XYLANASE; METHANOL;

ARTICLE; ASPERGILLUS NIGER; CELL DENSITY; CULTURE MEDIUM; DRY WEIGHT; ENZYME KINETICS; ENZYME SYNTHESIS; FED BATCH CULTURE; FEEDING; GENETIC CODE; IN VITRO STUDY; MOLECULAR CLONING; MOLECULAR WEIGHT; NONHUMAN; PH MEASUREMENT; PICHIA PASTORIS; PROTEIN EXPRESSION; RECOMBINANT GENE; RICE BRAN; SOYBEAN; TEMPERATURE DEPENDENCE;

ANIMALIA; ASPERGILLUS NIGER; GLYCINE MAX; PICHIA PASTORIS;

EID: 34248385655     PISSN: 01410229     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.enzmictec.2006.11.019     Document Type: Article

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