Efficient Nε-lauroyl-l-lysine production by recombinant ε-lysine acylase from Streptomyces mobaraensis

Journal of Biotechnology

Volumn 141, Issue 3-4, 2009, Pages 160-165

  Koreishi, Mayuko ^a   Kawasaki, Ryoko ^a   Imanaka, Hiroyuki ^a   Imamura, Koreyoshi ^a   Takakura, Yasuaki ^b   Nakanishi, Kazuhiro ^a  

^a OKAYAMA UNIVERSITY   (Japan)

^b AJINOMOTO CO INC   (Japan)

Author keywords

Lysine acylase; Actinomycete; N Lauroyl l lysine; Streptomyces mobaraensis

Indexed keywords

ACTINOMYCETE; AMIDE BONDS; AMIDOHYDROLASE; AMINO ACID PROTEINS; AQUEOUS BUFFER SOLUTIONS; CELL-FREE EXTRACTS; CULTURE SUPERNATANT; HYDROLASE; L-LYSINE HYDROCHLORIDES; L-LYSINE PRODUCTIONS; LAURIC ACIDS; OPEN READING FRAMES; SPECIFIC ACTIVITIES; STREPTOMYCES LIVIDANS; STREPTOMYCES MOBARAENSIS; WILD TYPES;

AMIDES; AMINES; CELL CULTURE; METAL REFINING; ORGANIC ACIDS; PURIFICATION;

AMINO ACIDS;

AMIDASE; AMINO ACID; BACTERIAL ENZYME; BUFFER; CELL EXTRACT; CHLORIDE; EPSILON LYSINE ACYLASE; HYDROLASE; LAURIC ACID; LYSINE DERIVATIVE; N EPSILON LAUROYL LYSINE; RECOMBINANT ENZYME; UNCLASSIFIED DRUG; DRUG DERIVATIVE; LAURIC ACID DERIVATIVE; LYSINE; RECOMBINANT PROTEIN;

AMINO ACID SEQUENCE; AMINO ACID SYNTHESIS; ARTICLE; BACTERIAL CELL; BACTERIAL GENE; CATALYSIS; CELL CULTURE; CHEMICAL BOND; CONTROLLED STUDY; ENZYME ACTIVITY; ENZYME ANALYSIS; ENZYME MECHANISM; ENZYME PURIFICATION; EXPRESSION VECTOR; GENE SEQUENCE; GENE VECTOR; HYDROLYSIS; MOLECULAR CLONING; MOLECULAR WEIGHT; NONHUMAN; NUCLEOTIDE SEQUENCE; OPEN READING FRAME; PRIORITY JOURNAL; PROTEIN INTERACTION; STREPTOMYCES; STREPTOMYCES LIVIDANS; STREPTOMYCES MOBARAENSIS; SUPERNATANT; WILD TYPE; CELL FREE SYSTEM; ENZYMOLOGY; ESCHERICHIA COLI; GENETICS; METABOLISM; MOLECULAR GENETICS; SEQUENCE ALIGNMENT;

STREPTOMYCES LIVIDANS; STREPTOMYCES MOBARAENSIS;

AMIDOHYDROLASES; AMINO ACID SEQUENCE; CELL-FREE SYSTEM; CLONING, MOLECULAR; ESCHERICHIA COLI; LAURIC ACIDS; LYSINE; MOLECULAR SEQUENCE DATA; RECOMBINANT PROTEINS; SEQUENCE ALIGNMENT; STREPTOMYCES; STREPTOMYCES LIVIDANS;

EID: 67349231972     PISSN: 01681656     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jbiotec.2009.03.008     Document Type: Article

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