Enzymatic properties of a novel highly active and chelator resistant protease from a Pseudomonas aeruginosa PD100

Enzyme and Microbial Technology

Volumn 39, Issue 7, 2006, Pages 1433-1440

  Najafi, Mohsen Fathi ^a   Deobagkar, Dileep N ^b   Mehrvarz, Mohsen ^a   Deobagkar, Deepti D ^b  

^a RAZI VACCINE AND SERUM RESEARCH INSTITUTE   (Iran)

^b UNIVERSITY OF PUNE   (India)

Author keywords

Acid PAGE; Collagen; Disulfide bonds; Inhibitors; P. aeruginosa; Protease

Indexed keywords

COLLAGEN; ENZYME IMMOBILIZATION; IONS; PH EFFECTS; PURIFICATION; SOILS;

ACID-PAGE; DISULFIDE BONDS; INHIBITORS; P. AERUGINOSA; PROTEASE;

ENZYMES;

AMINO ACID; CHELATING AGENT; COLLAGEN; COPPER; CYSTEINE; DETERGENT; ENZYME INHIBITOR; HISTIDINE; MERCAPTOETHANOL; METAL ION; NICKEL; PROTEINASE; SILVER; TRYPTOPHAN;

ARTICLE; BACTERIAL STRAIN; BACTERIUM ISOLATION; DISULFIDE BOND; ENZYME ACTIVITY; ENZYME INACTIVATION; ENZYME PURIFICATION; ENZYME SPECIFICITY; ENZYME STABILITY; ENZYME SUBSTRATE; ENZYME SYNTHESIS; INDIA; MOLECULAR WEIGHT; NONHUMAN; NUCLEOTIDE SEQUENCE; PH; POLYACRYLAMIDE GEL ELECTROPHORESIS; PROTEIN DEGRADATION; PSEUDOMONAS AERUGINOSA; SOIL; TEMPERATURE; THERMOSTABILITY; WASTE;

PSEUDOMONAS AERUGINOSA;

EID: 33748751474     PISSN: 01410229     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.enzmictec.2006.03.031     Document Type: Article

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