脲酶 来源于刀豆

尿素酶

Urea amidohydrolase

U128713-1g

1g

EnzymoPure™

≥45 units/mg dry weight

Jespersen (1975) reports that ammonium carbamate is produced in citrate and Tris buffer. Urease occurs in many bacteria, several species of yeast and a number of higher plants. Varner (1960) has reviewed it. Two of the best sources are: Jack beans (Canavlia ensiformis) from which it has been crystallized and thoroughly studied, and Bacillus pasteurii. The enzyme is important in assaying for urea. See Guilbault and Montalvo (1970). Its immobilization has been reported: et al. (1974), James and Pring (1975), Messing (1974), Nakamoto et al. (1975), Sundaram (1973) and Tran-Minh and Broun (1975). Characteristics of Urease from Jack Bean: Km: 1.3mM in Tris⋅HCl (Cesareo and Langton, 1992). Specificity Urease is specific for urea and hydroxyurea (Fishbein and Carbone 1965). See also Sundaram and Laidler (1970). Composition Monomeric (a)urease can polymerize to form six unit polymers of about three million daltons. (Fishbein et al. 1970; Fishbein and Nagarajan 1972a). Andrews and Reithel (1970) report on the sulfhydryl groups. Contaxis and Reithel (1971) indicate the molecule can be split in half with no loss of activity. See also Contaxis and Reithel (1972), Fishbein and Nagarajan (1972b), Lynn (1970), and Bailey and Boulter (1969). Optimal pH：7.4 Stabilizers EDTA in concentrations of 1 X 10-3 M. 50% glycerol solutions protect urease crystalline suspension for several months at 4°C. Inhibitors Heavy metals. NH4+ ions formed. See also Fishbein and Carbone (1965). Sodium and potassium ions are inhibitors (Cesareo and Langton, 1992). Urease Assay Method Worthington has adopted an assay method where the hydrolysis of urea is measured by coupling ammonia production to a glutamate dehydrogenase reaction. formulas One unit results in the oxidation of one micromole of NADH per minute at 25°C and pH 7.6 under the specified conditions. In addition to increased sensitivity, the assay method possesses the advantage that it can be manipulated to permit quantitation of urea. Reagents 0.1 M Potassium phosphate buffer, pH 7.6 0.023 M Adenosine-5'-diphosphate (ADP) in phosphate buffer 0.0072 M NADH in phosphate buffer 0.026 M a-Ketoglutarate in phosphate buffer 1.8 M Urea in phosphate buffer Glutamate Dehydrogenase: Dilute to approximately 500 units/ml in 50% glycerol or phosphate buffer. Store cold during use. Enzyme Dissolve enzyme at one mg/ml in 0.1 M phosphate buffer, pH 7.6. Immediately prior to use, dilute further in buffer to obtain a rate of 0.02-0.04 ΔA/minute. Procedure Adjust spectrophotometer to 340 nm and 25°C. Pipette into each cuvette as follows: 0.10 M Phosphate buffer, pH 7.6 2.4 ml

尿素酶催化尿素水解为二氧化碳和氨。尿素酶参与氮代谢和尿素降解。鱼腥草中的尿素酶每个亚基结合 2 个镍离子。