Purification and characterization of a low-molecular-weight bovine kidney acid phosphatase
An. acad. bras. ciênc
;
69(4): 451-60, 1997. ilus, tab, graf
Article
in English
| LILACS
| ID: lil-209330
RESUMO
A relative low molecular mass bovine kidney acid phosphatase was purified 1,640-fold to homogeneity, with 7 percent recovery. The purified enzyme (specific activity 100 mumol min-1 mg-1) was electrophoretically homogeneous with a relative molecular massa of 17.8 kDa, as determined by SDS-polyacrylamide gel electrophoresis. A broad pH optimum of 4.0-5.5 and a maximal enzyme activity at 60 degrees Celsius were determined for the p-nitrophenyl phosphate hydrolysis. Apparent Km values of 0.14 mM, 0.4 mM, 0.3 mM and 7.9 mM were obtained, at 37 degrees Celsius and pH 5.0, for the best substrates p-nitrophenyl phosphate, beta-naphtyl-phosphate, flavin mononucleotide and tyrosine-phosphate, respectively. The enzyme activity was enhanced by guanosine but inhibited by ZnCl2 and CuSO4, p-cloromercuribenzoate and ammonium molybdate. Vanadate (Ki 0.47 muM), pyridoxal 5'-phosphate (Ki 2.2 muM), inorganic phosphate (Ki 0.77 mM) are competitive inhibitors. Both glycerol and methanol increased significantly the acide phosphatase activity, acting as good phosphate acceptors in the transphosphorylation reaction.
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Index:
LILACS (Americas)
Main subject:
Acid Phosphatase
/
Kidney
Limits:
Animals
Language:
English
Journal:
An. acad. bras. ciênc
Journal subject:
Science
Year:
1997
Type:
Article
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