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A novel phospholipase C inhibitor, S-PLI produced by Streptomyces sp. strain no. A-6288.
- Source :
-
Journal of enzyme inhibition [J Enzyme Inhib] 1996; Vol. 10 (3), pp. 177-86. - Publication Year :
- 1996
-
Abstract
- S-PLI, an inhibitor of phospholipase C (PLC) produced by Streptomyces sp. strain No. 6288, was purified from the culture filtrate by salting-out with solid ammonium sulfate, column chromatography on CM-cellulose and gel filtration on Sephadex G-75. The molecular weight of S-PLI was estimated to be 65,000 by SDS-polyacrylamide gel electrophoresis. The inhibitor was found to be a glycoprotein with a composition of 609 amino acids and 19 glucose residues having an isoelectric point at 7.8. S-PLI was stable from pH 3 to 10 at 37 degrees C and up to 40 degrees at pH 6.0. The inhibitory activity showed pH- and temperature-dependence with a maximum around pH 7.0 at 50 degrees C. S-PLI inhibited phospholipase C in a competitive manner (Ki value; 9.5 x 10(-6) mM), but did not inhibit S-Hemolysin, phospholipase A2; phospholipase B, phospholipase D and phosphatases. S-PLI is the first reported example of a glycoproteinaceous inhibitor of microbial origin which is able to specifically inhibit phospholipase C.
- Subjects :
- Amino Acids analysis
Culture Media chemistry
Culture Media pharmacology
Electrophoresis, Polyacrylamide Gel
Enzyme Inhibitors isolation & purification
Enzyme Stability
Fungal Proteins isolation & purification
Glucose analysis
Hydrogen-Ion Concentration
Hydrolases antagonists & inhibitors
Hydrolases drug effects
Isoelectric Point
Kinetics
Molecular Weight
Phosphatidylcholines metabolism
Sphingomyelins metabolism
Temperature
Type C Phospholipases metabolism
Enzyme Inhibitors pharmacology
Fungal Proteins pharmacology
Streptomyces chemistry
Type C Phospholipases antagonists & inhibitors
Subjects
Details
- Language :
- English
- ISSN :
- 8755-5093
- Volume :
- 10
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Journal of enzyme inhibition
- Publication Type :
- Academic Journal
- Accession number :
- 8835943
- Full Text :
- https://doi.org/10.3109/14756369609030311