Activity assessment of microbial fibrinolytic enzymes

Appl Microbiol Biotechnol. 2013 Aug;97(15):6647-65. doi: 10.1007/s00253-013-5052-1. Epub 2013 Jun 29.

Abstract

Conversion of fibrinogen to fibrin inside blood vessels results in thrombosis, leading to myocardial infarction and other cardiovascular diseases. In general, there are four therapy options: surgical operation, intake of antiplatelets, anticoagulants, or fibrinolytic enzymes. Microbial fibrinolytic enzymes have attracted much more attention than typical thrombolytic agents because of the expensive prices and the side effects of the latter. The fibrinolytic enzymes were successively discovered from different microorganisms, the most important among which is the genus Bacillus. Microbial fibrinolytic enzymes, especially those from food-grade microorganisms, have the potential to be developed as functional food additives and drugs to prevent or cure thrombosis and other related diseases. There are several assay methods for these enzymes; this may due to the insolubility of substrate, fibrin. Existing assay methods can be divided into three major groups. The first group consists of assay of fibrinolytic activity with natural proteins as substrates, e.g., fibrin plate methods. The second and third groups of assays are suitable for kinetic studies and are based on the determination of hydrolysis of synthetic peptide esters. This review will deal primarily with the microorganisms that have been reported in literature to produce fibrinolytic enzymes and the first review discussing the methods used to assay the fibrinolytic activity.

Publication types

  • Review

MeSH terms

  • Amino Acid Sequence
  • Bacteria / enzymology
  • Enzymes / chemistry
  • Enzymes / metabolism*
  • Fibrinolysis*
  • Fungi / enzymology
  • Models, Molecular
  • Molecular Sequence Data
  • Seaweed / enzymology

Substances

  • Enzymes