Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: EC:3.2.1.36 (hyaluronidase)
 4,606 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

114 strains of anaerobic and microaerophilic coryneform bacteria from different origins were investigated for production of free extracellular hyaluronidase (hyaluronate glycanohydrolase, EC 3.2.1.36). A quantitative technique was applied measuring the release of N-acetyl-glucosamine groups from purified human potassium hyaluronate. The strains belonged to the following species: Propionibacterium acnes, P. avidum, P. granulosum, P. lymphophilum, the formerly so-called Corynebacterium parvum, P. freudenreichii subsp. freudenreichii and shermanii, P. thoenii, P. acidi-propionici, C. minutissimum, and Arachnia propionica. All together, 59 out of 114 (approximately 51.8%) tested strains showed clearly measurable hyaluronidase activities. P. acnes, the propionibacterium species most frequently found in acne vulgaris lesions, proved to be the most active species tested, 44 out of 64 (approximately 68.8%) P. acnes strains being positive. 5 strains producing hyaluronate glycanohydrolase activities of more than 60 mU/ml in thioglycollate broth cultures could be detected. P. avidum and P. granulosum strains were positive in only 45.0% and 33.3%, respectively, and their mean hyaluronidase activities were significantly lower. Differences in hyaluronidase activities of P. acnes strains isolated from acne vulgaris lesions and strains from normal human skin could not be found. The possible pathogenic role of propionibacteria hyaluronidase in acne vulgaris is discussed.
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PMID:Production of hyaluronidase by propionibacteria from different origins. 4 4

The molecular weight distribution of pMP-derived glycosaminoglycans (GAG), i.e. non-sulfated GAG, chondroitin sulfate (CS), and heparin sulfate (HS)-like material was determined. The peritoneal macrophages (pMP) were harvested from rats normal or stimulated by i.p. injection of thioglycolate, carrageenan or BCG, and maintained in culture. The GAG of cell layer and medium were isolated separately after labeling with 35S-sulfate and 3H-acetate. Treatment with nitrous acid served to remove HS-like material. Labeling with 3H-acetate served to detect synthesis of the high m. w. hyaluronic acid (HA). Gel chromatic separation was done using Sephadex G-200 columns. The maximal size of 35S-labeled GAG, especially HS (36 kDa), was reduced in cultural medium and cell layer after stimulation in vivo. Reduction was most pronounced after application of carrageenan followed by thioglycolate and BCG/LPS stimulation. The extracellular GAG of BCG-stimulated pMP were smallest, probably due to degradation. Heparan sulfate-like material made up a larger proportion in monolayer and medium, comprising the total m.w. range up to 36 kDa. The GAG sensitive to nitrous acid were maximal in cultures of carrageenan-stimulated pMP and minimal in those of thioglycolate-stimulated pMP. This type of HS was sensitive to hyaluronidase, too. Any synthesis of high molecular hyaluronic acid was not found in normal or stimulated rat pMP. Therefore MP-associated HA must be adsorbed from other sources or synthesized by early forms of macrophages.
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PMID:The glycosaminoglycans in cultures of stimulated rat peritoneal macrophages. 2. Gel chromatographic studies and the behaviour of heparan sulfate. 832 74