Isolation, properties, immunological specificity and localization of mouse testicular hyaluronidase

G. S. Gupta*, E. Goldberg

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

12 Scopus citations


Hyaluronidase (hyaluronate 4-glycanohydrolase, EC was purified from mouse testes by ion-exchange chromatography, Sephadex G-200 filtration and Con A-agarose affinity chromatography. The final preparation had 94-fold purity and 12.2 units spec. act. of the enzyme (unit of specific activity = μmol N-acetylglucosamine released/h per mg protein at 37°C and pH 4.5). Hyaluronidase is relatively heat stable and loses 10-20% of its activity at 50-55°C for 10 min. Ea for heat denaturation of enzyme is 42-45 kcal between 45 and 63°C. The Michaelis constant of mouse testicular hyaluronidase is 1.1 mg/ml hyaluronic acid. Antibodies to the purified enzyme were produced in rabbits and showed a single precipitin line by Ouchterlony gel diffusion. Antiserum to hyaluronidase inhibited enzyme activity by 25%. Immunologically, mouse testicular hyaluronidase is species specific. Tissue extracts of mouse vital organs, except testes and epididymis did not react with the antisera, though nonspecific precipitation occurred between intestinal extracts and anti-hyaluronidase serum. Hyaluronidase was localized in testis sections by indirect immunofluorescence. A specific dark green fluorescence was localized on cell boundaries extending from spermatogonia to spermatids and appeared on the sperm acrosome. Cytoplasm of spermatogonia and spermatocytes showed light green fluorescence, whereas interstitial tissue was devoid of fluorescence.

Original languageEnglish (US)
Pages (from-to)364-373
Number of pages10
JournalBBA - Enzymology
Issue number2
StatePublished - Feb 13 1981


  • Hyaluronidase
  • Immunological specificity (Mouse testis)
  • Localization

ASJC Scopus subject areas

  • General Medicine


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