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. 1959 Mar 25;5(2):279–288. doi: 10.1083/jcb.5.2.279

Further Studies on the Lyo and Desmo Components of Several Hydrolytic Enzymes and Their Histochemical Significance

Mark J Hannibal 1, Marvin M Nachlas 1
PMCID: PMC2224658  PMID: 13654449

Abstract

This report describes additional studies of the lyo and desmo components of esterase, alkaline phosphatase, acid phosphatase, leucine aminopeptidase, and β-glucuronidase. The techniques used have already been reported (7). Enzyme diffusion occurs to different degrees in different fixatives, and varies somewhat with each enzyme. Loss of enzymatic activity during fixation occurs as a result of both inactivation due to the chemical reaction of the fixative with the enzymic protein, and diffusion of the lyo component into the fixative. The amount of diffusion into formalin can be reduced by the addition of salts, sucrose, or methocel. The pH of the aqueous medium significantly influences the removal of the lyo fraction from the tissue section. A striking similarity can be noted in the proportions of each fraction of enzyme present in the kidney of the rat, dog, and man. The procedure of fixation and paraffin embedding of tissue blocks does not wholly prevent the diffusion of the lyo component from the tissue sections when they are subsequently immersed in the aqueous incubation medium.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BAKER J. R., FISHMAN W. H. Cellular localization of beta-glucuronidase in rat tissues. J Histochem Cytochem. 1956 Nov;4(6):570–587. doi: 10.1177/4.6.570. [DOI] [PubMed] [Google Scholar]
  2. DEFENDI V., PEARSE A. G. Significance of coupling rate in histochemical azo dye methods for enzymes. J Histochem Cytochem. 1955 May;3(3):203–211. doi: 10.1177/3.3.203. [DOI] [PubMed] [Google Scholar]
  3. HOLT S. J. The value of fundamental studies of staining reactions in enzyme histochemistry, with reference to indoxyl methods for esterases. J Histochem Cytochem. 1956 Nov;4(6):541–554. doi: 10.1177/4.6.541. [DOI] [PubMed] [Google Scholar]
  4. NACHLAS M. M., PRINN W., SELIGMAN A. M. Quantitative estimation of lyo- and desmoenzymes in tissue sections with and without fixation. J Biophys Biochem Cytol. 1956 Sep 25;2(5):487–502. doi: 10.1083/jcb.2.5.487. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. NACHLAS M. M., YOUNG A. C., SELIGMAN A. M. Problems of enzymatic localization by chemical reactions applied to tissue sections. J Histochem Cytochem. 1957 Nov;5(6):565–583. doi: 10.1177/5.6.565. [DOI] [PubMed] [Google Scholar]
  6. RUTENBURG A. M., SELIGMAN A. M. The histochemical demonstration of acid phosphatase by a post-incubation coupling technique. J Histochem Cytochem. 1955 Nov;3(6):455–470. doi: 10.1177/3.6.455. [DOI] [PubMed] [Google Scholar]
  7. SELIGMAN A. M., CHAUNCEY H. H., NACHLAS M. M. Effect of formalin fixation on the activity of five enzymes of rat liver. Stain Technol. 1951 Jan;26(1):19–23. doi: 10.3109/10520295109113172. [DOI] [PubMed] [Google Scholar]
  8. Stafford R. O., Atkinson W. B. Effect of Acetone and Alcohol Fixation and Paraffin Embedding on Activity of Acid and Alkaline Phosphatases in Rat Tissues. Science. 1948 Mar 12;107(2776):279–281. doi: 10.1126/science.107.2776.279. [DOI] [PubMed] [Google Scholar]

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