Localization of chitinolytic enzymes in blood of turbot, Scophthalmus maximus, and their possible roles in defence

The intracellular localizations ofchitinase and β‐N‐acetylglucosaminidase were detected in turbot blood smears, using a novel method employing fluorogenic substrates. The two enzymes showed different distributions, with chitinase being more generally distributed and N‐acetylglucosaminidase being str...

Full description

Bibliographic Details
Published in:Journal of Fish Biology
Main Authors: Manson, F. D. C., Fletcher, T. C., Gooday, G. W.
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 1992
Subjects:
Online Access:http://dx.doi.org/10.1111/j.1095-8649.1992.tb02637.x
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1095-8649.1992.tb02637.x
https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1095-8649.1992.tb02637.x
id crwiley:10.1111/j.1095-8649.1992.tb02637.x
record_format openpolar
spelling crwiley:10.1111/j.1095-8649.1992.tb02637.x 2024-06-02T08:14:11+00:00 Localization of chitinolytic enzymes in blood of turbot, Scophthalmus maximus, and their possible roles in defence Manson, F. D. C. Fletcher, T. C. Gooday, G. W. 1992 http://dx.doi.org/10.1111/j.1095-8649.1992.tb02637.x https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1095-8649.1992.tb02637.x https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1095-8649.1992.tb02637.x en eng Wiley http://onlinelibrary.wiley.com/termsAndConditions#vor Journal of Fish Biology volume 40, issue 6, page 919-927 ISSN 0022-1112 1095-8649 journal-article 1992 crwiley https://doi.org/10.1111/j.1095-8649.1992.tb02637.x 2024-05-03T11:28:37Z The intracellular localizations ofchitinase and β‐N‐acetylglucosaminidase were detected in turbot blood smears, using a novel method employing fluorogenic substrates. The two enzymes showed different distributions, with chitinase being more generally distributed and N‐acetylglucosaminidase being strongly associated with distinct intracellular bodies, probably lysosomes. The fluorogenic substrates were used to analyse soluble and membrane fractions of homogenates of red and white blood cells prepared on Percoll gradients. In the leucocytes, the chitinase and N‐acetylglucosaminidase activities were mostly in the soluble fraction. In the erythrocytes the activities were lower, at about one‐hundredth and one‐tenth specific activities, respectively, and were distributed between soluble and membrane‐bound fractions at about 2 : 1 and 3 : 1, respectively. In contrast, lysozyme had a soluble distribution in leucocytes and was not detected in erythrocytes. Plasma was rich in chitinase and lysozyme activities but had no detectable N‐acetylglucosaminidase. Two possible roles for the chitinolytic enzymes are discussed: defence against pathogens and processing of glycoproteins or glucosaminoglycans. Evidence for a defence role for the chitinase and lysozyme is provided by demonstrating that they had inhibitory activity against the chitinous fungus Mucor mucedo . Article in Journal/Newspaper Scophthalmus maximus Turbot Wiley Online Library Journal of Fish Biology 40 6 919 927
institution Open Polar
collection Wiley Online Library
op_collection_id crwiley
language English
description The intracellular localizations ofchitinase and β‐N‐acetylglucosaminidase were detected in turbot blood smears, using a novel method employing fluorogenic substrates. The two enzymes showed different distributions, with chitinase being more generally distributed and N‐acetylglucosaminidase being strongly associated with distinct intracellular bodies, probably lysosomes. The fluorogenic substrates were used to analyse soluble and membrane fractions of homogenates of red and white blood cells prepared on Percoll gradients. In the leucocytes, the chitinase and N‐acetylglucosaminidase activities were mostly in the soluble fraction. In the erythrocytes the activities were lower, at about one‐hundredth and one‐tenth specific activities, respectively, and were distributed between soluble and membrane‐bound fractions at about 2 : 1 and 3 : 1, respectively. In contrast, lysozyme had a soluble distribution in leucocytes and was not detected in erythrocytes. Plasma was rich in chitinase and lysozyme activities but had no detectable N‐acetylglucosaminidase. Two possible roles for the chitinolytic enzymes are discussed: defence against pathogens and processing of glycoproteins or glucosaminoglycans. Evidence for a defence role for the chitinase and lysozyme is provided by demonstrating that they had inhibitory activity against the chitinous fungus Mucor mucedo .
format Article in Journal/Newspaper
author Manson, F. D. C.
Fletcher, T. C.
Gooday, G. W.
spellingShingle Manson, F. D. C.
Fletcher, T. C.
Gooday, G. W.
Localization of chitinolytic enzymes in blood of turbot, Scophthalmus maximus, and their possible roles in defence
author_facet Manson, F. D. C.
Fletcher, T. C.
Gooday, G. W.
author_sort Manson, F. D. C.
title Localization of chitinolytic enzymes in blood of turbot, Scophthalmus maximus, and their possible roles in defence
title_short Localization of chitinolytic enzymes in blood of turbot, Scophthalmus maximus, and their possible roles in defence
title_full Localization of chitinolytic enzymes in blood of turbot, Scophthalmus maximus, and their possible roles in defence
title_fullStr Localization of chitinolytic enzymes in blood of turbot, Scophthalmus maximus, and their possible roles in defence
title_full_unstemmed Localization of chitinolytic enzymes in blood of turbot, Scophthalmus maximus, and their possible roles in defence
title_sort localization of chitinolytic enzymes in blood of turbot, scophthalmus maximus, and their possible roles in defence
publisher Wiley
publishDate 1992
url http://dx.doi.org/10.1111/j.1095-8649.1992.tb02637.x
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1095-8649.1992.tb02637.x
https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1095-8649.1992.tb02637.x
genre Scophthalmus maximus
Turbot
genre_facet Scophthalmus maximus
Turbot
op_source Journal of Fish Biology
volume 40, issue 6, page 919-927
ISSN 0022-1112 1095-8649
op_rights http://onlinelibrary.wiley.com/termsAndConditions#vor
op_doi https://doi.org/10.1111/j.1095-8649.1992.tb02637.x
container_title Journal of Fish Biology
container_volume 40
container_issue 6
container_start_page 919
op_container_end_page 927
_version_ 1800737905764728832