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Book ChapterDOI

[53] Collagenolytic protease from fiddler crab (Uca pugilator)

Gregory A. Grant, +2 more
- 01 Jan 1981 - 
- Vol. 80, pp 722-734
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TLDR
The procedure described in the chapter uses the glands from 8000 crabs, received in shipments of 1000 each, to produce approximately 100-150 mg of homogeneous crab protease from the glands of 8000 fiddler crabs.
Abstract
Publisher Summary This chapter presents the procedure for purification and assaying of crab collagenolytic protease. The procedure described in the chapter uses the glands from 8000 crabs, received in shipments of 1000 each. The purification steps are following: preparation of acetone powder; first gel filtration; ion-exchange chromatography; hydroxyapatite chromatography; second gel filtration. This procedure produces approximately 100-150 mg of homogeneous crab protease from the glands of 8000 fiddler crabs. The enzyme is stable for several months in slightly acidic solution (pH -6.0) at –20°C, and can be stored indefinitely as a lyophilized powder. Crab collagenase can be assayed specifically for collagenolytic activity with a standard assay, which quantitates the release of soluble [14C]glycine-containing peptides from native reconstituted guinea pig skin collagen fibrils, or spectrophotometrically by following esterase or amidase activity with synthetic substrates.

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Citations
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Journal ArticleDOI

A gene required for the specification of dorsal-ventral pattern in Drosophila appears to encode a serine protease

TL;DR: The molecular cloning of the gene and analysis of a complementary DNA sequence suggest that the gene encodes a serine protease which is structurally similar to proteases involved in blood clotting, peptide processing, and complement fixation pathways.
Journal ArticleDOI

Characterization of a collagenolytic serine proteinase from the Atlantic cod (gadus morhua)

TL;DR: Calcium binding stabilized the cod collagenase against thermal inactivation, but even in the presence of calcium, the enzyme was unstable at temperatures above 30 degrees C and the pH optimum of the enzymes was between pH 8.0 and 9.0.
Journal ArticleDOI

The midgut chymotrypsins of shrimps (Penaeus monodon, Penaeus japonicus and Penaeus penicillatus).

TL;DR: The results suggest that most Crustacea decapods contain chymotrypsins as one of the major digestive endopeptidases.
Journal ArticleDOI

The isolation and properties of collagenolytic proteases from crab hepatopancreas.

TL;DR: It seems that crab collagenolytic proteases and true metalloenzyme vertebrate and microbial collagenases have certain common structural features particularly in the regions of their substrate binding site.
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Purification, biochemical characterization and N-terminal sequence of a serine-protease with chymotrypsic and collagenolytic activities in a tropical shrimp, penaeus vannamei (crustacea, decapoda)

TL;DR: Two chymotrypsin variants, with collagenolytic activities, were purified from the hepatopancreas of Penaeus vannamei using radioactive protein as the substrate and n-terminal amino acid sequences of both variants are identical and are very close to other known crustacean serine proteases.
References
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Journal ArticleDOI

Role of a Buried Acid Group in the Mechanism of Action of Chymotrypsin

TL;DR: Polarization of the system due to the buried negative charge of the aspartic acid residue would make the serine oxygen strongly nucleophilic and would explain its reactivity towards amides and esters.
Journal ArticleDOI

Human skin collagenase: isolation of precursor and active forms from both fibroblast and organ cultures.

TL;DR: Human skin procollagenase has been isolated, in pure form, from the medium of fibroblasts cultured in the presence or absence of added serum, suggesting that a serum-inhibitable proteolytic system is present in these cultures which, like trypsin, converts procollsagenase to the active enzyme forms that can be isolated from serum-free organ culture medium.
Journal ArticleDOI

Three-dimensional structure of tosyl-elastase.

TL;DR: Amino-acid sequence studies and crystallographic evidence are used to construct an atomic model of elastase, which is compared with the structure of α-chymotrypsin, which shows opposite polarity.
Journal ArticleDOI

Studies on the formation of collagen. I. Properties and fractionation of neutral salt extracts of normal guinea pig connective tissue.

TL;DR: Some properties of cold neutral salt extracts of fresh guinea pig dermis have been described in terms of viscosity, electrophoresis and sedimentation patterns, partial composition, the collagen content, conditions for extraction of collagen, and the effect of certain enzymes.
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