GB804608A - Proteolytic enzyme - Google Patents
Proteolytic enzymeInfo
- Publication number
- GB804608A GB804608A GB28364/55A GB2836455A GB804608A GB 804608 A GB804608 A GB 804608A GB 28364/55 A GB28364/55 A GB 28364/55A GB 2836455 A GB2836455 A GB 2836455A GB 804608 A GB804608 A GB 804608A
- Authority
- GB
- United Kingdom
- Prior art keywords
- enzyme
- acetone
- specified
- sources
- aqueous
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/14—Hydrolases (3)
- C12N9/48—Hydrolases (3) acting on peptide bonds (3.4)
- C12N9/50—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25)
- C12N9/58—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from fungi
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Genetics & Genomics (AREA)
- Organic Chemistry (AREA)
- Zoology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Wood Science & Technology (AREA)
- Molecular Biology (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Biomedical Technology (AREA)
- Medicinal Chemistry (AREA)
- Biochemistry (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Mycology (AREA)
- Food Preservation Except Freezing, Refrigeration, And Drying (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
A proteolytic enzyme, which is an amorphous powder having a molecular weight of 30,000, an isoelectric point of 10.2, a sedimentation constant of 2.5 X 10-13, a diffusion constant of 8.2 X 10-7, an electrophoretic mobility of 0.08 X 10-5 in glycine buffer of pH 10.5 and of 0.43 X 10-5 in barbitol buffer of pH 8.5, optional proteolytic activity at pH 9.0 measured against casein, which is stable over pH 4.0 to 11.0 and gives a positive precipitin reaction against a 1 in 1000 dilution of specific rabbit antiserum, is produced by fermenting a fungus of the order Entomophthorales, family Entomophthoraceae in an aqueous nutrient medium containing assimilable sources of carbon and nitrogen and preferably inorganic salts. The fungi are of the genera Entomophthora, Bacidiobolus, Conidiobolus, Completoria, Massaspora and Ancyclistes. Species specified are E. apiculata, E. coronata, E. sphaerosperma, B. ranarum, C. villosus and C. brefeldianus. Sources of carbon for the nutrient medium are pentoses such as arabinose, ribose and xylose, monosaccharides such as mannose, levulose and galactose, disaccharides such as trehalose, maltose, lactose, cellibiose and sucrose, polysaccharides such as starch, and alcohols such as glycerol, mannitol, sorbitol, inositol and ethyl alcohol. Nitrogen sources are animal or vegetable proteins, soybean meal, casein, peptones, polypeptides, amino acids, animal stick liquor, sodium nitrate, asparagine urea, histidine and guanine. Inorganic salts are phosphates, sulphates and chlorides of alkali and alkaline earth metals and trace metals, e.g. cobalt, iron, magnesium and manganese. The medium is adjusted to pH 5.0 to 9.0 and preferably 6.0 to 8.0, the temperature of cultivation is 20 to 30 and especially 25 to 30 DEG C. and the duration is 24 to 90 hours especially 48 to 90 hours. Anti-foaming agents such as olein and brominated castor oil may be present. The enzyme is recovered from the filtered or unfiltered broth by adsorption at pH 6.5 to 8.5. Specified adsorbents are diatomaceous earths, magnesium silicates, fuller's earth, activated charcoal, lamp black, titanium oxide, alumina silica catalyst and zeolites such as "Permutit" (Registered Trade Mark). Elution is by dilute aqueous mineral acid such as hydrochloric or sulphuric at pH 9.0 to 11.5 especially 10.5, preferably in the presence of sodium chloride. For stability the pH is then adjusted to 6.0 to 8.0 and may be used as such in dry cleaning, hide bating or desizing cloth. For pharmaceutical use, bread-baking and baby foods it is further purified by adding acetone to an aqueous solution. The final product may be (a) dissolved in 1 per cent aqueous sodium chloride, lyophilized, (c) dried by suspension in an anhydrous water-miscible solvent such as acetone, (d) mixed with protecting and/or bulking agents. Specified protecting agents are sorbitol, corn syrup, lactose, dextrose, gelatin and gum acacia. The bulking agents may be starch, wood pulp, magnesium silicate and diatomaceous earth. For use in leather manufacture, the enzyme may be precipitated from the fermentation beer with a protein precipitant such as tannic acid, phosphotungstic acid, zinc chloride and ferric chloride. A protective agent may be added. The tannic acid precipitate may be slurred in water and treated with a watermiscible solvent such as acetone or methyl, ethyl, propyl or butyl alcohols in order to precipitate the enzyme.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US804608XA | 1954-10-25 | 1954-10-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB804608A true GB804608A (en) | 1958-11-19 |
Family
ID=22157527
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB28364/55A Expired GB804608A (en) | 1954-10-25 | 1955-10-05 | Proteolytic enzyme |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB804608A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1403274A1 (en) * | 2002-09-30 | 2004-03-31 | Meristem Therapeutics | Process for the purification of recombinant proteins from complex media and purified proteins obtained thereby |
WO2011104630A1 (en) * | 2010-02-26 | 2011-09-01 | Council Of Scientific & Industrial Research | Enzymes from conidiobolus brefeldianus and process for preparation thereof |
CN109761439A (en) * | 2019-01-23 | 2019-05-17 | 陈卫红 | Sewage equipment and its processing method |
-
1955
- 1955-10-05 GB GB28364/55A patent/GB804608A/en not_active Expired
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1403274A1 (en) * | 2002-09-30 | 2004-03-31 | Meristem Therapeutics | Process for the purification of recombinant proteins from complex media and purified proteins obtained thereby |
WO2004029078A1 (en) * | 2002-09-30 | 2004-04-08 | Meristem Therapeutics | Process for the purification of recombinant proteins from complex media and purified proteins obtained thereby |
WO2011104630A1 (en) * | 2010-02-26 | 2011-09-01 | Council Of Scientific & Industrial Research | Enzymes from conidiobolus brefeldianus and process for preparation thereof |
CN109761439A (en) * | 2019-01-23 | 2019-05-17 | 陈卫红 | Sewage equipment and its processing method |
CN109761439B (en) * | 2019-01-23 | 2023-08-25 | 陈卫红 | Papermaking sewage treatment equipment and treatment method thereof |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
McGrath | Protein measurement by ninhydrin determination of amino acids released by alkaline hydrolysis | |
Colowick | [11] Separation of proteins by use of adsorbents | |
Yim et al. | Characteristics of guanosine triphosphate cyclohydrolase I purified from Escherichia coli. | |
Moss et al. | Isolation of an avian erythrocyte protein possessing ADP-ribosyltransferase activity and capable of activating adenylate cyclase | |
Frére et al. | [51] Exocellular dd-carboxypeptidases-transpeptidases from Streptomyces | |
JP2884188B2 (en) | Method of hydrolysis of hemicellulose by immobilized enzyme and product comprising immobilized hemicellulose degrading enzyme | |
US4264738A (en) | Process for purification of proteolytic enzymes | |
Silink et al. | Gamma-glutamyl hydrolase conjugase). Purification and properties of the bovine hepatic enzyme. | |
Kobayashi et al. | Biochemical studies on sulfate-reducing bacteria XI. Purification and some properties of sulfite reductase, desulfoviridin | |
Eickbush et al. | A chromatin-bound proteolytic activity with unique specificity for histone H2A | |
Markovitz et al. | Purification, crystallization, and properties of the α-amylase of Pseudomonas saccharophila | |
Muzzarelli et al. | Isolation of lysozyme on chitosan | |
GB804608A (en) | Proteolytic enzyme | |
US2936265A (en) | Proteolytic enzyme and methods for its production | |
Ghosh et al. | Purification and properties of xylan hydrolase from mushroom Termitomyces clypeatus | |
Stedman et al. | The purification of choline-esterase | |
Singh et al. | Chloroplast DNA codes for the ribulose diphosphate carboxylase catalytic site on fraction I proteins of Nicotiana species | |
Shuster et al. | [86] 3′-Nucleotidase from rye grass | |
Cruz et al. | On the nucleotide binding domain of fructose-1, 6-bisphosphatase | |
Berghäuser et al. | Properties of adenylate kinase after modification of Arg-97 by phenylglyoxal | |
Kamra et al. | Crosslinked concanavalin AO-(diethylaminoethyl)-cellulose—an affinity medium for concanavalin A-interacting glycoproteins | |
Osada et al. | Purification and characterization of ascamycin-hydrolysing aminopeptidase from Xanthomonas citri | |
Pacaud | Purification of protease II from Escherichia coli by affinity chromatography and separation of two enzyme species from cells harvested at late log phase | |
US4146432A (en) | Immobilized proteases | |
GB1352270A (en) | Recovering and purifying antibiotics |