GB804608A - Proteolytic enzyme - Google Patents

Proteolytic enzyme

Info

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
Application number
GB28364/55A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Wyeth Holdings LLC
Original Assignee
American Cyanamid Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by American Cyanamid Co filed Critical American Cyanamid Co
Publication of GB804608A publication Critical patent/GB804608A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14Hydrolases (3)
    • C12N9/48Hydrolases (3) acting on peptide bonds (3.4)
    • C12N9/50Proteinases, e.g. Endopeptidases (3.4.21-3.4.25)
    • C12N9/58Proteinases, 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.
GB28364/55A 1954-10-25 1955-10-05 Proteolytic enzyme Expired GB804608A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (5)

* Cited by examiner, † Cited by third party
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

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