CS274966B2 - Method of general-purpose chromolytic substrate preparation for proteinasa's enzyme activity determination - Google Patents

Method of general-purpose chromolytic substrate preparation for proteinasa's enzyme activity determination

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Publication number
CS274966B2
CS274966B2 CS540288A CS540288A CS274966B2 CS 274966 B2 CS274966 B2 CS 274966B2 CS 540288 A CS540288 A CS 540288A CS 540288 A CS540288 A CS 540288A CS 274966 B2 CS274966 B2 CS 274966B2
Authority
CS
Czechoslovakia
Prior art keywords
weight
percent
egg white
stage
proteinases
Prior art date
Application number
CS540288A
Other languages
Czech (cs)
Other versions
CS8805402A1 (en
Inventor
Ludovit Ing Csc Kuniak
Angela Ing Matusova
Original Assignee
Slovenskej Vysokej Skoly Tech
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 Slovenskej Vysokej Skoly Tech filed Critical Slovenskej Vysokej Skoly Tech
Priority to CS540288A priority Critical patent/CS274966B2/en
Publication of CS8805402A1 publication Critical patent/CS8805402A1/en
Publication of CS274966B2 publication Critical patent/CS274966B2/en

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  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)

Abstract

Whole egg white, without preliminary treatment is cross-linked at a temperature of 15 to 25 degrees C in the first stage by epichlorhydrine in quantity of 3 to 5 percent by weight per the weight of egg white dry matter and is coloured by colouring agent Remazol Brillant Blue R (disodium salt of 8-amino-5-[3-(sulfoethylsulfonyl)anilino]6-anthraquinone sulfonic acid in the amount of 8 to 12 percent by weight per the weight of egg white dry matter in alkaline environment in concentration of 0.9 to 1.3 percent by weight of sodium hydroxide for a period of 12 to 16 hours. In the second stage the reaction product is defibred in mixer in such a volume of ethanol so that its resulting concentration in the reaction product would be 50 percent by weight. After mixing the chromological substrate is washed on filter with distilled water for a period of time necessary for the filtrate to be colourless and for the phenol phthalein not to colour in red. In the third stage water is displaced by ethanol, with 0.5 percent by weight of previously dissolved sodium chloride. Finally the gel is dried of methanol, ground on particles with dimensions ranging from 0.06 to 0.35 micrometers using standard method.The solution can be used in analytics of proteinase enzymes, selection of microorganisms for production of proteinases, interoperation monitoring of production of proteinases and in meat contamination control.
CS540288A 1988-08-02 1988-08-02 Method of general-purpose chromolytic substrate preparation for proteinasa's enzyme activity determination CS274966B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CS540288A CS274966B2 (en) 1988-08-02 1988-08-02 Method of general-purpose chromolytic substrate preparation for proteinasa's enzyme activity determination

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CS540288A CS274966B2 (en) 1988-08-02 1988-08-02 Method of general-purpose chromolytic substrate preparation for proteinasa's enzyme activity determination

Publications (2)

Publication Number Publication Date
CS8805402A1 CS8805402A1 (en) 1990-10-12
CS274966B2 true CS274966B2 (en) 1991-12-17

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ID=5398869

Family Applications (1)

Application Number Title Priority Date Filing Date
CS540288A CS274966B2 (en) 1988-08-02 1988-08-02 Method of general-purpose chromolytic substrate preparation for proteinasa's enzyme activity determination

Country Status (1)

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CS (1) CS274966B2 (en)

Also Published As

Publication number Publication date
CS8805402A1 (en) 1990-10-12

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