• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    Kinetic determination of enzyme substrates by means of coupled reactions comprising selecting the reaction parameters so that the most specific part reaction of a reaction sequence becomes rate-determining for the whole reaction sequence wherein the rate-determining part reaction follows first or pseudo-first order kinetics.
    公开号:SU1055346A3
    申请号:SU762432255
    申请日:1976-12-24
    公开日:1983-11-15
    发明作者:Цигенхорн Иоахим；Вильхельм Валефельд Аугуст；Хаген Александер；Грубер Вольфганг；Ульрих Бергмейер Ханс
    申请人:Берингер Маннхайм Гмбх (Фирма)；
    IPC主号:
    专利说明:

    O; l: l
    : / s
    35 The invention relates to analytical biochemistry, and specifically to methods for determining the concentration of enzyme substrates, and can be used in biochemistry and medicine to determine substrates. A known method for kinetic determination of the concentration of an enzyme substrate, including addition of an appropriate enzyme to the solution, carrying out a reaction, measuring the concentration of the resulting product at a certain time interval, and calculating the concentration of the substrate to be determined. It is essential that the reaction in the selected time interval proceeds in the first or pseudo-first order. In this case, the measured value of the change in 1 substrate permeation in a selected time interval is directly proportional to the desired initial concentration of the substrate ij to be determined. However, this method is applicable mainly for one-step reactions. A known method for kinetic determination of an enzyme substrate by means of conjugate reactions, includes carrying out the main reaction before the complete conversion of the detected substrate into the product and determination of the product obtained by means of an auxiliary reaction by the kinetic method 2. However, the known method of the reaction, since the auxiliary reaction is carried out only after termination of the main reaction. The aim of the invention is to accelerate the determination of the concentration of the enzyme substrate. This goal is achieved by the fact that in the process of kinetic determination of the concentration of the enzyme substrate, using conjugate reactions, the main and conjugate reactions are carried out simultaneously, and the substrates or enzymes of conjugate reactions are taken in excess. The method is carried out as follows. The reaction mixture containing the substrate to be determined is added simultaneously to the farm — the main and auxiliary reactions, as well as all the necessary substrates for the auxiliary reactions. To determine the substrate concentration by the kinetic method, 462 enzymes or substrates of auxiliary reactions are added in excess. In this case, the main reaction limits the speed of the whole process. The main reaction of a chain of reactions is understood to be that partial reaction, which has the greatest specificity with respect to the initial substance, and, in addition, due to the appropriate choice of reaction parameters, it can become a reaction that determines the speed of the whole process. It is also necessary for the main reaction to proceed according to the first or. pseudo-first order. Next, the change in substrate concentration over a certain period of time is determined. Then, using the ratio, 4 & C s where Cn is the initial concentration of the substrate to be determined; the rate constant of the main reaction; the change in the concentration of the substrate to be determined in the time interval (), H by keeping the values of K, t and to constant, determines the concentration of the enzyme substrate. and mer. Determination of glucose in the blood. The test sample is placed in a reaction medium containing 80-120 mM phosphate buffer {pH 7.0); 0.8 u / ml or more peroxidase (EC 1.11.1.7); 12 u / mp more glucose oxidase (K 1. 1.3.4); 0.6-, 8; G.M. 4-aminoanipirin and 3.0-13.5 mM phenol. The determination is carried out according to the following reactions: oi-D-glucose-D glucose glucose |) -O-glucose + H O-H, - 0 oxidase glucose acid + HnO H 502 - phenol + 4 peroxidase aminoantipyrin quinoid rasitel + 2H20. . The first reaction is the base, and the second and third are conjugated to it. The reactions were carried out simultaneously in a centrifugal analyzer, the first reading of the instrument was taken approximately 35 seconds after placing the reagent with the test plate, and the second one 1.5-1.3 minutes later. The peroxidase enzyme is added at such an increased dose that the basic reaction proceeding with the pseudo-first process limits the rate of the whole process. The glucose concentration is determined by spectral variation of the concentration of the chioid dye. Bes analysis takes 4-5 minutes.
    Definition of triglycerides. . Triglycerides are enzymatically cleaved into glycerol and fatty acids. Glycerin is determined according to the following reactions:
    glycerokinase
    glycerin + ATP ---- glycerin "3 phosphate + ADP
    pyruvate kinase
    ADP + phospho enolpyruv at ATP + pyruv at
    lactate dehydrogenase
    pyruvate-NADH + H
    - lactate + OVER,
    The method is carried out kinetically with the following reagents. : Reagent I: 45-55 mM phosphate buffer (pH 7.0); 4.6-3.1 mM magnesium sulfate; 300m400 mI sodium dodecyl sulfate; 2.3-3.5 mM ATP; 280-420Ш
    phosphoenolpyruvate; 120-230 mM OVER; 7.7- iCTj u / l or more lynase; 5,8JO ,, u / l or more esterase; 9.6 W units / l or more pyruvatcliosis (EC 2.7.1.40); 5.3-10 u / l or more lactate dehydrogenase (KF ... 27).
    Reagent 2t 2,910 u / l or more glycerokinase (EC 2.7.1.ZO)
    The concentration of glycerol is judged by measuring the formation of IADN by a centrifugal analyzer at 340 nm and 25 C. By increasing the concentration of HTF. and the addition of enzymes to auxiliary reactions; the main reaction determines the speed of the whole process.,
    For carrying out the method, mix 10 µl of the serum sample under study with 30-50 µl of physiological sodium chloride solution and 500,600 µl of reagent 1 and incubate for 10 min. Reagent 2 is then added and after 50 seconds the first is removed.
    and after 150-200 seconds, the second reading of the device.
    The proposed method allows to significantly speed up the analysis (3-10 times compared with the known),
    权利要求:
    Claims (1)
    [1]
    METHOD FOR KINETIC DETERMINATION OF ENZYME SUBSTRATE CONCENTRATION using conjugated reactions, characterized in that, in order to accelerate the analysis, the main and conjugated reactions are carried out simultaneously, while the substrates or enzymes of the conjugated reactions are taken in excess.
    类似技术:
    公开号 | 公开日 | 专利标题
    Jaworek et al.1974|Adenosine-5′-diphosphate and adenosine-5′-monophosphate
    CA1125151A|1982-06-08|Triglycerides assay and reagents therefor
    SU797592A3|1981-01-15|Method of determining substrate or enzymic activity in biological material
    Allred et al.1969|Determination of coenzyme A and acetyl CoA in tissue extracts
    Babson et al.1973|Kinetic colorimetric measurement of serum lactate dehydrogenase activity
    US4517287A|1985-05-14|Method and reagent for the enzymatic determination of enzyme substrates
    RU2004117087A|2005-04-27|ANALYSIS OF HOMOCYSTEIN AND CYSTATIONIONINE BY ENZYMATIC CYCLIC TRANSFORMATION
    US4120755A|1978-10-17|Kinetic method for determination of glucose concentrations with glucose dehydrogenase
    GB2115926A|1983-09-14|Method for the quantitative determination of physiological components in biological fluids
    SU1055346A3|1983-11-15|Method for kinetically determining concentration of enzimatic substrate
    US4097338A|1978-06-27|Fluorimetric demonstration and determination of a reduced coenzyme or derivative in an aqueous system
    EP0116307B1|1988-01-07|Composition, analytical element and method for the quantification of creatine kinase
    SU641884A3|1979-01-05|Reagent for determining triglycerides
    US4271265A|1981-06-02|Method and reagent for the determination of glutamate-oxalacetate transaminase and glutamate-pyruvate transaminase
    US4001089A|1977-01-04|Method for determination of triglycerides and glycerol
    US4565780A|1986-01-21|Method for determination of cholinesterase activity
    JP3036708B2|2000-04-24|Highly sensitive method for quantifying D-glucose-6-phosphate and composition for quantification
    KR880012754A|1988-11-29|Novel monoglyceride lipase, preparation method thereof and analysis method using the same
    US4142938A|1979-03-06|Determination of triglycerides and glycerol
    Rietz et al.1975|Fluorometric assay of serum acid or alkaline phosphatase, either in solution or on a semisolid surface
    Isobe et al.1987|A rapid enzymatic assay for total blood polyamines
    CN100547390C|2009-10-07|Fastly inspecting glutamic-pyruvic transaminase by optical reagent
    Rindfrey et al.1977|Kinetic determination of glucose concentrations with glucose dehydrogenase
    JP3036709B2|2000-04-24|Highly sensitive method for determining L-glycerol-3-phosphate or dihydroxyacetone phosphate and composition for determination
    EP0071087B1|1985-04-24|Improved determination of creatine phosphokinase in body fluids
    同族专利:
    公开号 | 公开日
    GB1571899A|1980-07-23|
    SE441364B|1985-09-30|
    AU2083276A|1978-06-29|
    US4229527A|1980-10-21|
    DD127909A5|1977-10-19|
    CH625272A5|1981-09-15|
    DE2558536A1|1977-07-07|
    SE7614226L|1977-06-25|
    FI60887C|1982-04-13|
    HU174894B|1980-04-28|
    FR2336682B1|1982-10-22|
    FI60887B|1981-12-31|
    JPS5282387A|1977-07-09|
    DE2558536C3|1991-03-07|
    JPS5934116B2|1984-08-20|
    DE2558536B2|1979-07-12|
    IT1064332B|1985-02-18|
    BE849804A|1977-06-23|
    FR2336682A1|1977-07-22|
    CA1100022A|1981-04-28|
    AU511225B2|1980-08-07|
    NL7613819A|1977-06-28|
    FI763653A|1977-06-25|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    JPS5033795B1|1970-11-25|1975-11-04|
    IT986838B|1972-05-12|1975-01-30|Sclavo Inst Sieroterapeut|COMPLEX OF REAGENTS FOR THE ENZYMATIC DETER MINATION OF GLUCOSE GLUCOSE SYSTEM OXIDASE PEROXIDASE DASES WITH MANUAL AND AUTOMATED METHODS CO WITH READING AT TERM OR IN KINETICS|
    AT324282B|1972-06-19|1975-08-25|Boehringer Mannheim Gmbh|METHOD AND REAGENT FOR DETERMINATION OF TRIGLYCERIDES|
    DE2349819A1|1973-10-04|1975-04-17|Eppendorf Geraetebau Netheler|PROCEDURE FOR THE ENZYMKINETIC CONCENTRATION OF A SUBSTRATE|
    DK678474A|1974-02-15|1975-10-13|Hoffmann La Roche|DE2833723A1|1978-08-01|1980-02-21|Boehringer Mannheim Gmbh|METHOD AND REAGENT FOR DETERMINING AN OXIDIZED PYRIDINE COENZYME|
    DE2950381A1|1979-12-14|1981-06-19|Boehringer Mannheim Gmbh, 6800 Mannheim|METHOD AND REAGENT FOR DETERMINING TRIGLYCERIDES|
    AT4328T|1980-09-19|1983-08-15|Boehringer Mannheim Gmbh|METHOD AND REAGENT FOR DETERMINING GLYCERIN.|
    DE3046241A1|1980-12-08|1982-07-15|Boehringer Mannheim Gmbh, 6800 Mannheim|METHOD AND REAGENT FOR DETERMINING CHOLESTERIN|
    DE3208253A1|1982-03-08|1983-09-15|Boehringer Mannheim Gmbh, 6800 Mannheim|METHOD FOR SPECIFIC DETERMINATION OF THE CHOLESTERIN OF THE LDL FRACTION IN SERUM|
    DE3340709A1|1983-11-10|1985-05-23|Boehringer Mannheim Gmbh, 6800 Mannheim|COMPETITIVE INHIBITOR FOR GK|
    DE3439181C2|1984-10-23|1994-01-20|Lange Gmbh Dr Bruno|Method for the photometric determination of the concentration of a substance|
    CN109596551A|2018-12-24|2019-04-09|苏州科铭生物技术有限公司|A kind of cellulase activity assay kit and its method based on micromethod|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    DE2558536A|DE2558536C3|1975-12-24|1975-12-24|
    [返回顶部]