SE337492B - - Google Patents

Info

Publication number
SE337492B
SE337492B SE11081/66A SE1108166A SE337492B SE 337492 B SE337492 B SE 337492B SE 11081/66 A SE11081/66 A SE 11081/66A SE 1108166 A SE1108166 A SE 1108166A SE 337492 B SE337492 B SE 337492B
Authority
SE
Sweden
Prior art keywords
phosphate
glucose
transferase
acylate
donor
Prior art date
Application number
SE11081/66A
Inventor
H Bergmeyer
H Moellering
Original Assignee
Boehringer Mannheim Gmbh
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 Boehringer Mannheim Gmbh filed Critical Boehringer Mannheim Gmbh
Publication of SE337492B publication Critical patent/SE337492B/xx

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/02Food
    • G01N33/14Beverages
    • G01N33/143Beverages containing sugar
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/54Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving glucose or galactose
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00Chemistry: molecular biology and microbiology
    • Y10S435/8215Microorganisms
    • Y10S435/822Microorganisms using bacteria or actinomycetales
    • Y10S435/823Acetobacter

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Zoology (AREA)
  • Food Science & Technology (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Wood Science & Technology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Pathology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biotechnology (AREA)
  • Microbiology (AREA)
  • Molecular Biology (AREA)
  • Medicinal Chemistry (AREA)
  • Emergency Medicine (AREA)
  • General Physics & Mathematics (AREA)
  • Biophysics (AREA)
  • General Engineering & Computer Science (AREA)
  • Genetics & Genomics (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
  • Investigating Or Analysing Materials By The Use Of Chemical Reactions (AREA)
  • Interface Circuits In Exchanges (AREA)

Abstract

Glucose is determined by a sequence of reactions comprising converting glucose into glucose-6-phosphate by means of a phosphate donor and a transferase, converting the glucose-6-phosphate into 6-phosphogluconic acid by means of triphosphopyridine-nucleotide in the presence of glucose-6-phosphoric acid dehydrogenase, reduced triphosphopyridine-nucleotide being formed at the same time, and then determining the latter spectrophotometrically: characterised in that phosphate donor is a compound of the general formula:- <FORM:1108770/B1-B2/1> in which R is an organic radical, said radical not possessing a negative charge in the immediate neighbourhood of the phospate group, and wherein the transferase is acylphosphate: glucose p transferase. Specified phosphate donors are the following phosphates:-benzoyl, nicotoyl, acetyl, propionyl, N-benzoyl, glycoyl, carbonyl, glutaroyl, succinyl, and 3-phosphoglyceric acid-1-phosphate. The phosphate donor may be synthesized immediately before glucose determination by reacting acylate ions and an acylate-phosphokinase (e.g. acetyl phosphate from an acetate, adenosine triphosphate by means of acetate - kinase, and carbamyl phosphate from carbamic acid and ATP by means of carbamatephosphokinase.) Examples describe the analysis of various fruit juices and blood for glucose. Fructose, if present, does not interfere. In one Example, the acyl phosphate used is derived from a glycocollacetate buffer of pH 9.0, and magnesium chloride is also be present. The sample to be determined is mixed with all the reactant except the acyl phosphate-glucose transferase, and the latter is then added to start the reaction. Glucose is determined spectrophotometrically after some minutes. The invention also comprises a composition comprising the above defined phosphate donor, acyl phosphate: glucose transferase, glucose-6-phosphate-dehydrogenase and triphosphopyridine nucleotide: or a similar composition in which the phosphate donor is replaced by adenosine triphosphate, acylate ions and an acylate-phosphokinase.
SE11081/66A 1951-01-28 1966-08-16 SE337492B (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19511598067 DE1598067A1 (en) 1951-01-28 1951-01-28 Methods and diagnostic agents for the enzymatic determination of glucose
DEB0083297 1965-08-17

Publications (1)

Publication Number Publication Date
SE337492B true SE337492B (en) 1971-08-09

Family

ID=25753451

Family Applications (1)

Application Number Title Priority Date Filing Date
SE11081/66A SE337492B (en) 1951-01-28 1966-08-16

Country Status (9)

Country Link
US (1) US3509025A (en)
JP (1) JPS503674B1 (en)
BE (1) BE685538A (en)
CH (1) CH488186A (en)
DE (1) DE1598067A1 (en)
GB (1) GB1108770A (en)
NL (1) NL6611550A (en)
NO (1) NO117818B (en)
SE (1) SE337492B (en)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56169598A (en) 1980-05-26 1981-12-26 Mitsubishi Petrochem Co Ltd Measuring composition
JPS59151899A (en) * 1983-02-16 1984-08-30 Unitika Ltd Determination composition
JPS62232555A (en) * 1986-04-02 1987-10-13 Unitika Ltd Oxygen sensor
US4935346A (en) * 1986-08-13 1990-06-19 Lifescan, Inc. Minimum procedure system for the determination of analytes
US6458326B1 (en) 1999-11-24 2002-10-01 Home Diagnostics, Inc. Protective test strip platform
TWI275795B (en) * 2001-02-14 2007-03-11 Sysmex Corp Novel assay method
US6525330B2 (en) 2001-02-28 2003-02-25 Home Diagnostics, Inc. Method of strip insertion detection
US6562625B2 (en) 2001-02-28 2003-05-13 Home Diagnostics, Inc. Distinguishing test types through spectral analysis
US6541266B2 (en) 2001-02-28 2003-04-01 Home Diagnostics, Inc. Method for determining concentration of an analyte in a test strip

Also Published As

Publication number Publication date
GB1108770A (en) 1968-04-03
DE1598067A1 (en) 1970-03-26
US3509025A (en) 1970-04-28
DE1598067C3 (en) 1974-04-18
NO117818B (en) 1969-09-29
JPS503674B1 (en) 1975-02-07
BE685538A (en) 1967-02-16
DE1598067B2 (en) 1973-09-27
NL6611550A (en) 1967-02-20
CH488186A (en) 1970-03-31

Similar Documents

Publication Publication Date Title
Abrams et al. TRANSFORMATION OF INOSINIC ACID TO ADENYLIC AND GUANYLIC ACIDS IN A SOLUBLE ENZYME SYSTEM1
Benson et al. Photosynthesis of galactolipids
Higashi et al. Biosynthesis of the Peptidoglycan of Bacterial Cell Walls: XIX. ISOPRENOID ALCOHOL PHOSPHOKINASE
DE2122255C3 (en) Method for the specific determination of creatinine
IL44480A (en) Process for the determination of total cholesterol or bound cholesterol and reagent therefor
Ichikawa et al. Efficient chemical synthesis of GDP-fucose
SE337492B (en)
ES473296A1 (en) Process and reagent for the determination of alpha -amylase
GB1359473A (en) Polyenic antibiotic
GB1508018A (en) Radioimmunoassay for determining the digoxin content of a sample
Nath et al. Studies on cyclic AMP levels and phosphodiesterase activity in developing sea urchin eggs: Effects of puromycin, 6-dimethylamino purine and aminophylline
GB1276230A (en) Diagnostic agent and process for the determination of glucose
Hirst et al. 196. The quantitative determination of galactose, mannose, arabinose, and rhamnose
US2906673A (en) Metabolic processes
Johnson Jr et al. SYNTHESIS OF POTENTIAL ANTICANCER AGENTS. II. 1 6-MERCAPTO-9-β-D-RIBOFURANOSYLPURINE
Nakamura The sucrose-synthesizing enzyme in the beans
Augustinsson Comparison between the acetylcholinesterases of Helix blood and cobra venom. I. The hydrolysis of acetylcholine and its inhibition by various compounds
GB1318488A (en) Preparation of lincomycins
Corlett et al. Analysis of periodate oxidation of carbohydrates by polarography
JPH05304996A (en) Determination of 1,5-anhydroglucitol
McL The Measurement of Cyclic Adenylate in Tissues
GB1319303A (en) Sugar derivatives
Callaway et al. A new method for the bioassay of cholinesterase inhibitors
Midelfort et al. [50] Applications of kinetic methods to aminoacyl-tRNA synthetases
Albaum Adenosine diphosphate, adenosine triphosphate