Enzyme Kinetics Determined Using Calorimetry: A General Assay for Enzyme Activity? (Record no. 46390)
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| fixed length control field | 01949nam a2200181Ia 4500 |
| 003 - CONTROL NUMBER IDENTIFIER | |
| control field | MX-MdCICY |
| 005 - DATE AND TIME OF LATEST TRANSACTION | |
| control field | 20250625140704.0 |
| 040 ## - CATALOGING SOURCE | |
| Transcribing agency | CICY |
| 090 ## - LOCALLY ASSIGNED LC-TYPE CALL NUMBER (OCLC); LOCAL CALL NUMBER (RLIN) | |
| Classification number (OCLC) (R) ; Classification number, CALL (RLIN) (NR) | B-12179 |
| 008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION | |
| fixed length control field | 250602s9999 xx |||||s2 |||| ||und|d |
| 245 10 - TITLE STATEMENT | |
| Title | Enzyme Kinetics Determined Using Calorimetry: A General Assay for Enzyme Activity? |
| 490 0# - SERIES STATEMENT | |
| Volume/sequential designation | Analytical BioChemistry, 296(2), p.179-187, 2001 |
| 520 3# - SUMMARY, ETC. | |
| Summary, etc. | Two techniques for determining enzyme kinetic constants using isothermal titration microcalorimetry are presented. The methods are based on the proportionality between the rate of a reaction and the thermal power (heat/time)generated. (i)An enzyme can be titrated with increasing amounts of substrate, while pseudo-first-order conditions are maintained. (ii)Following a single injection, the change in thermal power as substrate is depleted can be continuously monitored. Both methods allow highly precise kinetic characterization in a single experiment and can be used to measure enzyme inhibition. Applicability is demonstrated using a representative enzyme from each EC classification, including (i)oxidation-reduction activity of DHFR (EC 1.5.1.3); (ii)transferase activity of creatine phosphokinase (EC 2.7.3.2)and hexokinase (EC 2.7.1.1); (iii)hydrolytic activity of Heliobacter pylori urease (EC 3.5.1.5), trypsin (EC 3.4.21.4), and the HIV-1 protease (EC 3.4.21.16); (iv)lyase activity of heparinase (EC 4.1.1.7); and (v)ligase activity of pyruvate carboxylate (EC 6.4.1.1). This nondestructive method is completely general, enabling precise analysis of reactions in spectroscopically opaque solutions, using physiological substrates. Such a universal assay may have wide applicability in functional genomics. |
| 700 12 - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Todd, M.J. |
| 700 12 - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Gomez, J. |
| 856 40 - ELECTRONIC LOCATION AND ACCESS | |
| Uniform Resource Identifier | <a href="https://drive.google.com/file/d/1fav1bL9-Ga24DPPHN-42UiFfdJBBI1A_/view?usp=drivesdk">https://drive.google.com/file/d/1fav1bL9-Ga24DPPHN-42UiFfdJBBI1A_/view?usp=drivesdk</a> |
| Public note | Para ver el documento ingresa a Google con tu cuenta: @cicy.edu.mx |
| 942 ## - ADDED ENTRY ELEMENTS (KOHA) | |
| Source of classification or shelving scheme | Clasificación local |
| Koha item type | Documentos solicitados |
| Lost status | Source of classification or shelving scheme | Damaged status | Not for loan | Collection | Home library | Current library | Shelving location | Date acquired | Total checkouts | Full call number | Date last seen | Price effective from | Koha item type |
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| Clasificación local | Ref1 | CICY | CICY | Documento préstamo interbibliotecario | 25.06.2025 | B-12179 | 25.06.2025 | 25.06.2025 | Documentos solicitados |
