ENZYME-KINETICS BY MIDINFRARED SPECTROSCOPY - BETA-FRUCTOSIDASE STUDY BY A ONE-STEP ASSAY
被引:22
作者:
CADET, F
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FAC SCI ST DENIS,LA REUNION CTICS,FRANCE DOM LAB CHIM ORGAN,RECH & DEV LAB,F-97464 ST DENIS,FRANCEFAC SCI ST DENIS,LA REUNION CTICS,FRANCE DOM LAB CHIM ORGAN,RECH & DEV LAB,F-97464 ST DENIS,FRANCE
CADET, F
[1
]
PIN, FW
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FAC SCI ST DENIS,LA REUNION CTICS,FRANCE DOM LAB CHIM ORGAN,RECH & DEV LAB,F-97464 ST DENIS,FRANCEFAC SCI ST DENIS,LA REUNION CTICS,FRANCE DOM LAB CHIM ORGAN,RECH & DEV LAB,F-97464 ST DENIS,FRANCE
PIN, FW
[1
]
ROUCH, C
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FAC SCI ST DENIS,LA REUNION CTICS,FRANCE DOM LAB CHIM ORGAN,RECH & DEV LAB,F-97464 ST DENIS,FRANCEFAC SCI ST DENIS,LA REUNION CTICS,FRANCE DOM LAB CHIM ORGAN,RECH & DEV LAB,F-97464 ST DENIS,FRANCE
ROUCH, C
[1
]
ROBERT, C
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FAC SCI ST DENIS,LA REUNION CTICS,FRANCE DOM LAB CHIM ORGAN,RECH & DEV LAB,F-97464 ST DENIS,FRANCEFAC SCI ST DENIS,LA REUNION CTICS,FRANCE DOM LAB CHIM ORGAN,RECH & DEV LAB,F-97464 ST DENIS,FRANCE
ROBERT, C
[1
]
BARET, P
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FAC SCI ST DENIS,LA REUNION CTICS,FRANCE DOM LAB CHIM ORGAN,RECH & DEV LAB,F-97464 ST DENIS,FRANCEFAC SCI ST DENIS,LA REUNION CTICS,FRANCE DOM LAB CHIM ORGAN,RECH & DEV LAB,F-97464 ST DENIS,FRANCE
BARET, P
[1
]
机构:
[1] FAC SCI ST DENIS,LA REUNION CTICS,FRANCE DOM LAB CHIM ORGAN,RECH & DEV LAB,F-97464 ST DENIS,FRANCE
来源:
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY
|
1995年
/
1246卷
/
02期
关键词:
MID-FTIR;
ATTENUATED TOTAL REFLECTION;
PRINCIPAL COMPONENT REGRESSION;
ENZYME KINETICS;
BETA-FRUCTOSIDASE;
D O I:
10.1016/0167-4838(94)00193-K
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
An alternate method for enzyme study is proposed. Multidimensional statistical analysis applied on mid-infrared attenuated total reflectance spectra (Cadet et al. (1991) Appl. Spectrosc. 42, 166-172) collected during a kinetic allows a direct and fast quantification of the remaining substrate, as well as a one step enzymatic assay. Furthermore, the combination of these techniques may be used as a structural tool. The method applied to the study of beta-fructosidase is developed in this paper as an example. With appropriate calibration, the method may be extend to any enzyme.