Spelling suggestions: "subject:"oxygenases"" "subject:"dioxygenases""
11 |
Probing the interactions between component B and the hydroxylase of methane monooxygenase /Wallar, Bradley James. January 2000 (has links)
Thesis (Ph.D.)--University of Minnesota, 2000. / Includes bibliographical references. Also available on the World Wide Web as a PDF file.
|
12 |
Active site studies and design of ligands for affinity column separation of 2,5-dihydroxyacetanilide epoxidase (DHAE) I and IIAllen, Scott E. 03 September 2002 (has links)
A series of compounds, 7-8 and 20-25, were tested as competitive inhibitors
of 2,5-dihydroxyacetanilide epoxidase I (DHAE I) and DHAE II. A Hammett plot
was constructed for each enzyme to determine the effect of electron density on
inhibition. DHAE I gave a linear, highly correlated plot (r²=0.91) that signifies
the importance of the amide oxygen in 1 on substrate binding. The plot for DHAE
11 is curved showing the greatest degree of inhibition with 7 suggesting steric
factors within the active site control substrate binding. From these data, we
conclude that each enzyme binds substrate in an opposite fashion and that this
alone controls the stereochemistry of epoxide formation in 2 and 3.
Alternative substrates, 26-29 and 33, were also synthesized and tested for
product formation. All compounds, except 29, were accepted as alternative
substrates, although the rates varied significantly. Surprisingly, 33 was accepted as
an alternative substrate of DHAE II suggesting that the conformation of the amide
bond in 33 is similar to the conformation required for catalytic activity in this
enzyme.
This information was then used to design ligands for affinity column
separation of DHAE I and DHAE II from their protein mixtures. 35 and 36 were
synthesized and attached to carbonyl di-imidazole activated agarose. Column I
was tested three times with DHAE I enzyme preparations. The first attempt did not
result in active enzyme being eluted from the column. The second attempt
maintained the resin in the oxidized state. Protein was found to elute very quickly:
no protein was found after fraction 4. The third attempt resulted in active enzyme
in fractions 4-23. Column 2 was used twice for the attempted isolation of DHAE
II from its protein mixture. The second attempt for column 2 mirrored the results
for the third attempt with column 1. Neither column resulted in homogeneous
enzyme by SDS-PAGE. / Graduation date: 2003
|
13 |
Mechanistic studies on non-heme monooxygenases : dopamine [beta]-monooxygenase and pseudomonas oleovorans monooxygenase systemWimalasena, Kandatege 08 1900 (has links)
No description available.
|
14 |
Multiphase biochemistry : Liquid membranes and the affinity chromatography of oxygenasesLandgraff, Laura Mastrogianni 05 1900 (has links)
No description available.
|
15 |
Transition state studies on protocatechuate 3,4-dioxygenaseKaighobadi, Joni N. 12 1900 (has links)
No description available.
|
16 |
Isolation of phenylalanine hydroxylases and enzymatic studies with 3- and 4- pyridylalanineHan, Jin Hee 05 1900 (has links)
No description available.
|
17 |
A kinetic and resonance Raman spectroscopic investigation of protocatechuate-3,4-dioxygenasePhillips, Robert Stephen 08 1900 (has links)
No description available.
|
18 |
Interplay between 2-oxoglutarate oxygenases and cancer : studies on the aspartyl/asparaginyl-β-hydroxylasePfeffer, Inga January 2014 (has links)
No description available.
|
19 |
Xenobiotic monooxygenase activity and the response to inducers of cytochrome P-450 during embryonic and larval development in fish /Binder, Robert L. January 1981 (has links)
Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Biology, 1981. / Supervised by John J. Stegeman. Vita. Includes bibliographical references (leaves 239-262).
|
20 |
CRYSTALLIZATION AND CHARACTERIZATION OF RIBULOSE-1,5-BISPHOSPHATE CARBOXYLASE/OXYGENASE FROM HIGHER PLANTSJohal, Sarjit Singh January 1980 (has links)
No description available.
|
Page generated in 0.1152 seconds