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Cape baboon Cytochrome P450 11β-hydroxylases : the characterization of two functional enzymesBrown, Natasja 03 1900 (has links)
Dissertation (PhD)--University of Stellenbosch, 2007. / ENGLISH ABSTRACT: This study:
1. Describes the localization of CYP11B1 in the Cape baboon adrenal gland using Western
blot analysis. CYP11B1 was localized to the adrenal cortex and medulla.
2. Describes the catalytic activity of CYP11B1 towards 11-deoxycorticosterone and
corticosterone in adrenal cortical- and medullary tissue homogenates. Aldosterone
formation in the adrenal medulla was identified using an atmospheric pressure chemical
ionization-mass spectrometry method, which was developed in our department.
3. Compares the catalytic activity of three recombinant Cape baboon CYP11B1 cDNAs,
expressed in COS-1 cells, towards 11-deoxycorticosterone and 11-deoxycortisol.
4. Describes the determination of the Michaelis-Menten constants and maximum reaction
rates of 11-deoxycorticosterone and 11-deoxycortisol utilization by two functional
recombinant Cape baboon CYP11B1 cDNAs, respectively. 11-Deoxycorticosterone
metabolites were quantified using an enzyme immunoassay kit. 11-Deoxycortisol
metabolites were quantified using a liquid chromatography-mass spectrometry method,
which was developed in our department.
5. Describes the homology modeling of two isoforms of Cape baboon CYP11B1 using
CYP102 and CYP2C5 as structural templates. The influence of three amino acid residue
substitutions, located in the predicted D-E helix, on the catalytic activity of the two
CYP11B1 isoforms was examined. / AFRIKAANSE OPSOMMING: Hierdie studie:
1. Beskryf die lokalisering van CYP11B1 in die bynier van die Kaapse bobbejaan deur
gebruik te maak van die Western kladtegniek. CYP11B1 is gelokaliseer tot die adrenale
korteks en medulla.
2. Beskryf die metabolisme van 11-deoksikortikosteroon en kortikosteroon in adrenale
korteks- and medulla weefsel preparate, onderskeidelik. Die produksie van aldosteroon in
die medulla is geïdentifiseer deur gebruik te maak van ‘n atmosferiese druk chemiese
ionisasie-massa spektrometrie metode wat in ons departement ontwikkel is.
3. Vergelyk die katalitiese aktiwiteit van drie rekombinante Kaapse bobbejaan CYP11B1
cDNAs, getransfekteer in COS-1 selle, ten opsigte van 11-deoksikortikosteroon en 11-
deoksikortisol metabolisme.
4. Beskryf die bepaling van die Michaelis-Menten konstantes en maksimum snelhede van
twee funksionele rekombinante Kaapse bobbejaan CYP11B1 cDNAs, getransfekteer in
COS-1 selle, ten opsigte van 11-deoksikortikosteroon en 11-deoksikortisol metabolisme.
11-Deoksikortikosteroon metaboliete is gekwantifiseer deur gebruik te maak van ‘n
ensiem immunotoets. 11-Deoksikortisol metaboliete is gekwantifiseer deur middel van ‘n
vloeistofchromatografie-massaspektrometrie metode, ontwikkel in ons departement.
5. Beskryf die modelering van drie-dimensionele strukture van twee funksionele Kaapse
bobbejaan CYP11B1 isoensieme deur CYP102 en CYP2C5 as template te gebruik. Die
effek van drie aminosuurresiduveranderinge in die voorspelde D-E heliks op die
katalitiese aktiwiteit van die twee CYP11B1 isoforme is bepaal.
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A structure/function investigation into baboon cytochrome P450 side-chain cleavage (CYP11A1)Storbeck, Karl-Heinz 12 1900 (has links)
Thesis (MSc (Biochemistry))--University of Stellenbosch, 2005. / This study describes:
1. The cloning of baboon cytochrome P450 side-chain cleavage (CYP11A1) cDNA by in
vitro site-directed mutagenesis.
2. The identification and sequencing of three baboon CYP11A1 mutants: CYP11A1a,
CYP11A1b and CYP11A1c.
3. The expression and characterisation of baboon and human CYP11A1 cDNA,
CYP11A1a, CYP11A1b and CYP11A1c in nonsteroidogenic COS-1 cells. The Km and
V-values for the metabolism of 25-hydroxycholesterol were determined.
4. The construction of the first homology model of CYP11A1, using both mammalian
(CYP2C5) and bacterial (CYP102) cytochromes P450 crystal structures as templates.
5. A structure/function study into the role of the amino acid residues Ile98, Lys103 and
Thr291 in substrate binding and enzymatic activity.
6. The proposal of a topological model of the CYP11A1 active pocket as determined by
substrate docking studies.
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