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2 Acta Biochimica Polonica

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Purification of geranylgeranyl diphosphate synthase from bovine brain

100%

Sagami H. , Morita Y. , Korenaga T. , Ogura K.

1994

tom 41

nr 3

Geranylgeranyl diphosphate (GGPP) synthase was purified to homogeneity from bovine brain in a one-step affinity column procedure. For the construction of the affinity column, a farnesyl diphosphate (FPP) analog, CM6-amino-l-hexyl)-P- -farnesylmethyl phosphonophosphate, was synthesized and linked to the spacer of the matrix of Affigel 10 via the amino group. The native enzyme appeared to be homooligomer (150-195 kDa) with a molecular mass of the monomer of 37.5 kDa. The pi for the enzyme was 6.2. The Km values for dimethylallyl diphosphate (DMAPP), geranyl diphosphate (GPP) and FTP were estimated to be 33 uM, 0.80 uM and 0.74 uM, respectively. The Km value for isopentenyl diphosphate (IPP) in the presence of both IPP and FPP mixture was 2|iM. The ratio of the reaction velocity for formation of GGPP from DMAPP, GPP or FPP was 0.004:0.145:1. The intermediate FPP was formed in the reaction with GPP as an allylic primer. FPP synthase catalyzing the formation of FPP from DMAPP and IPP was also purified to homogeneity from the same organ by a similar affinity chromatography procedure using a GPP analog, 0-(6-amino-l-hexyl)- -P-geranylmethyl phosphonophosphate as a ligand. The enzyme was a homodimer with a monomeric molecular mass of 40.0 kDa. These results indicate that GGPP, a lipid precursor for the biosynthesis of a majority of prenylated proteins, is synthesized from DMAPP and IPP by the action of FPP synthase catalyzing the reactions C5->C15 followed by the action of GGPP synthase catalyzing the reaction C15->C20.

Heterogeneity of the bovine brain glutathione-S-transferase

100%

Baranczyk-Kuzma A. , Drobisz D.

nr 1