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Pre-steady-state kinetic analysis of the trichodiene synthase reaction pathway
Author(s): Cane DE, Chiu HT, Liang PH, Anderson KS
Source: BIOCHEMISTRY    Volume: 36    Issue: 27    Pages: 8332-8339    Published: JUL 8 1997  
Times Cited: 25     References: 34     
Abstract: The pre-steady-state kinetics of the trichodiene synthase reaction were investigated by rapid chemical quench methods. The single-turnover rate was found to be 3.5-3.8 s(-1), a rate 40 times faster than the steady-state catalytic rate (k(cat) = 0.09 s(-1)) for trichodiene synthase-catalyzed conversion of farnesyl diphosphate (FPP) to trichodiene at 15 degrees C. In a multiturnover experiment, a burst phase (k(b) = 4.2 s(-1)) corresponding to the accumulation of trichodiene on the surface of the enzyme was followed by a slower, steady-stale release of products (k(lin) = 0.086 s(-1)) which corresponds to k(cat). These results strongly suggest that the release of trichodiene from the enzyme active site is the rate-limiting step in the overall reaction, while the consumption of FPP is the step which limits chemical catalysis at the active site. Single-turnover experiments with trichodiene synthase mutant D101E, for which the steady-slate rate constant k(cat) is 1/3 of that of wild type, revealed that the mutation actually depresses the face of FPP consumption by a factor of 100. The deuterium isotope effect on the consumption of [1-H-2,1,2-C-14]FPP was found to be 1.11 +/- 0.06. Single turnover reactions of [1,2-C-14]FPP catalyzed by trichodiene synthase were carried out at 4, 15, or 30 degrees C in an effort to provide direct observation of the proposed intermediate nerolidyl diphosphate (NPP). However, no NPP was detected, indicating that the conversion of NPP must be too fast to be observed within the detection limits of the assay. Taken together, these observations suggest that the isomerization of FPP to NPP is the step which limits the rate of chemical catalysis in the trichodiene synthase reaction pathway.
Document Type: Article
Language: English
Reprint Address: Cane, DE (reprint author), BROWN UNIV, DEPT CHEM, BOX H, PROVIDENCE, RI 02912 USA
Addresses:
1. YALE UNIV, SCH MED, DEPT PHARMACOL, NEW HAVEN, CT 06520 USA
Publisher: AMER CHEMICAL SOC, 1155 16TH ST, NW, WASHINGTON, DC 20036
Subject Category: Biochemistry & Molecular Biology
IDS Number: XK094
ISSN: 0006-2960
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