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PMID: 7873527 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Trichodiene synthase. Identification of active site residues by site-directed mutagenesis.

Biochemistry ·Vol. 34 ·No. 8 ·1995-02-28 ·Pages 2480-8

Cane DE, Shim JH, Xue Q, Fitzsimons BC, Hohn TM

Abstract

Derivatization of 5,5'-dithiobis(2-nitrobenzoic acid)-treated trichodiene synthase with [methyl-14C]methyl methanethiosulfonate and analysis of the derived tryptic peptides suggested the presence of two cysteine residues at the active site. The corresponding C146A and C190A mutants were constructed by site-directed mutagenesis. The C190A mutant displayed partial but significantly reduced activity, with a reduction in kcat/Km of 3000 compared to the wild-type trichodiene synthase, while the C146A mutant was essentially inactive. A hybrid trichodiene synthase, constructed from amino acids 1-309 of the Fusarium sporotrichioides enzyme and amino acids 310-383 of the Gibberella pulicaris cyclase, had steady state kinetic parameters nearly identical to those of the wild-type F. sporotrichioides enzyme. From this parent hybrid, a series of mutants was constructed by site-directed mutagenesis in which the amino acids in the base-rich region, 302-306 (DRRYR), were systematically modified. Three of these mutants were overexpressed and purified to homogeneity. The importance of Arg304 for catalysis was established by the observation that the R304K mutant showed a more than 25-fold increase in Km, as well as a 200-fold reduction in kcat. In addition, analysis of the incubation products of the R304K mutant by gas chromatography-mass spectrometry (GC-MS) indicated that farnesyl diphosphate was converted not only to trichodiene but to at least two additional C15H24 hydrocarbons, mle 204. Replacement of the Tyr305 residue of trichodiene synthase with Phe had little effect on kcat, while increasing the Km by a factor of ca. 7-8.(ABSTRACT TRUNCATED AT 250 WORDS)

MeSH Terms
Amino Acid Sequence Base Sequence Binding Sites/genetics Carbon-Carbon Lyases Catalysis Cloning, Molecular Cysteine/chemistry DNA Primers/genetics DNA, Fungal/genetics Escherichia coli/genetics Fusarium/enzymology,genetics Kinetics Lyases/chemistry,genetics,metabolism Methyl Methanesulfonate/analogs & derivatives,pharmacology Molecular Sequence Data Molecular Structure Mutagenesis, Site-Directed Polyisoprenyl Phosphates/chemistry Sesquiterpenes Substrate Specificity
Chemicals
DNA Primers DNA, Fungal Polyisoprenyl Phosphates Sesquiterpenes methyl methanethiosulfonate farnesyl pyrophosphate Methyl Methanesulfonate Lyases Carbon-Carbon Lyases trichodiene synthetase Cysteine
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Cane D E
Department of Chemistry, Brown University, Providence, Rhode Island 02912, USA.
Shim J H
Xue Q
Fitzsimons B C
Hohn T M
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
1995-02-28
Pages
2480-8
Language
English
Region
United States
NLM ID
0370623
Subset
IM
Grants
NIGMS NIH HHS · GM-30301 · United States
Corrections
ErratumIn
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