(Q34225449)

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Alternative termination chemistries utilized by monoterpene cyclases: chimeric analysis of bornyl diphosphate, 1,8-cineole, and sabinene synthases

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Europe PubMed Central

PubMed publication ID

31 July 2017

Alternative termination chemistries utilized by monoterpene cyclases: chimeric analysis of bornyl diphosphate, 1,8-cineole, and sabinene synthases (English)

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Europe PubMed Central

PubMed publication ID

31 July 2017

Reuben J. Peters

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Reuben J Peters

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Rodney B Croteau

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31 July 2017

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1 September 2003

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31 July 2017

Archives of Biochemistry and Biophysics

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31 July 2017

417

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31 July 2017

2

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31 July 2017

203-211

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31 July 2017

Plant terpenoid synthases: molecular biology and phylogenetic analysis

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Biosynthesis of monoterpenes: Preliminary characterization of bornyl pyrophosphate synthetase from sage (Salvia officinalis) and demonstration that geranyl pyrophosphate is the preferred substrate for cyclization

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7 January 2021

Biosynthesis of monoterpenes: partial purification, characterization, and mechanism of action of 1,8-cineole synthase

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Mechanism of the pyrophosphate migration in the enzymatic cyclization of geranyl and linalyl pyrophosphates to (+)- and (-)-bornyl pyrophosphates

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Evidence for the ionization steps in monoterpene cyclization reactions using 2-fluorogeranyl and 2-fluorolinalyl pyrophosphates as substrates

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Stereochemical disposition of the geminal dimethyl groups in the enzymatic cyclization of geranyl diphosphate to (+)-bornyl diphosphate by recombinant (+)-bornyl diphosphate synthase from Salvia officinalis

1 reference

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Mechanism of monoterpene cyclization: stereochemical aspects of the transformation of noncyclizable substrate analogs by recombinant (-)-limonene synthase, (+)-bornyl diphosphate synthase, and (-)-pinene synthase

1 reference

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Syn stereochemistry of cyclic ether formation in 1,8-cineole biosynthesis catalyzed by recombinant synthase from Salvia officinalis

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Monoterpene synthases from common sage (Salvia officinalis). cDNA isolation, characterization, and functional expression of (+)-sabinene synthase, 1,8-cineole synthase, and (+)-bornyl diphosphate synthase

1 reference

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Bornyl diphosphate synthase: structure and strategy for carbocation manipulation by a terpenoid cyclase

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Truncation of limonene synthase preprotein provides a fully active 'pseudomature' form of this monoterpene cyclase and reveals the function of the amino-terminal arginine pair

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Identifying functional domains within terpene cyclases using a domain-swapping strategy

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Structural basis for cyclic terpene biosynthesis by tobacco 5-epi-aristolochene synthase

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Domain swapping of Citrus limon monoterpene synthases: impact on enzymatic activity and product specificity

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Crystal structure of pentalenene synthase: mechanistic insights on terpenoid cyclization reactions in biology

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Crystal structure determination of aristolochene synthase from the blue cheese mold, Penicillium roqueforti

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Structure of trichodiene synthase from Fusarium sporotrichioides provides mechanistic inferences on the terpene cyclization cascade

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SWISS-MODEL and the Swiss-PdbViewer: an environment for comparative protein modeling

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Bifunctional abietadiene synthase: free diffusive transfer of the (+)-copalyl diphosphate intermediate between two distinct active sites

1 reference

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Bifunctional abietadiene synthase: mutual structural dependence of the active sites for protonation-initiated and ionization-initiated cyclizations

1 reference

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Mechanism of abietadiene synthase catalysis: stereochemistry and stabilization of the cryptic pimarenyl carbocation intermediates

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Identifiers

10.1016/S0003-9861(03)00347-3

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

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