Results 341 to 350 of about 83,469 (387)
Progress in the Metabolic Engineering of Yarrowia lipolytica for the Synthesis of Terpenes. [PDF]
Liu SC+6 more
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Integrated multi-omics analysis unravels the floral scent characteristics and regulation in "Hutou" multi-petal jasmine. [PDF]
Fang J+9 more
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Journal of Integrative Plant Biology, 2022
Jasmonic acid (JA) is a key regulator of plants defense responses. Although the transcription factor MYC2, the master regulator of the JA signaling pathway, orchestrates a hierarchical transcriptional cascade that regulates the JA responses, only a few ...
Yunyun Cao+10 more
semanticscholar +1 more source
Jasmonic acid (JA) is a key regulator of plants defense responses. Although the transcription factor MYC2, the master regulator of the JA signaling pathway, orchestrates a hierarchical transcriptional cascade that regulates the JA responses, only a few ...
Yunyun Cao+10 more
semanticscholar +1 more source
Phase-Separated Multienzyme Compartmentalization for Terpene Biosynthesis in a Prokaryote.
Angewandte Chemie, 2022Liquid-liquid phase separation (LLPS) forms biomolecular condensates or coacervates in cells. Metabolic enzymes can form phase-separated subcellular compartments that enrich enzymes, co-factors, and substrates.
Yue Wang+9 more
semanticscholar +1 more source
Journal of Agricultural and Food Chemistry, 2021
Terpenes and their derivatives are important biomarkers of grape quality as they contribute to the flavor and aroma of grapes. However, the molecular basis of terpene biosynthesis throughout the grapevine phenological developmental cycle remains elusive.
Wu Wang+7 more
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Terpenes and their derivatives are important biomarkers of grape quality as they contribute to the flavor and aroma of grapes. However, the molecular basis of terpene biosynthesis throughout the grapevine phenological developmental cycle remains elusive.
Wu Wang+7 more
semanticscholar +1 more source
Terpenes and terpene derivatives-22
Tetrahedron, 1987Abstract Isocanambrin ( 1 ) and 6-epi-isocordilin ( 21 ) were synthesized by twofold application of a reaction sequence starting from an α, β-unsaturated carbonyl compound via Wittig-Horner reaction , selective hydrogenation, epoxidation, and solvolysis to give a hydroxy-γ-lactone. Thus, aldehyde 4 was converted (→ 5 ,→ 8 ,→ 9
Peter Weyerstahl+3 more
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Biotechnology Advances, 2006
The main application of terpenes as fragrances and flavors depends on the absolute configuration of the compounds because enantiomers present different organoleptic properties. Biotransformations allow the production of regio- and stereoselective compounds under mild conditions. These products may be labeled as "natural".
M. Manuela R. da Fonseca+1 more
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The main application of terpenes as fragrances and flavors depends on the absolute configuration of the compounds because enantiomers present different organoleptic properties. Biotransformations allow the production of regio- and stereoselective compounds under mild conditions. These products may be labeled as "natural".
M. Manuela R. da Fonseca+1 more
openaire +2 more sources
Biochimica et Biophysica Acta, 1961
Abstract Chromatography of peppermint oil terpenes on silicic acid chromatoplates, using hexane containing ethyl acetate as the developing solvent, effectively separates known constituents of the oil. A sequence of examinations of the plates makes possible the detection and recovery of numerous components of commercial peppermint oil and of extracts ...
R.L. Dunning, W.D. Looms, J. Battaile
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Abstract Chromatography of peppermint oil terpenes on silicic acid chromatoplates, using hexane containing ethyl acetate as the developing solvent, effectively separates known constituents of the oil. A sequence of examinations of the plates makes possible the detection and recovery of numerous components of commercial peppermint oil and of extracts ...
R.L. Dunning, W.D. Looms, J. Battaile
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ChemInform Abstract: CARBONYLATION OF TERPENES [PDF]
1. The most active and selective catalysts for carbonylation of L-menthol, D,L-menthol, p-menthene, and 2,6-dimethyl-2,7-octadiene are BF3·2C2H5COOH, BF3·2CH3COOH, BF3·2CH2C1COOH, BF3·2CH2C1COOH, and BF3·2CH2C1COOH-BF3·2CH3COOH (3∶1). 2. The primary products of the carbonylation of L-menthol, D,L-menthol, and p-menthene-1 are trans- and ...
K. G. Ryabova+4 more
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