Compounds > 2,2-dimethyl-1,3-dioxolane-4-methanol
Page last updated: 2024-08-18

2,2-dimethyl-1,3-dioxolane-4-methanol and glycerol

2,2-dimethyl-1,3-dioxolane-4-methanol has been researched along with glycerol in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (50.00)29.6817
2010's3 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Gandolfi, R; Kroppenstedt, RM; Marinelli, F; Molinari, F; Romano, D1
Boersma, YL; Cool, RH; Dijkstra, BW; Dröge, MJ; Pijning, T; Quax, WJ; van der Sloot, AM1
Fernández, L; Höbenreich, H; Reetz, MT; Soni, P1
Godinho, LF; Poelarends, GJ; Quax, WJ; Reis, CR; Tepper, PG1
Dekker, FJ; Dijkstra, BW; Godinho, LF; Poelarends, GJ; Quax, WJ; Reis, CR; Rozeboom, HJ1
Barbiroli, A; Bolognesi, M; Contente, ML; De Vitis, V; Gourlay, LJ; Milani, M; Molinari, F; Nakhnoukh, C; Pinto, A; Romano, D1

Other Studies

6 other study(ies) available for 2,2-dimethyl-1,3-dioxolane-4-methanol and glycerol

ArticleYear
Newly isolated Streptomyces spp. as enantioselective biocatalysts: hydrolysis of 1,2-O-isopropylidene glycerol racemic esters.
    Journal of applied microbiology, 2005, Volume: 99, Issue:4

    Topics: Alkenes; Butyrates; Carboxylesterase; Catalysis; Culture Media; DNA, Fungal; DNA, Ribosomal; Esterases; Esters; Freeze Drying; Glycerol; Hydrogen-Ion Concentration; Hydrolysis; Mycelium; Phylogeny; Sequence Analysis, DNA; Solvents; Streptomyces; Temperature

2005
A novel genetic selection system for improved enantioselectivity of Bacillus subtilis lipase A.
    Chembiochem : a European journal of chemical biology, 2008, May-05, Volume: 9, Issue:7

    Topics: Alkenes; Aspartic Acid; Bacillus subtilis; Directed Molecular Evolution; Escherichia coli; Gene Expression Regulation, Bacterial; Gene Library; Glycerol; Hydrolysis; Lipase; Mutation; Periplasm; Stereoisomerism; Substrate Specificity

2008
A genetic selection system for evolving enantioselectivity of enzymes.
    Chemical communications (Cambridge, England), 2008, Nov-21, Issue:43

    Topics: Alkenes; Candida; Catalysis; Directed Molecular Evolution; Esters; Fungal Proteins; Glycerol; Kinetics; Lipase; Molecular Structure; Stereoisomerism; Substrate Specificity

2008
Discovery of an Escherichia coli esterase with high activity and enantioselectivity toward 1,2-O-isopropylideneglycerol esters.
    Applied and environmental microbiology, 2011, Volume: 77, Issue:17

    Topics: Alkenes; Cloning, Molecular; Escherichia coli; Escherichia coli Proteins; Esterases; Esters; Gene Expression; Gene Knockout Techniques; Glycerol; Models, Molecular; Recombinant Proteins; Stereoisomerism; Substrate Specificity

2011
Enhancement of the enantioselectivity of carboxylesterase A by structure-based mutagenesis.
    Journal of biotechnology, 2012, Mar-31, Volume: 158, Issue:1-2

    Topics: Alkenes; Amino Acid Sequence; Bacillus subtilis; Carboxylesterase; Catalysis; Catalytic Domain; Escherichia coli; Esters; Glycerol; Kinetics; Models, Molecular; Molecular Sequence Data; Mutagenesis, Site-Directed; Protein Conformation; Recombinant Proteins; Substrate Specificity

2012
A stereospecific carboxyl esterase from Bacillus coagulans hosting nonlipase activity within a lipase-like fold.
    The FEBS journal, 2018, Volume: 285, Issue:5

    Topics: Alkenes; Bacillus coagulans; Bacterial Proteins; Carboxylesterase; Circular Dichroism; Crystallography, X-Ray; Glycerol; Models, Molecular; Molecular Docking Simulation; Protein Binding; Protein Conformation; Protein Denaturation; Protein Domains; Protein Folding; Recombinant Proteins; Substrate Specificity

2018