Methods to increase enantioselectivity of lipases and esterases (Q35025978)

5 August 2017

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title

Methods to increase enantioselectivity of lipases and esterases (English)

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5 August 2017

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1

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5 August 2017

1 December 2002

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Current Opinion in Biotechnology

5 August 2017

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5 August 2017

13

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5 August 2017

6

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5 August 2017

543-547

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Lipases: Interfacial Enzymes with Attractive Applications

5 August 2017

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7 January 2021

Improved biocatalysts by directed evolution and rational protein design

1 reference

https://api.crossref.org/works/10.1016%2FS0958-1669%2802%2900350-6

7 January 2021

Controlling lipase enantioselectivity for organic synthesis.

1 reference

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7 January 2021

Enzymes in organic synthesis. 42. Investigation of the effects of the isozymal composition of pig liver esterase on its stereoselectivity in preparative-scale ester hydrolysis of asymmetric synthetic value

1 reference

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7 January 2021

By Overexpression in the YeastPichia pastoris to Enhanced Enantioselectivity: New Aspects in the Application of Pig Liver Esterase

1 reference

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7 January 2021

Enantioselective Hydrolysis ofd,l-Menthyl Benzoate toL-(-)-Menthol by RecombinantCandida rugosa Lipase LIP1

1 reference

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7 January 2021

Molecular modeling and biocatalysis: explanations, predictions, limitations, and opportunities

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7 January 2021

Tailoring new enzyme functions by rational redesign

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7 January 2021

Engineering enzyme specificity.

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https://api.crossref.org/works/10.1016%2FS0958-1669%2802%2900350-6

7 January 2021

Improved enantioselectivity of a lipase by rational protein engineering.

1 reference

https://api.crossref.org/works/10.1016%2FS0958-1669%2802%2900350-6

7 January 2021

Creation of an enantioselective hydrolase by engineered substrate-assisted catalysis.

1 reference

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7 January 2021

Stereoselectivity of Pseudomonas cepacia lipase toward secondary alcohols: a quantitative model

1 reference

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7 January 2021

Activity of Lipases and Esterases towards Tertiary Alcohols: Insights into Structure��Function Relationships

1 reference

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7 January 2021

Novel methods for biocatalyst screening

1 reference

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7 January 2021

Directed evolution of biocatalysts

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https://api.crossref.org/works/10.1016%2FS0958-1669%2802%2900350-6

7 January 2021

Directed evolution of an enantioselective lipase

1 reference

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7 January 2021

Directed Evolution of an Enantioselective Enzyme through Combinatorial Multiple-Cassette Mutagenesis

1 reference

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7 January 2021

Ionic Liquids-New "Solutions" for Transition Metal Catalysis

1 reference

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7 January 2021

Lipase-catalyzed reactions in ionic liquids

1 reference

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7 January 2021

Enzyme catalysis in ionic liquids: lipase catalysed kinetic resolution of 1-phenylethanol with improved enantioselectivity

1 reference

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7 January 2021

Biocatalysis in ionic liquids: markedly enhanced enantioselectivity of lipase

1 reference

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7 January 2021

Improved preparation and use of room-temperature ionic liquids in lipase-catalyzed enantio- and regioselective acylations.

1 reference

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7 January 2021

Enhanced enantioselectivity of lipase from Pseudomonas sp. at high temperatures and fixed water activity in the ionic liquid, 1-butyl-3-methylimidazolium bis[(trifluoromethyl)sulfonyl]amide

1 reference

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7 January 2021

Enzyme catalysis in ionic liquids

1 reference

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7 January 2021

Separation of Enantiomers by Extraction Based on Lipase-Catalyzed Enantiomer-Selective Fluorous-Phase Labeling.

1 reference

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7 January 2021

Resolution of 1-(2-naphthyl)ethanol by a combination of an enzyme-catalyzed kinetic resolution with a fluorous triphasic separative reaction

1 reference

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7 January 2021

Molecular basis for enantioselectivity of lipase from Chromobacterium viscosum toward the diesters of 2,3-dihydro-3-(4'-hydroxyphenyl)-1,1,3-trimethyl-1H-inden-5-ol

1 reference

https://api.crossref.org/works/10.1016%2FS0958-1669%2802%2900350-6

7 January 2021

10.1016/S0958-1669(02)00350-6

Identifiers

DOI

1 reference

5 August 2017

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PubMed ID

12482512