Lipases as practical biocatalysts (Q34662058)

3 August 2017

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title

Lipases as practical biocatalysts (English)

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3 August 2017

1

Manfred T Reetz

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3 August 2017

1 April 2002

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Current Opinion in Chemical Biology

3 August 2017

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3 August 2017

6

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3 August 2017

2

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3 August 2017

145-150

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Lipases: Interfacial Enzymes with Attractive Applications

3 August 2017

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https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

Bacterial biocatalysts: molecular biology, three-dimensional structures, and biotechnological applications of lipases

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https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

Enzymes for chemical synthesis

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https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

Industrial biocatalysis today and tomorrow

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https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

Improving enzymes by using them in organic solvents

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https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

Enhancing the enantioselectivity of lipase in transesterification by substrate matching: an enzyme memory based approach.

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

Computer-aided control of water activity for lipase-catalyzed esterification in solvent-free systems

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https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

At what temperature can enzymes maintain their catalytic activity?

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https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

Effects of substituent and temperature on enantioselectivity for lipase-catalyzed esterification of 2-(4-substituted phenoxy) propionic acids in organic solvents

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https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

Comparison of hydrolytic activity in water and heptane for thirty-two commercial lipase preparations

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https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

Enhanced activities of lipase pretreated with organic solvents

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https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

Lipase-catalyzed reactions in ionic liquids

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https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

Biocatalysis in ionic liquids: markedly enhanced enantioselectivity of lipase

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https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

1 reference

7 January 2021

Tuning lipase enantioselectivity in organic media using solid-state buffers

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https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

Improving lipase enantioselectivity in organic solvents by forming substrate salts with chiral agents

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https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

Parallel kinetic resolution under catalytic conditions: a three-phase system allows selective reagent activation using two catalysts.

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https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

Enzyme immobilization in silica-hardened organogels

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https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

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

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https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

Rational design of enantioselective enzymes requires considerations of entropy

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https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

Computer simulations of enantioselective ester hydrolyses catalyzed by Pseudomonas cepacia lipase

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https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

How do lipases and esterases work: the electrostatic contribution

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https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

Lipase protein engineering

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https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

Improved enantioselectivity of a lipase by rational protein engineering.

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

Combinatorial and computational challenges for biocatalyst design

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https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

Directed Evolution and Biocatalysis

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https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

Dynamic kinetic resolution of alpha-hydroxy acid esters

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https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

Chemoenzymatic construction of a four-component Ugi combinatorial library

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

The synthesis of (+)-allopumiliotoxin 323B'.

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https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

Enantioselective Synthesis of the Ricciocarpins A and B This work was supported by the Deutsche Forschungsgemeinschaft (Graduierten-Kolleg "Struktur-Eigenschafts-Beziehungen bei Heterocyclen") and the Fonds der Chemischen Industrie. We thank Prof. D

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https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

A highly chemo- and stereoselective synthesis of beta-keto esters via a polymer-supported lipase catalyzed transesterfication

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https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

Enzymatic kinetic resolution of piperidine atropisomers: synthesis of a key intermediate of the farnesyl protein transferase inhibitor, SCH66336

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

Regioselective enzymatic aminoacylation of lobucavir to give an intermediate for lobucavir prodrug

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

Enzyme-labile protecting groups in peptide synthesis: development of glucose- and galactose-derived urethanes

1 reference

https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

Reversible Michael reaction-enzymatic hydrolysis: a new variant of dynamic resolution

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https://api.crossref.org/works/10.1016%2FS1367-5931%2802%2900297-1

7 January 2021

10.1016/S1367-5931(02)00297-1

Identifiers

DOI

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3 August 2017

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PubMed ID

12038997