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Enzyme Engineering for Nonaqueous Solvents: Random Mutagenesis to Enhance Activity of Subtilisin E in Polar Organic Media

Chen, Keqin and Arnold, Frances H. (1991) Enzyme Engineering for Nonaqueous Solvents: Random Mutagenesis to Enhance Activity of Subtilisin E in Polar Organic Media. Bio/Technology, 9 (11). pp. 1073-1077. ISSN 0733-222X. https://resolver.caltech.edu/CaltechAUTHORS:20181113-134920984

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Abstract

Enzyme activity is often dramatically reduced in polar organic solvents, even under conditions where the folded structures are stable. We have utilized random mutagenesis by polymerase chain reaction (PCR) techniques combined with screening for enhanced activity in the presence of dimethylformamide (DMF) to probe mechanisms by which improved enzymes for chemical synthesis in polar organic media might be obtained. Two amino acid substitutions which enhance subtilisin E activity in the presence of DMF, Q103R and D60N, were identified by screening on agar plates containing DMF and casein. The two substitutions are located near the substrate binding pocket or in the active site, and their effects on the catalytic efficiency k_(cat)/K_M for the hydrolysis of a peptide substrate are additive. The effects of D60N are apparent only in the presence of DMF, highlighting the importance of screening in the organic solvent. Protein engineering is an effective approach to enhancing enzyme activity in organic media: the triple mutant D60N+Q103R+N218S is 38 times more active than wild–type subtilisin E in 85% DMF. An evolutionary approach consisting of multiple steps of random muta–genesis and screening in continually higher concentrations of organic solvent should result in enzymes that are substantially more active in organic media.


Item Type:Article
Related URLs:
URLURL TypeDescription
https://doi.org/10.1038/nbt1191-1073DOIArticle
ORCID:
AuthorORCID
Arnold, Frances H.0000-0002-4027-364X
Additional Information:© 1991 Nature Publishing Group. Published 01 November 1991.
Issue or Number:11
Record Number:CaltechAUTHORS:20181113-134920984
Persistent URL:https://resolver.caltech.edu/CaltechAUTHORS:20181113-134920984
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:90874
Collection:CaltechAUTHORS
Deposited By: Tony Diaz
Deposited On:13 Nov 2018 22:39
Last Modified:03 Oct 2019 20:29

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