Abstract
The engineering of crops for selected fatty acid production is one of the major goals of plant biotechnology. The Garm FatA1, an acyl-acyl carrier protein (ACP) thioesterase isolated from Garcinia mangostana, generates an elevated stearate (18:0) phenotype in transgenic Brassica plants. By site- directed mutagenesis, we generated seven mutants that showed up to a 13-fold increase in specific enzyme activity toward 18:0-ACP in vitro. The seed- specific expression of mutant S111A/V193A in Brassica plants results in transgenic plants that accumulate 55-68% more stearate than plants expressing the wild-type enzyme. Our results demonstrate that a thioesterase can be engineered to increase specific activity and that its improved function demonstrated in vitro is retained in vivo.
Original language | English |
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Pages (from-to) | 593-597 |
Number of pages | 5 |
Journal | Nature Biotechnology |
Volume | 17 |
Issue number | 6 |
DOIs | |
State | Published - Jun 1999 |
Keywords
- Alanine scanning
- Protein engineering
- Site-directed mutagenesis
- Stearate
- Transgenic plants
ASJC Scopus subject areas
- Biotechnology
- Bioengineering
- Applied Microbiology and Biotechnology
- Molecular Medicine
- Biomedical Engineering