Improved stearate phenotype in transgenic canola expressing a modified acyl-acyl carrier protein thioesterase

被引:45
作者
Facciotti, MT [1 ]
Bertain, PB [1 ]
Yuan, L [1 ]
机构
[1] Calgene Inc, LLC, Davis, CA 95616 USA
关键词
alanine scanning; site-directed mutagenesis; stearate; transgenic plants; protein engineering;
D O I
10.1038/9909
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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.
引用
收藏
页码:593 / 597
页数:5
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