Unleashing the innate ability of Escherichia coli to produce D-Allose

被引:0
|
作者
Luu, Bryant [1 ]
Palur, Dileep Sai Kumar [2 ]
Taylor, Jayce E. [2 ]
Didzbalis, John [3 ]
Siegel, Justin B. [1 ,2 ,4 ,5 ]
Atsumi, Shota [1 ,2 ]
机构
[1] Univ Calif Davis, Biochem Mol Cellular & Dev Biol Grad Grp, Davis, CA 95616 USA
[2] Univ Calif Davis, Dept Chem, Davis, CA 95616 USA
[3] Mars Inc, 6885 Elm St, Mclean, VA 22101 USA
[4] Univ Calif Davis, Genome Ctr, Davis, CA 95616 USA
[5] Univ Calif Davis, Dept Biochem & Mol Med, Sacramento, CA 95616 USA
关键词
Rare sugars; D-allose; Metabolic engineering; CEREBRAL ISCHEMIA/REPERFUSION INJURY; L-RHAMNOSE ISOMERASE; RARE SUGAR; RIBOSE-5-PHOSPHATE ISOMERASE; D-PSICOSE; EXPRESSION; SEPARATION; GLUCOSE; GENOME;
D O I
10.1016/j.ymben.2025.01.007
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
D-allose is a rare monosaccharide, found naturally in low abundances. Due to its low-calorie profile and similar taste to sucrose, D-allose has the potential to become an ideal sugar substitute. D-allose also displays unique properties and health benefits that can be applied to various fields, including food and medicine. D-allose can be produced using two enzymatic steps in vitro: the epimerization of D-fructose, then the isomerization of the resulting D-psicose. This method suffers from poor yield due to the reversible nature of both reactions. We found that Escherichia coli possesses all of the required enzymes to convert D-glucose to D-allose with a thermodynamically favorable pathway, through a series of phosphorylation-epimerization-isomerizationdephosphorylation steps. To increase carbon flux toward D-allose production, the pathway genes were additionally expressed, and the competing pathways were removed. The engineered strains achieved production of Dallose, at a titer of 56.4 g L- 1 , a productivity of 0.65 g L- 1 hr- 1 , and a yield of 41.4% under test tube conditions.
引用
收藏
页码:206 / 214
页数:9
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