Quercetin Glucoside Production by Engineered Escherichia coli

被引:18
|
作者
Xia, Tian [1 ]
Eiteman, Mark A. [1 ]
机构
[1] Univ Georgia, Coll Engn, BioChem Engn, Athens, GA 30602 USA
关键词
Glycosylation; Glucose-6-phosphate isomerase; Glucose-6-phosphate; 1-dehydrogenase; SPONTANEOUSLY HYPERTENSIVE-RATS; CENTRAL CARBON METABOLISM; IN-VITRO; PHOSPHOGLUCOSE ISOMERASE; REGIOSELECTIVE SYNTHESIS; FLAVONOID QUERCETIN; GENE-EXPRESSION; FLUX ANALYSIS; CELL-GROWTH; GLYCOSIDES;
D O I
10.1007/s12010-017-2403-x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Escherichia coli strains expressing the O-glucosyltransferases UGT73B3 or UGT84B1 were compared for the production of glucosides from quercetin supplied into a defined medium. The formation of quercetin-3-glucoside (Q3G) by UGT73B3 showed a maximum at 33 degrees C, while the formation of quercetin-7-glucoside by UGT84B1 increased with increasing temperature to 37 degrees C. The highest concentrations of Q3G were attained by strains having a deletion in the pgi gene-coding phosphoglucose isomerase, which effectively blocked the entry of glucose-6P into the Embden-Meyerhof-Parnas pathway. Formation of Q3G was improved in 1-L controlled bioreactors compared to shake flask cultures, a result attributed to the greater oxygen transfer rate in bioreactors. Under batch conditions with 30 g/L glucose as the sole carbon source, E. coli MEC367 (MG1655 pgi) expressing UGT73B3 generated 3.9 g/L Q3G in 56 h.
引用
收藏
页码:1358 / 1370
页数:13
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