3.9 Article

Overcoming glutamate auxotrophy in Escherichia coli itaconate overproducer by the Weimberg pathway

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ELSEVIER
DOI: 10.1016/j.mec.2021.e00190

关键词

Weimberg pathway; Glutamate auxotroph; Itaconic acid

资金

  1. Ministry of Science and Technology (Taiwan) [MOST 106-2622-8-007-017, MOST 108-2221-E-007-070-MY3]

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Engineering efficient itaconate producers often requires elimination of isocitrate dehydrogenase to preserve cis-aconitate, leading to auxotrophy for 2-ketoglutarate. This study presents a novel approach by introducing the Weimberg pathway for 2-ketoglutarate biosynthesis, overcoming the need for glutamate supplementation. Through careful tuning of xylose concentration, the final strain produced 20 g/L of itaconate in minimal medium without the need for antibiotics.
Biosynthesis of itaconic acid occurs through decarboxylation of the TCA cycle intermediate cis-aconitate. Engineering of efficient itaconate producers often requires elimination of the highly active isocitrate dehydrogenase to conserve cis-aconitate, leading to 2-ketoglutarate auxotrophy in the producing strains. Supplementation of glutamate or complex protein hydrolysate then becomes necessary, often in large quantities, to support the high cell density desired during itaconate fermentation and adds to the production cost. Here, we present an alternative approach to overcome the glutamate auxotrophy in itaconate producers by synthetically introducing the Weimberg pathway from Burkholderia xenovorans for 2-ketoglutarate biosynthesis. Because of its independence from natural carbohydrate assimilation pathways in Escherichia coli, the Weimberg pathway is able to provide 2-ketoglutarate using xylose without compromising the carbon flux toward itaconate. With xylose concentration carefully tuned to minimize excess 2-ketoglutarate flux in the stationary phase, the final strain accumulated 20 g/L of itaconate in minimal medium from 18 g/L of xylose and 45 g/L of glycerol. Necessity of the recombinant Weimberg pathway for growth also allowed us to maintain multi-copy plasmids carrying in operon the itaconateproducing genes without addition of antibiotics. Use of the Weimberg pathway for growth restoration is applicable to other production systems with disrupted 2-ketoglutarate synthesis.

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