Metabolic Engineering of Escherichia coli for Efficient Production of Ectoine

IF 6.2 1区 农林科学 Q1 AGRICULTURE, MULTIDISCIPLINARY Journal of Agricultural and Food Chemistry Pub Date : 2024-12-26 DOI:10.1021/acs.jafc.4c07640
Ke Wang, Xitong Song, Boya Cui, Yi Wang, Wei Luo
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Abstract

Ectoine is a valuable compatible solute with extensive applications in bioengineering, cosmetics, medicine, and the food industry. While certain halophilic bacteria can naturally produce ectoine, as a model organism for biomanufacturing, Escherichia coli offers significant advantages to be engineered for potentially high-level ectoine production. However, complex metabolic flux distributions and byproduct formation present bottlenecks that limit ectoine production in E. coli. In this study, we aimed to enhance ectoine production in E. coli BL21(DE3) through systematic metabolic engineering strategies. We investigated the effects of the ectABC gene cluster sequence, plasmid copy number, and key gene copy number on ectoine synthesis. Using the original ectABC sequence with the high-copy-number plasmid pRSFDuet-1 resulted in the highest level of ectoine production. Knocking out genes encoding homoserine dehydrogenase and diaminopimelate decarboxylase reduced competing pathways, further increasing ectoine yield. Overexpression of aspartate semialdehyde dehydrogenase, aspartate kinase I (thrA*), aspartate aminotransferase, and aspartate ammonia-lyase (aspA) was performed, and optimal gene copy numbers were determined. When the copy numbers of thrA* and aspA were both three, ectoine synthesis improved, reaching 1.91 g/L. Enhancing the oxaloacetate pool by overexpressing phosphoenolpyruvate carboxylase (ppc) or introducing pyruvate carboxylase (pyc) from Corynebacterium glutamicum further increased ectoine production to 4.99 g/L. Balancing NADPH and ATP levels through cofactor engineering contributed to additional production improvements. Combining these strain engineering strategies, we ultimately constructed strain C24, which produced 35.33 g/L ectoine in a 5 L fermenter with a glucose conversion rate of 0.21 g/g. These results demonstrate that targeted metabolic engineering can significantly enhance ectoine production in E. coli, providing a foundation for industrial-scale production.

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高效生产艾克托因的大肠杆菌代谢工程
依托碱是一种有价值的相容性溶质,在生物工程、化妆品、医药和食品工业中有着广泛的应用。虽然某些嗜盐细菌可以自然产生异托碱,但作为生物制造的模式生物,大肠杆菌为潜在的高水平异托碱生产提供了显著的优势。然而,复杂的代谢通量分布和副产物形成存在瓶颈,限制了大肠杆菌的肠外泌素生产。在本研究中,我们旨在通过系统代谢工程策略提高大肠杆菌BL21(DE3)的异托因产量。我们研究了ectABC基因簇序列、质粒拷贝数和关键基因拷贝数对外托因合成的影响。将原始的ectABC序列与高拷贝数质粒pRSFDuet-1结合使用,可以产生最高水平的ectABC。敲除编码同丝氨酸脱氢酶和二氨基苯甲酸脱羧酶的基因减少了竞争途径,进一步提高了外托氨酸的产量。通过过表达天冬氨酸半醛脱氢酶、天冬氨酸激酶I (thrA*)、天冬氨酸转氨酶和天冬氨酸解氨酶(aspA),确定最佳基因拷贝数。当thrA*和aspA拷贝数均为3时,异托因的合成提高,达到1.91 g/L。通过过表达磷酸烯醇丙酮酸羧化酶(ppc)或引入谷氨酸棒状杆菌的丙酮酸羧化酶(pyc)来增强草酰乙酸池,进一步将外托氨酸产量提高到4.99 g/L。通过辅因子工程平衡NADPH和ATP水平有助于进一步提高产量。结合这些菌株工程策略,我们最终构建了菌株C24,该菌株在5l发酵罐中产生35.33 g/L的异黄酮,葡萄糖转化率为0.21 g/g。这些结果表明,靶向代谢工程可以显著提高大肠杆菌的异托因产量,为工业规模生产提供了基础。
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来源期刊
Journal of Agricultural and Food Chemistry
Journal of Agricultural and Food Chemistry 农林科学-农业综合
CiteScore
9.90
自引率
8.20%
发文量
1375
审稿时长
2.3 months
期刊介绍: The Journal of Agricultural and Food Chemistry publishes high-quality, cutting edge original research representing complete studies and research advances dealing with the chemistry and biochemistry of agriculture and food. The Journal also encourages papers with chemistry and/or biochemistry as a major component combined with biological/sensory/nutritional/toxicological evaluation related to agriculture and/or food.
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