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A Novel Muconic Acid Biosynthesis Approach by Shunting Tryptophan Biosynthesis via Anthranilate

机译:通过邻氨基苯甲酸转移色氨酸生物合成的新型粘康酸生物合成方法

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摘要

Muconic acid is the synthetic precursor of adipic acid, and the latter is an important platform chemical that can be used for the production of nylon-6,6 and polyurethane. Currently, the production of adipic acid relies mainly on chemical processes utilizing petrochemicals, such as benzene, which are generally considered environmentally unfriendly and nonrenewable, as starting materials. Microbial synthesis from renewable carbon sources provides a promising alternative under the circumstance of petroleum depletion and environment deterioration. Here we devised a novel artificial pathway in Escherichia coli for the biosynthesis of muconic acid, in which anthranilate, the first intermediate in the tryptophan biosynthetic branch, was converted to catechol and muconic acid by anthranilate 1,2-dioxygenase (ADO) and catechol 1,2-dioxygenase (CDO), sequentially and respectively. First, screening for efficient ADO and CDO from different microbial species enabled the production of gram-per-liter level muconic acid from supplemented anthranilate in 5 h. To further achieve the biosynthesis of muconic acid from simple carbon sources, anthranilate overproducers were constructed by overexpressing the key enzymes in the shikimate pathway and blocking tryptophan biosynthesis. In addition, we found that introduction of a strengthened glutamine regeneration system by overexpressing glutamine synthase significantly improved anthranilate production. Finally, the engineered E. coli strain carrying the full pathway produced 389.96 ± 12.46 mg/liter muconic acid from simple carbon sources in shake flask experiments, a result which demonstrates scale-up potential for microbial production of muconic acid.
机译:粘康酸是己二酸的合成前体,后者是一种重要的平台化学品,可用于生产尼龙6,6和聚氨酯。当前,己二酸的生产主要依赖于利用石油化学产品如苯的化学方法作为起始原料,该化学产品通常被认为对环境不利且不可再生,例如苯。在石油枯竭和环境恶化的情况下,由可再生碳源合成微生物提供了一种有前途的替代方法。在这里,我们设计了一种用于大肠杆菌粘菌酸生物合成的新型人工途径,其中色氨酸生物合成分支的第一个中间体邻氨基苯甲酸被邻氨基苯甲酸1,2-二加氧酶(ADO)和邻苯二酚1转化为邻苯二酚和粘康酸。 ,2-二加氧酶(CDO),依次和分别。首先,从不同微生物中筛选有效的ADO和CDO能够在5小时内从补充的邻氨基苯甲酸生产每克克级粘康酸。为了进一步实现从简单碳源生物合成粘康酸,通过在sh草酸酯途径中过表达关键酶并阻断色氨酸的生物合成来构建邻氨基苯甲酸过生产者。此外,我们发现通过过量表达谷氨酰胺合酶引入增强的谷氨酰胺再生系统可以显着提高邻氨基苯甲酸的产生。最后,携带完整途径的工程大肠杆菌菌株在摇瓶实验中从简单的碳源产生了389.96±12.46 mg / L粘康酸,这一结果证明了微生物生产粘康酸的规模化潜力。

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