Junping Zhou , Zheng Zhang , Xinyuan Xin , Yinan Xue , Yihong Wang , Xueyun Feng , Bo Zhang , Man Zhao , Zhiqiang Liu , Yuguo Zheng
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Upon confirmation that the <span>d</span>-pantothenate biosynthetic pathway could be used for <span>d</span>-panthenol biosynthesis, a fermentation medium and pyruvate pool of the strain were first optimized, enhancing the <span>d</span>-pantothenol production from 31.6 mg L<sup>−1</sup> to 184.2 mg L<sup>−1</sup>. Moreover, structure-guided rational protein engineering of pantothenate synthase (PS) was also applied for improving the catalytic activities towards 3-aminopropanol, variant M3 (F62L/R123Q/R189I), which destroyed the hydrogen network between the residues R123/R189 and the carboxyl group of β-alanine and showed a 3.77-fold increase in <span>d</span>-panthenol production compared to that of the wild-type PS. In order to enhance the supply of NADPH, genes for cofactor regeneration and the pentose phosphate pathway (PPP) were enhanced, along with the knockdown of the NADPH depletion pathway. It was found that the reduction of the <em>pgi</em> gene resulted in the enhancement of the transcription level in the PPP pathway, which led to a relatively balanced ratio of NADPH/NADP<sup>+</sup>. The obtained strain DPN13 reached a peak of 1469.3 mg L<sup>−1</sup><span>d</span>-pantothenol in the shake flask. Fed-batch fermentation was then carried out, and the titers of <span>d</span>-pantoate and <span>d</span>-pantothenol of the final strain in a 5 L bioreactor reached 24.1 g L<sup>−1</sup> and 13.2 g L<sup>−1</sup>, respectively, which were the highest of biosynthesized <span>d</span>-pantoate and <span>d</span>-pantothenol reported to date. Overall, with the systematic metabolic engineering of the strain for the <em>de novo</em> biosynthesis of <span>d</span>-panthenol, the green production of <span>d</span>-panthenol with industrial sustainability would be easily achieved.</div></div>","PeriodicalId":78,"journal":{"name":"Green Chemistry","volume":"27 6","pages":"Pages 1806-1819"},"PeriodicalIF":9.2000,"publicationDate":"2025-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Metabolic engineering of Escherichia coli for the production of d-panthenol from 3-aminopropanol and glucose†\",\"authors\":\"Junping Zhou , Zheng Zhang , Xinyuan Xin , Yinan Xue , Yihong Wang , Xueyun Feng , Bo Zhang , Man Zhao , Zhiqiang Liu , Yuguo Zheng\",\"doi\":\"10.1039/d4gc06142j\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div> <span>d</span>-Panthenol is an important chemical widely utilized in the feed, medicine and cosmetic industries. For industrial production, <span>d</span>-panthenol is converted by chemical condensation with 3-aminopropanol and <span>d</span>-pantolactone, in which <span>d</span>-pantolactone is produced by enzymatic racemization from chemically synthesized <span>dl</span>-pantolactone. In this study, the <em>de novo</em> biosynthesis of <span>d</span>-panthenol in engineered <em>Escherichia coli</em> from glucose with the supplementation of 3-aminopropanol was established for the first time. Upon confirmation that the <span>d</span>-pantothenate biosynthetic pathway could be used for <span>d</span>-panthenol biosynthesis, a fermentation medium and pyruvate pool of the strain were first optimized, enhancing the <span>d</span>-pantothenol production from 31.6 mg L<sup>−1</sup> to 184.2 mg L<sup>−1</sup>. Moreover, structure-guided rational protein engineering of pantothenate synthase (PS) was also applied for improving the catalytic activities towards 3-aminopropanol, variant M3 (F62L/R123Q/R189I), which destroyed the hydrogen network between the residues R123/R189 and the carboxyl group of β-alanine and showed a 3.77-fold increase in <span>d</span>-panthenol production compared to that of the wild-type PS. In order to enhance the supply of NADPH, genes for cofactor regeneration and the pentose phosphate pathway (PPP) were enhanced, along with the knockdown of the NADPH depletion pathway. It was found that the reduction of the <em>pgi</em> gene resulted in the enhancement of the transcription level in the PPP pathway, which led to a relatively balanced ratio of NADPH/NADP<sup>+</sup>. The obtained strain DPN13 reached a peak of 1469.3 mg L<sup>−1</sup><span>d</span>-pantothenol in the shake flask. Fed-batch fermentation was then carried out, and the titers of <span>d</span>-pantoate and <span>d</span>-pantothenol of the final strain in a 5 L bioreactor reached 24.1 g L<sup>−1</sup> and 13.2 g L<sup>−1</sup>, respectively, which were the highest of biosynthesized <span>d</span>-pantoate and <span>d</span>-pantothenol reported to date. 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引用次数: 0
摘要
d -泛醇是一种广泛应用于饲料、医药、化妆品等行业的重要化学品。在工业生产中,d -泛醇与3-氨基丙醇和D-pantolactone通过化学缩合转化,其中D-pantolactone由化学合成的DL-pantolactone经酶外消旋作用生成D-pantolactone。本研究首次建立了以葡萄糖为原料,在工程大肠杆菌中添加3-氨基丙醇的新生物合成d -泛醇的方法。在确认d -泛酸生物合成途径可用于d -泛酸生物合成后,首先对菌株的发酵培养基和丙酮酸池进行了优化,将d -泛酸产量从31.6 mg L−1提高到184.2 mg L−1。此外,还利用结构导向的泛酸合成酶(PS)合理蛋白工程技术提高了变体M3 (F62L/R123Q/R189I)对3-氨基丙醇的催化活性,该变体M3 (F62L/R123Q/R189I)破坏了残基R123/R189与β-丙氨酸羧基之间的氢网络,与野生型PS相比,d-泛酸合成酶的产量增加了3.77倍。辅助因子再生和戊糖磷酸途径(PPP)基因增强,NADPH耗竭途径下调。我们发现pgi基因的减少导致PPP通路中转录水平的增强,从而导致NADPH/NADP+的比例相对平衡。得到的菌株DPN13在摇瓶中达到峰值1469.3 mg L−1d -泛酸醇。然后进行补料分批发酵,最终菌株在5l生物反应器中D-pantoate和D-pantothenol的滴度分别达到24.1 g L−1和13.2 g L−1,这是迄今为止报道的生物合成D-pantoate和D-pantothenol的最高滴度。综上所述,通过对菌株进行系统的代谢工程,实现d -泛醇的从头生物合成,将很容易实现具有工业可持续性的d -泛醇绿色生产。
Metabolic engineering of Escherichia coli for the production of d-panthenol from 3-aminopropanol and glucose†
d-Panthenol is an important chemical widely utilized in the feed, medicine and cosmetic industries. For industrial production, d-panthenol is converted by chemical condensation with 3-aminopropanol and d-pantolactone, in which d-pantolactone is produced by enzymatic racemization from chemically synthesized dl-pantolactone. In this study, the de novo biosynthesis of d-panthenol in engineered Escherichia coli from glucose with the supplementation of 3-aminopropanol was established for the first time. Upon confirmation that the d-pantothenate biosynthetic pathway could be used for d-panthenol biosynthesis, a fermentation medium and pyruvate pool of the strain were first optimized, enhancing the d-pantothenol production from 31.6 mg L−1 to 184.2 mg L−1. Moreover, structure-guided rational protein engineering of pantothenate synthase (PS) was also applied for improving the catalytic activities towards 3-aminopropanol, variant M3 (F62L/R123Q/R189I), which destroyed the hydrogen network between the residues R123/R189 and the carboxyl group of β-alanine and showed a 3.77-fold increase in d-panthenol production compared to that of the wild-type PS. In order to enhance the supply of NADPH, genes for cofactor regeneration and the pentose phosphate pathway (PPP) were enhanced, along with the knockdown of the NADPH depletion pathway. It was found that the reduction of the pgi gene resulted in the enhancement of the transcription level in the PPP pathway, which led to a relatively balanced ratio of NADPH/NADP+. The obtained strain DPN13 reached a peak of 1469.3 mg L−1d-pantothenol in the shake flask. Fed-batch fermentation was then carried out, and the titers of d-pantoate and d-pantothenol of the final strain in a 5 L bioreactor reached 24.1 g L−1 and 13.2 g L−1, respectively, which were the highest of biosynthesized d-pantoate and d-pantothenol reported to date. Overall, with the systematic metabolic engineering of the strain for the de novo biosynthesis of d-panthenol, the green production of d-panthenol with industrial sustainability would be easily achieved.
期刊介绍:
Green Chemistry is a journal that provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998), which defines green chemistry as the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry aims to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. The journal welcomes submissions on all aspects of research relating to this endeavor and publishes original and significant cutting-edge research that is likely to be of wide general appeal. For a work to be published, it must present a significant advance in green chemistry, including a comparison with existing methods and a demonstration of advantages over those methods.