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Exploring the metabolic fate of propanol in industrial erythromycin-producing strain via 13C labeling experiments and enhancement of erythromycin production by rational metabolic engineering of Saccharopolyspora erythraea
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  • Feng Xu,
  • Ming Hong,
  • Ming-Zhi Huang,
  • Chongchong Chen,
  • Xiwei Tian,
  • Haifeng Hang,
  • Ju Chu
Feng Xu
East China University of Science and Technology State Key Laboratory of Bioreactor Engineering
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Ming Hong
East China University of Science and Technology State Key Laboratory of Bioreactor Engineering
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Ming-Zhi Huang
East China University of Science and Technology State Key Laboratory of Bioreactor Engineering
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Chongchong Chen
East China University of Science and Technology State Key Laboratory of Bioreactor Engineering
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Xiwei Tian
East China University of Science and Technology State Key Laboratory of Bioreactor Engineering
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Haifeng Hang
East China University of Science and Technology
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Ju Chu
East China University of Science and Technology State Key Laboratory of Bioreactor Engineering
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Abstract

Propanol have been widely used as a precursor for erythromycin synthesis in industrial production. However, the knowledge on the exact metabolic fate of propanol was still unclear. In the present study, the metabolic fate of propanol in industrial erythromycin-producing strain S. erythraea E3 was explored via 13C labeling experiments. An unexpected pathway in which propanol was channeled into tricarboxylic acid cycle was uncovered, resulting in uneconomic catabolism of propanol. By deleting the sucC gene, which encodes succinyl-CoA synthetase that catalyse a reaction in the unexpected propanol utilization pathway, a novel strain E3-ΔsucC was constructed. The strain E3-ΔsucC showed a significant enhancement in erythromycin production in the chemically defined medium compared to E3 (786.61 vs 392.94 mg/L). Isotopic dilution mass spectrometry metabolomics and isotopically nonstationary 13C metabolic flux analysis were employed to characterize the metabolic differences between S. erythraea E3 and E3-ΔsucC. The results showed that compared with the starting strain E3, the fluxes of pentose phosphate pathway in E3-△sucC increased by almost 200%. The most significant difference located in the tricarboxylic acid cycle was also found. The flux of the metabolic reaction catalyzed by succinyl-CoA synthetase in E3-ΔsucC was almost zero, while the glyoxylate bypass flux significantly increased. These new insights into the precursor utilization of antibiotic biosynthesis by rational metabolic engineering in S. erythraea provide the new vision in increasing industrial production of secondary metabolites.