1. Academic Validation
  2. Metabolic Engineering of Escherichia coli for Production of α-Santalene, a Precursor of Sandalwood Oil

Metabolic Engineering of Escherichia coli for Production of α-Santalene, a Precursor of Sandalwood Oil

  • J Agric Food Chem. 2021 Nov 10;69(44):13135-13142. doi: 10.1021/acs.jafc.1c05486.
Yan Wang 1 Shenting Zhou 1 Qian Liu 1 Seong-Hee Jeong 2 Liyan Zhu 1 Xiangming Yu 1 Xiaojian Zheng 1 Gongyuan Wei 1 Seon-Won Kim 2 Chonglong Wang 1
Affiliations

Affiliations

  • 1 School of Biology and Basic Medical Sciences, Soochow University, Suzhou 215006, People's Republic of China.
  • 2 Division of Applied Life Science (BK21 Plus), PMBBRC, Gyeongsang National University, Jinju 52828, Republic of Korea.
Abstract

α-Santalene belongs to a class of natural compounds with many physiological functions and medical applications. Advances in metabolic engineering enable non-native hosts (e.g., Escherichia coli) to produce α-santalene, the precursor of sandalwood oil. However, imbalances in enzymatic activity often result in a metabolic burden on hosts and repress the synthetic capacity of the desired product. In this work, we manipulated ribosome binding sites (RBSs) to optimize an α-santalene synthetic operon in E. coli, and the best engineered E. coli NA-IS3D strain could produce α-santalene at a titer of 412 mg·L-1. Concerning the observation of the inverse correlation between indole synthesis and α-santalene production, this study speculated that indole-associated amino acid metabolism would be competitive to the synthesis of α-santalene rather than indole toxicity itself. The deletion of tnaA could lead to a 1.5-fold increase in α-santalene production to a titer of 599 mg·L-1 in E. coli tnaA- NA-IS3D. Our results suggested that the optimization of RBS sets of the synthetic module and attenuation of the competitive pathway are promising approaches for improving the production of Terpenoids including α-santalene.

Keywords

Escherichia coli; RBS manipulation; indole; metabolic engineering; α-santalene.

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