Metabolic Engineering of Escherichia coli for Production of alpha-Santalene, a Precursor of Sandalwood Oil
- Authors
- Wang, Yan; Zhou, Shenting; Liu, Qian; Jeong, Seong-Hee; Zhu, Liyan; Yu, Xiangming; Zheng, Xiaojian; Wei, Gongyuan; Kim, Seon-Won; Wang, Chonglong
- Issue Date
- Nov-2021
- Publisher
- American Chemical Society
- Keywords
- alpha-santalene; indole; RBS manipulation; metabolic engineering; Escherichia coli
- Citation
- Journal of Agricultural and Food Chemistry, v.69, no.44, pp 13135 - 13142
- Pages
- 8
- Indexed
- SCIE
SCOPUS
- Journal Title
- Journal of Agricultural and Food Chemistry
- Volume
- 69
- Number
- 44
- Start Page
- 13135
- End Page
- 13142
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/2999
- DOI
- 10.1021/acs.jafc.1c05486
- ISSN
- 0021-8561
1520-5118
- Abstract
- alpha-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 alpha-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 alpha-santalene synthetic operon in E. coli, and the best engineered E. coli NA-IS3D strain could produce alpha-santalene at a titer of 412 mg.L-1. Concerning the observation of the inverse correlation between indole synthesis and alpha-santalene production, this study speculated that indoleassociated amino acid metabolism would be competitive to the synthesis of alpha-santalene rather than indole toxicity itself. The deletion of tnaA could lead to a 1.5-fold increase in alpha-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 alpha-santalene.
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