Abstract
Carminic acid is an aromatic polyketide found in scale insects (i.e., Dactylopius coccus) and is a widely used natural red colorant. It has long been produced by the cumbersome farming of insects followed by multistep purification processes. Thus, there has been much interest in producing carminic acid by the fermentation of engineered bacteria. Here we report the complete biosynthesis of carminic acid from glucose in engineered Escherichia coli. We first optimized the type II polyketide synthase machinery from Photorhabdus luminescens, enabling a high-level production of flavokermesic acid upon coexpression of the cyclases ZhuI and ZhuJ from Streptomyces sp. R1128. To discover the enzymes responsible for the remaining two reactions (hydroxylation and C-glucosylation), biochemical reaction analyses were performed by testing enzyme candidates reported to perform similar reactions. The two identified enzymes, aklavinone 12-hydroxylase (DnrF) from Streptomyces peucetius and C-glucosyltransferase (GtCGT) from Gentiana triflora, could successfully perform hydroxylation and C-glucosylation of flavokermesic acid, respectively. Then, homology modeling and docking simulations were performed to enhance the activities of these two enzymes, leading to the generation of beneficial mutants with 2-5-fold enhanced conversion efficiencies. In addition, the GtCGT mutant was found to be a generally applicable C-glucosyltransferase in E. coli, as was showcased by the successful production of aloesin found in Aloe vera. Simple metabolic engineering followed by fed-batch fermentation resulted in 0.63 ± 0.02 mg/L of carminic acid production from glucose. The strategies described here will be useful for the design and construction of biosynthetic pathways involving unknown enzymes and consequently the production of diverse industrially important natural products.
Original language | English |
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Journal | Journal of the American Chemical Society |
Volume | 143 |
Issue number | 14 |
Pages (from-to) | 5364-5377 |
ISSN | 0002-7863 |
DOIs | |
Publication status | Published - 2021 |
Bibliographical note
Funding Information:The authors thank Dr. Seon Young Park and Dr. Kyeong Rok Choi for helpful discussions, Eunju Lee at UC Davis Economics Department for advice on statistics, Yu Ri Lee at Chungnam National University Center for Research Facilities for LC-HRMS analyses, Dr. Yun-Cheol Na at Korea Basic Science Institute (KBSI), Western Seoul Center, for LC-MS/MS analyses, Ji Won Kim at KAIST Bio Core Center for LC-MS (MRM) analyses, and Jae Hyun Lee at KBSI, Western Seoul Center, for NMR analysis. This work was supported by the Technology Development Program to Solve Climate Changes on Systems Metabolic Engineering for Biorefineries (Grants NRF-2012M1A2A2026556 and NRF-2012M1A2A2026557) of the Ministry of Science and ICT (MSIT) through the National Research Foundation (NRF) of Korea and the KAIST Cross-Generation Collaborative Lab project; S.Y.L. and D.Y. were also supported by Novo Nordisk Foundation grant NNF16OC0021746.
Publisher Copyright:
© 2021 American Chemical Society.