Abstract
Tetrahydropapaveroline (THP), a benzylisoquinoline alkaloid (BIA) found in diverse pharmaceutical compounds, is used as a starting material for the production of BIA. THP also has various neurobiological properties but is difficult to synthesize. Therefore, a simple method for THP production is desired. Recent studies have shown that microbes, especially bacteria, can serve as platforms for synthesizing these complex compounds; however, because bacteria lack organelles, the designed synthetic pathway cannot be compartmentalized. Thus, the metabolic flow is frequently inhibited or disrupted by undesirable reactions. Indeed, in the first attempt to synthesize THP using a single strain of engineered Escherichia coli, the yield was quite low (<5 μM), mainly because of the oxidation of THP by tyrosinase, an essential enzyme in our production system. To circumvent these problems, we constructed a stepwise (R,S)-THP production system, in which the dopamine-producing step and the subsequent THP-producing step were separated. The yield of (R,S)-THP reached 1.0 mM (287 mg/L), the highest yielding BIA production method using a microbe reported to date. Furthermore, we demonstrated that (R,S)-THP produced by stepwise fermentation is useful for the production of reticuline, an important BIAs intermediate. Based on these observations, applying the stepwise fermentation method is discussed.
Highlights
Tetrahydropapaveroline (THP), a benzylisoquinoline alkaloid (BIA) found in diverse pharmaceutical compounds, is used as a starting material for the production of B enzylisoquinoline alkaloids (BIAs)
THP is naturally produced by the condensation reaction of dopamine and 3,4-dyhydroxyphenylacetaldehyde (3,4-DHPAA), which is synthesized from dopamine by an endogenous monoamine oxidase (MAO) in humans
Whereas tyrosine hydroxylase activity is essential for L-DOPA synthesis in the microbial production system of BIA (Fig. 1), o-diphenolase activity is undesirable because it results in the oxidation of the hydroxyl groups of the intermediate compounds, L-DOPA and dopamine, to their quinone derivatives[17]
Summary
(R,S)-Tetrahydropapaveroline production by stepwise fermentation using engineered Escherichia coli Akira Nakagawa[1], Chiaki Matsuzaki[1], Eitaro Matsumura[1], Takashi Koyanagi[1], Takane Katayama[1], Kenji Yamamoto[1], Fumihiko Sato[2], Hidehiko Kumagai1 & Hiromichi Minami[1]. Whereas tyrosine hydroxylase activity is essential for L-DOPA synthesis in the microbial production system of BIA (Fig. 1), o-diphenolase activity is undesirable because it results in the oxidation of the hydroxyl groups of the intermediate compounds, L-DOPA and dopamine, to their quinone derivatives[17]. In addition to these two compounds, we speculated that THP was oxidized by the o-diphenolase activity of tyrosinase. We report that THP is oxidized by tyrosinase and to avoid oxidation, we employed stepwise fermentative production of (R,S)-THP by using dopamine production and MAO expression strains
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