Nakagawa Akira, Matsuzaki Chiaki, Matsumura Eitaro, Koyanagi Takashi, Katayama Takane, Yamamoto Kenji, Sato Fumihiko, Kumagai Hidehiko, Minami Hiromichi
Research Institute for Bioresources and Biotechnology, Ishikawa Prefectural University, Nonoichi-shi, Ishikawa 921-8836, Japan.
Division of Integrated Life Science, Graduate School of Biostudies, Kyoto University, Oiwake-cho, Kitashirakawa, Sakyo-ku, Kyoto 606-8502, Japan.
Sci Rep. 2014 Oct 21;4:6695. doi: 10.1038/srep06695.
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.
四氢罂粟碱(THP)是一种存在于多种药物化合物中的苄基异喹啉生物碱(BIA),用作生产BIA的起始原料。THP还具有多种神经生物学特性,但难以合成。因此,需要一种简单的THP生产方法。最近的研究表明,微生物,尤其是细菌,可以作为合成这些复杂化合物的平台;然而,由于细菌缺乏细胞器,设计的合成途径无法进行区室化。因此,代谢流经常受到不良反应的抑制或干扰。事实上,在首次尝试使用单一工程化大肠杆菌菌株合成THP时,产量相当低(<5 μM),主要是因为酪氨酸酶(我们生产系统中的一种必需酶)对THP的氧化作用。为了解决这些问题,我们构建了一个分步生产(R,S)-THP的系统,其中多巴胺生产步骤和随后的THP生产步骤是分开的。(R,S)-THP的产量达到了1.0 mM(287 mg/L),这是迄今为止报道的使用微生物生产BIA的最高产量方法。此外,我们证明了通过分步发酵产生的(R,S)-THP可用于生产重要的BIA中间体网状番荔枝碱。基于这些观察结果,讨论了分步发酵方法的应用。