Hawkins Kristy M, Smolke Christina D
Division of Chemistry and Chemical Engineering, California Institute of Technology, 1200 East California Boulevard, MC 210-41, Pasadena, California 91125, USA.
Nat Chem Biol. 2008 Sep;4(9):564-73. doi: 10.1038/nchembio.105.
The benzylisoquinoline alkaloids (BIAs) are a diverse class of metabolites that exhibit a broad range of pharmacological activities and are synthesized through plant biosynthetic pathways comprised of complex enzyme activities and regulatory strategies. We have engineered yeast to produce the key intermediate reticuline and downstream BIA metabolites from a commercially available substrate. An enzyme tuning strategy was implemented that identified activity differences between variants from different plants and determined optimal expression levels. By synthesizing both stereoisomer forms of reticuline and integrating enzyme activities from three plant sources and humans, we demonstrated the synthesis of metabolites in the sanguinarine/berberine and morphinan branches. We also demonstrated that a human P450 enzyme exhibits a novel activity in the conversion of (R)-reticuline to the morphinan alkaloid salutaridine. Our engineered microbial hosts offer access to a rich group of BIA molecules and associated activities that will be further expanded through synthetic chemistry and biology approaches.
苄基异喹啉生物碱(BIAs)是一类多样的代谢产物,具有广泛的药理活性,通过由复杂酶活性和调控策略组成的植物生物合成途径合成。我们对酵母进行了工程改造,使其能够从一种市售底物生产关键中间体网状番荔枝碱和下游BIA代谢产物。实施了一种酶优化策略,该策略确定了来自不同植物的变体之间的活性差异,并确定了最佳表达水平。通过合成网状番荔枝碱的两种立体异构体形式,并整合来自三种植物来源和人类的酶活性,我们展示了血根碱/小檗碱和吗啡喃分支中代谢产物的合成。我们还证明,一种人类细胞色素P450酶在将(R)-网状番荔枝碱转化为吗啡喃生物碱salutaridine时表现出一种新的活性。我们改造后的微生物宿主提供了获取丰富的BIA分子和相关活性的途径,这些将通过合成化学和生物学方法进一步扩展。