Self-Sufficient In Vitro Multi-Enzyme Cascade for Efficient Synthesis of Danshensu from l-DOPA.
Ruizhi HanKe GaoYulin JiangJieyu ZhouGuochao XuJinjun DongUlrich SchwanebergYu JiYe NiPublished in: ACS synthetic biology (2022)
Danshensu (DSS), a traditional Chinese medicine, is widely used for the treatment of cardiovascular and cancer diseases. Here, a one-pot multi-enzyme cascade pathway was designed for DSS synthesis from l-DOPA using tyrosine aminotransferase from Escherichia coli ( Ec TyrB) and d-isomer-specific 2-hydroxyacid dehydrogenase from Lactobacillus frumenti ( Lf D2-HDH). Glutamate dehydrogenase from Clostridium difficile ( Cd gluD) was also introduced for a self-sufficient system of α-ketoglutaric acid and NADH. Under optimal conditions (35 °C, pH 7.0, Ec TyrB: Lf D2-HDH: Cd gluD = 3:2:1, glutamate:NAD + = 1:1), 98.3% yield (at 20 mM l-DOPA) and space-time yield of 6.61 g L -1 h -1 (at 40 mM l-DOPA) were achieved. Decreased yields of DSS at elevated l-DOPA concentrations (100 mM) could be attributed to an inhibited Cd gluD activity caused by NH 4 + accumulation. This developed multi-enzyme cascade pathway (including Ec TyrB, Lf D2-HDH, and Cd gluD) provides an efficient and sustainable approach for the production of DSS from l-DOPA.