Prof. Liang, Zhao-Xun
Our lab focuses on discovering novel enzymes, pathways, and mechanisms involved in natural product biosynthesis and bacterial pathogenesis. We leverage genomics, biochemistry, and synthetic biology to awaken cryptic biosynthetic pathways, revealing new enzymatic strategies for building and modifying molecular scaffolds. Building on nature's biosynthetic diversity, we also strive to engineer microbes to produce "unnatural" natural products. With powerful DNA synthesis and genome editing tools, we redesign entire pathways by combining enzymes from different systems or creating entirely new biochemical routes. This synthetic biology approach will expand nature's chemical repertoire for drug discovery applications. Another focus of our research examines cyclic dinucleotides, key signaling molecules that regulate critical bacterial processes. These bacterial messengers function through sophisticated networks of enzymes and effector proteins, which ensure precise spatiotemporal control over bacterial behaviour. By elucidating these signaling pathways, we seek to uncover novel therapeutic targets for disrupting pathogenic infections, aiming to develop innovative antimicrobial and biofilm-disrupting strategies.
Research Areas
Research Assistant
Research Fellow
PhD Student
PhD Student
PhD Student
Research Assistant
PhD Student
PhD Student
Research Assistant
Research Fellow
PhD Student
- Ma, G.L., Candra, H., Pang, L.M., Xiong, J., Ding, Y., Tran, H.T., Low, Z.J., Ye, H., Liu, M., Zheng, J., Fang, M., Cao, B., and Liang, Z.-X. “Biosynthesis of tasikamides via pathway coupling and diazonium-mediated hydrazone formation.” Journal of the American Chemical Society 144 (2022): 1622–1633. https://doi.org/10.1021/jacs.1c10369
- Ma, G.-L., Tran, H.T., Low, Z.J., Candra, H., Pang, L.M., Chang, Q.W., Fan, M.L., and Liang, Z.-X. “Pathway retrofitting yields insights into the biosynthesis of anthraquinone-fused enediynes.” Journal of the American Chemical Society 143 (2021): 11500–11509. https://doi.org/10.1021/jacs.1c03911
- Low, Z.J., Ma, G.-L., Tran, H.T., Zou, Y., Juan, X., Pang, L., Nuryyeva, S., Hong, Y., Hu, J., Houk, K.N., and Liang, Z.-X. “Sungeidines from a non-canonical enediyne biosynthetic pathway.” Journal of the American Chemical Society 142 (2020): 1673–1679. https://doi.org/10.1021/jacs.9b10086
- Xu, L.H., Xing, L.Y., Zeng, Y., Yam, J.K.H., Ding, Y., Venkataramani, P., Cheang, Q.W., Yang, X., Tang, X., Zhang, L.-H., Chiam, K.-H., Yang, L., and Liang, Z.-X. “A cyclic di-GMP–binding adaptor protein interacts with a chemotaxis methyltransferase to control flagellar motor switching.” Science Signaling 9 (2016): ra102. https://doi.org/10.1126/scisignal.aaf7584
- Ho, C.L., Chong, K.S.J., Oppong, J.A., Chuah, M.L.C., Tan, S.M., and Liang, Z.-X. “Visualizing the perturbation of cellular cyclic di-GMP levels in bacterial cells.” Journal of the American Chemical Society 135 (2013): 566–569. https://doi.org/10.1021/ja310497x