photo: The Hong Kong University of Science and Technology
New research from a team of scientists from Hong Kong University of Science and Technology (HKUST), UC Berkeley and Scripps Institution of Oceanography of University of California, San Diego (SCRIPPS) has used synthetic biology to determine the active mechanism of E. Coli toxin in breaking down DNA.
While human gut microbes like E. coli help digest food and regulate our immune system, they also contain toxins that could arrest cell cycle and eventually cause cell death. Scientists have long known that colibactin – a genotoxin produced by E. coli, can induce DNA double-strand breaks in eukaryotic cells and increase the risk of colorectal cancer in humans. However, how colibactin causes DNA damage had remained a mystery as reconstructing colibactin metabolites is extremely difficult due to the compound’s instability, low titer and complexity of its biosynthetic pathway.
Led by Prof. Qian Peiyuan, Chair Professor of HKUST’s Department of Ocean Science and Division of Life Science, the research group unearthed the missing link using a novel biosynthetic method. The team not only succeeded in cloning the colibactin gene cluster, but also found a way to mass produce the genes for testing and validation. After repeated assays of various sets of colibactin precursors, the team eventually identified colibactin-645 as the culprit of the DNA double-strand breaks, and uncovered colibactin metabolite’s biosynthetic pathway as well as its mechanism of causing DNA damage.
Prof. Qian said, “Although a few colibactin metabolites have been reported to damage DNA via DNA crosslinking activity, the genotoxic colibactin that possesses DNA double-strands directly is yet-to-be-identified. Our research has confirmed colibactin-645 exerts direct DNA double-strand breaks, that unearthed the missing link that correlates colibactin to its health effects on human beings.”
LI Zhongrui, a graduate student in the lab of Wenjun Zhangsaid the restructuring of colibactin’s molecular scaffold provides a model for designing and synthesizing potent DNA cleaving agents – such as synthetic restriction “enzymes” or chemotherapeutic agents.
The research article is available at Nature Chemistry https://doi.org/10.1038/s41557-019-0317-7
This announcement originally appeared in sciencemag.com>>