Postdoc. University of California, Davis
Ph.D. The Royal Vet and Ag University, Denmark
M.S., The Chinese Academy of Sciences
B.S. Yunnan University, China
Biosynthetic mechanism and metabolic engineering of novel antifungal and anti-MRSA antibiotics from gliding Gram-negative bacteria, mycotoxins and other bioactive natural products from plant pathogenic fungi and endophytes.
- Molecular mechanism for the biosynthesis of new antibiotics, mycotoxins and other bioactive natural products
- Discovery of new antibiotics and other bioactive natural products from Lysobacter bacteria, endophytic fungi, and other underexplored sources
- Metabolic pathway engineering
Research in the Du group is at the interface of chemistry and biology. Specifically, we are studying the molecular mechanisms by which organisms (bacteria, fungi and plants) make structurally complex, biologically active natural products. Our goal is to use this knowledge to produce new products through genetic engineering that will be beneficial to humans. The studies involve tools and knowledge from biochemistry, molecular biology, genetics, and chemistry. Currently, we are working on three main projects.
1. Biosynthetic mechanism for fungal polyketides
Polyketides are probably the most significant group of natural products in terms of their importance to human medicines. To date, most of the studies have focused on polyketides isolated from bacteria. Although fungi produce numerous polyketides, their biosynthetic mechanism is still not very clear. We have chosen a group of polyketides, including mycotoxin fumonisins, as a model system for our studies. Fumonisins are produced by the pathogenic fungus Fusarium verticillioides, which is a widespread contaminant of corn and maize-derived food and feed (Biopolymers 2010). The ingestion of fumonisin-contaminated corn causes fatal diseases in livestock and imposes cancer risk to humans. We have developed a genetic system that can specifically change the biosynthetic genes in filamentous fungi. Using this system, we have created mutants for the biosynthetic genes, determined biosynthetic intermediates in the mutants, and established a biosynthetic pathway. Through engineering the polyketide synthase gene, we successfully turned the mycotoxin-producing fungus into an antifungal metabolite-producer (JACS 2007). In addition, we have been using E. coli and bakerí»s yeast as heterologous hosts to express and study the fungal genes (Biochem 2006). Our studies revealed an unprecedented PLP-dependent polyketide chain-releasing mechanism, in which a discrete 2-oxoamine synthase catalyzes a decarboxylative condensation between L-alanine and acyl-S-ACP (JACS 2009). The reaction results in the termination and offloading of the polyketide chain, as well as the introduction of a new carbon-carbon bond and an amino group to the chain. The mechanism is fundamentally different from the thioesterase/cyclase-catalyzed polyketide chain-releasing mechanism found in bacterial and other fungal polyketide biosyntheses (NPR 2010).
2. New antibiotics from a group of ubiquitous environmental bacteria
Lysobacter is a genus of Gram-negative bacteria that are ubiquitous in soil and aquatic environments. Several Lysobacter species are prolific producers of bioactive natural products and emerging as new biocontrol agents (NPR 2012). From the biocontrol agent Lysobacter enzymogenes, we have isolated a potent antifungal compound HSAF, which appears to have a novel mode of action (MBC 2006) and possesses new structural features distinct from any existing fungicides and antifungal drugs (AAC 2007). We have identified the genes for HSAF biosynthesis and investigated the biosynthetic mechanism (JACS 2011; Biochem 2012). These studies revealed a previously unrecognized biosynthetic mechanism for hybrid polyketide-peptide. In addition, we isolated a group of potent anti-MRSA cyclic lipodepsipeptides WAP-8294A and identified the WAP biosynthetic gene cluster from the bacterium (AAC 2011). These works establish the foundation for future exploitation of Lysobacter species for new antibiotics.
3. New Anticancer Natural Products from Plant Endophytic Fungi
Plant endophytic microorganisms represent a largely unexploited resource for new bioactive natural products. It is estimated that each of the ~300,000 plant species on the earth has at least one endophyte. Collaborating with Prof. Yuemao Shen at the School of Life Science, Shandong University, we have isolated a family of structurally distinct and biologically active natural products from a new marine fungal strain, Phomopsis sp A123, which is an endophyte of the costal mangrove plants. These compounds, including mycoepoxydiene (MED) and deacetylmycoepoxydiene (DAM), exhibit a variety of biological properties including anticancer, anti-inflammatory and antimicrobial activities. Most interestingly, the compounds possess a rare structural feature, a cyclooctadiene with an oxygen bridge. To investigate the molecular mechanism for the biosynthesis of these compounds, we have cloned the biosynthetic genes from the endophytic fungus and used RNAi to verify the genes.
For more information, please visit the Du Research Group Homepage.
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12. Li Y, Chen H, Ding Y, Xie Y, Wang H, Cerny RL, Shen Y, and Du L. 2014. Iterative assembly of two separate polyketide chains by the same single-module bacterial polyketide synthase in the biosynthesis of HSAF. Angewandte Chemie International Edition 53: 7524-7530. pdf
11. Wang Y, Qian G, Liu F, Li Y-Z, Shen Y, and Du L. 2013. Facile method for site-specific gene integration in Lysobacter enzymogenes for yield improvement of the anti-MRSA antibiotics WAP-8294A and the antifungal antibiotic HSAF. ACS Synthetic Biology 2: 670-678. pdf
10. Wang Y, Qian G, Li Y, Wang YS, Wang YL, Wright S, Li Y-Z, Shen Y, Liu F, and Du L. 2013. Biosynthetic mechanism for sunscreens of the biocontrol agent Lysobacter enzymogenes. PLOS One 8(6): e66633. pdf
9. Xie Y, Wright S, Shen Y, and Du L. 2012. Bioactive natural products from Lysobacter. Natural Product Reports 29: 1277-1287. pdf
8. Lou L, Chen H, Cerny RL, Li Y, Shen Y, and Du L. 2012. Unusual activities of the thioesterase domain for the biosynthesis of the polycyclic tetramate macrolactam HSAF in Lysobacter enzymogenes C3. Biochemistry 51, 4-6. pdf. (Highlighted onBiochemistry website, January, 2012).
7. Zhang W, Li Y, Qian G, Wang Y, Chen H, Li Y-Z, Liu F, Shen Y, Du L. 2011. Identification and characterization of the anti-Methicillin-Resistant Staphylococcus aureus WAP-8294A2 biosynthetic gene cluster from Lysobacter enzymogenes OH11. Antimicrobial Agents and Chemotherapy 55: 5581-5589. pdf.
6. Lou L, Qian G, Xie Y, Hang J, Chen H, Zaleta-Rivera K, Li Y, Shen Y, Dussault PH, and Du L. 2011. Biosynthesis of HSAF, a tetramic acid-containing macrolactam from Lysobacter enzymogenes. Journal of American Chemical Society 133: 643-645. pdf.
5. Du L, Lou L. 2010. PKSs and NRPSs release mechanisms. Natural Product Reports 27: 255-278. pdf.
4. Gerber R, Lou L, and Du L. 2009. A PLP-dependent polyketide chain releasing mechanism in the biosynthesis of mycotoxin fumonisins in Fusarium verticillioides. Journal of American Chemical Society 131:3148-3149. pdf. (Highlighted on JACS website, March, 2009).
3. Zhu X, Yu F, Li X-C, and Du L. 2007. Production of dihydroisocoumarins in Fusarium verticillioides by swapping the ketosynthase domain of the fungal iterative modular polyketide synthase Fum1p with that of lovastatin diketide synthase. Journal of American Chemical Society 129: 36-37. pdf.
2. Yu F, Zaleta-Rivera K, Zhu X, Huffman J, Millet J, Harris SD, Yuen G, Li X, and Du L. 2007. Structure and biosynthesis of HSAF, a broad spectrum antimycotic with a novel mode of action. Antimicrobial Agents and Chemotherapy 51: 64-72. pdf. Cited by Faculty of 1000 Biology (Evaluated by D. Newman, NIH, March 8, 2007) pdf.
1. Zaleta-Rivera K, Xu C, Yu F, Butchko RAE, Proctor RH, Lara MEH, Raza A, Dussault PH, and Du L. 2006. A bidomain nonribosomal peptide synthetase encoded by FUM14 catalyzes the formation of tricarballylic esters in the biosynthesis of fumonisins. Biochemistry 45: 2561-2569. pdf
An undergraduate, graduate, or postdoctoral associate in my group can expect to receive training in both chemistry and biology, including:
For more information, please visit the Du Research Group website.
If you are seeking an exciting graduate career that helps you develop research skills at the interface of chemistry and biology, and are a self-motivated and creative individual, please email a letter of interest or resume to Prof. Du at email@example.com.