{"id":133,"date":"2014-02-20T13:12:25","date_gmt":"2014-02-20T19:12:25","guid":{"rendered":"http:\/\/chemweb.unl.edu\/ldu\/?page_id=133"},"modified":"2025-07-01T14:36:10","modified_gmt":"2025-07-01T19:36:10","slug":"recent-publications","status":"publish","type":"page","link":"http:\/\/chemweb.unl.edu\/ldu\/recent-publications\/","title":{"rendered":"Recent Publications"},"content":{"rendered":"<h3>For a complete list of publications, click <a href=\"http:\/\/chemweb.unl.edu\/ldu\/?page_id=31\">here<\/a><\/h3>\n<h3>For citations and h-index, click <a href=\"http:\/\/scholar.google.com\/citations?user=1fl9dpEAAAAJ&amp;amp;hl=en&amp;amp;oi=ao\">here<\/a><a title=\"Citations and H-index\" href=\"http:\/\/scholar.google.com\/citations?user=1fl9dpEAAAAJ&amp;hl=en&amp;oi=ao\"><br \/>\n<\/a><\/h3>\n<p>&nbsp;<\/p>\n<h4><strong>Selected Recent Publications<\/strong><\/h4>\n<p>&nbsp;<\/p>\n<p>Xie X, Li F, Mu Y, Lu M, Luo J, Wang H, Shen Y, <strong>Du L<\/strong>, Zhu D, and Li Y<strong>. 2025<\/strong>. Structural basis for medium-chain dehydrogenase\/reductase-catalyzed reductive cyclization in polycyclic tetramate macrolactam biosynthesis.<strong><em> Journal of American Chemical Society<\/em><\/strong> 147: 19153-19261. <a href=\"https:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/jacs.5c04971?ref=article_openPDF\">pdf<\/a><\/p>\n<p>Li X, Pan C, Wang H, Shen Y, Li Y, and <strong>Du L. 2025<\/strong>. Heterologous production of phenazines in the biocontrol agent <em>Lysobacter enzymogenes<\/em> C3. <em><strong>Journal of Agricultural and Food Chemistry<\/strong><\/em> 73: 1345-1355. <a href=\"https:\/\/pubs.acs.org\/doi\/epdf\/10.1021\/acs.jafc.4c09518?ref=article_openPDF\">pdf<\/a><\/p>\n<p>Zhang F, Liu J, Jiang L, Zheng Y, Yu L, and <strong>Du L.<\/strong> <strong>2024<\/strong>. Production of the siderophore lysochelin in rich media through maltose-promoted high-density growth of <em>Lysobacter<\/em> sp. 3655. <strong><em>Frontiers in Microbiology <\/em><\/strong>15:1433983. <a href=\"https:\/\/www.frontiersin.org\/journals\/microbiology\/articles\/10.3389\/fmicb.2024.1433983\/full?utm_source=Email_to_authors_&amp;utm_medium=Email&amp;utm_content=T1_11.5e1_author&amp;utm_campaign=Email_publication&amp;field&amp;journalName=Frontiers_in_Microbiology&amp;id=1433983\">pdf<\/a><\/p>\n<p>Miller A, Li S, Eichhorn CD, Zheng Y, and <strong>Du L.<\/strong> <strong>2023<\/strong>. Identification and biosynthetic study of the siderophore lysochelin in the biocontrol Agent<em> Lysobacter enzymogenes<\/em>. <strong><em>Journal of Agricultural and Food Chemistry <\/em><\/strong>71: 7418-7426. <a href=\"https:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/acs.jafc.3c01250\">pdf<\/a><\/p>\n<p>Han W, Zhai Y, Zhang R, Gong X, Li J, Xu G, Lei X, <strong>Du L<\/strong>, and Gao J<strong>.<\/strong> <strong>2023<\/strong>. Tricrilactones A\u2212H, potent antiosteoporosis macrolides with distinctive ring skeletons from <em>Trichocladium crispatum<\/em>, an alpine moss-associated fungus. <strong><em>Angewandte Chemie International Edition <\/em><\/strong>62: e202300773. <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/epdf\/10.1002\/anie.202300773\">pdf<\/a>.<\/p>\n<p>Yue H, Miller A, Khetrapal V, Jayasekera V, Wright S, and <strong>Du L.<\/strong> <strong>2022<\/strong>. Biosynthesis, regulation, and engineering of natural products from <em>Lysobacter<\/em>. <strong><em>Natural Product Reports<\/em><\/strong> 39: 842 \u2013 874. <a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlepdf\/2022\/np\/d1np00063b\">pdf<\/a><\/p>\n<p>Yue H, Jiang J, Taylor A, Leite A, Dodds E, and <strong>Du L.<\/strong>\u00a0<strong>2021<\/strong>. Outer membrane vesicles-mediated co-delivery of the antifungal HSAF metabolites and lytic polysaccharide monooxygenase in the predatory <em>Lysobacter enzymogenes<\/em>.<strong><em> ACS Chemical Biology <\/em><\/strong>16: 1079-1089. <a href=\"https:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/acschembio.1c00260\">pdf<\/a><\/p>\n<p>Yu L, Li H, Zhou Z, Liu F, and <strong>Du L.<\/strong>\u00a0<strong>2021<\/strong>. An antifungal polycyclic tetramate macrolactam HSAF is a novel oxidative stress modulator in <em>Lysobacter enzymogenes<\/em>.<strong><em> Applied and Environmental Microbiology<\/em><\/strong> 87: e03105-20. <a href=\"https:\/\/aem.asm.org\/content\/aem\/87\/10\/e03105-20.full.pdf\">pdf<\/a><\/p>\n<p>Yu L, Du F, Chen X, Zheng Y, Morton M, Liu F, and <strong>Du L.<\/strong>\u00a0<strong>2020<\/strong>. Identification of the biosynthetic gene cluster for the anti-MRSA lysocins through gene cluster activation using strong promoters of housekeeping genes and production of new analogs in <em>Lysobacter<\/em> sp. 3655.<strong><em> ACS Synthetic Biology<\/em><\/strong> 9: 1989-1997. <a href=\"https:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/acssynbio.0c00067\">pdf<\/a><\/p>\n<p>Sang M, Wang H, Shen Y, Rodrigues de Almeida N, Conda-Sheridan M, Li S, Li Y, and\u00a0<strong>Du L.<\/strong>\u00a0<strong>2019<\/strong>. Identification of an anti-MRSA cyclic lipodepsipeptide, WBP-29479A1, by genome mining of\u00a0<em>Lysobacter antibioticus<\/em>.\u00a0<strong><em>Organic Letters<\/em><\/strong> 21: 6432-6436. <a href=\"https:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/acs.orglett.9b02333?ai=6562\">pdf<\/a>.<\/p>\n<p>Li X, Wang H, Shen Y, Li Y, and\u00a0<strong>Du L. 2019.<\/strong>\u00a0OX4 is an NADPH-dependent dehydrogenase catalyzing an extended Michael addition reaction to form the six-membered ring in the antifungal HSAF.\u00a0<strong><i>Biochemistry<\/i><\/strong> 58: 5245\u22125248. <a href=\"https:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/acs.biochem.9b00280\">pdf<\/a><\/p>\n<p>Li Y, Wang H, Liu Y, Jiao Y, Li S, Shen Y, and\u00a0<strong>Du L.\u00a02018.<\/strong>\u00a0Biosynthesis of the polycyclic system in the antifungal HSAF and analogues from\u00a0<em>Lysobacter enzymogenes<\/em>.<em><strong>\u00a0Angewandte Chemie International Edition\u00a0<\/strong><\/em>57: 6221-6225.\u00a0<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/epdf\/10.1002\/anie.201802488\">pdf<\/a><\/p>\n<p>Jiang J, Guiza-Beltran D, Schacht A, Wright S, Zhang L, and <strong>Du L. 2018.<\/strong> Functional and structural analysis of phenazine <em>O<\/em>-methyltransferase LaPhzM from <em>Lysobacter antibioticus<\/em> OH13 and one-pot enzymatic synthesis of the antibiotic myxin. <em><strong>ACS Chemical Biology<\/strong><\/em>\u00a013: 1003-1012.\u00a0<a href=\"https:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/acschembio.8b00062\">pdf<\/a>.<\/p>\n<p>Yu L, Su W, Fey P, Liu F, and\u00a0<strong>Du L.\u00a02018.<\/strong>\u00a0Yield improvement of the anti-MRSA antibiotics WAP-8294A by CRISPR\/dCas9 combined with refactoring self-protection genes in\u00a0<em>Lysobacter enzymogenes<\/em>\u00a0OH11.\u00a0<em><strong>ACS Synthetic Biology\u00a0<\/strong><\/em>7: 258\u2212266.\u00a0<a href=\"http:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/acssynbio.7b00293\">pdf<\/a>.<\/p>\n<p>Li S, Wu X, L Zhang, Shen Y, and\u00a0<strong>Du L. 2017.\u00a0<\/strong>Activation of a cryptic gene cluster in\u00a0<em>Lysobacter enzymogenes\u00a0<\/em>revealed a module\/domain portable mechanism of nonribosomal peptide synthetases in the biosynthesis of pyrrolopyrazines.\u00a0<strong><em>Organic Letters<\/em><\/strong>\u00a019: 5010\u22125013. <a href=\"http:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/acs.orglett.7b01611\">pdf<\/a>.<\/p>\n<p>Han Y, Wang Y, Yu Y, Chen H, Shen Y, and\u00a0<strong>Du L. 2017.<\/strong>\u00a0Indole-induced reversion of intrinsic multi-antibiotic resistance in\u00a0<em>Lysobacter enzymogenes<\/em>.\u00a0<em><strong>Applied and Environmental Microbiology<\/strong><\/em>\u00a083:e00995-17. <a href=\"http:\/\/aem.asm.org\/content\/83\/17\/e00995-17.full.pdf+html\">pdf<\/a>.<\/p>\n<p>Zhao Y, Qian G, Ye Y, Wright S, Chen H, Shen Y, Liu F, and\u00a0<strong>Du L. 2016.<\/strong> Heterocyclic aromatic <i>N<\/i>-oxidation in the biosynthesis of phenazine antibiotics from <i>Lysobacter antibioticus<\/i>. <em><strong>Organic Letters <\/strong><\/em>18: 2495-2498.\u00a0<a href=\"http:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/acs.orglett.6b01089\">pdf<\/a><\/p>\n<p>Wang M, Zhang W, Xu W, Shen Y, and\u00a0<strong>Du L. 2016.<\/strong>\u00a0Optimization of genome shuffling for high yield production of the antitumor deacetylmycoepoxydiene in an endophytic fungus of mangrove plants.\u00a0<em><strong>Applied Microbiology and Biotechnology<\/strong><\/em>\u00a0100: 7491\u20137498.\u00a0<a href=\"http:\/\/download.springer.com\/static\/pdf\/563\/art%253A10.1007%252Fs00253-016-7457-0.pdf?originUrl=http%3A%2F%2Flink.springer.com%2Farticle%2F10.1007%2Fs00253-016-7457-0&amp;token2=exp=1471553512~acl=%2Fstatic%2Fpdf%2F563%2Fart%25253A10.1007%25252Fs00253-016-7457-0.pdf%3ForiginUrl%3Dhttp%253A%252F%252Flink.springer.com%252Farticle%252F10.1007%252Fs00253-016-7457-0*~hmac=db1ad3d49fd5abefebc7bcabd6481eff5da0aefd29a30ad833e27e0706817de1\">pdf<\/a><\/p>\n<p>Han Y, Wang Y, Tombosa S, Wright S, Huffman J, Yuen G, Qian G, Liu F, Shen Y, and <strong>Du L. 2015<\/strong>. Identification of a small molecule signaling factor that regulates the biosynthesis of the antifungal polycyclic tetramate macrolactam HSAF in <em>Lysobacter enzymogenes<\/em>. <em><strong>Applied Microbiology and Biotechnology<\/strong><\/em><i><\/i><b><i>\u00a0<\/i><\/b>99: 801-811.\u00a0<a href=\"http:\/\/link.springer.com\/article\/10.1007\/s00253-014-6120-x\">pdf<\/a><a href=\"http:\/\/download.springer.com\/static\/pdf\/599\/art%253A10.1007%252Fs00253-014-6120-x.pdf?auth66=1423856775_df2f0663335b61fe3d6fa65dd72b7829&amp;ext=.pdf\"><br \/>\n<\/a><\/p>\n<p>Li Y, Chen H, Ding Y, Xie Y, Wang H, Cerny RL, Shen Y, and\u00a0<strong>Du L.\u00a02014<\/strong>. Iterative assembly of two separate polyketide chains by the same single-module bacterial polyketide synthase in the biosynthesis of HSAF.\u00a0<em><strong>Angewandte Chemie International Edition<\/strong><\/em>\u00a053: 7524-7530.\u00a0<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.201403500\/pdf\">pdf<\/a><\/p>\n<p>Wang Y, Qian G, Liu F, Li Y-Z, Shen Y, and\u00a0<strong>Du L.\u00a02013<\/strong>. Facile method for site-specific gene integration in\u00a0<i>Lysobacter enzymogenes<\/i>\u00a0for yield improvement of the anti-MRSA antibiotics WAP-8294A and the antifungal antibiotic HSAF.\u00a0<strong><i>ACS Synthetic Biology<\/i><\/strong>\u00a02: 670-678. <a href=\"http:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/sb4000806\">pdf<\/a><\/p>\n<p>Zhao PJ, Yang YL,\u00a0<strong>Du L<\/strong>, Liu JK, and Zeng Y.\u00a0<strong>2013<\/strong>. Elucidating the biosynthetic pathway for vibralactone: A pancreatic lipase inhibitor with a fused bicyclic \u00df-lactone<em>.\u00a0<strong>Angewandte Chemie International Edition<\/strong><\/em>\u00a052: 1-6.\u00a0<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.201208182\/pdf\">pdf<\/a><\/p>\n<p>Xie Y, Wright S, Shen Y, and <strong>Du L. 2012.<\/strong> Bioactive natural products from <i>Lysobacter. <strong><i>Natural Product Reports<\/i>\u00a0<\/strong><\/i>29: 1277-1287.\u00a0<a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlepdf\/2012\/np\/c2np20064c\">pdf<\/a><\/p>\n<p>Lou L, Chen H, Cerny RL, Li Y, Shen Y, and <strong>Du L. 2012.<\/strong><b> <\/b>Unusual activities of the thioesterase domain for the biosynthesis of the polycyclic tetramate macrolactam HSAF in <i>Lysobacter enzymogenes<\/i> C3<i>. <\/i><strong><i>Biochemistry<\/i><\/strong><i> <\/i>51, 4-6. <a href=\"http:\/\/pubs.acs.org\/doi\/ipdf\/10.1021\/bi2015025\">pdf<\/a>. (<span style=\"text-decoration: underline;\">Highlighted on\u00a0<\/span><strong><span style=\"text-decoration: underline;\"><i>Biochemistry<\/i><\/span><\/strong><span style=\"text-decoration: underline;\"> website, January, 2012<\/span>).<\/p>\n<p>Zhang W, Li Y, Qian G, Wang Y, Chen H, Li Y-Z, Liu F, Shen Y, and\u00a0<strong>Du L. 2011.<\/strong> Identification and characterization of the anti-Methicillin-Resistant <i>Staphylococcus aureus<\/i> WAP-8294A2 biosynthetic gene cluster from <i>Lysobacter enzymogenes<\/i> OH11.<strong><i> Antimicrobial Agents and Chemotherapy<\/i><\/strong> 55: 5581-5589.\u00a0<a href=\"http:\/\/aac.asm.org\/content\/55\/12\/5581.full.pdf+html\">pdf.<\/a><\/p>\n<p>Lou L, Qian G, Xie Y, Hang J, Chen H, Zaleta-Rivera K, Li Y, Shen Y, Dussault PH, Liu F, and\u00a0<strong>Du L. 2011.<\/strong><b> <\/b>Biosynthesis of HSAF, a tetramic acid-containing macrolactam from <i>Lysobacter enzymogenes. <\/i><strong><i>Journal of the American Chemical Society<\/i><\/strong><i> <\/i>133: 643-645. <a href=\"http:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/ja105732c\">pdf<\/a>.<\/p>\n<p><strong>Du L <\/strong>and\u00a0Lou L. <strong>2010.<\/strong> PKSs and NRPSs release mechanisms. <strong><i>Natural Product Reports<\/i><\/strong> 27: 255-278.<span style=\"text-decoration: underline;\"> <a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlepdf\/2010\/np\/b912037h\">pdf<\/a><\/span>.<\/p>\n<p>Gerber R, Lou L, and <strong>Du L. 2009.<\/strong>\u00a0A PLP-dependent polyketide chain releasing mechanism in the biosynthesis of mycotoxin fumonisins in <i>Fusarium verticillioides<\/i>. <strong><i>Journal of the American Chemical Society<\/i><\/strong><i> <\/i>131: 3148-3149. <a href=\"http:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/ja8091054\">pdf<\/a>. \u00a0(<span style=\"text-decoration: underline;\">Highlighted on<\/span><strong><span style=\"text-decoration: underline;\"> <i>JACS<\/i> <\/span><\/strong><span style=\"text-decoration: underline;\">website, March, 2009<\/span>).<\/p>\n<p>Zhu X, Yu F, Li X-C, and <strong>Du L. 2007.<\/strong> Production of dihydroisocoumarins in<i> Fusarium verticillioides<\/i> by swapping the ketosynthase domain of the fungal iterative modular polyketide synthase Fum1p with that of lovastatin diketide synthase. <strong><i>Journal of the American Chemical Society <\/i><\/strong>129: 36-37. <a href=\"http:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/ja0672122\">pdf<\/a>.<\/p>\n<p>Yu F, Zaleta-Rivera K, Zhu X, Huffman J, Millet J, Harris SD, Yuen G, Li X, and <strong>Du L. 2007.<\/strong> Structure and biosynthesis of HSAF, a broad spectrum antimycotic with a novel mode of action. <strong><i>Antimicrobial Agents and Chemotherapy<\/i><\/strong> 51: 64-72. <a href=\"http:\/\/aac.asm.org\/content\/51\/1\/64.full.pdf\">pdf<\/a>. <span style=\"text-decoration: underline;\">Cited by<\/span><strong><span style=\"text-decoration: underline;\"> Faculty of 1000 Biology<\/span> <\/strong>(Evaluated by D. Newman, NIH, March 8,\u00a02007)<b> <\/b><a href=\"http:\/\/www.f1000biology.com\/article\/id\/1067750\/evaluation\">pdf<\/a><b>.<\/b><\/p>\n<p>Zaleta-Rivera K, Xu C, Yu F, Butchko RAE, Proctor RH, Lara MEH, Raza A, Dussault PH, and\u00a0<strong>Du L.\u00a02006.\u00a0<\/strong>A bidomain nonribosomal peptide synthetase encoded by <i>FUM14<\/i> catalyzes the formation of tricarballylic esters in the biosynthesis of fumonisins.\u00a0<strong><i>Biochemistry<\/i><i>\u00a0<\/i><\/strong>45: 2561-2569.\u00a0<a href=\"http:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/bi052085s\">pdf<\/a><b><i><\/i><\/b><\/p>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>For a complete list of publications, click here For citations and h-index, click here &nbsp; Selected Recent Publications &nbsp; Xie X, Li F, Mu Y, Lu M, Luo J, Wang H, Shen Y, Du L, Zhu D, and Li Y. 2025. Structural basis for medium-chain dehydrogenase\/reductase-catalyzed reductive cyclization in polycyclic tetramate macrolactam biosynthesis. Journal of<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"open","template":"","meta":[],"guten_post_layout_featured_media_urls":{"full":false,"thumbnail":false,"medium":false,"medium_large":false,"large":false,"1536x1536":false,"2048x2048":false,"guten_post_layout_landscape_large":false,"guten_post_layout_portrait_large":false,"guten_post_layout_square_large":false,"guten_post_layout_landscape":false,"guten_post_layout_portrait":false,"guten_post_layout_square":false,"featured_image":false,"frontpage_image":false,"custom_header_image":false},"_links":{"self":[{"href":"http:\/\/chemweb.unl.edu\/ldu\/wp-json\/wp\/v2\/pages\/133"}],"collection":[{"href":"http:\/\/chemweb.unl.edu\/ldu\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"http:\/\/chemweb.unl.edu\/ldu\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"http:\/\/chemweb.unl.edu\/ldu\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/chemweb.unl.edu\/ldu\/wp-json\/wp\/v2\/comments?post=133"}],"version-history":[{"count":83,"href":"http:\/\/chemweb.unl.edu\/ldu\/wp-json\/wp\/v2\/pages\/133\/revisions"}],"predecessor-version":[{"id":1465,"href":"http:\/\/chemweb.unl.edu\/ldu\/wp-json\/wp\/v2\/pages\/133\/revisions\/1465"}],"wp:attachment":[{"href":"http:\/\/chemweb.unl.edu\/ldu\/wp-json\/wp\/v2\/media?parent=133"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}