Publications

2022 | 2021  |  2020  |  2019  |  2018  |  2017  |  2016  |  2015  |  2014  |  2013  |  2012  |  2011

2022

Shi, Y.-M., Hirschmann, M., Shi, Y.-N., Ahmed, S., Abebew, D., Tobias, N. J., Grün, P., Crames, J. J., Pöschel, L., Kuttenlochner, W., Richter, C., Herrmann, J., Müller, R., Thanwisai, A., Pidot, S. J., Stinear, T. P., Groll, M., Kim, Y. & Bode, H. B. (2022)
Global analysis of biosynthetic gene clusters reveals conserved and unique natural products in entomopathogenic nematode-symbiotic bacteria. Nat. Chem. doi: 10.1038/s41557-41022-00923-41552.

2021

Reyes-Fernández, E. Z., Shi, Y.-M., Grün, P., Bode, H. B. & Bölker, M. (2021)
An Unconventional Melanin Biosynthetic Pathway in Ustilago maydis. Appl. Environ. Microbiol. 87 (3), AEM.01510-01520. doi: 10.1128/aem.01510-20.

2020

Machado, R. A. R., Thönen, L., Arce, C. C. M., Theepan, V., Prada, F., Wüthrich, D., Robert, C. A. M., Vogiatzaki, E., Shi, Y.-M., Schaeren, O. P., Notter, M., Bruggmann, R., Hapfelmeier, S., Bode, H. B. & Erb, M. (2020)
Engineering bacterial symbionts of nematodes improves their biocontrol potential to counter the western corn rootworm. Nat. Biotechnol. 38 (5), 600-608. doi: 10.1038/s41587-020-0419-1.

Lee, J., Shi, Y.-M., Grün, P., Gube, M., Feldbrügge, M., Bode, H. & Hennicke, F. (2020)
Identification of Feldin, an Antifungal Polyyne from the Beefsteak Fungus Fistulina hepatica. Biomolecules 10 (11), 1502. doi: 10.3390/biom10111502.

2019

Wang, G., Zhao, Z., Ke, J., Engel, Y., Shi, Y.-M., Robinson, D., Bingol, K., Zhang, Z., Bowen, B., Louie, K., Wang, B., Evans, R., Miyamoto, Y., Cheng, K., Kosina, S., De Raad, M., Silva, L., Luhrs, A., Lubbe, A., Hoyt, D. W., Francavilla, C., Otani, H., Deutsch, S., Washton, N. M., Rubin, E. M., Mouncey, N. J., Visel, A., Northen, T., Cheng, J.-F., Bode, H. B. & Yoshikuni, Y. (2019)
CRAGE enables rapid activation of biosynthetic gene clusters in undomesticated bacteria. Nat. Microbiol. 4 (12), 2498-2510. doi: 10.1038/s41564-019-0573-8.

Tobias, N. J., Parra-Rojas, C., Shi, Y.-N., Shi, Y.-M., Simonyi, S., Thanwisai, A., Vitta, A., Chantratita, N., Hernandez-Vargas, E. A. & Bode, H. B. (2019)
Cyclo(tetrahydroxybutyrate) production is sufficient to distinguish between Xenorhabdus and Photorhabdus isolates in Thailand. Environ. Microbiol. 21 (8), 2921-2932. doi: 10.1111/1462-2920.14685.

Shi, Y.-N., Pusch, S., Shi, Y.-M., Richter, C., Maciá-Vicente, J. G., Schwalbe, H., Kaiser, M., Opatz, T. & Bode, H. B. (2019)
(±)-Alternarlactones A and B, Two Antiparasitic Alternariol-like Dimers from the Fungus Alternaria alternata P1210 Isolated from the Halophyte Salicornia sp. J. Org. Chem. 84 (17), 11203-11209. doi: 10.1021/acs.joc.9b01229.

Shi, Y.-M., Brachmann, A. O., Westphalen, M. A., Neubacher, N., Tobias, N. J. & Bode, H. B. (2019)
Dual phenazine gene clusters enable diversification during biosynthesis. Nat. Chem. Biol. 15 (4), 331-339. doi: 10.1038/s41589-019-0246-1.

Grammbitter, G. L. C., Schmalhofer, M., Karimi, K., Shi, Y. M., Schoner, T. A., Tobias, N. J., Morgner, N., Groll, M. & Bode, H. B. (2019)
An Uncommon Type II PKS Catalyzes Biosynthesis of Aryl Polyene Pigments. J. Am. Chem. Soc. 141 (42), 16615-16623. doi: 10.1021/jacs.8b10776.

Drummond, L., Kschowak, M. J., Breitenbach, J., Wolff, H., Shi, Y.-M., Schrader, J., Bode, H. B., Sandmann, G. & Buchhaupt, M. (2019)
Expanding the Isoprenoid Building Block Repertoire with an IPP Methyltransferase from Streptomyces monomycini. ACS Synth. Biol. 8 (6), 1303-1313. doi: 10.1021/acssynbio.8b00525.

Bode, E., Heinrich, A. K., Hirschmann, M., Abebew, D., Shi, Y.-N., Vo, T. D., Wesche, F., Shi, Y.-M., Grün, P., Simonyi, S., Keller, N., Engel, Y., Wenski, S., Bennet, R., Beyer, S., Bischoff, I., Buaya, A., Brandt, S., Cakmak, I., Çimen, H., Eckstein, S., Frank, D., Fürst, R., Gand, M., Geisslinger, G., Hazir, S., Henke, M., Heermann, R., Lecaudey, V., Schäfer, W., Schiffmann, S., Schüffler, A., Schwenk, R., Skaljac, M., Thines, E., Thines, M., Ulshöfer, T., Vilcinskas, A., Wichelhaus, T. A. & Bode, H. B. (2019)
Promoter activation in Δhfq mutants as an efficient tool for specialized metabolite production enabling direct bioactivity testing. Angew. Chem. Int. Ed. 58 (52), 18957-18963. doi: 10.1002/anie.201910563.

2018

Tobias, N. J., Shi, Y.-M. & Bode, H. B. (2018)
Refining the Natural Product Repertoire in Entomopathogenic Bacteria. Trends Microbiol. 26 (10), 833-840. doi: 10.1016/j.tim.2018.04.007.

Shi, Y.-M., Richter, C., Challinor, V. L., Grün, P., Girela del Rio, A., Kaiser, M., Schüffler, A., Piepenbring, M., Schwalbe, H. & Bode, H. B. (2018)
Georatusin, a Specific Antiparasitic Polyketide–Peptide Hybrid from the Fungus Geomyces auratus. Org. Lett. 20 (6), 1563-1567. doi: 10.1021/acs.orglett.8b00293.

Shi, Y.-M. & Bode, H. B. (2018)
Chemical language and warfare of bacterial natural products in bacteria-nematode-insect interactions. Nat. Prod. Rep.35 (4), 309-335. doi: 10.1039/c7np00054e.

Shi, Y.-M., Hu, K., Pescitelli, G., Liu, M., Li, X.-N., Du, X., Xiao, W.-L., Sun, H.-D. & Puno, P.-T. (2018)
Schinortriterpenoids with Identical Configuration but Distinct ECD Spectra Generated by Nondegenerate Exciton Coupling. Org. Lett. 20 (6), 1500-1504. doi: 10.1021/acs.orglett.8b00149.

2017

Tobias, N. J., Wolff, H., Djahanschiri, B., Grundmann, F., Kronenwerth, M., Shi, Y.-M., Simonyi, S., Grün, P., Shapiro-Ilan, D., Pidot, S. J., Stinear, T. P., Ebersberger, I. & Bode, H. B. (2017)
Natural product diversity associated with the nematode symbionts Photorhabdus and Xenorhabdus. Nat. Microbiol. 2 (12), 1676-1685. doi: 10.1038/s41564-017-0039-9.

Shi, Y.-M. & Bode, H. B. (2017)
Microbiology: A new language for small talk. Nat. Chem. Biol. 13 (5), 453-454. doi: 10.1038/nchembio.2362.

Cai, X., Shi, Y.-M., Pöhlmann, N., Revermann, O., Bahner, I., Pidot, S. J., Wesche, F., Lackner, H., Büchel, C., Kaiser, M., Richter, C., Schwalbe, H., Stinear, T. P., Zeeck, A. & Bode, H. B. (2017)
Structure and Biosynthesis of Isatropolones, Bioactive Amine-Scavenging Fluorescent Natural Products from Streptomyces Gö66. Angew. Chem. Int. Ed. 56 (18), 4945-4949. doi: 10.1002/anie.201701223.

Hu, Z.-X., Li, X.-N., Shi, Y.-M., Wang, W.-G., Du, X., Li, Y., Zhang, Y.-H., Pu, J.-X. & Sun, H.-D. (2017)
Lanostane-type triterpenoids from Kadsura coccinea. Tetrahedron 73 (20), 2931-2937. doi: 10.1016/j.tet.2017.03.087.

2016

Shi, Y. M., Cai, S. L., Li, X. N., Liu, M., Shang, S. Z., Du, X., Xiao, W. L., Pu, J. X. & Sun, H. D. (2016)
LC–UV-Guided Isolation and Structure Determination of Lancolide E: A Nortriterpenoid with a Tetracyclo[5.4.0.02,4.03,7]undecane-Bridged System from a “Talented” Schisandra Plant. Org. Lett. 18 (1), 100-103. doi: 10.1021/acs.orglett.5b03334.

Hu, Z. X., Hu, K., Shi, Y. M., Wang, W. G., Du, X., Li, Y., Zhang, Y. H., Pu, J. X. & Sun, H. D. (2016)
Rearranged 6/6/5/6-Fused Triterpenoid Acids from the Stems of Kadsura coccinea. J. Nat. Prod. 79 (10), 2590-2598. doi: 10.1021/acs.jnatprod.6b00508.

Hu, Z.-X., Shi, Y.-M., Wang, W.-G., Tang, J.-W., Zhou, M., Du, X., Zhang, Y.-H., Pu, J.-X. & Sun, H.-D. (2016)
Structural Characterization of Kadcoccinin A: A Sesquiterpenoid with a Tricyclo[4.4.0.03,10]decane Scaffold from Kadsura coccinea. Org. Lett. 18 (9), 2284-2287. doi: 10.1021/acs.orglett.6b00919.

Gao, Z.-H., Shi, Y.-M., Qiang, Z., Wang, X., Shang, S.-Z., Yang, Y., Du, B.-W., Peng, H.-P., Ji, X., Li, H., Wang, F. & Xiao, W.-L. (2016)
Plasiatine, an Unprecedented Indole–Phenylpropanoid Hybrid from Plantago asiatica as a Potent Activator of the Nonreceptor Protein Tyrosine Phosphatase Shp2. Sci. Rep. 6, 24945. doi: 10.1038/srep24945.

2015

Wang, W.-G., Tang, J.-W., Shi, Y.-M., Du, X., Li, X.-N., Wu, H.-Y., Jiang, H.-Y., Li, Y., Pu, J.-X. & Sun, H.-D. (2015)
Laxiflorol A, the first example of 7,8:15,16-di-seco-15-nor-21-homo-ent-kauranoid from Isodon eriocalyx var. laxiflora. RSC Adv. 5 (8), 6132-6135. doi: 10.1039/c4ra12704h.

Shi, Y. N., Yang, L., Zhao, J. H., Shi, Y. M., Qu, Y., Zhu, H. T., Wang, D., Yang, C. R., Li, X. C., Xu, M. & Zhang, Y. J. (2015)
Chemical constituents from Piper wallichii. Nat. Prod. Res. 29 (14), 1372-1375. doi: 10.1080/14786419.2014.998217.

Shi, Y. N., Shi, Y. M., Yang, L., Li, X. C., Zhao, J. H., Qu, Y., Zhu, H. T., Wang, D., Cheng, R. R., Yang, C. R., Xu, M. & Zhang, Y. J. (2015)
Lignans and aromatic glycosides from Piper wallichii and their antithrombotic activities. J. Ethnopharmacol. 162, 87-96. doi: 10.1016/j.jep.2014.12.038.

Shi, Y. M., Xiao, W. L., Pu, J. X. & Sun, H. D. (2015)
Triterpenoids from the Schisandraceae family: an update. Nat. Prod. Rep. 32 (3), 367-410. doi: 10.1039/c4np00117f.

Liu, M., Luo, Y. Q., Wang, W. G., Shi, Y. M., Wu, H. Y., Du, X., Pu, J. X. & Sun, H. D. (2015)
Two New 18-Norschiartane-type Schinortriterpenoids from Schisandra lancifolia. Nat. Prod. Commun. 10 (12), 2045-2047. doi: 10.1177/1934578X1501001208.

Liang, C.-Q., Shi, Y.-M., Wang, W.-G., Hu, Z.-X., Li, Y., Zheng, Y.-T., Li, X.-N., Du, X., Pu, J.-X., Xiao, W.-L., Zhang, H.-B. & Sun, H.-D. (2015)
Kadcoccinic Acids A–J, Triterpene Acids from Kadsura coccinea. J. Nat. Prod. 78 (8), 2067-2073. doi: 10.1021/acs.jnatprod.5b00392.

Hu, Z. X., Shi, Y. M., Wang, W. G., Li, X. N., Du, X., Liu, M., Li, Y., Xue, Y. B., Zhang, Y. H., Pu, J. X. & Sun, H. D. (2015)
Kadcoccinones A-F, New Biogenetically Related Lanostane-Type Triterpenoids with Diverse Skeletons from Kadsura coccinea. Org. Lett. 17 (18), 4616-4619. doi: 10.1021/acs.orglett.5b02360.

2014

Shi, Y. M., Zhong, W. M., Chen, H., Wang, R. R., Shang, S. Z., Liang, C. Q., Gao, Z. H., Zheng, Y. T., Xiao, W. L. & Sun, H. D. (2014)
New Lignans from the Leaves and Stems of Schisandra chinensis and Their Anti-HIV-1 Activities. Chin. J. Chem. 32 (8), 734-740. doi: 10.1002/cjoc.201400001.

Shi, Y. M., Yang, J., Xu, L., Li, X. N., Shang, S. Z., Cao, P., Xiao, W. L. & Sun, H. D. (2014)
Structural Characterization and Antioxidative Activity of Lancifonins: Unique Nortriterpenoids from Schisandra lancifolia. Org. Lett. 16 (5), 1370-1373. doi: 10.1021/ol5001186.

Shi, Y.-M., Wang, L.-Y., Zou, X.-S., Li, X.-N., Shang, S.-Z., Gao, Z.-H., Liang, C.-Q., Luo, H.-R., Li, H.-L., Xiao, W.-L. & Sun, H.-D. (2014)
Nortriterpenoids from Schisandra chinensis and Their Absolute Configurational Assignments by Electronic Circular Dichroism Study. Tetrahedron 70 (4), 859-868. doi: 10.1016/j.tet.2013.12.023.

Liu, Z.-K., Wu, D.-R., Shi, Y.-M., Zeng, T., Liu, S.-H., Du, X., Dang, Y.-J., Xiao, W.-L. & Sun, H.-D. (2014)
Three New Diterpenoids from Leonurus japonicus. Chin. Chem. Lett. 25 (5), 677-679. doi: 10.1016/j.cclet.2014.01.047.

Liang, C. Q., Luo, R. H., Yan, J. M., Li, Y., Li, X. N., Shi, Y. M., Shang, S. Z., Gao, Z. H., Yang, L. M., Zheng, Y. T., Xiao, W. L., Zhang, H. B. & Sun, H. D. (2014)
Structure and Bioactivity of Triterpenoids from the Stems of Schisandra sphenanthera. Archives of Pharmacal Research 37 (2), 168-174. doi: 10.1007/s12272-013-0133-3.

2013

Shi, Y. M., Wang, X. B., Li, X. N., Luo, X., Shen, Z. Y., Wang, Y. P., Xiao, W. L. & Sun, H. D. (2013)
Lancolides, Antiplatelet Aggregation Nortriterpenoids with Tricyclo[6.3.0.02,11]undecane-Bridged System from Schisandra lancifolia. Org. Lett. 15 (19), 5068-5071. doi: 10.1021/ol402414z.

Shang, S. Z., Kong, L. M., Yang, L. P., Jiang, J., Huang, J., Zhang, H. B., Shi, Y. M., Zhao, W., Li, H. L., Luo, H. R., Li, Y., Xiao, W. L. & Sun, H. D. (2013)
Bioactive Phenolics and Terpenoids from Manglietia insignis. Fitoterapia 84, 58-63. doi: 10.1016/j.fitote.2012.10.010.

Shang, S. Z., Chen, H., Liang, C. Q., Gao, Z. H., Du, X., Wang, R. R., Shi, Y. M., Zheng, Y. T., Xiao, W. L. & Sun, H. D. (2013)
Phenolic Constituents from Parakmeria yunnanensis and Their Anti-HIV-1 Activity. Archives of Pharmacal Research 36 (10), 1223-1230. doi: 10.1007/s12272-013-0070-1.

Shang, S.-Z., Han, Y.-S., Shi, Y.-M., Du, X., Liang, C.-Q., Wainberg, M. A., Gao, Z.-H., Xiao, W.-L. & Sun, H.-D. (2013)
Four New Lignans from the Leaves and Stems of Schisandra propinqua var. sinensis. Nat. Prod. Bioprospect. 3 (2), 56-60. doi: 10.1007/s13659-013-0017-8.

Liang, C. Q., Shi, Y. M., Li, X. Y., Luo, R. H., Li, Y., Zheng, Y. T., Zhang, H. B., Xiao, W. L. & Sun, H. D. (2013)
Kadcotriones A–C: Tricyclic Triterpenoids from Kadsura coccinea. J. Nat. Prod. 76 (12), 2350-2354. doi: 10.1021/np400546z.

Liang, C. Q., Hu, J., Shi, Y. M., Shang, S. Z., Du, X., Zhan, R., Xiong, W. Y., Zhang, H. B., Xiao, W. L. & Sun, H. D. (2013)
Schisphenlignans A–E: Five New Dibenzocyclooctadiene Lignans from Schisandra sphenanthera. Chem. Pharm. Bull.61 (1), 96-100. doi: 10.1248/cpb.c12-00700.

Liang, C. Q., Hu, J., Luo, R. H., Shi, Y. M., Shang, S. Z., Gao, Z. H., Wang, R. R., Zheng, Y. T., Xiong, W. Y., Zhang, H. B., Xiao, W. L. & Sun, H. D. (2013)
Six New Lignans from the Leaves and Stems of Schisandra sphenanthera. Fitoterapia 86, 171-177. doi: 10.1016/j.fitote.2013.03.008.

Liang, C.-Q., Hu, J., Shi, Y.-M., Shang, S.-Z., Du, X., Zhan, R., Wang, W.-G., Xiong, W.-Y., Xiao, W.-L., Zhang, H.-B. & Sun, H.-D. (2013)
Five New Nortriterpenoids from the Stems of Schisandra neglecta. Helv. Chim. Acta 96 (7), 1376-1385. doi: 10.1002/hlca.201200392.

He, F., Bao, J., Zhang, X. Y., Tu, Z. C., Shi, Y. M. & Qi, S. H. (2013)
Asperterrestide A, a Cytotoxic Cyclic Tetrapeptide from the Marine-Derived Fungus Aspergillus terreus SCSGAF0162. J. Nat. Prod. 76 (6), 1182-1186. doi: 10.1021/np300897v.

2012

Zou, J., Du, X., Pang, G., Shi, Y.-M., Wang, W.-G., Zhan, R., Kong, L.-M., Li, X.-N., Li, Y., Pu, J.-X. & Sun, H.-D. (2012)
Ternifolide A, a New Diterpenoid Possessing a Rare Macrolide Motif from Isodon ternifolius. Org. Lett. 14 (12), 3210-3213. doi: 10.1021/ol3013205.

Shang, S.-Z., Yan, J.-M., Zhang, H.-B., Shi, Y.-M., Gao, Z.-H., Du, X., Li, Y., Xiao, W.-L. & Sun, H.-D. (2012)
Two New Neolignans from Manglietia insignis. Nat. Prod. Bioprospect. 2 (5), 227-230. doi: 10.1007/s13659-012-0063-7.

Luo, X., Shi, Y. M., Luo, R. H., Luo, S. H., Li, X. N., Wang, R. R., Li, S. H., Zheng, Y. T., Du, X., Xiao, W. L., Pu, J. X. & Sun, H. D. (2012)
Schilancitrilactones A–C: Three Unique Nortriterpenoids from Schisandra lancifolia. Org. Lett. 14 (5), 1286-1289. doi: 10.1021/ol300099e.

Liang, C. Q., Shi, Y. M., Luo, R. H., Li, X. Y., Gao, Z. H., Li, X. N., Yang, L. M., Shang, S. Z., Li, Y., Zheng, Y. T., Zhang, H. B., Xiao, W. L. & Sun, H. D. (2012)
Kadcoccitones A and B, Two New 6/6/5/5-Fused Tetracyclic Triterpenoids from Kadsura coccinea. Org. Lett. 14 (24), 6362-6365. doi: 10.1021/ol303168y.

Gao, Z.-H., Kong, L.-M., Zou, X.-S., Shi, Y.-M., Shang, S.-Z., Luo, H.-R., Liang, C.-Q., Li, X.-N., Li, Y., Du, X., Xiao, W.-L. & Sun, H.-D. (2012)
Four new indole alkaloids from Plantago asiatica. Nat. Prod. Bioprospect. 2 (6), 249-254. doi: 10.1007/s13659-012-0082-4.

2011

Yang, G.-Y., Li, Y.-K., Zhang, X.-J., Li, X.-N., Yang, L.-M., Shi, Y.-M., Xiao, W.-L., Zheng, Y.-T. & Sun, H.-D. (2011)
Three New Nortriterpenoids from Schisandra wilsoniana and Their Anti-HIV-1 Activities. Nat. Prod. Bioprospect. 1 (1), 33-36. doi: 10.1007/s13659-011-0008-6.

Shi, Y. M., Li, X. Y., Li, X. N., Luo, X., Xue, Y. B., Liang, C. Q., Zou, J., Kong, L. M., Li, Y., Pu, J. X., Xiao, W. L. & Sun, H. D. (2011)
Schicagenins A–C: Three Cagelike Nortriterpenoids from Leaves and Stems of Schisandra chinensis. Org. Lett. 13 (15), 3848-3851. doi: 10.1021/ol201366d.

Luo, X., Pu, J. X., Fan, P., Shi, Y. M., Yang, G. Y., Li, X. N., Lei, C., Gao, X. M., Zhang, H. B., Xiao, W. L. & Sun, H. D. (2011)
Four New Dibenzocyclooctadiene Lignans from Schisandra rubriflora. Chin. J. Nat. Med. 9 (3), 167-172. doi: 10.3724/sp.j.1009.2011.00167.

 

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