1. Shi J., Zang X., Zhao Z., Shen Z., Li W., Zhao G., Jiahai Zhou#, and Du Y.L.# (2023) Conserved Enzymatic Cascade for Bacterial Azoxy Biosynthesis. J. Am. Chem. Soc. 145, 49, 27131–27139.
2. He J, Wu L., Wei W., Meng S., Liu Z.T., Xu X., Pan H.X., Yang S., Liang Y.#, Zhou J.#, Tang G.L.#, (2023) Enzymatic catalysis favours eight-membered over five-membered ring closure in bicyclomycin biosynthesis. Nature Catalysis, 6, 637–648.
3. Liu J., Lu J., Zhang C., Zhou Q., Jamieson C.S., Shang C., Houk K.N.#, Zhou J.#, Hu Y.# (2023). Tandem intermolecular [4 + 2] cycloadditions are catalysed by glycosylated enzymes for natural product biosynthesis. Naure Chemistry, 15, 1083–1090.
4. Ohashi M., Tan D., Lu J., Jamieson C.S., Kanayama D., Zhou J.#, Houk K.N.#, Tang Y.# (2023) Enzymatic cis-Decalin Formation in Natural Product Biosynthesis. J Am Chem Soc, 145(6): 3301-3305.
5. Zhang J., Hou X., Chen Z., Ko Y., Ruszczycky M.W., Chen Y., Zhou J.#, Liu H.W.# (2022) Dioxane bridge formation during the biosynthesis of spectinomycin involves a twitch radical SAM dehydrogenase that may have evolved from an epimerase. J Am Chem Soc, 144(22): 9910-9919.
6. Lee Y.H., Hou X., Chen R., Feng X., Liu X., Ruszczycky M.W., Gao J.M.#, Wang B.#, Zhou J.#, Liu H.W.# (2022) Radical S-Adenosyl methionine enzyme BlsE catalyzes a radical-mediated 1,2-diol dehydration during the biosynthesis of Blasticidin S. J Am Chem Soc, 144(10): 4478-4486.
7. Wu L., Wang Z., Cen Y.#, Wang B.#, Zhou J.# (2022) Structural insight into the catalytic mechanism of the endoperoxide synthase FtmOx1. Angew Chem Int Ed, 61(12): e202112063.
8. Wen W., Zhang Y., Zhang Y., Yu Q., Jiang C., Tang M., Pu J., Wu L., Zhao Y., Shi T., Zhou J.#, Tang G.L.# (2021) Reductive inactivation of the hemiaminal pharmacophore for resistance against tetrahydroisoquinoline antibiotics. Nat Communications, 12(1): 7085.
9. Liu N., Wu L., Feng J., Sheng X.#, Li J., Chen X., Li J., Liu W., Zhou J.#, Wu Q.#, Zhu D.# (2021) Crystal structures and catalytic mechanism of L-erythro-3,5-diaminohexanoate dehydrogenase and rational engineering for asymmetric synthesis of β-amino acids, Angew Chem Int Ed, 60: 10203-10.
10. Gao D., Jamieson C.S., Wang G., Yan Y., Zhou J.#, Houk K.N.#, Tang Y.# (2021) A polyketide cyclase that forms medium-ring lactones. J Am Chem Soc, 143: 80-84.
11. Yan Y., Zang X., Jamieson C.S., Lin H., Houk K.N., Zhou J.#, Tang Y.# (2020). Biosynthesis of the fungal glyceraldehyde-3-phosphate dehydrogenase inhibitor heptelidic acid and mechanism of self-resistance. Chem Sci, 11(35): 9554-9562.
12. Ohashi M., Jamieson C.S., Cai Y., Tan D., Kanayama D., Tang M.C., Anthony S.M., Chari J.V., Barber J.S., Picazo E., Kakule T.B., Cao S., Garg N.K., Zhou J.#, Houk K.N.#, Tang Y.# (2020) An enzymatic Alder-ene reaction. Nature, 586(7827): 64-69.
13. Li A., Acevedo-Rocha C.G., D'Amore L., Chen J., Peng Y., Garcia-Borras M., Gao C., Zhu J., Rickerby H., Osuna S.#, Zhou J.#, Reetz M.T.# (2020) Regio- and stereoselective steroid hydroxylation at C7 by cytochrome P450 monooxygenase mutants. Angew Chem Int Ed, 59(30): 12499-12505.
14. Chen T., Chen J., Tang Y., Zhou J.#, Guo Y.#, Chang W.# (2020) Pathway from N-alkylglycine to alkylisonitrile catalyzed by Iron (II) and 2-oxoglutarate-dependent oxygenases. Angew Chem Int Ed, 59(19): 7367-7371.
15. Cai, Y., Hai Y., Ohashi M., Jamieson C.S., Garcia-Borras M., Houk K.N.#, Zhou J.#, Tang Y.# (2019) Structural basis for stereoselective dehydration and hydrogen-bonding catalysis by the SAM-dependent pericyclase LepI. Nature Chemistry, 11(9): 812-820.
16. Cen Y., Singh W., Arkin M., Moody T.S., Huang M., Zhou J.#, Wu Q.#, Reetz M.T.# (2019) Artificial cysteine-lipases with high activity and altered catalytic mechanism created by laboratory evolution. Nature Communications, 10(1): 3198.
17. Xu J., Cen Y., Singh W., Fan J., Wu L., Lin X., Zhou J.#, Huang M.#, Reetz M.T.#, Wu Q.# (2019) Stereodivergent protein engineering of a lipase to access all possible stereoisomers of chiral esters with two stereocenters. J Am Chem Soc, 141(19): 7934-7945.
18. Zhou J., Wang Y., Xu G., Wu L., Han R., Schwaneberg U., Rao Y., Zhao Y.L., Zhou J.#, Ni Y.# (2018) Structural insight into enantioselective inversion of an alcohol dehydrogenase reveals a "polar gate" in stereorecognition of diaryl ketones. J Am Chem Soc, 140(39): 12645-12654.
19. Yan Y., Liu Q., Zang X., Yuan S., Bat-Erdene U., Nguyen C., Gan J., Zhou J.#, Jacobsen S.E.#, Tang Y.# (2018) Resistance-gene-directed discovery of a natural-product herbicide with a new mode of action. Nature, 559(7714): 415-418.
20. Li Y., Zhang W., Zhang H., Tian W., Wu L., Wang S., Zheng M., Zhang J., Sun C., Deng Z., Sun Y., Qu X.#, Zhou J.# (2018) Structural basis of a broadly selective acyltransferase from the polyketide synthase of splenocin. Angew Chem Int Ed, 57(20): 5823-5827.
21. Sun Z., Wu L., Bocola M., Chan H.C.S., Lonsdale R., Kong X.D., Yuan S.#, Zhou J.#, Reetz M.T.# (2018) Structural and computational insight into the catalytic mechanism of limonene epoxide hydrolase mutants in stereoselective transformations. J Am Chem Soc, 140(1): 310-318.
22. Yuan H., Zhang J., Cai Y., Wu S., Yang K., Chan H.C.S., Huang W., Jin W.B., Li Y., Yin Y., Igarashi Y., Yuan S.#, Zhou J.#, Tang G.L.# (2017) GyrI-like proteins catalyze cyclopropanoid hydrolysis to confer cellular protection. Nature Communications, 8(1): 1485.
23. Zhang J., Liu N., Cacho R.A., Gong Z., Liu Z., Qin W., Tang C., Tang Y.#, Zhou J.# (2016). Structural basis of nonribosomal peptide macrocyclization in fungi. Nature Chemical Biology, 12(12): 1001-1003.
24. Sun Z., Lonsdale R., Kong X., Xu J., Zhou J.#, Reetz M.R.# (2015). Reshaping an enzyme binding pocket for enhanced and inverted stereoselectivity: use of smallest amino acid alphabets in directed evolution. Angew Chem Int Ed, 54(42): 12410-12415.
25. Kong X., Yuan S., Li L., Chen S., Xu J.#, Zhou J.# (2014) Engineering of an epoxide hydrolase for efficient bioresolution of bulky pharmaco substrates. Proc Natl Acad Sci USA, 111(44): 15717-15722.
26. Kong X., Ma Q., Zhou J.#, Zeng B.#, Xu J.# (2014). A smart library of epoxide hydrolase variants and the top hits for synthesis of (S)-β-blocker precursors. Angew Chem Int Ed, 53(26): 6641-6644.