发表论文
[1] Yu Li, Peiyuan Yao, Shiqing Zhang, Jinhui Feng, Hao Su, Xiangtao Liu, Xiang Sheng, Qiaqing Wu, Dunming Zhu, Yanhe Ma. Creating a new benzaldehyde lyase for atom-economic synthesis of chiral 1,2,4-butanetriol and 2-aminobutane-1,4-diol from formaldehyde. CHEM CATALYSIS. 2023, 3(1): http://dx.doi.org/10.1016/j.checat.2022.11.006.[2] Li, Ming, Cui, Yunfeng, Xu, Zefei, Chen, Xi, Feng, Jinhui, Wang, Min, Yao, Peiyuan, Wu, Qiaqing, Zhu, Dunming. Asymmetric Synthesis of N-Substituted gamma-Amino Esters and gamma-Lactams Containing alpha,gamma-Stereogenic Centers via a Stereoselective Enzymatic Cascade. ADVANCED SYNTHESIS & CATALYSIS[J]. 2022, 364(2): 372-379, http://dx.doi.org/10.1002/adsc.202100953.[3] Zhan, Zhuangzhuang, Xu, Zefei, Yu, Shanshan, Feng, Jinhui, Liu, Fufeng, Yao, Peiyuan, Wu, Qiaqing, Zhu, Dunming. Stereocomplementary Synthesis of a Key Intermediate for Tofacitinib via Enzymatic Dynamic Kinetic Resolution-Reductive Amination. ADVANCED SYNTHESIS & CATALYSIS[J]. 2022, 364(14): 2380-2386, http://dx.doi.org/10.1002/adsc.202200361.[4] Yang, Linsong, Li, Jianjiong, Xu, Zefei, Yao, Peiyuan, Wu, Qiaqing, Zhu, Dunming, Ma, Yanhe. Asymmetric Synthesis of Fused-Ring Tetrahydroisoquinolines and Tetrahydro-beta-carbolines from 2-Arylethylamines via a Chemoenzymatic Approach. ORGANIC LETTERS[J]. 2022, 24(36): 6531-6536, http://dx.doi.org/10.1021/acs.orglett.2c02466.[5] Li, Jiacheng, Li, Jianjiong, Cui, Yunfeng, Wang, Min, Feng, Jinhui, Yao, Peiyuan, Wu, Qiaqing, Zhu, Dunming. Asymmetric Synthesis of Both Enantiomers of Dimethyl 2-Methylsuccinate by the Ene-Reductase-Catalyzed Reduction at High Substrate Concentration. CATALYSTS[J]. 2022, 12(10): http://dx.doi.org/10.3390/catal12101133.[6] Li, Jianjiong, Yu, Shanshan, Wang, Yingang, Yao, Peiyuan, Wu, Qiaqing, Zhu, Dunming. Simultaneous Preparation of (S)-2-Aminobutane and D-Alanine or D-Homoalanine via Biocatalytic Transamination at High Substrate Concentration. ORGANIC PROCESS RESEARCH & DEVELOPMENT[J]. 2022, 26(7): 2013-2020, [7] Li, Yu, Hu, Na, Xu, Zefei, Cui, Yunfeng, Feng, Jinhui, Yao, Peiyuan, Wu, Qiaqing, Zhu, Dunming, Ma, Yanhe. Asymmetric Synthesis of N-Substituted 1,2-Amino Alcohols from Simple Aldehydes and Amines by One-Pot Sequential Enzymatic Hydroxymethylation and Asymmetric Reductive Amination. ANGEWANDTECHEMIEINTERNATIONALEDITION[J]. 2022, 61(17): http://dx.doi.org/10.1002/anie.202116344.[8] Marshall, James R, Yao, Peiyuan, Montgomery, Sarah L, Finnigan, James D, Thorpe, Thomas W, Palmer, Ryan B, MangasSanchez, Juan, Duncan, Richard A M, Heath, Rachel S, Graham, Kirsty M, Cook, Darren J, Charnock, Simon J, Turner, Nicholas J. Screening and characterization of a diverse panel of metagenomic imine reductases for biocatalytic reductive amination. NATURE CHEMISTRY[J]. 2021, 13(2): https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7116802/.[9] Peiyuan Yao, James R Marshall, Zefei Xu, Jesmine Lim, Simon J Charnock, Dunming Zhu, Nicholas J Turner. Asymmetric Synthesis of N ‐Substituted α‐Amino Esters from α‐Ketoesters via Imine Reductase‐Catalyzed Reductive Amination. ANGEWANDTE CHEMIE (INTERNATIONAL ED. IN ENGLISH). 2021, 60(16): 8717-8721, https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8048798/.[10] Wang, Yingang, Feng, Jinhui, Dong, Wenyue, Chen, Xi, Yao, Peiyuan, Wu, Qiaqing, Zhu, Dunming. Improving Catalytic Activity and Reversing Enantio-Specificity of omega-Transaminase by Semi-Rational Engineering en Route to Chiral Bulky beta-Amino Esters. CHEMCATCHEM[J]. 2021, 13(15): 3396-3400, http://dx.doi.org/10.1002/cctc.202100503.[11] Yu, Shanshan, Li, Jinlong, Yao, Peiyuan, Feng, Jinhui, Cui, Yunfeng, Li, Jianjiong, Liu, Xiangtao, Wu, Qiaqing, Lin, Jianping, Zhu, Dunming. Inverting the Enantiopreference of Nitrilase-Catalyzed Desymmetric Hydrolysis of Prochiral Dinitriles by Reshaping the Binding Pocket with a Mirror-Image Strategy. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION[J]. 2021, 60(7): 3679-3684, http://dx.doi.org/10.1002/anie.202012243.[12] Xu, Zefei, Yao, Peiyuan, Sheng, Xiang, Li, Jinlong, Li, Jianjiong, Yu, Shanshan, Feng, Jinhui, Wu, Qiaqing, Zhu, Dunming. Biocatalytic Access to 1,4-Diazepanes via Imine Reductase-Catalyzed Intramolecular Asymmetric Reductive Amination. ACS CATALYSIS[J]. 2020, 10(15): 8780-8787, http://dx.doi.org/10.1021/acscatal.0c02400.[13] 董文玥, 姚培圆, 吴洽庆. 纳米材料固定化酶的研究进展. 微生物学通报[J]. 2020, 47(7): 2161-2176, http://lib.cqvip.com/Qikan/Article/Detail?id=7102497488.[14] Dong, Yijie, Yao, Peiyuan, Cui, Yunfeng, Wu, Qiaqing, Zhu, Dunming, Li, Guangyue, Reetz, Manfred T. Manipulating the stereoselectivity of a thermostable alcohol dehydrogenase by directed evolution for efficient asymmetric synthesis of arylpropanols. BIOLOGICAL CHEMISTRY[J]. 2019, 400(3): 313-321, https://www.webofscience.com/wos/woscc/full-record/WOS:000458628400006.[15] Yu, Shanshan, Yao, Peiyuan, Li, Jinlong, Feng, Jinhui, Wu, Qiaqing, Zhu, Dunming. Improving the catalytic efficiency and stereoselectivity of a nitrilase from Synechocystis sp. PCC6803 by semi-rational engineering en route to chiral gamma-amino acids. CATALYSIS SCIENCE & TECHNOLOGY[J]. 2019, 9(6): 1504-1510, https://www.webofscience.com/wos/woscc/full-record/WOS:000462662100016.[16] Yao, Peiyuan, Xu, Zefei, Yu, Shanshan, Wu, Qiaqing, Zhu, Dunming. Imine Reductase-Catalyzed Enantioselective Reduction of Bulky alpha,beta-Unsaturated Imines en Route to a Pharmaceutically Important Morphinan Skeleton. ADVANCED SYNTHESIS & CATALYSIS[J]. 2019, 361(3): 556-561, https://www.webofscience.com/wos/woscc/full-record/WOS:000457795500024.[17] Liu, Na, Feng, Jinhui, Zhang, Rui, Chen, Xi, Li, Xuemei, Yao, Peiyuan, Wu, Qiaqing, Ma, Yanhe, Zhu, Dunming. Efficient microbial synthesis of key steroidal intermediates from bio-renewable phytosterols by genetically modified Mycobacterium fortuitum strains. GREEN CHEMISTRY[J]. 2019, 21(15): 4076-4083, [18] Zhang, Mujiao, Yao, Peiyuan, Yu, Shanshan, Zhang, Tongcun, Wu, Qiaqing, Zhu, Dunming. Efficient selective hydrolysis of terephthalonitrile to 4-cyanobenzoic acid catalyzed by a novel nitrilase from Pantoea sp. PROCESS BIOCHEMISTRY[J]. 2018, 75: 152-156, http://dx.doi.org/10.1016/j.procbio.2018.09.020.[19] Li, Xuemei, Chen, Xi, Wang, Yu, Yao, Peiyuan, Zhang, Rui, Feng, Jinhui, Wu, Qiaqing, Zhu, Dunming, Ma, Yanhe. New product identification in the sterol metabolism by an industrial strain Mycobacterium neoaurum NRRL B-3805. STEROIDS[J]. 2018, 132: 40-45, http://dx.doi.org/10.1016/j.steroids.2018.02.001.[20] Gong, Rui, Yao, Peiyuan, Chen, Xi, Feng, Jinhui, Wu, Qiaqing, Lau, Peter C K, Zhu, Dunming. Accessing d-Valine Synthesis by Improved Variants of Bacterial Cyclohexylamine Oxidase. CHEMCATCHEM[J]. 2018, 10(2): 387-390, https://www.webofscience.com/wos/woscc/full-record/WOS:000423197900007.[21] Zhang, Xuemei, Ren, Jie, Yao, Peiyuan, Gong, Rui, Wang, Min, Wu, Qiaqing, Zhu, Dunming. Biochemical characterization and substrate profiling of a reversible 2,3-dihydroxybenzoic acid decarboxylase for biocatalytic Kolbe-Schmitt reaction. ENZYME AND MICROBIAL TECHNOLOGY[J]. 2018, 113: 37-43, http://dx.doi.org/10.1016/j.enzmictec.2018.02.008.[22] Qu, Ge, Lonsdale, Richard, Yao, Peiyuan, Li, Guangyue, Liu, Beibei, Reetz, Manfred T, Sun, Zhoutong. Methodology Development in Directed Evolution: Exploring Options when Applying Triple-Code Saturation Mutagenesis. CHEMBIOCHEM[J]. 2018, 19(3): 239-246, https://www.webofscience.com/wos/woscc/full-record/WOS:000424105700008.[23] Yao, Peiyuan, Cong, Peiqian, Gong, Rui, Li, Jinlong, Li, Guangyue, Ren, Jie, Feng, Jinhui, Lin, Jianping, Lau, Peter C K, Wu, Qiaqing, Zhu, Dunming. Biocatalytic Route to Chiral 2-Substituted-1,2,3,4-Tetrahydroquinolines Using Cyclohexylamine Oxidase Muteins. ACS CATALYSIS[J]. 2018, 8(3): 1648-1652, https://www.webofscience.com/wos/woscc/full-record/WOS:000426804100004.[24] Zhang, Yan, Yao, Peiyuan, Cui, Yunfeng, Wu, Qiaqing, Zhu, Dunming. One-Pot Enzymatic Synthesis of Cyclic Vicinal Diols from Aliphatic Dialdehydes via Intramolecular C-C Bond Formation and Carbonyl Reduction Using Pyruvate Decarboxylases and Alcohol Dehydrogenases. ADVANCED SYNTHESIS & CATALYSIS[J]. 2018, 360(21): 4191-4196, [25] Li, Guangyue, Yao, Peiyuan, Gong, Rui, Li, Jinlong, Liu, Pi, Lonsdale, Richard, Wu, Qiaqing, Lin, Jianping, Zhu, Dunming, Reetz, Manfred T. Simultaneous engineering of an enzyme's entrance tunnel and active site: the case of monoamine oxidase MAO-N. 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Enzymatic synthesis of 3-hydroxypropionic acid at high productivity by using free or immobilized cells of recombinant Escherichia coli. JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC[J]. 2016, 129: 37-42, http://dx.doi.org/10.1016/j.molcatb.2016.03.011.[32] 王雷, 袁京, 姚培圆, 程丽华, 解美仙, 贾荣荣, 冯进辉, 王敏, 吴洽庆, 朱敦明. 一种来源于运动替斯崔纳菌KA081020-065的新型卤醇脱卤酶的表达纯化及性质分析. 生物工程学报[J]. 2015, 31(5): 659-669, http://sciencechina.cn/gw.jsp?action=detail.jsp&internal_id=5428708&detailType=1.[33] Yao, Peiyuan, Wang, Lei, Yuan, Jing, Cheng, Lihua, Jia, Rongrong, Xie, Meixian, Feng, Jinhui, Wang, Min, Wu, Qiaqing, Zhu, Dunming. Efficient Biosynthesis of Ethyl (R)-3-Hydroxyglutarate through a One-Pot Bienzymatic Cascade of Halohydrin Dehalogenase and Nitrilase. CHEMCATCHEM[J]. 2015, 7(9): 1438-1444, https://www.webofscience.com/wos/woscc/full-record/WOS:000353974300006.[34] Zhang, Dalong, Chen, Xi, Zhang, Rui, Yao, Peiyuan, Wu, Qiaqing, Zhu, Dunming. Development of beta-Amino Acid Dehydrogenase for the Synthesis of beta-Amino Acids via Reductive Amination of beta-Keto Acids. ACS CATALYSIS[J]. 2015, 5(4): 2220-2224, http://124.16.173.210/handle/834782/1452.[35] 姚培圆, 任杰, 吴洽庆, 朱敦明. 化学生物融合转化反应研究的最新进展及挑战. 中国科学. 化学[J]. 2015, 45(5): 479-500, https://www.sciengine.com/doi/10.1360/N032014-00283.[36] Chao Han, Peiyuan Yao, Jing Yuan, Yitao Duan, Jinhui Feng, Min Wang, Qiaqing Wu, Dunming Zhu. Nitrilase-catalyzed hydrolysis of 3-aminopropionitrile at high concentration with a tandem reaction strategy for shifting the reaction to β-alanine formation. JOURNAL OF MOLECULAR CATALYSIS. B, ENZYMATIC. 2015, 115: 113-118, http://dx.doi.org/10.1016/j.molcatb.2015.02.007.[37] Duan, Yitao, Yao, Peiyuan, Chen, Xi, Liu, Xiangtao, Zhang, Rui, Feng, Jinhui, Wu, Qiaqing, Zhu, Dunming. Exploring the synthetic applicability of a new carboxylic acid reductase from Segniliparus rotundus DSM 44985. 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