教师简介

李新林,助理研究员(讲师),甘肃陇南人,博士毕业于中国科学院大学(中国科学院分子植物科学卓越创新中心,原中国科学院上海生命科学研究院)

联系方式(Email):xinlinli@sdu.edu.cn; 

ORCID ID:https://orcid.org/my-orcid?orcid=0000-0002-6094-0577

地址:山东省济南市历下区文化西路44号山东大学齐鲁医学院(药学院)


教育经历
  • 2019-9 — 2023-6
    中国科学院大学
    理学博士学位
  • 2016-9 — 2019-7
    首都医科大学
    医学硕士学位
  • 2010-9 — 2014-7
    天津中医药大学
    理学学士
工作经历
  • 2023-09 — 至今
     山东大学  齐鲁医学院(药学院) 
    助理研究员(讲师)
研究方向
论文成果

(1) Xin-Lin Li, Yanlei Sun, Ying Yin, Shuai Zhan, Chengshu Wang*.A bacterial-like Pictet-Spenglerase drives the evolution of fungi to produce β-carboline glycosides together with separate genes.Proceedings of the National Academy of Sciences of the United States of America.2023,120 :e2303327120.

(2) Xin-Lin Li#, Yu-Xing Xu#, Yuan Li, Rui Zhang, Tian-Yuan Hu, Ping Su, Man Zhou, Ting Tang, Ying Zeng, Yan-Long Yang*, Wei Gao*.Rapid discovery and functional characterization of diterpene synthases from basidiomycete fungi by genome mining.Fungal Genetics and Biology.2019,128 :36-42.

(3) Yuan Li, Xin-Lin Li, Chang-Jiang-Sheng Lai, Rui-Shan Wang, Li-Ping Kang, Ting Ma, Zhen-Hua Zhao, Wei Gao*, Lu-Qi Huang*.Functional characterization of three flavonoid glycosyltransferases from Andrographis paniculata.Royal Society Open Science.2019,6 :190150.

(4) Yanlei Sun#, Bo Chen#, Xin-Lin Li, Ying Yin, Chengshu Wang*.Orchestrated biosynthesis of the secondary metabolite cocktails enables the producing fungus to combat diverse bacteria.mBio.2022,13 :e0180022.

(5) Tianyuan Hu, Jiawei Zhou, Yuru Tong, Ping Su, Xin-Lin Li, Yuan Liu, Nan Liu, Xiaoyi Wu, Yifeng Zhang, Jiadian Wang, Linhui Gao, Lichan Tu, Yun Lu, Zhouqian Jiang, Yongjin J Zhou, Wei Gao*, Luqi Huang*.Engineering chimeric diterpene synthases and isoprenoid biosynthetic pathways enables high-level production of miltiradiene in yeast.Metabolic Engineering.2020,60 :87-96.

(6) Yuan Li, Hui-Xin Lin, Jian Wang, Jian Yang, Chang-Jiang-Sheng Lai, Xing Wang, Bao-Wei Ma, Jin-Fu Tang, Yong Li, Xin-Lin Li, Juan Guo, Wei Gao*, Lu-Qi Huang*.Glucosyltransferase capable of catalyzing the last step in Neoandrographolide biosynthesis.Organic Letters.2018,20 :5999-6002.

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