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  Location: Home >> TIB PI

ZHANG Xueli, Ph.D.

Principal Investigator, TIB, Tianjin, China

Tel: 022-84861983

Fax: 022-84861983



1996-2000  School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, B.S. 

2000-2005  School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Ph.D. 

Professional Experience 

2005-2007  Department of Microbiology and Cell Science, University of Florida, Post-doctoral 

2007-2010  Department of Microbiology and Cell Science, University of Florida, Research Assistant Professor 

2010-          Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Professor

2015-          The Key Laboratory of Systems Microbial Biotechnology, Chinese Academy of Sciences, Director  

Research Interest

Our group has been interested in constructing microbial cell factories for production of bulk chemicals and plant-derived natural products through metabolic engineering and synthetic biology. Research interests include:

(1) Identification of new enzymes for natural products synthesis using metabolic engineering platforms, followed by enzyme optimization.

(2) Design and construction of synthetic pathways, followed by pathway optimization through coordinated gene expression, cofactor engineering and metabolic evolution.

(3) Optimization of cell physiology through adaptive evolution, followed by characterization of their genetic mechanisms.

(4) Development of new genome editing methods.

Selected Publications

1. Dai Z, Liu Y, Sun Z, Wang D, Qu G, Ma X, Fan F, Zhang L, Li S, Zhang X*. Identification of a novel cytochrome P450 enzyme that catalyzes the C-2α hydroxylation of pentacyclic triterpenoids and its application in yeast cell factories. Metab Eng. 2019. 51:70-78

2. Wu T, Li S, Ye L, Zhao D, Fan F, Li Q, Zhang B, Bi C*, Zhang X*. Engineering an Artificial Membrane Vesicle Trafficking System (AMVTS) for the Excretion of β-Carotene in Escherichia coli. ACS Synth Biol. 2019. 8(5):1037-1046.

3. Li Q, Fan F, Gao X, Yang C, Bi C, Tang J, Liu T, Zhang X*. Balanced activation of IspG and IspH to eliminate MEP intermediate accumulation and improve isoprenoids production in Escherichia coli. Metab Eng. 2017. 44:13-21

4. Wu T, Ye L, Zhao D, Li S, Li Q, Bi C*, Zhang X*. Membrane engineering - A novel strategy to enhance the production and accumulation of β-carotene in Escherichia coli. Metab Eng. 2017, 43:85-91.

5. Zhu X, Zhao D, Qiu H, Fan F, Man S, Bi C*, Zhang X*. The CRISPR/Cas9-facilitated multiplex pathway optimization (CFPO) technique and its application to improve the Escherichia coli xylose utilization pathway. Metab Eng. 2017. 43:37-45.

6. Zhu X, Tan Z, Xu H, Chen J, Tang J, Zhang X*. Metabolic evolution of two reducing equivalent-conserving pathways for high-yield succinate production in Escherichia coli. Metab Eng. 2014, 24:87-96.

7. Dai Z, Liu Y, Zhang X, Shi M, Wang B, Huang L*, Zhang X*. Metabolic engineering of Saccharomyces cerevisiae for production of ginsenosides. Metab Eng. 2013, 20:146-156.

8. Zhao J, Li Q, Sun T, Zhu X, Xu H, Tang J, Zhang X*, Ma Y. Engineering central metabolic modules of Escherichia coli for improving β-carotene production. Metab Eng. 2013, 17: 42-50.

9. Shi A, Zhu X, Lu J, Zhang X*, Ma Y. Combinatorial activation of transhydrogenase and NAD kinase for improving isobutanol production. Metab Eng. 2013, 16:1-10.

10. Dai Z, Liu Y, Huang L, Zhang X*Production of miltiradiene by metabolically engineered Saccharomyces cerevisiaeBiotechnol Bioeng. 2012, 109(11): 2845–2853.



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