Principal Investigator,Professor : Microbial Natural Product Biosynthesis and Synthetic Biology

 

PAN Guohui
Address:NO.1 West Beichen Road, Chaoyang District, Beijing 100101, China
Telephone/fax:010-64806056
E-mail:panguohui@im.ac.cn
Research Interests
Our lab works on the discovery, biosynthesis, and synthetic biology study of microbial natural product drugs, with interdisciplinary techniques such as microbiology, bioinformatics, molecular biology and gene editing, biochemistry, and natural product chemistry.
1. Exploitation of microbial resources and targeted mining of natural product drugs.
2. Biosynthetic mechanism of complex natural products and development of enzyme catalysts.
3. Synthetic biology creation of natural product drugs.
Education/degrees
2004.9-2008.9 B.E., Bioengineering, China University of Mining and Technology (Beijing), Beijing, China
2008.9-2014.2 Ph.D., Biochemistry and Molecular Biology, Institute of Microbiology, Chinese Academy of Sciences (IMCAS), Beijing, China
Work experience
Postdoctoral Fellow Training
2014.2-2019.8 Postdoc., Department of Chemistry, The Scripps Research Institute, Florida, U.S.A.
Professional Appointments
2019.8-present Professor, IMCAS, Beijing, China

 

Editorial Board
mLife, Junior Editorial Board, 2024-
Chinese Journal of Natural Medicines, Youth Editorial Board, 2021-2025
Frontiers in Bioengineering and Biotechnology, Review Editor, 2017-
Frontiers in Microbiology, Review Editor, 2022-
Microbiology China, Editorial Board, 2021-

The main research areas
Discovery, biosynthesis, and synthetic biology study of microbial natural product drugs.
Publication
* Corresponding authors # Co-first authors
1. Steele AD#, Jiang H#, Pan G, Lim SK, Kalkreuter E, Kwong T, Ju J, Rajski S, Shen B*. Discrete acyltransferases and thioesterases in iso-migrastatin and lactimidomycin biosynthesis. Biochemistry. 2024, 63, 4, 563–75.

 

2. Gao J#, Li L#, Shen S, Ai G, Wang B, Guo F, Yang T, Han H, Xu Z, Pan G*, Fan K*. Cofactor-independent C–C bond cleavage reactions catalyzed by the AlpJ family of oxygenases in atypical angucycline biosynthesis. Beilstein J. Org. Chem. 2024, 20, 1198–1206.

3. Kong Y, Liu Y, Wang K, Wang T, Wang C, Ai B, Jia H, Pan G, Yin M, Xu Z*. Confirmation of the stereochemistry of spiroviolene. Beilstein J. Org. Chem. 2024, 20, 852–858.

4. Zhang C, Zhao Y, Li Z, Wang W, Huang Y, Pan G, Fan K*. Molecular mechanism of GylR-mediated regulation of glycerol metabolism in Streptomyces clavuligerus NRRL 3585. Front Microbiol. 2022, 13, 1078293.

5. Wang H#, Wang L#, Fan K, Pan G*. Tetracycline family natural products: discovery, biosynthesis and engineering. Chin J Nat Medicines. 2022, 20(10):773-794.

6. Zhang Z, Li P*, Wang M, Zhang Y, Wu B, Tao Y, Pan G*, Chen Y*. (S)-3-aminopiperidine-2,6-dione is a biosynthetic intermediate of microbial blue pigment indigoidine. mLife. 2022, 1(2):146–155

7. Wang J#, Li Z#, Wang W, Pang S, Yao Y, Yuan F, Wang H, Xu Z, Pan G, Liu Z, Chen Y*, Fan K*. Dynamic control strategy to produce riboflavin with lignocellulose hydrolysate in the thermophile geobacillus thermoglucosidasius. ACS Synth Biol. 2022, 11(6):2163-2174.

8. Meng S#, Steele AD#, Yan W#, Pan G, Kalkreuter E, Liu YC, Xu Z, Shen B*. Thiocysteine lyases as polyketide synthase domains installing hydropersulfide into natural products and a hydropersulfide methyltransferase. Nat Commun. 2021, 12(1):5672.

9. Wang L, Fan K, Wang H, Hu H, Xiang L, Ai G, Pan G*. Bioinformatics-directed discovery of dehydrated linear trimer and dimer of 2,3-dihydroxybenzoyl-L-serine from Streptomyces albofaciens JCM 4342. Microbiology China, 2021, 48(7): 2307-2317.

10. Yuan F, Yin S, Xu Y, Xiang L, Wang H, Li Z, Fan K*, Pan G*. The richness and diversity of catalases in bacteria. Front. Microbiol. 2021, 12:645477.

11. Zhang Q#, Ren JW#, Wang W, Zhai J, Yang J, Liu N, Huang Y, Chen Y, Pan G*, Fan K*. A versatile transcription-translation in one approach for activation of cryptic biosynthetic gene clusters. ACS Chem Biol. 2020, 15(9), 2551-2557.

12. Kalkreuter E, Pan G, Cepeda AJ, Shen B*. Targeting bacterial genomes for natural product discovery. Trends Pharmacol Sci. 2020, 41(1):13-26.

13. Steele AD, Kalkreuter E, Pan G, Meng S, Shen B*. Hybrid peptide-polyketide natural product biosynthesis. In: Hung-Wen (Ben) Liu, Tadhg P. Begley (eds.) Comprehensive Natural Products III: Chemistry and Biology. vol. 2, 2020, pp. 284-335. Elsevier.

14. McAlpine et al. The value of universally available raw NMR data for transparency, reproducibility, and integrity in natural product research. Nat Prod Rep. 2019, 36(1):35-107.

15. Xu Z#, Pan G#, Zhou H, Shen B*. Discovery and characterization of 1-aminocyclopropane-1-carboxylic acid synthase of bacterial origin. J Am Chem Soc. 2018, 140(49):16957-16961. (Hot off the press)

16. Kwong T#, Ma M#, Pan G, Hindra, Yang D, Yang C, Lohman JR, Rudolf JD, Cleveland JL, Shen B*. P450-catalyzed tailoring steps in leinamycin biosynthesis featuring regio- and stereoselective hydroxylations and substrate promiscuities. Biochemistry. 2018, 57(33):5005–5013.

17. Pan G#, Xu Z#, Guo Z, Hindra, Ma M, Yang D, Zhou H, Gansemans Y, Zhu X, Huang Y, Zhao LX, Jiang Y, Cheng J, Van Nieuwerburgh F, Suh JW, Duan Y, Shen B*. Discovery of the leinamycin family of natural products by mining actinobacterial genomes. Proc Natl Acad Sci U S A. 2017, 114(52):E11131-E11140. (Highlighted by F1000)

18. Zhang B#, Xu Z#, Teng Q#, Pan G, Ma M, Shen B*. A Long-range acting dehydratase domain as the missing link for C17-dehydration in iso-migrastatin biosynthesis. Angew. Chem. Int. Ed. 2017, 56(25):7247-7251.

19. Li L#, Pan G#, Zhu X, Fan K, Gao W, Ai G, Ren J, Shi M, Olano C, Salas J, Yang K*. Engineered jadomycin analogues with altered sugar moieties revealing JadS as a substrate flexible O-glycosyltransferase. Appl Microbiol Biotechnol. 2017, 101(13):5291-5300.

20. Pan G#, Gao X#, Fan K#, Liu J, Meng B, Gao J, Wang B, Zhang C, Han H, Ai G, Chen Y, Wu D*, Liu ZJ*, Yang K*. Structure and function of a C-C bond cleaving oxygenase in atypical angucycline biosynthesis. ACS Chem Biol. 2017, 12(1):142-152.

21. Guo Z, Pan G, Xu Z, Yang D, Hindra, Zhu X, Huang Y, Zhao LX, Jiang Y, Duan Y, Shen B*. New isofuranonaphthoquinones and isoindolequinones from Streptomyces sp. CB01883. J Antibiot. 2017, 70(4):414-422.

22. Huang Y#, Yang D#, Pan G, Tang GL, Shen B*. Characterization of LnmO as a pathway-specific Crp/Fnr-type positive regulator for leinamycin biosynthesis in Streptomyces atroolivaceus and its application for titer improvement. Appl Microbiol Biotechnol. 2016, 100(24):10555-10562.

23. Huang Y, Tang GL, Pan G, Chang CY, Shen B. Characterization of the ketosynthase and acyl carrier protein domains at the LnmI nonribosomal peptide synthetase-polyketide synthase interface for leinamycin biosynthesis. Org Lett. 2016, 18(17):4288-4291.

24. Zhang B#, Yang D#, Yan Y, Pan G, Xiang W*, Shen B*. Overproduction of lactimidomycin by cross-overexpression of genes encoding Streptomyces antibiotic regulatory proteins. Appl Microbiol Biotechnol. 2016, 100(5):2267-2277.

25. Medema MH et al. (2015) Minimum information about a biosynthetic gene cluster. Nat Chem Biol. 2015, 11(9):625-631. (Highlighted by F1000)

26. Wang B#, Ren J#, Li L, Guo F, Pan G, Ai G, Aigle B, Fan K*, Yang K*. Kinamycin biosynthesis employs a conserved pair of oxidases for B-ring contraction. Chem Commun. 2015, 51(42):8845-8848.

27. Liu Y, Ryu H, Ge B, Pan G, Sun L, Park K, Zhang K*. Improvement of wuyiencin biosynthesis in Streptomyces wuyiensis CK-15 by identification of a key regulator, WysR. J Microbiol Biotechnol. 2014, 24(12):1644-1653.

28. Wang W#, Ji J#, Li X, Wang J, Li S, Pan G, Fan K, Yang K*. Angucyclines as signals modulate the behaviors of Streptomyces coelicolor. Proc Natl Acad Sci U S A. 2014, 111(15):5688-5693.

29. Zhang Y#, Pan G#, Zou Z, Fan K, Yang K*, Tan H*. JadR*-mediated feed-forward regulation of cofactor supply in jadomycin biosynthesis. Mol Microbiol. 2013, 90(4):884-897.

30. Fan K#, Pan G#, Peng X, Zheng J, Gao W, Wang J, Wang W, Li Y, Yang K*. Identification of JadG as the B ring opening oxygenase catalyzing the oxidative C-C bond cleavage reaction in jadomycin biosynthesis. Chem Biol. 2012, 19(11):1381-1390.