51cg

Professor Hai Deng

Professor Hai Deng
Professor Hai Deng
Professor Hai Deng

Personal Chair

51cg
Email Address
h.deng@abdn.ac.uk
Telephone Number
+44 (0)1224 272953
Office Address
038 Meston Building
Old Aberdeen Campus
Meston Walk
AB24 3UE

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School/Department
School of Natural and Computing Sciences


Biography

08/2022 -                 Personal Chair, 51cg, UK

08/2018 - 07/2022   Reader, 51cg, UK

08/2014 - 07/2018  Senior Lecturer, 51cg, UK

10/2008 - 07/2014   Lecturer, 51cg, UK 

06/2002 - 09/2008   Postdoctoral fellow, University of St Andrews, UK 

1999 - 2002             Ph.D.   University of Wales Swansea, UK 

 

Memberships and Affiliations

Internal Memberships

Director of Research

PGR coordinator

CM2514 course coordinator

External Memberships

BBSRC pool of expert

MRC and BBSRC panel members

UKRI FLF peer review colleague

External reviewer for a series of peer-reviewed journals within my area of interest, including Nature, Nat. Chen. ACIE, Sci. Adv. Chem. Sci., Chem Comm., ACS Chem. Biol., ChemBioChem, Marine Biotechnology, Org & Biomol. Chem, FEMS Microbiology Ecology, Chemistry today, Marine Drugs, Fish and Shellfish Immunology, and Virulence.

A reviewer of research councils, BBSRC (UK) and FCT (Fundação para a Ciência e a Tecnologia in the field of Chemistry and Biochemistry, 2010-2011), Fonds de recherche du Québec - Nature et technologies, Québec, Canada (2015-2016) and charities, Leverhulme Trust (UK).

Research

Research Overview

My research carries on the great tradition of UK natural product biosynthesis activity. We have  all the required skills to succeed in such an enterprise, involving discovery of new families of specialised metabolites, bacterial genomics, chemical synthesis and the associated molecular biology to manipulate genomes to enzymology and the reconstruction of biochemistry. All of this is focussed on understanding the molecular basis and mechanism of natural products assembly.

Recent contributions involve the understanding of a group of unsaturated amino acids called dehydroamino acids (dhAAs). dhAAs are key components in many peptidyl therapeutics and versatile building blocks in peptide chemistry where organic chemists generate peptidyl derivatives through Michael additions, cross couplings and cycloaddition. They are used as bio-orthogonal handles for later stage modification of biomolecules. However, accessing dhAAs in structurally complex molecules presents a synthetic challenge, often resulting in poor atomic economy.

Among approximately 40 dhAAs found in the natural product inventory, only two, dehydroalanine (Dha) and (Z)-dehydrobutyrine (ZDhb), are well-studied. In this context our lab has elucidated the formation of several understudied dhAAs in newly discovered bacterial peptide-related metabolites, such as pyrrolizidine alkaloids (PAs) (Angew Chem. Int. Ed. 2015, 54, 12697, Nat. Comm. 2022, 13, 62), short dehydrated non-ribosomal peptides (Angew Chemie. Int. Ed. 2021, 60, 3229) and a new family of ribosomally synthesized and posttranslationally modified peptides (RiPPs) (Nat. Comm. 2022, 13, 5044) as shown below. Apart from this, we have also accumulated an outstanding body of work from bioactive natural product discovery to new enzymology as evidenced in our publication profile.

The discovery we made offers an alternative to rational engineering of pathways to generate bioactive peptides. As such we have obtained grants from various funding bodies (i.e. UKRI, Leverhulm Trust, Royal Society, Royal Society of Edinburgh, IBIOIC, EC) to further investigate potential applications of novel enzymes identified in these pathways towards the development of pharmaceuticals. 

rep papers 2023.jpg

Research Areas

Biological and Environmental Sciences

Research Specialisms

  • Industrial Biotechnology
  • Biochemistry
  • Organic Chemistry
  • Applied Chemistry

Our research specialisms are based on the Higher Education Classification of Subjects (HECoS) which is , published under the licence.

Past Research

My team has accumulated a good body of work on bioactive natural product discovery (from polyketides and peptides to alkaloids)  and their biosynthesis, and new enzyme investigation as shown below. Collectively it is a combination of both its range and illustration and  these new organic molecules and new enzymes my team has discovered will find applications for the development of pharmaceuticals and agrochemicals or new ways to biosciences.

All specialised metabolites 2023.jpg

Collaborations

Professor Mathew Jenner, Department of Chemistry, University of Warwick, UK

Professor Steven Cobb, Department of Chemistry, University of Durham, UK

Dr Jioji Tabudravu, School of Natural Sciences, University of Central Lancashire, UK

Dr David Clarke, EastChem, School of Chemistry, University of Edinburgh, Edinburgh, EH9 3FJ, UK

Professor Bruce Milne, Department of Physics, University of Coimbra, Rua Larga, 3004-516, Coimbra, Portugal

Professor Yi Yu, School of Pharmaceutical Sciences, Wuhan University, Wuhan 430071, China

Professor Kwaku Kyeremeh, Department of Chemistry, University of Ghana, Ghana

NCIMB Ltd and Ingenza Ltd

Funding and Grants

We gratefully thank the funding bodies below for financial supports of our research

MRC, BBSRC, Leverhulm Trust, EC, IBIOIC, The Royal Society and The Royal Society of Edinburgh.

Funding bodies.png

 

 

 

Teaching

Teaching Responsibilities

CM4518 Biological origin of natural products

CM1020 Chemistry for Biosciences 1

CM1512 Chemistry for Biosciences 2

CM3534 Organic and Biological Chemistry

 

Publications

Page 3 of 11 Results 21 to 30 of 110

  • Digyalipopeptide A, an antiparasitic cyclic peptide from the Ghanaian Bacillus sp. strain DE2B.

    Nartey, A. P., Dofuor, A. K., Owusu, K. B. A., Camas, A. S., Deng, H., Jaspars, M., Kyeremeh, K.
    Beilstein journal of organic chemistry, vol. 18, pp. 1763-1771
    Contributions to Journals: Articles
  • A ribosomally synthesised and post-translationally modified peptide containing a β-enamino acid and a macrocyclic motif

    Wang, S., Lin, S., Fang, Q., Gyampoh, R., Lu, Z., Gao, Y., Clarke, D. J., Wu, K., Trembleau, L., Yu, Y., Kyeremeh, K., Milne, B. F., Tabudravu, J., Deng, H.
    Nature Communications, vol. 13, no. 1, 5044
    Contributions to Journals: Articles
  • A Second Near-Infrared Ru(II) Polypyridyl Complex for Synergistic Chemo-Photothermal Therapy

    Liu, Y., Li, Q., Gu, M., Lu, D., Xiong, X., Zhang, Z., Pan, Y., Liao, Y., Ding, Q., Gong, W., Chen, D. S., Guan, M., Wu, J., Tian, Z., Deng, H., Gu, L., Hong, X., Xiao, Y.
    Journal of Medicinal Chemistry, vol. 65, no. 3, pp. 2225-2237
    Contributions to Journals: Articles
  • Organic NIR-II dyes with ultralong circulation persistence for image-guided delivery and therapy

    Li, Y., Gao, J., Wang, S., Li, S., Hou, X., Pan, Y., Gao, J., Qiao, X., Tian, Z., Chen, D., Deng, H., Deng, Z., Hong, X., Xiao, Y.
    Journal of Controlled Release, vol. 342, pp. 157-169
    Contributions to Journals: Articles
  • Aminoacyl chain translocation catalysed by a type II thioesterase domain in an unusual non-ribosomal peptide synthetase

    Wang, S., Brittain, W. D., Zhang, Q., Lu, Z., Tong, M. H., Wu, K., Kyeremeh, K., Jenner, M., Yu, Y., Cobb, S. L., Deng, H.
    Nature Communications, vol. 13, no. 1, 62
    Contributions to Journals: Articles
  • Characterization of a class II ketol-acid reductoisomerase from Mycobacterium tuberculosis

    Valera, A., Wang, S., Carr, R., Trembleau, L., Deng, H.
    RSC Advances, vol. 12, no. 17, pp. 10540-10544
    Contributions to Journals: Articles
  • The chemical profile of activated secondary metabolites by overexpressing LaeA in Aspergillus niger

    Wang, B., Li, X., Tabudravu, J., Wang, S., Deng, H., Pan, L.
    Microbiological Research, vol. 248, 126735
    Contributions to Journals: Articles
  • Peculiarities of promiscuous l-threonine transaldolases for enantioselective synthesis of β-hydroxy-α-amino acids

    Deng, H., Wang, S.
    Applied Microbiology and Biotechnology, vol. 105, pp. 3507–3520
    Contributions to Journals: Articles
  • Bacterial Pathogens: Threat or Treat? (a review on bioactive natural products from bacterial pathogens)

    Maglangit, F., Yu, Y., Deng, H.
    Natural Product Reports, vol. 38, no. 4, pp. 782-821
    Contributions to Journals: Review articles
  • Genomic scanning enabling discovery of a new antibacterial bicyclic carbamate-containing alkaloid

    Fang, Q., Wu, L., Urwald, C., Mugat, M., Wang, S., Kyeremeh, K., Philips, C., Law, S., Zhou, Y., Deng, H.
    Synthetic and Systems Biotechnology, vol. 6, no. 1, pp. 12-19
    Contributions to Journals: Articles
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