Professor Hai Deng

Professor Hai Deng
Professor Hai Deng
Professor Hai Deng

Personal Chair

About
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, University of Aberdeen, UK

08/2018 - 07/2022   Reader, University of Aberdeen, UK

08/2014 - 07/2018  Senior Lecturer, University of Aberdeen, UK

10/2008 - 07/2014   Lecturer, University of Aberdeen, 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 HESA open data, published under the Creative Commons Attribution 4.0 International 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 10 of 10 Results 91 to 100 of 100

  • Fluorinase mediated C--18 F bond formation, an enzymatic tool for PET labelling

    Deng, H., Cobb, S. L., Gee, A. D., Lockhart, A., Martarello, L., McGlinchey, R. P., O'hagan, D., Onega, M.
    Chemical Communications, no. 6, pp. 652-654
    Contributions to Journals: Articles
  • Substrate specificity in enzymatic fluorination. The fluorinase from Streptomyces cattleya accepts 2'-deoxyadenosine substrates

    Cobb, S. L., Deng, H., McEwan, A. R., Naismith, J. H., O'hagan, D., Robinson, D. A.
    Organic & Biomolecular Chemistry, no. 8, pp. 1458-1460
    Contributions to Journals: Articles
  • The identification of 5'-fluoro-5-deoxyinosine as a shunt product in cell free extracts of Streptomyces cattleya

    Cobb, S. L., Deng, H., Hamilton, J. T. G., McGlinchey, R. P., O'hagan, D., Schaffrath, C.
    Bioorganic Chemistry, vol. 33, no. 5, pp. 393-401
    Contributions to Journals: Articles
  • Enzymatic fluorination in Streptomyces cattleya takes place with an inversion of configuration consistent with an SN2 reaction mechanism

    Cadicamo, C. D., Courtieu, J., Deng, H., Meddour, A., O'Hagan, D.
    ChemBioChem, vol. 5, no. 5, pp. 685-690
    Contributions to Journals: Articles
  • Crystal structure and mechanism of a bacterial fluorinating enzyme

    Dong, C., Hang, F., Deng, H., Schaffrath, C., Spencer, J. B., O'hagan, D., Naismith, J. H.
    Nature, vol. 427, no. 6974, pp. 561-565
    Contributions to Journals: Articles
  • Identification of 5-fluoro-5-deoxy-D-ribose-1-phosphate as an intermediate in fluorometabolite biosynthesis in Streptomyces cattleya

    Cobb, S. L., Deng, H., Hamilton, J. T. G., McGlinchey, R. P., O’Hagan, D.
    Chemical Communications, vol. 5, pp. 592-593
    Contributions to Journals: Articles
  • Fluorometabolite biosynthesis and the fluorinase from Streptomyces cattleya

    Deng, H., O’Hagan, D., Schaffrath, C.
    Natural Product Reports, vol. 21, no. 6, pp. 773-784
    Contributions to Journals: Articles
  • The first enzymatic method for C–18F bond formation: the synthesis of 5′‐[18F]‐fluoro‐5′‐deoxyadenosine for imaging with PET

    Martarello, L., Schaffrath, C., Deng, H., Gee, A. D., Lockhart, A., O’Hagan, D.
    Journal of Labelled Compounds and Radiopharmaceuticals, vol. 46, no. 13, pp. 1181-1189
    Contributions to Journals: Articles
  • Isolation and characterisation of 5'-fluorodeoxyadenosine synthase, a fluorination enzyme from Streptomyces cattleya

    Schaffrath, C., Deng, H., O'Hagan, D.
    FEBS LETTERS, vol. 547, no. 1-3, pp. 111-114
    Contributions to Journals: Articles
  • Crystallization and X-ray diffraction of 5'-fluoro-5'-deoxyadenosine synthase, a fluorination enzyme from Streptomyces cattleya

    Dong, C., Deng, H., Dorward, M., Schaffrath, C., O’Hagan, D., Naismith, J. H.
    Acta Crystallographica Section D: Biological Crystallography, vol. 59, no. 12, pp. 2292-2293
    Contributions to Journals: Articles
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