Dr Richard Daniel
Senior Lecturer

  • Email: richard.daniel@ncl.ac.uk
  • Telephone: +44 (0) 191 208 3239
  • Fax: +44 (0) 191 208 7424
  • Address: The Centre for Bacterial Cell Biology
    Baddily Clark Building
    Newcastle University
    Richardson Road
    Newcastle upon Tyne
    NE2 4AX
    United Kingdom

 Education and qualifications:

10/1996 – 11/2000      D.Phil. (Physiological Sciences) at Sir William Dunn School of Pathology, University of Oxford, Supervisor: Prof. J. Errington           

10/1986 – 07/1989      BSc with Hons. (Bacteriology and Molecular Genetics) University of Bristol,

                                  Part II Supervisor: Dr. J Grinsted

Positions held: 

2010 -              Senior Lecturer, Centre for Bacterial Cell Biology Newcastle University

2006 -  2009    Lecturer, ICaMB, University of Newcastle

2004 – 2006    University Research Lecturer, Sir William Dunn School of Pathology, Oxford University

2000 – 2006    Consultant, Prolysis Ltd, Oxford

2000 – 2004    Senior Research assistant (RS II), Sir William Dunn School of Pathology, Oxford
                        University

1990 - 1999     Research Assistant, Sir William Dunn School of Pathology, Oxford University

1989 – 1990    Medical Laboratory Scientific Officer, Dept. of Paediatrics, John Radcliffe Hospital, 
                        Oxford University

External Responsibilities
BBSRC Peer review panel BBSRC Committee B:  Plants, Microbes, Food and Sustainability panel since 2012 

Internal Responsibilities:
Management of the CBCB Microscopy facility.
Member of the Bio Imaging committee for the Medical Faculty
Member of the Robotics committee for the Medical Faculty

Current lab members: 

Post Graduate Students:

Karzan Sidiq - (international funding)
Jad Sassine -
(MC studentship - AMBER project)
Man Chow - (Self funded)

Postdoctoral Research Fellows:

Aurelie Guyet (BBSRC)

Gabriella Henriques (MC visiting fellowship) 

 

 

VACANCIES - I am always open to informal enquiries for PhD or Post-doctoral positions in this lab, and often find a way to fund good candidates. Please feel free to email me if you are interested (Richard.Daniel@ncl.ac.uk ).   

 Research Interests.

A bacterial cell as a gross simplification is sometimes described as a collection of enzymes and nucleic acid enclosed in a lipid bag. In reality this is far from the truth, the bacterial cell has levels of organisation and complexity comparable to higher organisms, but due the difference in scale these properties were invisible. Recent advances in imaging techniques are just beginning to reveal these complexities that at almost at the limit of resolution for light microscopy and invisible to electron microscopy. Characterising and understanding the processes that generate and maintain this organisation represents the next challenge. 

Research in this lab predominantly utilises the Gram-positive bacterium Bacillus subtilis as a model system,  but may also use Listeria spp. Corynebacterium glutamicum, Staph. aureus and Strep. pneumonia for comparison due to their interesting morphological diversity. To support this work we are able to utilise a wide range of techniques most of which are available in the Centre.
Currently the main areas of research are focused on:-

 The physical properties of the cell envelope of Bacillus subtilis:
The interface the bacterial cell and its environment has an intricate role in biology. It must permit the selective passage of material too and from the cell membrane, but be structurally robust enough to prevent osmotic lysis of the cell, the entry of large toxic molecules and repel the attacks of enzymes and bacteriophages. However it must also be capable for dynamic remodelling to allow the enlargement and division of the cell. Thus an understanding of the composition of the cell wall and the roles of the individual components is critical.

Current projects: 
Determination of the composition of the cell wall and how it changes according to the phase of growth or environmental conditions. (K. Sidiq)

Design and characterisation of probes to investigate the bacterial cell wall and its basic physical properties as extracted sacculi as well as in vivo. (Man Chow)

Bacterial cell wall biosynthesis:
Bacterial cell wall helps to maintain cell shape but most importantly it provides protection to the cells, and has been one of the targets for antibiotics. However, the mechanisms involved in cell wall biosynthesis are still poorly understood. Most of the analysis has been restricted to either the biosynthetic pathway required for synthesis of the major cell wall precursors (e.g. mur or mra genes) or the final steps of peptidoglycan synthesis (carried out by penicillin-binding proteins). Very little is known about the intermediate steps whereby the precursors are exported from the cytoplasm to the outside of the cell and incorporated into the existing structure to allow cell enlargement or division. Recent studies have provided evidence for specific complexes, (cytoskeletal structures) central to these events. However, the mechanism and the functional components of these complexes have yet to be clearly defined. Thus, there are many areas to explore, including peptidoglycan precursor export and incorporation, cell wall maturation and degradation, secondary polymer biosynthesis, export and incorporation (e.g. teichoic acids).

Current projects:
Defining the roles of specific PBPs in peptidoglycan synthesis and maturation (A. Guyet)

Constructing strains with the minimum complement of enzymes necessary for normal growth and division (A. Bone and G. Henriques)

Understanding the mechanisms that coordinate peptidoglycan synthesis and degradation, to allow controlled growth and division (A. Guyet)

Determination of antibiotic resistance determinants and their mode of action - primarily focusing on wall active compounds (K. Sidiq)

Biological role of membrane proteins
Following on form the "omic" revolutions, we now have a vast data base of genes that are present in bacteria, but a limited understanding of their biological function. One sub class of proteins that are generally very variable are the membrane spanning proteins, many of which are annotated with potential functions, but not definitive experimental data supports these predictions. To correct this gap in our understanding we are looking at systematic methods to identify the functions of this sub set of proteins using classical genetic techniques combined with robotics. This work is designed to aid the development of the minimal genome by defining genes that are either redundant in function or are unnecessary except under specific condition.
    The ultimate objective being the construction of strains with the minimal gene content for viable replication that can be customised with a specific gene complement (set of bio-bricks) to fulfil a specific function.

 Current projects:
High throughput genetic manipulation of strains using various selection systems and screening methods for phenotypic characterisation (G. Henriques)

 

 

Current teaching at undergraduate and masters level:
Lectures: 
MIC2026   Microbial Cell Biology                                                                  Module Leader

MIC2028   Practical Skills in Medical Microbiology                                          Practical Supervisor

MIC3044   Integrated Microbiology and Immunology                                      Lecturer

MMB8008  Cell Cycle Control and Cell Signalling in Health and Disease            Lecturer

Pastoral Tutor for undergraduates in years 1, 2 and 3.

Research project supervision: 

Undergraduate project supervisor

MRes and MSci project supervisor

M. Phil supervisor for M. Chow (2014).

PhD supervisor for M. Xu ( D.Phil in Oxford 2008), P. Gamba (2011), A. Doble (2012), S. Moore (2013), K Sidiq (2012-2015), and Jad Sassine (2013-2016).