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Staff Profile

Dr Richard Daniel

Senior Lecturer

  • Telephone: +44 (0) 191 208 3239
  • Address: The Centre for Bacterial Cell Biology
    Baddily Clark Building
    Newcastle University
    Richardson Road
    Newcastle upon Tyne
    NE2 4AX
    United Kingdom

Background

 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

External examiner for Liverpool University

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: 


Dr. L. Wu - Senior Research Associate and BBSRC funded Co-I

(https://www.ncl.ac.uk/cbcb/staff/profile/ljwu.html#background)


Post Graduate Students:

Alaa Aljohani - SACB

Yousef Alanazi - SACB

Amirah Alofi - SACB

Areej Aljohani - SACB

Sahar Aljahdali - SACB

Marwa S. Ahmed - Egyptian funding

Muad Khalefah - SACB

Christodoulos Astriaos



Previous member of the research group:


R. Emmins - PDRA (2007-2010)

A. Guyet - PDRA ( 2011-2023)


M. Duchene - Erasmus student (2011)

D. Wolf - MC visiting fellowship (2010)

A. Gronwewold- Erasmus student (2012)

G. Henriques - MC visiting fellowship (2014)

E. Lauwers - Erasmus student (2016)

L. Keller - Erasmus student (2018)

R. Du - Visiting student from Hong Kong (2019)

Y. Wade - visiting MC fellow from Bath University (2019)

Robert Warneke - Visiting student from Goettingen, Germany (2023)

Muhammad Rauf - IRSIP Program, HEC, Pakistan (2024)


Directly supervised PhD students:

M. Xu - PhD student completed 2008

P. Gamba - PhD completed 2010

K. Sidiq - PhD completed 2016

J. Sassine - PhD completed 2018

F. Alatawi - PhD completed 2020

Man Chow - PhD completed 2022

Grace Goldsmith - PhD completed 2022


 

Research

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 ). 

The laboratory is based in the Centre for Bacterial Cell Biology, part of the Bioscience Institute of Newcastle University (NUBI).

 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 / Enterococcus faecium 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. (M. Khalefah)

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

Analysis of nutrient uptake systems (Areej Aljohani)

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 (Yousef Alanazi)

Constructing strains with the minimum complement of enzymes necessary for normal growth and division (Yousef Alanazi and Amirah Alofi)

Understanding the mechanisms that coordinate peptidoglycan synthesis and degradation, to allow controlled growth and division (Alaa Aljohani)

Mechanisms altering gene expression in response to environmental conditions (Marwa Ahmed)

Changes in the bacterial cell envelope in response to environmental conditions ( Muad Khalefah)

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 (  )

Functional roles of conserved cell envelope components is assimilation of metals (Sahar Aljahdali)

Synthetic biology

 Exploitation of basic cellular processes and the consequences of mutations in synthetic biology ( )

 

Teaching

Current teaching at masters level:
Modules: 

MMB8106  Molecular Microbiology

MMB8008  Cell Cycle Control and Cell Signalling in Health and Disease

Pastoral Tutor for undergraduates in years 1, 2 and 3 and second supervisor for PhD projects.

Primary Research supervision for: 

Undergraduate final year projects, MRes and MSci projects and PhD projects.

Previous PhD students:

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

Main supervisor for completed PhDs:

 M. Xu ( D.Phil in Oxford 2008), P. Gamba (2011), A. Doble (2012), S. Moore (2013), K Sidiq (2012), Jad Sassine (2013), F. Alatawi (2020) M. Chow (2022)

Current PhD students:

G. Goldsmith - compartmentalised gene expression

A. Aljohani - cell wall metabolism.

A. Alofi - Autolytic enzymes

Y. Alanazi - Roles of PBPs in B. subtilis 

Areej Aljohani - Uptake systems

Saj Aljahdali - Metal ion assimilation

Marwa Ahmed - Sigma factor activation

Publications