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MSc Microbiology and Infection

University of Birmingham, United Kingdom
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Course Overview

Our Microbiology and Infection MSc provides you with sound theoretical and hands-on laboratory experience in cutting-edge microbiology. The course is set within the context of the Institute of Microbiology and Infection at the University of Birmingham, the largest grouping of microbiologists in the UK.

This MSc programme is built on the combined expertise in microbiology and infection that has been assembled through the establishment of the Institute of Microbiology and Infection at Birmingham.

It draws on the internationally recognized expertise of members of both the College of Life and Environmental Sciences and College of Medical and Dental Sciences to provide a course that will be attractive to aspiring biomedical scientists and clinical microbiologists worldwide.

Students graduating from this course can look forward to gaining a thorough grounding in this important area, with job opportunities throughout the public and private sector, as well as in research settings.

This course will provide graduates in the Biosciences with a sound theoretical background and hands-on laboratory experience in leading-edge microbiology. Students will gain specialist knowledge and insight in key aspects of bacterial infection.

The course will enable students to develop basic abilities and skills on which to build professional capability in a healthcare or related microbiology or biomedical research setting.

General Eligibility

Minimum lower second class (2.ii) Honours degree (or equivalent overseas degree) in a suitable Biosciences or biomedical subject, such as; Microbiology, Molecular Biology, Biological Sciences, Biology, Biosciences, Biotechnology, Biochemistry, Medicine, Dentistry, Veterinary medicine or Biomedical sciences.

Part Time Work Details

20 Hours of Work permit weekly for international students.

What You'll Study

1 Module
  • Characterization of a cell‐wall hydrolase from Mycobacterium tuberculosis

  • Implementation of the CRISPR‐Cas9 to tag genes in yeast

  • Promoter organization in bacteria

  • Sepsis and other clinical outcomes in burn trauma: applying metabolism to understand sepsis and clinical outcomes

  • How does metabolism differ in different human samples (biofluids and tissues)?

  • Enzyme‐responsive nanomaterials to deliver antimicrobial peptides

  • A multidisciplinary approach to studying the behavior of bacterial communities in artificial cellular environments

  • Turning gene regulation inside out: prevalence of promoters within genes in bacterial chromosomes

  • Interaction of the partitioning proteins KorB and IncC with DNA and other protein partners

  • Transcription rate variability and gene regulatory network dynamics

  • Probing the structure and function of the Bam complex, the Gram negative bacterial outer membrane protein folding machinery

  • Retrograde lipid transport in E. coli

  • Using novel methods to purify a membrane protein complex

  • Towards a structure for the neurodegeneration protein Cln3

  • Individual‐based modelling of biofilms

  • Transfer of antibiotic resistance carrying plasmids in spatially structured multispecies communities

  • High throughput determination of substrate affinity in a microfluidic device

  • Gene regulation in bacteria

  • Understanding the pH sensing mechanism of E. coli

  • Understanding the link between genotype and phenotype in laboratory‐evolved strains of stress‐resistant bacteria

  • Understanding and manipulating mupirocin and thiomarinol biosynthesis to create novel biologically active molecules

  • Dissecting plasmid host range determinants

  • Regulation of antibiotic production in marine bacteria

  • Phenotypic characterisation of exopolyphosphatase‐deficient mutants in Mycobacterium smegmatis. Elucidating the role of ppxs genes in phosphate metabolism

  • Isolation of interacting proteins of the MmpL3 transporter from Mycobacterium tuberculosis using the Yeast Two‐Hybrid (Y2H) system

  • Structural bioinformatics for the reengineering of the mupirocin and thiomarinol antibiotic biosynthesis pathways

  • Sequence and structural comparison of ketosynthase domains from trans‐AT polyketide synthase systems

  • The behaviour of lab‐evolved stress resistant strains of bacteria under fermentation conditions

  • Cloning and expression of the lectinolysin gene from Streptococcus mitis

Language Requirement

  • IELTS6.5
  • TOEFL93
  • PTE65
  • Duolingo89

English requirements

IELTS - 6.5

TOEFL - 88

Ready to get started?

For any enquiries or further details, please don't hesitate to contact us. Let's take the next step in your academic journey together.

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