Matthew A. Jorgenson profile photo

Matthew A. Jorgenson

Federal Grant PI

Assistant Professor

University of Arkansas for Medical Sciences

faculty

Microbiology & Immunology, College of Medicine

10 h-index 24 pubs 882 cited

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Biography and Research Information

OverviewAI-generated summary

Matthew A. Jorgenson is an Assistant Professor in the Department of Microbiology & Immunology at the University of Arkansas for Medical Sciences. His research focuses on the biosynthesis and function of bacterial cell envelope glycans, particularly those in Gram-negative bacteria like *Escherichia coli* and Gram-positive bacteria such as *Staphylococcus aureus*. He investigates the stepwise assembly of these complex carbohydrate structures and their roles in bacterial physiology and pathogenesis.

Dr. Jorgenson's work involves understanding how specific enzymes and metabolic pathways contribute to glycan production. He has explored the regulation of these processes, including how disruptions in nucleotide sugar metabolism can lead to defects in cell division and surface polysaccharide expression. His research also examines the substrate sequestration properties of these glycans and their impact on the bacterial cell envelope. He is currently funded by the National Institute of General Medical Sciences (NIH/NIGMS) for a project aimed at manipulating undecaprenyl phosphate levels to decipher mechanisms of competing cell envelope assembly pathways in *Escherichia coli*.

His scholarship metrics include an h-index of 10, with 24 total publications and 882 total citations. Dr. Jorgenson collaborates with researchers at the University of Arkansas for Medical Sciences, including Joseph C. Bryant, Chia Y. Lee, and Alongkorn Kurilung.

Metrics

  • h-index: 10
  • Publications: 24
  • Citations: 882

Selected Publications

  • Dysregulation of a nucleotidyltransferase induces division and surface glycan defects in <i>Escherichia coli</i> by altering related metabolite levels (2026) DOI
  • Pardon the interruption: how Und-P sequestration has reshaped our understanding of the bacterial cell envelope (2025) DOI
  • The DigH glycosyl hydrolase is conditionally required for daughter cell separation in <i>Escherichia coli</i> (2025) DOI
  • Characterization of Ssc, an <i>N</i> -acetylgalactosamine-containing <i>Staphylococcus aureus</i> surface polysaccharide (2024) DOI
  • Engineering Escherichia coli for increased Und-P availability leads to material improvements in glycan expression technology (2024) DOI
  • Tracking Colanic Acid Repeat Unit Formation from Stepwise Biosynthesis Inactivation in <i>Escherichia coli</i> (2021) DOI
  • Making the Enterobacterial Common Antigen Glycan and Measuring Its Substrate Sequestration (2021) DOI

Federal Grants 1 $376,625 total

NIH/National Institute of General Medical Sciences Contact PI Jun 2024 - Apr 2029

Manipulating undecaprenyl phosphate levels to decipher mechanisms of competing cell envelope assembly pathways in Escherichia coli

National Institute of General Medical Sciences $376,625 R35

Grants & Funding

  • Composition and characteristics of cell poles as a measure of bacterial growth history US Department of the Army Co-Investigator
  • Bacterial cell wall synthesis, shape and septation NIH Co-Investigator
  • In vitro and cellular tools for complex polysaccharide biosynthesis NIH Co-Investigator
  • Center for Microbial Pathogenesis and Host Inflammatory Responses NIH Co-Investigator
  • Center for Microbial Pathogenesis and Host Inflammatory Responses NIH Co-Investigator
  • Manipulating undecaprenyl phosphate levels to decipher mechanisms of competing cell envelope assembly pathways in Escherichia coli NIH/Nat. Inst. of General Medical Sciences Principal Investigator

Collaborators

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