D-Ribose changes extracellular protein composition of E.coli Biofilms

Location

Bent Corridor, Science Center

Document Type

Poster - Open Access

Start Date

5-1-2026 12:00 PM

End Date

5-1-2026 2:00 PM

Abstract

Bacteria in the swimming, planktonic state can adhere to a surface, multiply, and form an interconnected community called biofilm. The extracellular network formed between bacterial cells, the extracellular polymeric substance (EPS), provides the community with several advantages that enhance overall bacterial viability. The formation of biofilm is especially problematic in the context of the medical and agricultural sectors, where biofilm growth can curb antibacterial efficacy. Past research in our lab demonstrated the modulation of biofilm growth and composition in the presence of environmental sugars. In this study, Escherichia coli strain PHL628 was grown in the presence of D-ribose, and changes in extracellular protein concentration were observed using SDS-PAGE. The expression of the transcripts of these putative proteins was quantified using qPCR. Biofilm grown in the presence of D-ribose at both 28 and 37 °C demonstrated upregulated expression of key transcripts involved in the folding and assembly of outer membrane proteins (OMPs), which play a consequential role in the biofilm’s antibiotic resistance profile. Future work will utilize immunoblotting and confocal microscopy to confirm specific protein presence and measure other EPS components affected by D-ribose. These findings characterize the complex interplay between sugar metabolism and EPS biosynthesis, identifying specific extracellular proteins as promising targets for novel antibiofilm strategies.

Keywords:

Biochemistry, Molecular biology, Bacterial culturing, Biofilm

Notes

Presenter: Dylan Hwang

Major

Biochemistry

Project Mentor(s)

Lisa Ryno, Chemistry and Biochemistry

2026

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May 1st, 12:00 PM May 1st, 2:00 PM

D-Ribose changes extracellular protein composition of E.coli Biofilms

Bent Corridor, Science Center

Bacteria in the swimming, planktonic state can adhere to a surface, multiply, and form an interconnected community called biofilm. The extracellular network formed between bacterial cells, the extracellular polymeric substance (EPS), provides the community with several advantages that enhance overall bacterial viability. The formation of biofilm is especially problematic in the context of the medical and agricultural sectors, where biofilm growth can curb antibacterial efficacy. Past research in our lab demonstrated the modulation of biofilm growth and composition in the presence of environmental sugars. In this study, Escherichia coli strain PHL628 was grown in the presence of D-ribose, and changes in extracellular protein concentration were observed using SDS-PAGE. The expression of the transcripts of these putative proteins was quantified using qPCR. Biofilm grown in the presence of D-ribose at both 28 and 37 °C demonstrated upregulated expression of key transcripts involved in the folding and assembly of outer membrane proteins (OMPs), which play a consequential role in the biofilm’s antibiotic resistance profile. Future work will utilize immunoblotting and confocal microscopy to confirm specific protein presence and measure other EPS components affected by D-ribose. These findings characterize the complex interplay between sugar metabolism and EPS biosynthesis, identifying specific extracellular proteins as promising targets for novel antibiofilm strategies.