Effect of L-arabinose on internal and external pH of PHL628 Escherichia coli

Presenter Information

Audrey Neighmond, Oberlin College

Location

CELA & Mary Church Terrell Library, First Floor

Document Type

Poster - Open Access

Start Date

4-25-2025 12:00 PM

End Date

4-25-2025 2:00 PM

Abstract

Understanding how environmental sugars influence intracellular pH (pHi) is crucial, as pHi homeostasis can be impacted through biofilm formation in Escherichia coli. Biofilms—structured communities of bacteria attached to surfaces—protect the cells from environmental stressors, including desiccation and exposure to antibiotics. Altered pHi regulation within biofilms may be able to affect bacterial metabolism, stress response pathways, and even the efficacy of antibiotics. In this project, we examined whether the presence of L-arabinose, a common pentose, affects the pHi of E. coli. Our previous transcriptomic data for PHL628 biofilm and planktonic cells in the presence of arabinose showed the activation of pH-responsive stress pathways and efflux pumps, among other changes to metabolic pathways. This protocol enables us to compare intracellular acidification in arabinose-treated and untreated cells. It provides insights into the role of araE, an arabinose symporter, in pH regulation and the metabolic response to L-arabinose. Our findings shed light on how E. coli adjusts its pHi under varying environmental conditions, with implications for biofilm formation and antibiotic resistance.

Keywords:

Bacteria, Biofilm, pH

Notes

Presenter: Audrey Neighmond

Major

Biology
Psychology

Project Mentor(s)

Lisa Ryno, Chemistry and Biochemistry

2025

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Apr 25th, 12:00 PM Apr 25th, 2:00 PM

Effect of L-arabinose on internal and external pH of PHL628 Escherichia coli

CELA & Mary Church Terrell Library, First Floor

Understanding how environmental sugars influence intracellular pH (pHi) is crucial, as pHi homeostasis can be impacted through biofilm formation in Escherichia coli. Biofilms—structured communities of bacteria attached to surfaces—protect the cells from environmental stressors, including desiccation and exposure to antibiotics. Altered pHi regulation within biofilms may be able to affect bacterial metabolism, stress response pathways, and even the efficacy of antibiotics. In this project, we examined whether the presence of L-arabinose, a common pentose, affects the pHi of E. coli. Our previous transcriptomic data for PHL628 biofilm and planktonic cells in the presence of arabinose showed the activation of pH-responsive stress pathways and efflux pumps, among other changes to metabolic pathways. This protocol enables us to compare intracellular acidification in arabinose-treated and untreated cells. It provides insights into the role of araE, an arabinose symporter, in pH regulation and the metabolic response to L-arabinose. Our findings shed light on how E. coli adjusts its pHi under varying environmental conditions, with implications for biofilm formation and antibiotic resistance.