Abstract

While multi-drug resistance in bacteria is an emerging concern in public health, using carbon dots (CDs) as a new source of antimicrobial activity is gaining popularity due to their antimicrobial and non-toxic properties. Here we prepared carbon dots from citric acid and β-alanine and demonstrated their ability to inhibit the growth of diverse groups of Gram-negative bacteria, including E. coli, Salmonella, Pseudomonas, Agrobacterium, and Pectobacterium species. Carbon dots were prepared using a one-pot, three-minute synthesis process in a commercial microwave oven (700 W). The antibacterial activity of these CDs was studied using the well-diffusion method, and their minimal inhibitory concentration was determined by exposing bacterial cells for 20 h to different concentrations of CDs ranging from 0.5 to 10 mg/mL. Our finding indicates that these CDs can be an effective alternative to commercially available antibiotics. We also demonstrated the minimum incubation time required for complete inhibition of bacterial growth, which varied depending on bacterial species. With 15-min incubation time, A. tumefaciens and P. aeruginosa were the most sensitive strains, whereas E. coli and S. enterica were the most resistant bacterial strains requiring over 20 h incubation with CDs.

Highlights

  • Due to their cell wall composition, Gram-negative bacteria are reported to be more resistant to antibiotics compared to Gram-positive bacteria [1,2]

  • We demonstrate the potential application of β-alanine based carbon dots (CDs) as novel antimicrobial agents against a diverse group of Gram-negative bacteria, including E. coli, Pseudomonas, Salmonella, Agrobacterium, and Pectobacterium

  • CDs synthesized in this study showed a zeta-potential value of −8.09 ± 5.68 mV measured by the Malvern Zetasizer Nano-ZS ZEN 3600 (Figure 3D)

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Summary

Introduction

Due to their cell wall composition, Gram-negative bacteria are reported to be more resistant to antibiotics compared to Gram-positive bacteria [1,2]. Gram-negative bacteria possess an extra protective outer membrane of lipopolysaccharides that limits the entry of certain antibiotics. The majority of commercially available antibiotics follow two pathways to enter the Gram-negative bacterial cell. Hydrophobic antibiotics use lipid-mediated pathways, whereas hydrophilic antibiotics enter the cells using diffusion porins [3]. Due to frequent modifications in lipid and protein compositions and porins in the outer membrane of Gram-negative bacteria, they are selective against larger hydrophilic antibiotics and are more resistant to antibiotics. Due to intensive prescription of antibiotics, many bacteria are becoming multi-drug resistant (MDR) [4]

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