Table 3.
The antimicrobial efficacy of LED in liquid system
Tested food product | LED used | Tested microorganisms | Quality and mode of action | Major findings | References |
---|---|---|---|---|---|
Suspension in suitable buffers | UV-A LED (365 nm); working distance, 20 mm | E. coli DH5α, Enteropathogenic E. coli, Vibrio parahaemolyticus, Staphylococcus aureus, and Salmonella enterica serovar Enteritidis | 3.9 log reduction in E. coli DH5α with 54 J/cm2 dose; the inactivation was higher at the illumination temperature of 20 °C and pH 8 and varied for different bacterial species | Mori et al. [85] | |
Suspension in PBS | UV-A LED (365 nm); maximum current of one diode was 0.5 A, the voltage was 4.5 V; intensity was 70 mW/cm2, working distance, 2 cm | E. coli DH5α, Enteropathogenic E. coli, Vibrio parahaemolyticus, Staphylococcus aureus and Salmonella enterica serovar Enteritidis | Oxidative DNA damage observed (2.6 folds higher 8-OHdG formation); involvement of ROS like OH− and H2O2 observed in the LED inactivation effect | E. coli DH5α, Enteropathogenic E. coli, Vibrio parahaemolyticus, Staphylococcus aureus were reduced by > 5 log CFU/ml by 75 min treatment with 315 J/cm2 dose; Salmonella was reduced by > 4 log CFU/ml with 672 J/cm2 dose for 160 min with UV-A LED | Hamamoto et al. [39] |
Ultrapure water, nutrient water and nutrient water with humic acids | UV LEDs (269 and 276 nm); sample volume 25 ml with stirring | E. coli K12 | 3 to 4 log CFU/cm3 reduction observed; presence of humic acids and turbidity affected the UV irradiation and inactivation caused; 269 nm LED was more effective | Vilhunen, Särkkä and Sillanpää [126] | |
Bacterial suspension in PBS | 265 nm LEDs; placed over a 6.5 mm wide aluminum channel 1 mm above the water surface; water depth, 7 mm; treatment dose, 0 to 20 mJ/cm2 | E. coli K12 | > 3 log CFU/ml reduction with 20 mJ/cm2 dose of UV LED treatment | Chatterley and Linden [17] | |
Bacterial suspension in appropriate buffers | 255, 280, 365, and 405 nm LEDs; pH tested, 6 and 8; treatment times, 60, 120 and 180 s | 3 strains of E. coli and 2 strains of E. faecalis | pH did not show any significant effect | 280/365 and 280/405 nm combination of LED treatment were most effective for bactericidal effect; 20 h after the UV irradiation all the tested samples showed 7 log reduction in all treated strains | Chevremont et al. [21] |
Bacterial suspension in deionized water | 269 and 282 nm LEDs | Bacillus subtilis | 269 nm LED produced better germicidal effect than 282 nm LED treatment | Rtele et al. [129] | |
Water samples from tertiary effluent from the City of Regina wastewater treatment plant (WWTP) and bacterial suspension in suitable broth | 260 nm UV LEDs | E. coli ATCC 25922 | High turbidity of WWTP resulted in inconsistent effect; 1–2.5 log reduction obtained with 20 and 50 min treatment in a time dependent manner | Nelson et al. [91] | |
Bacterial suspension in PBS | UV LEDs emitting wavelengths 265, 280 and 310 nm; 0.7, 1.3 and 1.1 mW output power, respectively; used for treatment individually and in combinations | E. coli K12 | 310 nm LED showed least antibacterial effect in batch system; 265 and 280 nm LEDs produced ~ 4 log reduction in both batch and flow-through system with dose of 10.8 and 13.8, and 16.4 and 25.5 mJ/cm2, respectively | Oguma et al. [92] | |
Bacterial suspension in 0.9% saline solution | UV-C LED (281.8 nm); Glass tube (quartz) and soda lime glass; 9 ml of bacterial suspension; treatment times, 10, 40, and 90 s; doses, 8.64, 34.59, and 77.82 mJ/cm2 | Escherichia coli DSM 498 and Bacillus subtilis DSM 402 | Quartz glass had better transmittance of light; B. subtilis was reduced by 1.04 (soda lime glass) and 1.79 log CFU/ml (quartz glass) and, E. coli was reduced by 1.85 (soda lime glass) and 2.8 log CFU/ml (quartz glass) with 90s treatment; mixing of the samples improved the inactivation | Gross et al. [37] | |
Bacterial suspension in appropriate buffer | 260 nm (UV) LEDs and low pressure UV lamp | Escherichia coli B, a non-enveloped virus (MS-2), and a bacterial spore Bacillus atrophaeus | Comparable inactivation efficacy for E. coli B and MS-2; LED produced better inactivation for Bacillus atrophaeus; dose required for 4 log reductions for UV LEDs were as follows: E. coli B, 6.2 mJ/cm2; MS-2, 58 mJ/cm2, and B. atrophaeus, 18.7 mJ/cm2 | Sholtes et al. [114] | |
Bacterial suspension in 0.05 M NaCl | Semi-commercial LED arrays (270–740 nm); treatment time, 6 h | Escherichia coli K12 ATCC W3110 and Enterococcus faecalis ATCC 19433 | 270, 365, 385, and 405 nm arrays produced > 5 log10 reduction; 430 and 455 nm LED arrays resulted in ≈ 4.2 and 2.3-log10 reduction in E. coli and E. faecalis cell counts; 310 nm produced insufficient disinfection doe commercial application; 525, 590, 623, 660, and 740 nm arrays produced insignificant disinfection | Lui et al. [76] | |
Four UV-LED units emitting wavelengths 265, 280 nm, the combination of 265/280 (50%), and 265/280 (75%) | E. coli | Photoreactivation and dark repair decreased in case of 280 nm LED treatment | 265 nm LED resulted in the maximum inactivation | Li et al. [70] | |
Microbes in appropriate buffers | UV-C LED emitting 260 and 280 nm LED and 260/280 nm combination used for treatment | Escherichia coli, MS2 coliphage, human adenovirus type 2 (HAdV2), and Bacillus pumilus spores | DNA and RNA damage observed for individual LED treatments | Over 3 log reduction observed in E. coli with all UV LEDs; 260 nm LED was most effective in the inactivation of MS2 coliphage; A dose of 122, 89, and 105 mJ/cm2 of 260, 280, and 260/280 nm LEDs required for 4-log reduction; 260 and 260/280 nm LED more effective for B. pumilis inactivation | Beck et al. [9] |
Real wastewater samples and suspension in laboratory water | UV LED (265 nm); sample volume, 50 ml; frequency tested, 0.1, 1, 10, 100, 1 kHz; duty rate-10, 25, 50, 75, 90% | E. coli ATCC 11229, coliphage MS2 ATCC 15597-B1 | No significant difference in the microbial inactivation observed between continuous and pulsed LED treatments | Song, Taghipour and Mohseni [119] | |
Dechlorinated tap water | UV LED (285 nm) | Heterotrophic plate count (HPC) | UV LED treatment showed decreased HPC for 5 days storage; Methylobacterium species was UV resistant | Oguma et al. [94] | |
Bacterial suspension in sterile distilled water | UV-A (365 nm) and UV-C (265 nm) LEDs; treatment times, 20 or 30 min (UV-A) and 5–16 min (UV-C); sample volume, 15 ml | E. coli (ATCC 25922, ATCC 700891, ATCC 15597, and ATCC 700891) | UVA pre-radiation showed: Insignificant effect in photo repair of bacteria; suppressed dark repair; no role of hydroxyl radical in the inactivation; improved CPD formation only in E. coli ATCC 15597 | Synergistic effect of UV-A and UV-C was effective for E. coli (ATCC 11229, ATCC 15597, and ATCC 700891) | Xiao et al. [131] |
Microbes in appropriate buffers | UV LEDs (265, 280, and 300 nm) | Pseudomonas aeruginosa and Legionella pneumophila, E. coli, Bacillus subtilis spores, and bacteriophage Qb | Energy consumption was least for 280 nm LED for 3 log reduction; linear curve observed for L. pneumophila and bacteriophage Qb; sigmoidal curve observed for E. coli, P. aeruginosa, and B. subtilis spores | Rattanakul and Oguma [107] | |
UHT skim milk (< 0.5% fat) | 405 (NUV-Vis), 433 and 460 nm (blue) LEDs; illumination temperature, 5–15 °C; treatment time, 0–90 min | E. coli ATCC 25922 | No significant effect on physicochemical properties of the LED treated milk | Highest inactivation at higher temperature and lower wavelengths; 406 nm LED treatment at 13.8 °C for 37.83 min can yield 5 log reduction with minimal color change | Srimagal, Ramesh and Sahu [120] |
Clear and cloudy apple juice | Four UV LEDs emitting wavelengths 254, 280, 365 and 405 nm; working distance, 1 cm; sample volume, 3 ml | E. coli K12 (ATCC 25253) | Highest inactivation of PPO enzyme obtained by 280/365 and 280/405 nm LED treatment; lowest color difference observed with 280/365 nm LED combination | UV LEDs most effective in clear apple juice; highest inactivation in cloudy apple was ~ 2 log CFU/ml by 280 nm and 280/365 nm LEDs; 280 nm LED produced 4.4 log reduction in clear apple juice | Akgün and Ünlütürk [2] |
Colored beverages and two different commercially available orange juices (A and B) | UV-A LED (365 nm); intensity, 70 mW/cm2; coloring pigment concentrations, 0.001, 0.01, 0.1, and 1.0%; treatment time, 30 min; dose, 126 J/cm2 | E. coli DH5α | Increasing the concentration of coloring agents decreased the antibacterial effect | Maximum log reduction was 1.75 log CFU/ml in the beverage containing 0.001% β carotene; orange juices (A and B) showed 0.35 and 1.58 log reduction, respectively | Lian et al. [74] |
Orange juice | Blue (460 nm) LED; irradiances used, 92, 147.7, and 254.7 mW/cm2; illumination temperatures, 4, 12, and 20 °C | Cocktail of Salmonella enterica serovars Gaminara, Montevideo, Newport, Typhimurium, and Saintpaul | Significant color changes observed | 2–5 log reduction observed in Salmonella cocktail; best treatment conditions obtained was an irradiance of 92 mW/cm2 for 13.58 h corresponding to dose of 4500 J/cm2 at 12 °C | Ghate et al. [35] |