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  • Characterization of cefalexin degradation capabilities of two Pseudomonas strains isolated from activated sludge.

Characterization of cefalexin degradation capabilities of two Pseudomonas strains isolated from activated sludge.

Journal of hazardous materials (2014-07-30)
Bokun Lin, Jinling Lyu, Xian-jin Lyu, Han-qing Yu, Zhong Hu, James C W Lam, Paul K S Lam
ABSTRACT

Pharmaceuticals have recently been regarded as contaminants of emerging concern. To date, there is limited knowledge about antibiotic-degrading microorganisms in conventional activated sludge treatment systems and their characteristics toward antibiotic degradation especially in the presence of a pharmaceutical mixture. As such, antibiotic-degrading microorganisms were investigated and isolated from the activated sludge, and their degradation capabilities were evaluated. Two strains of cefalexin-degrading bacteria CE21 and CE22 were isolated and identified as Pseudomonas sp. in the collected activated sludge. Strain CE22 was able to degrade over 90% of cefalexin, while CE21 was able to remove 46.7% of cefalexin after incubation for 24h. The removal efficiency of cefalexin by CE22, different from that of CE21, was not significantly affected by an increase in cefalexin concentration, even up to 10ppm, however the presence of 1ppm of other pharmaceuticals had a significant effect on the degradation of cefalexin by CE22, but no significant effect on CE21. The degradation product of cefalexin by the two strains was identified to be 2-hydroxy-3-phenyl pyrazine. Our results also indicated that CE21 and CE22 were able to degrade caffeine, salicylic acid and chloramphenicol. Moreover, CE21 was found to be capable of eliminating sulfamethoxazole and naproxen.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
N-Acetyl-D-penicillamine, for HPLC derivatization, ≥99.0% (T)
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Tetracycline, 98.0-102.0% (HPLC)
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Salicylic acid, ReagentPlus®, ≥99%
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Salicylic acid, ≥99%, FG
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Salicylic acid, ACS reagent, ≥99.0%
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Ibuprofen, meets USP testing specifications
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Erythromycin, BioReagent, suitable for cell culture
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Tetracycline, 98.0-102.0% (HPLC)
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Erythromycin, meets USP testing specifications
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Erythromycin, potency: ≥850 μg per mg
Supelco
Carbamazepine, Pharmaceutical Secondary Standard; Certified Reference Material
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Ibuprofen, Pharmaceutical Secondary Standard; Certified Reference Material
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Salicylic acid, Pharmaceutical Secondary Standard; Certified Reference Material
USP
Ibuprofen, United States Pharmacopeia (USP) Reference Standard
Ibuprofen for peak identification, European Pharmacopoeia (EP) Reference Standard
Ibuprofen, European Pharmacopoeia (EP) Reference Standard
USP
Salicylic acid, United States Pharmacopeia (USP) Reference Standard
Supelco
Caffeine, Pharmaceutical Secondary Standard; Certified Reference Material
Supelco
Sulfamethoxazole, certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland
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Chloramphenicol, VETRANAL®, analytical standard
Supelco
Ciprofloxacin, VETRANAL®, analytical standard
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Sulfamethoxazole, Pharmaceutical Secondary Standard; Certified Reference Material
Supelco
Ciprofloxacin, Pharmaceutical Secondary Standard; Certified Reference Material
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Caffeine, certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland
USP
Caffeine melting point standard, United States Pharmacopeia (USP) Reference Standard
Sigma-Aldrich
Caffeine, anhydrous, tested according to Ph. Eur.
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Ciprofloxacin, ≥98% (HPLC)
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Caffeine, anhydrous, 99%, FCC, FG
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Caffeine, Sigma Reference Standard, vial of 250 mg
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Caffeine, powder, ReagentPlus®