Skip to main navigation Skip to search Skip to main content

Chlortetracycline detoxification in maize via induction of glutathione S-transferases after antibiotic exposure

Research output: Contribution to journalArticlepeer-review

108 Scopus citations

Abstract

Soil contamination with nonmetabolized antibiotics is an emerging environmental concern, especially on agricultural croplands that receive animal manure as fertilizer. In this study, phytotoxicity of chlortetracycline (CTC) antibiotics on pinto beans (Phaseolus vulgaris) and maize (Zea mays) was investigated under controlled conditions. When grown in CTC-treated soil, a significant increase in the activities of the plant stress proteins glutathione S-transferases (GST) and peroxidases (POX) were observed in maize plants, but not in pinto beans. In vitro conjugation reactions demonstrated that the induced GST in maize catalyzed the conjugation of glutathione (GSH) with CTC, producing stable conjugates that were structurally characterized using liquid chromatography/mass spectrometry. The antibiotic-induced GST produced CTC-glutathione conjugate at relative concentrations 2-fold higher than that produced by constitutively expressed GST extracted from untreated maize. On the other hand, GST extracted from pinto beans (both treated and untreated) did not efficiently catalyze glutathione conjugation with CTC. These results suggest that maize is able to detoxify chlortetracycline via the glutathione pathway, whereas pinto beans cannot. This may explain the observed stunted growth of pinto beans after antibiotic treatment. This study demonstrates the importance of plant uptake in determining the fate of antibiotics in soil and their potential phytotoxicity to susceptible plants.

Original languageEnglish
Pages (from-to)1450-1456
Number of pages7
JournalEnvironmental Science and Technology
Volume41
Issue number4
DOIs
StatePublished - Feb 15 2007

Fingerprint

Dive into the research topics of 'Chlortetracycline detoxification in maize via induction of glutathione S-transferases after antibiotic exposure'. Together they form a unique fingerprint.

Cite this