The biodegradation of cefuroxime, cefotaxime and cefpirome by the synthetic consortium with probiotic Bacillus clausii and investigation of their potential biodegradation pathways.
Antibiotic-resistance genes
Bacillus clausii
Biodegradation
Cephalosporins
Co-culture
Journal
The Science of the total environment
ISSN: 1879-1026
Titre abrégé: Sci Total Environ
Pays: Netherlands
ID NLM: 0330500
Informations de publication
Date de publication:
15 Feb 2019
15 Feb 2019
Historique:
received:
06
03
2018
revised:
14
09
2018
accepted:
14
09
2018
pubmed:
22
9
2018
medline:
12
12
2018
entrez:
22
9
2018
Statut:
ppublish
Résumé
Cephalosporin residues in the environment are a great concern, but bioremediation options do exist. Bacillus clausii T reached a removal rate of 100% within 8 h when challenged with a mixture of cefuroxime (CFX), cefotaxime (CTX), and cefpirome (CPR). The co-culture of B. clausii T and B. clausii O/C displayed a higher removal efficiency for the mixture of CFX, CTX and CPR than a pure culture of B. clausii O/C. B. clausii T alleviated the biotoxicity of CFX and CPR. What's more, the biotoxicity of for CFX and CPR transformation products released by the co-culture of B. clausii T and B. clausii O/C was lower than that in pure cultures. Real-time PCR was applied to detect the changes in the expression levels of the relevant antibiotic-resistance genes of B. clausii T during CFX and CPR degradation. The results indicated that CFX and CPR enhanced the expression of the β-lactamase gene bcl1. Hydrolysis, deacetylation and decarboxylation are likely the major mechanisms of CTX biodegradation by B. clausii. These results demonstrate that B. clausii T is a promising strain for the bioremediation of environmental contamination by CFX, CTX, and CPR.
Identifiants
pubmed: 30236844
pii: S0048-9697(18)33632-5
doi: 10.1016/j.scitotenv.2018.09.187
pii:
doi:
Substances chimiques
Anti-Bacterial Agents
0
Cephalosporins
0
Cefotaxime
N2GI8B1GK7
Cefuroxime
O1R9FJ93ED
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
271-280Informations de copyright
Copyright © 2018 Elsevier B.V. All rights reserved.