Chronic impact of sulfamethoxazole on acetate utilization kinetics and population dynamics of fast growing microbial culture

G. Kor-Bicakci*, I. Pala-Ozkok, A. Rehman, D. Jonas, E. Ubay-Cokgor, D. Orhon

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

19 Citations (Scopus)

Abstract

The study evaluated the chronic impact of sulfamethoxazole on metabolic activities of fast growing microbial culture. It focused on changes induced on utilization kinetics of acetate and composition of the microbial community. The experiments involved a fill and draw reactor, fed with acetate and continuous sulfamethoxazole dosing of 50. mg/L. The evaluation relied on model evaluation of the oxygen uptake rate profiles, with parallel assessment of microbial community structure by 454-pyrosequencing. Continuous sulfamethoxazole dosing inflicted a retardation effect on acetate utilization in a way commonly interpreted as competitive inhibition, blocked substrate storage and accelerated endogenous respiration. A fraction of acetate was utilized at a much lower rate with partial biodegradation of sulfamethoxazole. Results of pyrosequencing with a replacement mechanism within a richer more diversified microbial culture, through inactivation of vulnerable fractions in favor of species resistant to antibiotic, which made them capable of surviving and competing even with a slower metabolic response.

Original languageEnglish
Pages (from-to)219-228
Number of pages10
JournalBioresource Technology
Volume166
DOIs
Publication statusPublished - Aug 2014

Funding

Authors thank The Scientific Research Fund of Istanbul Technical University (Project Nr: 33680 and 33742) and The Scientific and Technological Research Council of Turkey . Authors thank University of Kiel Institute of Clinical Molecular Biology for the technical assistance.

FundersFunder number
Türkiye Bilimsel ve Teknolojik Araştirma Kurumu
Istanbul Teknik Üniversitesi33742, 33680

    Keywords

    • 454-Pyrosequencing
    • Biodegradation
    • Chronic inhibition
    • Process kinetics
    • Sulfamethoxazole

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