Isolation and identification of an iopromide-degrading strain and its application in an A2/O system
► Isolate and identify an iopromide-degrading strain I-24. ► Evaluate the effects of various factors on IOPr degradation by strain I-24. ► Examine the enzymatic activity of I-24 supplied with different carbon sources. ► Apply strain I-24 to a lab-scale waste water treatment process. ► Analyse the 16...
Gespeichert in:
Veröffentlicht in: | Bioresource technology 2013-04, Vol.134, p.36-42 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | ► Isolate and identify an iopromide-degrading strain I-24. ► Evaluate the effects of various factors on IOPr degradation by strain I-24. ► Examine the enzymatic activity of I-24 supplied with different carbon sources. ► Apply strain I-24 to a lab-scale waste water treatment process. ► Analyse the 16S rDNA fragments obtained from the reactor by DGGE and UPGMA cluster.
An iopromide (IOPr)-degrading bacterium was isolated from activated sludge of a wastewater treatment plant in Shanghai. Based on its morphology, physiological-biochemical characteristics and a phylogenetic analysis of its 16S rRNA sequence, the bacterium was identified and named as Pseudomonas sp. I-24. The optimum condition for degrading IOPr was at 30°C and pH 7.0. After 5days, strain I-24 could degrade 30mg/L IOPr by 99% in a basal salts medium with a 5% (V/V) inoculum and 200mg/L starch as the primary substrate. When applied to an Anaerobic-Anoxic/Aerobic (A2/O) process, with the coexistence of other bacteria, the strain I-24 got lower (61.3%) IOPr removal, but in two A2/O systems (with and without I-24 inoculation), the CODcr removal were both approximately 95%. The trial dosed with strain I-24 showed better IOPr removal than the un-dosed one. I-24 sustained its abundance in the A2/O system during the experiment. |
---|---|
ISSN: | 0960-8524 1873-2976 |
DOI: | 10.1016/j.biortech.2013.02.043 |