Batch phenol biodegradation study and application of factorial experimental design

A bacterium, Pseudomonas aeruginosa (ATTC27853), was investigated for its ability to grow and to degrade phenol as solecarbon source, in aerobic batch culture. The parameters which affect the substrate biodegradation such as the adaptation ofbacteria to phenol, the temperature, and the nature of the...

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Main Authors: A. Hellal, A. Namane, N. Saidani, D. Hank
Format: Article
Language:English
Published: Eastern Macedonia and Thrace Institute of Technology 2010-01-01
Series:Journal of Engineering Science and Technology Review
Subjects:
Online Access:http://www.jestr.org/downloads/volume3/fulltext232010.pdf
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spelling doaj-103452bc9b044d6fbf76a2d22493fecb2020-11-25T01:42:31ZengEastern Macedonia and Thrace Institute of TechnologyJournal of Engineering Science and Technology Review1791-23772010-01-0131123127Batch phenol biodegradation study and application of factorial experimental designA. HellalA. NamaneN. SaidaniD. HankA bacterium, Pseudomonas aeruginosa (ATTC27853), was investigated for its ability to grow and to degrade phenol as solecarbon source, in aerobic batch culture. The parameters which affect the substrate biodegradation such as the adaptation ofbacteria to phenol, the temperature, and the nature of the bacteria were investigated. The results show that for a range oftemperature of 30 to 40°C, the best degradation of phenol for a concentration of 100mg/l was observed at 30°C. The regenerationof the bacterium which allows the reactivation of its enzymatic activity, shows that the degradation of 100 mg/ l ofsubstrate at 30° C required approximately 50 hours with revivified bacteria, while it only starts after 72 hours for those norevivified. Adapted to increasing concentrations, allows the bacteria to degrade a substrate concentration of about 400mg/l in less than 350 hours.A second part was consisted in the determination of a substrate degradation model using the factorial experiment design,as a function of temperature (30-40°C) and of the size of the inoculums (260.88 - 521.76mg/ l). The results were analyzedstatistically using the Student’s t-test, analysis of variance, and F-test. The value of R2 (0.99872) and adjusted R2 (0.9962)close to 1.0, verifies the good correlation between the observed and the predicted values, and provides the excellent relationshipbetween the independent variables (factors) and the response (the time of the phenol degradation). F-value found above200, indicates that the considered model is statistically significant.http://www.jestr.org/downloads/volume3/fulltext232010.pdfBiodegradationPhenolPseudomonas aeruginosaFactorial experimental design
collection DOAJ
language English
format Article
sources DOAJ
author A. Hellal
A. Namane
N. Saidani
D. Hank
spellingShingle A. Hellal
A. Namane
N. Saidani
D. Hank
Batch phenol biodegradation study and application of factorial experimental design
Journal of Engineering Science and Technology Review
Biodegradation
Phenol
Pseudomonas aeruginosa
Factorial experimental design
author_facet A. Hellal
A. Namane
N. Saidani
D. Hank
author_sort A. Hellal
title Batch phenol biodegradation study and application of factorial experimental design
title_short Batch phenol biodegradation study and application of factorial experimental design
title_full Batch phenol biodegradation study and application of factorial experimental design
title_fullStr Batch phenol biodegradation study and application of factorial experimental design
title_full_unstemmed Batch phenol biodegradation study and application of factorial experimental design
title_sort batch phenol biodegradation study and application of factorial experimental design
publisher Eastern Macedonia and Thrace Institute of Technology
series Journal of Engineering Science and Technology Review
issn 1791-2377
publishDate 2010-01-01
description A bacterium, Pseudomonas aeruginosa (ATTC27853), was investigated for its ability to grow and to degrade phenol as solecarbon source, in aerobic batch culture. The parameters which affect the substrate biodegradation such as the adaptation ofbacteria to phenol, the temperature, and the nature of the bacteria were investigated. The results show that for a range oftemperature of 30 to 40°C, the best degradation of phenol for a concentration of 100mg/l was observed at 30°C. The regenerationof the bacterium which allows the reactivation of its enzymatic activity, shows that the degradation of 100 mg/ l ofsubstrate at 30° C required approximately 50 hours with revivified bacteria, while it only starts after 72 hours for those norevivified. Adapted to increasing concentrations, allows the bacteria to degrade a substrate concentration of about 400mg/l in less than 350 hours.A second part was consisted in the determination of a substrate degradation model using the factorial experiment design,as a function of temperature (30-40°C) and of the size of the inoculums (260.88 - 521.76mg/ l). The results were analyzedstatistically using the Student’s t-test, analysis of variance, and F-test. The value of R2 (0.99872) and adjusted R2 (0.9962)close to 1.0, verifies the good correlation between the observed and the predicted values, and provides the excellent relationshipbetween the independent variables (factors) and the response (the time of the phenol degradation). F-value found above200, indicates that the considered model is statistically significant.
topic Biodegradation
Phenol
Pseudomonas aeruginosa
Factorial experimental design
url http://www.jestr.org/downloads/volume3/fulltext232010.pdf
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