Biosurfactant Production by Pseudomonas Aeruginosa 181

This study involves the screening of biosurfactant producers that have been isolated from crude oil bacteria degraders. The bacteria were isolated by qualitative screening on cetyltrimethylammonium bromide (CTAB) agar plates and quantitative screening for biosurfactant production in liquid media. A...

Full description

Saved in:
Bibliographic Details
Main Author: Yassin Al-Araji, Laith Issa
Format: Thesis
Language:English
English
Published: 2004
Online Access:http://psasir.upm.edu.my/id/eprint/4812/1/FBSB_2004_2.pdf
http://psasir.upm.edu.my/id/eprint/4812/
Tags: Add Tag
No Tags, Be the first to tag this record!
id my.upm.eprints.4812
record_format eprints
spelling my.upm.eprints.48122013-05-27T07:18:26Z http://psasir.upm.edu.my/id/eprint/4812/ Biosurfactant Production by Pseudomonas Aeruginosa 181 Yassin Al-Araji, Laith Issa This study involves the screening of biosurfactant producers that have been isolated from crude oil bacteria degraders. The bacteria were isolated by qualitative screening on cetyltrimethylammonium bromide (CTAB) agar plates and quantitative screening for biosurfactant production in liquid media. A biosurfactant producer identified as Pseudomonas aeruginosa 181 was selected for further analysis. Maximum biosurfactant production by Pseudomonas aeruginosa 181 was achieved after 120 h incubation at pH 7.0 and 37°C. Static condition and 5.0% bacterial inoculum’s gave the optimum biosurfactant yield. Culture medium containing glucose as the carbon source; and casamino acids as the organic nitrogen source gave the highest level of biosurfactant production. Corn steep liquor and ammonium nitrate on the other hand inhibited biosurfactant production. However, the addition of metal ions such as Fe, Mg and Mn maximized biosurfactant synthesis.The biosurfactant produced by Pseudomonas aeruginosa 181 was purified to homogeneity by acid precipitation and ammonium sulphate precipitation. Biosurfactant produced byPseudomonas aeruginosa 181 was stable and had a broad range of pH from 3.0 to 12.0 with the maximum activity (Surface Tension reduction and Emulsification Index (E24))exhibited at pH 7.0. The purified biosurfactant had a broad range of temperature and exhibited optimum activity at 30°C. This biosurfactant had high activity compared to many commercial surfactants with 0.1 mg critical micelle concentration (CMC). The purified biosurfactant had a maximum emulsification index (E24) of 86% with hexadecane,followed by 80% with nonane, dodecane,tridecane, pentadecane, octadecane and o- Xylene.Response surface methodology (RSM) was then used to study interactive effects of the parameters (pH, stirring rate, casamino acid concentration and incubation period) on the production of biosurfactants. Generally, simultaneously increasing surface tension reduction and emulsification index (E24) improved yields. Production carried out at larger volumes of 1L using Bioreactor under RSM-optimized conditions yielded 350.22 mg of products after purification by acid precipitation. Identities of isolated products were verified by using TLC, high performance liquid chromatography (HPLC), liquid chromatography–Mass spectrometry (LC-MS), mass spectrometry (MS-MS), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and infraredspectroscopy (FT-IR), from analysis carried out the rhamnolipids were monorhamnolipids and dirhamnolipids. 2004 Thesis NonPeerReviewed application/pdf en http://psasir.upm.edu.my/id/eprint/4812/1/FBSB_2004_2.pdf Yassin Al-Araji, Laith Issa (2004) Biosurfactant Production by Pseudomonas Aeruginosa 181. PhD thesis, Universiti Putra Malaysia. English
institution Universiti Putra Malaysia
building UPM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Putra Malaysia
content_source UPM Institutional Repository
url_provider http://psasir.upm.edu.my/
language English
English
description This study involves the screening of biosurfactant producers that have been isolated from crude oil bacteria degraders. The bacteria were isolated by qualitative screening on cetyltrimethylammonium bromide (CTAB) agar plates and quantitative screening for biosurfactant production in liquid media. A biosurfactant producer identified as Pseudomonas aeruginosa 181 was selected for further analysis. Maximum biosurfactant production by Pseudomonas aeruginosa 181 was achieved after 120 h incubation at pH 7.0 and 37°C. Static condition and 5.0% bacterial inoculum’s gave the optimum biosurfactant yield. Culture medium containing glucose as the carbon source; and casamino acids as the organic nitrogen source gave the highest level of biosurfactant production. Corn steep liquor and ammonium nitrate on the other hand inhibited biosurfactant production. However, the addition of metal ions such as Fe, Mg and Mn maximized biosurfactant synthesis.The biosurfactant produced by Pseudomonas aeruginosa 181 was purified to homogeneity by acid precipitation and ammonium sulphate precipitation. Biosurfactant produced byPseudomonas aeruginosa 181 was stable and had a broad range of pH from 3.0 to 12.0 with the maximum activity (Surface Tension reduction and Emulsification Index (E24))exhibited at pH 7.0. The purified biosurfactant had a broad range of temperature and exhibited optimum activity at 30°C. This biosurfactant had high activity compared to many commercial surfactants with 0.1 mg critical micelle concentration (CMC). The purified biosurfactant had a maximum emulsification index (E24) of 86% with hexadecane,followed by 80% with nonane, dodecane,tridecane, pentadecane, octadecane and o- Xylene.Response surface methodology (RSM) was then used to study interactive effects of the parameters (pH, stirring rate, casamino acid concentration and incubation period) on the production of biosurfactants. Generally, simultaneously increasing surface tension reduction and emulsification index (E24) improved yields. Production carried out at larger volumes of 1L using Bioreactor under RSM-optimized conditions yielded 350.22 mg of products after purification by acid precipitation. Identities of isolated products were verified by using TLC, high performance liquid chromatography (HPLC), liquid chromatography–Mass spectrometry (LC-MS), mass spectrometry (MS-MS), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and infraredspectroscopy (FT-IR), from analysis carried out the rhamnolipids were monorhamnolipids and dirhamnolipids.
format Thesis
author Yassin Al-Araji, Laith Issa
spellingShingle Yassin Al-Araji, Laith Issa
Biosurfactant Production by Pseudomonas Aeruginosa 181
author_facet Yassin Al-Araji, Laith Issa
author_sort Yassin Al-Araji, Laith Issa
title Biosurfactant Production by Pseudomonas Aeruginosa 181
title_short Biosurfactant Production by Pseudomonas Aeruginosa 181
title_full Biosurfactant Production by Pseudomonas Aeruginosa 181
title_fullStr Biosurfactant Production by Pseudomonas Aeruginosa 181
title_full_unstemmed Biosurfactant Production by Pseudomonas Aeruginosa 181
title_sort biosurfactant production by pseudomonas aeruginosa 181
publishDate 2004
url http://psasir.upm.edu.my/id/eprint/4812/1/FBSB_2004_2.pdf
http://psasir.upm.edu.my/id/eprint/4812/
_version_ 1643823006337728512
score 13.160551