Recovery of microquantities of human Epidermal Growth Factor from Esherichia coli homogenate and Pichia pastoris culture medium using expanded bed adsorption
A rational design of recovery of microquantities of human Epidermal Growth Factor (hEGF) from different complex feedstocks using STREAMLINE Direct HST in expanded bed adsorption (EBA) was approached. The highest adsorption yields were achieved at pH 4.5, which was close to the isoelectric point of p...
Saved in:
Main Authors: | , , , , |
---|---|
Format: | Article |
Published: |
Taylor & Francis Inc.
2014
|
Online Access: | http://psasir.upm.edu.my/id/eprint/35176/ http://www.tandfonline.com/doi/abs/10.1080/01496395.2013.867351 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
id |
my.upm.eprints.35176 |
---|---|
record_format |
eprints |
spelling |
my.upm.eprints.351762015-12-31T02:08:51Z http://psasir.upm.edu.my/id/eprint/35176/ Recovery of microquantities of human Epidermal Growth Factor from Esherichia coli homogenate and Pichia pastoris culture medium using expanded bed adsorption Rosti, Ira Amira Ramanan, Ramakrishnan Nagasundara Tan, Joo Shun Ling, Tau Chuan Ariff, Arbakariya A rational design of recovery of microquantities of human Epidermal Growth Factor (hEGF) from different complex feedstocks using STREAMLINE Direct HST in expanded bed adsorption (EBA) was approached. The highest adsorption yields were achieved at pH 4.5, which was close to the isoelectric point of protein by utilizing mixed interaction that was offered by the adsorbent. Escherichia coli treated with osmotic shock and Pichia pastoris culture medium spiked with hEGF were applied as feedstocks to evaluate bed stability in the presence of cells. A recovery of 90% was achieved for both cells at pH 4.5. Effects of pH on the P. pastoris culture medium and E. coli homogenate were similar, indicating that both cells have negatively charged surfaces at pH 4.5. The cell transmission index (T) showed that there was no tendency for E. coli homogenate and yeast cells to bind to the matrix at pH 4.5. Because the electrostatic properties of cells and protein are pH dependent, the method presented for screening conditions for biomass and adsorbent is convenient for designing robust and reliable EBA purification processes. Lower ionic strength improved purification of hEGF from E. coli homogenate. Taylor & Francis Inc. 2014 Article PeerReviewed Rosti, Ira Amira and Ramanan, Ramakrishnan Nagasundara and Tan, Joo Shun and Ling, Tau Chuan and Ariff, Arbakariya (2014) Recovery of microquantities of human Epidermal Growth Factor from Esherichia coli homogenate and Pichia pastoris culture medium using expanded bed adsorption. Separation Science and Technology , 49 (5). pp. 702-708. ISSN 0149-6395; ESSN:1520-5754 http://www.tandfonline.com/doi/abs/10.1080/01496395.2013.867351 10.1080/01496395.2013.867351 |
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/ |
description |
A rational design of recovery of microquantities of human Epidermal Growth Factor (hEGF) from different complex feedstocks using STREAMLINE Direct HST in expanded bed adsorption (EBA) was approached. The highest adsorption yields were achieved at pH 4.5, which was close to the isoelectric point of protein by utilizing mixed interaction that was offered by the adsorbent. Escherichia coli treated with osmotic shock and Pichia pastoris culture medium spiked with hEGF were applied as feedstocks to evaluate bed stability in the presence of cells. A recovery of 90% was achieved for both cells at pH 4.5. Effects of pH on the P. pastoris culture medium and E. coli homogenate were similar, indicating that both cells have negatively charged surfaces at pH 4.5. The cell transmission index (T) showed that there was no tendency for E. coli homogenate and yeast cells to bind to the matrix at pH 4.5. Because the electrostatic properties of cells and protein are pH dependent, the method presented for screening conditions for biomass and adsorbent is convenient for designing robust and reliable EBA purification processes. Lower ionic strength improved purification of hEGF from E. coli homogenate. |
format |
Article |
author |
Rosti, Ira Amira Ramanan, Ramakrishnan Nagasundara Tan, Joo Shun Ling, Tau Chuan Ariff, Arbakariya |
spellingShingle |
Rosti, Ira Amira Ramanan, Ramakrishnan Nagasundara Tan, Joo Shun Ling, Tau Chuan Ariff, Arbakariya Recovery of microquantities of human Epidermal Growth Factor from Esherichia coli homogenate and Pichia pastoris culture medium using expanded bed adsorption |
author_facet |
Rosti, Ira Amira Ramanan, Ramakrishnan Nagasundara Tan, Joo Shun Ling, Tau Chuan Ariff, Arbakariya |
author_sort |
Rosti, Ira Amira |
title |
Recovery of microquantities of human Epidermal Growth Factor from Esherichia coli homogenate and Pichia pastoris culture medium using expanded bed adsorption |
title_short |
Recovery of microquantities of human Epidermal Growth Factor from Esherichia coli homogenate and Pichia pastoris culture medium using expanded bed adsorption |
title_full |
Recovery of microquantities of human Epidermal Growth Factor from Esherichia coli homogenate and Pichia pastoris culture medium using expanded bed adsorption |
title_fullStr |
Recovery of microquantities of human Epidermal Growth Factor from Esherichia coli homogenate and Pichia pastoris culture medium using expanded bed adsorption |
title_full_unstemmed |
Recovery of microquantities of human Epidermal Growth Factor from Esherichia coli homogenate and Pichia pastoris culture medium using expanded bed adsorption |
title_sort |
recovery of microquantities of human epidermal growth factor from esherichia coli homogenate and pichia pastoris culture medium using expanded bed adsorption |
publisher |
Taylor & Francis Inc. |
publishDate |
2014 |
url |
http://psasir.upm.edu.my/id/eprint/35176/ http://www.tandfonline.com/doi/abs/10.1080/01496395.2013.867351 |
_version_ |
1643831375519809536 |
score |
13.160551 |