Loading…
Immobilization of Brevibacterium flavum cells on collagen for the production of glutamic acid in a recycle reactor
In this study, live cells of Brevibacterium flavum were immobilized for the production of glutamic acid. The reason for such a choice was that glutamic acid fermentation is an extensively studied fermentation and one which requires the viability of entire cellular faculties for the acid production....
Saved in:
Published in: | Biotechnology and bioengineering 1981-04, Vol.23 (4), p.899-916 |
---|---|
Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c3549-67192a6269720fd014d9c540c581a83ff090ec8bba6531fd976110c7e0cabb273 |
---|---|
cites | cdi_FETCH-LOGICAL-c3549-67192a6269720fd014d9c540c581a83ff090ec8bba6531fd976110c7e0cabb273 |
container_end_page | 916 |
container_issue | 4 |
container_start_page | 899 |
container_title | Biotechnology and bioengineering |
container_volume | 23 |
creator | Constantinides, Alkis Bhatia, Daleep Vieth, Wolf R. |
description | In this study, live cells of Brevibacterium flavum were immobilized for the production of glutamic acid. The reason for such a choice was that glutamic acid fermentation is an extensively studied fermentation and one which requires the viability of entire cellular faculties for the acid production. Brevibacterium flavum was chosen because it is an industrially used bacterium, and is very potent via a vis glutamic acid production. Studies were performed to find aeration and agitation conditions for optimal growth and glutamic acid productivity. Experiments were also done to find the optimum harvesting time. The cell activity peaks during the run of fermentation, and the time at which the peak occurs, was found. Conventional methods for immobilizing the cells on collagen were found to be lacking. The pH and drying were the two main reasons for loss of viability of the cells; the latter being more important. A modified immobilization procedure has been devised, which can immobilize live cells at any given pH and ionic strength, in contrast to the conventional method which requires the pH to be above 11 or below 3. This new method involves dialysis of collagen in suitable dialysis bags against water at pH7 (or buffer at any desired pH). The dialysed collagen blended at 20,000 rpm, resulted in a very smooth dispersion, unnoticeably different from collagen dispersion prepared at pH 11. The dispersed collagen was then cast and dried at an elevated temperature, and high air flow rate over the cast membrane, decreasing the time of drying from 6–8 hr ( in the conventional method) to 1.5–2 hr. The membrane has been tested for glutamic acid producing capabilities in a column reactor with the membrane spirally wound. The reactor has been operated under continuous conditions for 5–10 days with stable activities. |
doi_str_mv | 10.1002/bit.260230419 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_15294026</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>15294026</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3549-67192a6269720fd014d9c540c581a83ff090ec8bba6531fd976110c7e0cabb273</originalsourceid><addsrcrecordid>eNp9kM1PxCAQxYnRxPXj6J2Tt-pAW1iOanRdYzTGryOhFBSli0K7uv71YlaNJ08vk_zem5mH0A6BPQJA9xvX71EGtISKiBU0IiB4AVTAKhoBACvKWtB1tJHSUx75mLERitOuC43z7kP1LsxwsPgwmrlrlO5NdEOHrVfzLNp4n3AmdPBePZgZtiHi_tHglxjaQf-4H_zQq85prLRrsZthhaPRC-1N1hwa4hZas8ons_2tm-j25Pjm6LQ4v5xMjw7OC13WlSgYJ4IqRpngFGwLpGqFrivQ9ZiocWktCDB63DSK1SWxreCMENDcgFZNQ3m5iXaXufnA18GkXnYufb2hZiYMSZKaigooy2CxBHUMKUVj5Ut0nYoLSUB-NStzs_K32czzJf_mvFn8D8vD6c1f5_cml3rz_utU8VkyXvJa3l9MJDs7u7q7npzIq_IT6y6Mxg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>15294026</pqid></control><display><type>article</type><title>Immobilization of Brevibacterium flavum cells on collagen for the production of glutamic acid in a recycle reactor</title><source>Wiley Online Library All Backfiles</source><creator>Constantinides, Alkis ; Bhatia, Daleep ; Vieth, Wolf R.</creator><creatorcontrib>Constantinides, Alkis ; Bhatia, Daleep ; Vieth, Wolf R.</creatorcontrib><description>In this study, live cells of Brevibacterium flavum were immobilized for the production of glutamic acid. The reason for such a choice was that glutamic acid fermentation is an extensively studied fermentation and one which requires the viability of entire cellular faculties for the acid production. Brevibacterium flavum was chosen because it is an industrially used bacterium, and is very potent via a vis glutamic acid production. Studies were performed to find aeration and agitation conditions for optimal growth and glutamic acid productivity. Experiments were also done to find the optimum harvesting time. The cell activity peaks during the run of fermentation, and the time at which the peak occurs, was found. Conventional methods for immobilizing the cells on collagen were found to be lacking. The pH and drying were the two main reasons for loss of viability of the cells; the latter being more important. A modified immobilization procedure has been devised, which can immobilize live cells at any given pH and ionic strength, in contrast to the conventional method which requires the pH to be above 11 or below 3. This new method involves dialysis of collagen in suitable dialysis bags against water at pH7 (or buffer at any desired pH). The dialysed collagen blended at 20,000 rpm, resulted in a very smooth dispersion, unnoticeably different from collagen dispersion prepared at pH 11. The dispersed collagen was then cast and dried at an elevated temperature, and high air flow rate over the cast membrane, decreasing the time of drying from 6–8 hr ( in the conventional method) to 1.5–2 hr. The membrane has been tested for glutamic acid producing capabilities in a column reactor with the membrane spirally wound. The reactor has been operated under continuous conditions for 5–10 days with stable activities.</description><identifier>ISSN: 0006-3592</identifier><identifier>EISSN: 1097-0290</identifier><identifier>DOI: 10.1002/bit.260230419</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Brevibacterium flavum</subject><ispartof>Biotechnology and bioengineering, 1981-04, Vol.23 (4), p.899-916</ispartof><rights>Copyright © 1981 John Wiley & Sons, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3549-67192a6269720fd014d9c540c581a83ff090ec8bba6531fd976110c7e0cabb273</citedby><cites>FETCH-LOGICAL-c3549-67192a6269720fd014d9c540c581a83ff090ec8bba6531fd976110c7e0cabb273</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fbit.260230419$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fbit.260230419$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1415,27922,27923,46047,46471</link.rule.ids></links><search><creatorcontrib>Constantinides, Alkis</creatorcontrib><creatorcontrib>Bhatia, Daleep</creatorcontrib><creatorcontrib>Vieth, Wolf R.</creatorcontrib><title>Immobilization of Brevibacterium flavum cells on collagen for the production of glutamic acid in a recycle reactor</title><title>Biotechnology and bioengineering</title><addtitle>Biotechnol. Bioeng</addtitle><description>In this study, live cells of Brevibacterium flavum were immobilized for the production of glutamic acid. The reason for such a choice was that glutamic acid fermentation is an extensively studied fermentation and one which requires the viability of entire cellular faculties for the acid production. Brevibacterium flavum was chosen because it is an industrially used bacterium, and is very potent via a vis glutamic acid production. Studies were performed to find aeration and agitation conditions for optimal growth and glutamic acid productivity. Experiments were also done to find the optimum harvesting time. The cell activity peaks during the run of fermentation, and the time at which the peak occurs, was found. Conventional methods for immobilizing the cells on collagen were found to be lacking. The pH and drying were the two main reasons for loss of viability of the cells; the latter being more important. A modified immobilization procedure has been devised, which can immobilize live cells at any given pH and ionic strength, in contrast to the conventional method which requires the pH to be above 11 or below 3. This new method involves dialysis of collagen in suitable dialysis bags against water at pH7 (or buffer at any desired pH). The dialysed collagen blended at 20,000 rpm, resulted in a very smooth dispersion, unnoticeably different from collagen dispersion prepared at pH 11. The dispersed collagen was then cast and dried at an elevated temperature, and high air flow rate over the cast membrane, decreasing the time of drying from 6–8 hr ( in the conventional method) to 1.5–2 hr. The membrane has been tested for glutamic acid producing capabilities in a column reactor with the membrane spirally wound. The reactor has been operated under continuous conditions for 5–10 days with stable activities.</description><subject>Brevibacterium flavum</subject><issn>0006-3592</issn><issn>1097-0290</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1981</creationdate><recordtype>article</recordtype><recordid>eNp9kM1PxCAQxYnRxPXj6J2Tt-pAW1iOanRdYzTGryOhFBSli0K7uv71YlaNJ08vk_zem5mH0A6BPQJA9xvX71EGtISKiBU0IiB4AVTAKhoBACvKWtB1tJHSUx75mLERitOuC43z7kP1LsxwsPgwmrlrlO5NdEOHrVfzLNp4n3AmdPBePZgZtiHi_tHglxjaQf-4H_zQq85prLRrsZthhaPRC-1N1hwa4hZas8ons_2tm-j25Pjm6LQ4v5xMjw7OC13WlSgYJ4IqRpngFGwLpGqFrivQ9ZiocWktCDB63DSK1SWxreCMENDcgFZNQ3m5iXaXufnA18GkXnYufb2hZiYMSZKaigooy2CxBHUMKUVj5Ut0nYoLSUB-NStzs_K32czzJf_mvFn8D8vD6c1f5_cml3rz_utU8VkyXvJa3l9MJDs7u7q7npzIq_IT6y6Mxg</recordid><startdate>198104</startdate><enddate>198104</enddate><creator>Constantinides, Alkis</creator><creator>Bhatia, Daleep</creator><creator>Vieth, Wolf R.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>198104</creationdate><title>Immobilization of Brevibacterium flavum cells on collagen for the production of glutamic acid in a recycle reactor</title><author>Constantinides, Alkis ; Bhatia, Daleep ; Vieth, Wolf R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3549-67192a6269720fd014d9c540c581a83ff090ec8bba6531fd976110c7e0cabb273</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1981</creationdate><topic>Brevibacterium flavum</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Constantinides, Alkis</creatorcontrib><creatorcontrib>Bhatia, Daleep</creatorcontrib><creatorcontrib>Vieth, Wolf R.</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Biotechnology and bioengineering</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Constantinides, Alkis</au><au>Bhatia, Daleep</au><au>Vieth, Wolf R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immobilization of Brevibacterium flavum cells on collagen for the production of glutamic acid in a recycle reactor</atitle><jtitle>Biotechnology and bioengineering</jtitle><addtitle>Biotechnol. Bioeng</addtitle><date>1981-04</date><risdate>1981</risdate><volume>23</volume><issue>4</issue><spage>899</spage><epage>916</epage><pages>899-916</pages><issn>0006-3592</issn><eissn>1097-0290</eissn><abstract>In this study, live cells of Brevibacterium flavum were immobilized for the production of glutamic acid. The reason for such a choice was that glutamic acid fermentation is an extensively studied fermentation and one which requires the viability of entire cellular faculties for the acid production. Brevibacterium flavum was chosen because it is an industrially used bacterium, and is very potent via a vis glutamic acid production. Studies were performed to find aeration and agitation conditions for optimal growth and glutamic acid productivity. Experiments were also done to find the optimum harvesting time. The cell activity peaks during the run of fermentation, and the time at which the peak occurs, was found. Conventional methods for immobilizing the cells on collagen were found to be lacking. The pH and drying were the two main reasons for loss of viability of the cells; the latter being more important. A modified immobilization procedure has been devised, which can immobilize live cells at any given pH and ionic strength, in contrast to the conventional method which requires the pH to be above 11 or below 3. This new method involves dialysis of collagen in suitable dialysis bags against water at pH7 (or buffer at any desired pH). The dialysed collagen blended at 20,000 rpm, resulted in a very smooth dispersion, unnoticeably different from collagen dispersion prepared at pH 11. The dispersed collagen was then cast and dried at an elevated temperature, and high air flow rate over the cast membrane, decreasing the time of drying from 6–8 hr ( in the conventional method) to 1.5–2 hr. The membrane has been tested for glutamic acid producing capabilities in a column reactor with the membrane spirally wound. The reactor has been operated under continuous conditions for 5–10 days with stable activities.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><doi>10.1002/bit.260230419</doi><tpages>18</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0006-3592 |
ispartof | Biotechnology and bioengineering, 1981-04, Vol.23 (4), p.899-916 |
issn | 0006-3592 1097-0290 |
language | eng |
recordid | cdi_proquest_miscellaneous_15294026 |
source | Wiley Online Library All Backfiles |
subjects | Brevibacterium flavum |
title | Immobilization of Brevibacterium flavum cells on collagen for the production of glutamic acid in a recycle reactor |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-14T10%3A20%3A32IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Immobilization%20of%20Brevibacterium%20flavum%20cells%20on%20collagen%20for%20the%20production%20of%20glutamic%20acid%20in%20a%20recycle%20reactor&rft.jtitle=Biotechnology%20and%20bioengineering&rft.au=Constantinides,%20Alkis&rft.date=1981-04&rft.volume=23&rft.issue=4&rft.spage=899&rft.epage=916&rft.pages=899-916&rft.issn=0006-3592&rft.eissn=1097-0290&rft_id=info:doi/10.1002/bit.260230419&rft_dat=%3Cproquest_cross%3E15294026%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3549-67192a6269720fd014d9c540c581a83ff090ec8bba6531fd976110c7e0cabb273%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=15294026&rft_id=info:pmid/&rfr_iscdi=true |