Loading…
Variation in recombinant protein expression levels among clones of lepidopteran cell populations
Clones isolated from the heterogenous Spodoptera frugiperda IPLB-Sf-21-AE and Mamestra brassiace IZD-Mb-O503 insect cell populations have been compared in regards to their synthesis of recombinant Escherichia coli β-galactosidase (β-gal), human tissue plasminogen activator (t-PA), and human kidney r...
Saved in:
Published in: | Enzyme and microbial technology 1995, Vol.17 (2), p.168-174 |
---|---|
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-c395t-a37b2c1d8483a009aefeb51b5190f0dbb94d5aa54bfcbb5e75fc1ffc363fbd933 |
---|---|
cites | cdi_FETCH-LOGICAL-c395t-a37b2c1d8483a009aefeb51b5190f0dbb94d5aa54bfcbb5e75fc1ffc363fbd933 |
container_end_page | 174 |
container_issue | 2 |
container_start_page | 168 |
container_title | Enzyme and microbial technology |
container_volume | 17 |
creator | Pasumarthy, Murali K. Murhammer, David W. |
description | Clones isolated from the heterogenous
Spodoptera frugiperda IPLB-Sf-21-AE and
Mamestra brassiace IZD-Mb-O503 insect cell populations have been compared in regards to their synthesis of recombinant
Escherichia coli β-galactosidase (β-gal), human tissue plasminogen activator (t-PA), and human kidney renin. Significant differences were found among the clones in their expression levels of these proteins. In addition, the expression levels oft-PA and renin were considerably less than that of β-gal. Clone BC5 was the best producer of t-PA and renin among the Mb-O503 clones, whereas clone BB5 was the best producer of β-gal. The Sf-9 cell line and clone 2 were the best producers of t-PA and renin, respectively, among the Sf-21 clones. The Mb-O503 clones generally were better producers of t-PA than the Sf-21 clones, with the BC5 clone producing twice the levels of any other Mb-O503 or Sf-21 clone. The Sf-21 clones were generally better renin producers; the Mb-O503 clones were generally found to have β-gal expression levels superior to those reported previously for the Sf-21 clones. |
doi_str_mv | 10.1016/0141-0229(94)00018-M |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_16929401</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>014102299400018M</els_id><sourcerecordid>16929401</sourcerecordid><originalsourceid>FETCH-LOGICAL-c395t-a37b2c1d8483a009aefeb51b5190f0dbb94d5aa54bfcbb5e75fc1ffc363fbd933</originalsourceid><addsrcrecordid>eNqNkU1LAzEQhoMoWKv_wMMeRPSwOulm281FkOIXtHhRrzHJTiSyTdZkW_Tfm21LjyIMBIZn3hmeEHJK4YoCHV8DZTSH0YhfcHYJALTK53tkQKsJz4ED3yeDHXJIjmL87CHGYEDe32SwsrPeZdZlAbVfKOuk67I2-A5TD7_bgDH2RIMrbGImF959ZLrxDmPmTWq3tvZth0G6TGPTZK1vl806NR6TAyObiCfbd0he7-9epo_57PnhaXo7y3XByy6XxUSNNK0rVhUSgEs0qEqaioOBWinO6lLKkimjlSpxUhpNjdHFuDCq5kUxJOeb3HT31xJjJxY29sdIh34ZBR3zEWdA_wFWFKpxn8g2oA4-xoBGtMEuZPgRFETvXfRSRS9VcCbW3sU8jZ1t82XUsjFJirZxN1uwCeNQJuxmgyWjuLIYRNQWncbapl_oRO3t33t-ATaQmXc</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>16810863</pqid></control><display><type>article</type><title>Variation in recombinant protein expression levels among clones of lepidopteran cell populations</title><source>ScienceDirect Freedom Collection 2022-2024</source><creator>Pasumarthy, Murali K. ; Murhammer, David W.</creator><creatorcontrib>Pasumarthy, Murali K. ; Murhammer, David W.</creatorcontrib><description>Clones isolated from the heterogenous
Spodoptera frugiperda IPLB-Sf-21-AE and
Mamestra brassiace IZD-Mb-O503 insect cell populations have been compared in regards to their synthesis of recombinant
Escherichia coli β-galactosidase (β-gal), human tissue plasminogen activator (t-PA), and human kidney renin. Significant differences were found among the clones in their expression levels of these proteins. In addition, the expression levels oft-PA and renin were considerably less than that of β-gal. Clone BC5 was the best producer of t-PA and renin among the Mb-O503 clones, whereas clone BB5 was the best producer of β-gal. The Sf-9 cell line and clone 2 were the best producers of t-PA and renin, respectively, among the Sf-21 clones. The Mb-O503 clones generally were better producers of t-PA than the Sf-21 clones, with the BC5 clone producing twice the levels of any other Mb-O503 or Sf-21 clone. The Sf-21 clones were generally better renin producers; the Mb-O503 clones were generally found to have β-gal expression levels superior to those reported previously for the Sf-21 clones.</description><identifier>ISSN: 0141-0229</identifier><identifier>EISSN: 1879-0909</identifier><identifier>DOI: 10.1016/0141-0229(94)00018-M</identifier><identifier>CODEN: EMTED2</identifier><language>eng</language><publisher>Amsterdam: Elsevier Inc</publisher><subject>Biological and medical sciences ; Biotechnology ; clonal isolates ; Escherichia coli ; Fundamental and applied biological sciences. Psychology ; Genetic engineering ; Genetic technics ; Insect cells ; Methods. Procedures. Technologies ; Modification of gene expression level ; recombinant protein expression ; Spodoptera frugiperda</subject><ispartof>Enzyme and microbial technology, 1995, Vol.17 (2), p.168-174</ispartof><rights>1995</rights><rights>1995 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c395t-a37b2c1d8483a009aefeb51b5190f0dbb94d5aa54bfcbb5e75fc1ffc363fbd933</citedby><cites>FETCH-LOGICAL-c395t-a37b2c1d8483a009aefeb51b5190f0dbb94d5aa54bfcbb5e75fc1ffc363fbd933</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3474905$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Pasumarthy, Murali K.</creatorcontrib><creatorcontrib>Murhammer, David W.</creatorcontrib><title>Variation in recombinant protein expression levels among clones of lepidopteran cell populations</title><title>Enzyme and microbial technology</title><description>Clones isolated from the heterogenous
Spodoptera frugiperda IPLB-Sf-21-AE and
Mamestra brassiace IZD-Mb-O503 insect cell populations have been compared in regards to their synthesis of recombinant
Escherichia coli β-galactosidase (β-gal), human tissue plasminogen activator (t-PA), and human kidney renin. Significant differences were found among the clones in their expression levels of these proteins. In addition, the expression levels oft-PA and renin were considerably less than that of β-gal. Clone BC5 was the best producer of t-PA and renin among the Mb-O503 clones, whereas clone BB5 was the best producer of β-gal. The Sf-9 cell line and clone 2 were the best producers of t-PA and renin, respectively, among the Sf-21 clones. The Mb-O503 clones generally were better producers of t-PA than the Sf-21 clones, with the BC5 clone producing twice the levels of any other Mb-O503 or Sf-21 clone. The Sf-21 clones were generally better renin producers; the Mb-O503 clones were generally found to have β-gal expression levels superior to those reported previously for the Sf-21 clones.</description><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>clonal isolates</subject><subject>Escherichia coli</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genetic engineering</subject><subject>Genetic technics</subject><subject>Insect cells</subject><subject>Methods. Procedures. Technologies</subject><subject>Modification of gene expression level</subject><subject>recombinant protein expression</subject><subject>Spodoptera frugiperda</subject><issn>0141-0229</issn><issn>1879-0909</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><recordid>eNqNkU1LAzEQhoMoWKv_wMMeRPSwOulm281FkOIXtHhRrzHJTiSyTdZkW_Tfm21LjyIMBIZn3hmeEHJK4YoCHV8DZTSH0YhfcHYJALTK53tkQKsJz4ED3yeDHXJIjmL87CHGYEDe32SwsrPeZdZlAbVfKOuk67I2-A5TD7_bgDH2RIMrbGImF959ZLrxDmPmTWq3tvZth0G6TGPTZK1vl806NR6TAyObiCfbd0he7-9epo_57PnhaXo7y3XByy6XxUSNNK0rVhUSgEs0qEqaioOBWinO6lLKkimjlSpxUhpNjdHFuDCq5kUxJOeb3HT31xJjJxY29sdIh34ZBR3zEWdA_wFWFKpxn8g2oA4-xoBGtMEuZPgRFETvXfRSRS9VcCbW3sU8jZ1t82XUsjFJirZxN1uwCeNQJuxmgyWjuLIYRNQWncbapl_oRO3t33t-ATaQmXc</recordid><startdate>1995</startdate><enddate>1995</enddate><creator>Pasumarthy, Murali K.</creator><creator>Murhammer, David W.</creator><general>Elsevier Inc</general><general>Elsevier Science</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>1995</creationdate><title>Variation in recombinant protein expression levels among clones of lepidopteran cell populations</title><author>Pasumarthy, Murali K. ; Murhammer, David W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c395t-a37b2c1d8483a009aefeb51b5190f0dbb94d5aa54bfcbb5e75fc1ffc363fbd933</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>clonal isolates</topic><topic>Escherichia coli</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genetic engineering</topic><topic>Genetic technics</topic><topic>Insect cells</topic><topic>Methods. Procedures. Technologies</topic><topic>Modification of gene expression level</topic><topic>recombinant protein expression</topic><topic>Spodoptera frugiperda</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pasumarthy, Murali K.</creatorcontrib><creatorcontrib>Murhammer, David W.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Enzyme and microbial technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pasumarthy, Murali K.</au><au>Murhammer, David W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Variation in recombinant protein expression levels among clones of lepidopteran cell populations</atitle><jtitle>Enzyme and microbial technology</jtitle><date>1995</date><risdate>1995</risdate><volume>17</volume><issue>2</issue><spage>168</spage><epage>174</epage><pages>168-174</pages><issn>0141-0229</issn><eissn>1879-0909</eissn><coden>EMTED2</coden><abstract>Clones isolated from the heterogenous
Spodoptera frugiperda IPLB-Sf-21-AE and
Mamestra brassiace IZD-Mb-O503 insect cell populations have been compared in regards to their synthesis of recombinant
Escherichia coli β-galactosidase (β-gal), human tissue plasminogen activator (t-PA), and human kidney renin. Significant differences were found among the clones in their expression levels of these proteins. In addition, the expression levels oft-PA and renin were considerably less than that of β-gal. Clone BC5 was the best producer of t-PA and renin among the Mb-O503 clones, whereas clone BB5 was the best producer of β-gal. The Sf-9 cell line and clone 2 were the best producers of t-PA and renin, respectively, among the Sf-21 clones. The Mb-O503 clones generally were better producers of t-PA than the Sf-21 clones, with the BC5 clone producing twice the levels of any other Mb-O503 or Sf-21 clone. The Sf-21 clones were generally better renin producers; the Mb-O503 clones were generally found to have β-gal expression levels superior to those reported previously for the Sf-21 clones.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><doi>10.1016/0141-0229(94)00018-M</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0141-0229 |
ispartof | Enzyme and microbial technology, 1995, Vol.17 (2), p.168-174 |
issn | 0141-0229 1879-0909 |
language | eng |
recordid | cdi_proquest_miscellaneous_16929401 |
source | ScienceDirect Freedom Collection 2022-2024 |
subjects | Biological and medical sciences Biotechnology clonal isolates Escherichia coli Fundamental and applied biological sciences. Psychology Genetic engineering Genetic technics Insect cells Methods. Procedures. Technologies Modification of gene expression level recombinant protein expression Spodoptera frugiperda |
title | Variation in recombinant protein expression levels among clones of lepidopteran cell populations |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-30T20%3A05%3A39IST&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=Variation%20in%20recombinant%20protein%20expression%20levels%20among%20clones%20of%20lepidopteran%20cell%20populations&rft.jtitle=Enzyme%20and%20microbial%20technology&rft.au=Pasumarthy,%20Murali%20K.&rft.date=1995&rft.volume=17&rft.issue=2&rft.spage=168&rft.epage=174&rft.pages=168-174&rft.issn=0141-0229&rft.eissn=1879-0909&rft.coden=EMTED2&rft_id=info:doi/10.1016/0141-0229(94)00018-M&rft_dat=%3Cproquest_cross%3E16929401%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c395t-a37b2c1d8483a009aefeb51b5190f0dbb94d5aa54bfcbb5e75fc1ffc363fbd933%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=16810863&rft_id=info:pmid/&rfr_iscdi=true |