An immobilized whole yeast cell biocatalyst for enzymatic sucrose hydrolysis
A novel granular immobilized biocatalyst with invertase activity was prepared by mutual covalent bonding of native bakers' yeast cells Saccharomyces cerevisiae with polyethyleneimine and glutaraldehyde without the use of any solid carrier. The specific invertase activity of the biocatalyst was...
Gespeichert in:
Veröffentlicht in: | Enzyme and microbial technology 1992, Vol.14 (3), p.221-229 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 229 |
---|---|
container_issue | 3 |
container_start_page | 221 |
container_title | Enzyme and microbial technology |
container_volume | 14 |
creator | Hasal, Pavel Vojtíšek, Vladimír Čejková, Alena Kleczek, Pavel Kofroňová, Olga |
description | A novel granular immobilized biocatalyst with invertase activity was prepared by mutual covalent bonding of native bakers' yeast cells
Saccharomyces cerevisiae with polyethyleneimine and glutaraldehyde without the use of any solid carrier. The specific invertase activity of the biocatalyst was 300–1500 Ug
−1. The optimum pH value for the invertase activity was 4.6. The half-life of the invertase activity was 500–1000 h at reaction temperatures of 60–75°C. The activation energy of sucrose hydrolysis equaled 36.2 ± 5 kJ kmol
−1 at reaction temperatures below 65°C. The enzyme reaction was inhibited by substrate at concentrations above 1.0–1.5 mol l
−1, depending on the particle size. The biocatalyst was used for batch sucrose hydrolysis in laboratory-scale reactors at substrate concentrations of 10–70% (w/w), pH 4.6, and temperatures of 60–75°C. The specific productivity of the biocatalyst was 3–10 h
−1. The total biocatalyst productivity over the period of its lifetime was 2000–10,000 kg of sucrose hydrolysed per kilogram of the biocatalyst. The mechanical stability of the biocatalyst particles was quite satisfactory even during long-term operation in stirred reactors. The biocatalyst was stored at temperature +4°C for 1 year without appreciable loss of the invertase activity. The results of the biocatalyst exploration confirmed its applicability for enzymatic hydrolysis of even highly concentrated sucrose solutions under industrial conditions, especially at a high reaction temperature. |
doi_str_mv | 10.1016/0141-0229(92)90070-5 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_16194565</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>0141022992900705</els_id><sourcerecordid>16194565</sourcerecordid><originalsourceid>FETCH-LOGICAL-c400t-712b04b1213a578efc30d8a41efe811ac1b4d8270bb71a42aec6844497d06d933</originalsourceid><addsrcrecordid>eNp9kE1LxDAQhoMouH78Aw89iOihOpNNm-YiLOIXLHjRc0jTKRtpG026SvfX27qyR08DM8-8887L2BnCNQLmN4ACU-BcXSp-pQAkpNkem2EhVQoK1D6b7ZBDdhTjO8DYEDBjy0WXuLb1pWvchqrke-UbSgYysU8sNU1SOm9Nb5phbNQ-JNRthtb0ziZxbYOPlKyGKvhx7uIJO6hNE-n0rx6zt4f717undPny-Hy3WKZWAPSpRF6CKJHj3GSyoNrOoSqMQKqpQDQWS1EVXEJZSjSCG7J5IYRQsoK8UvP5MbvY6n4E_7mm2OvWxcmt6civo8YclcjybATFFpycxkC1_giuNWHQCHqKTk-56CkXrbj-jU5Pa-d_-iZa09TBdNbF3W7GuSykGLHbLUbjr1-Ogo7WUWepcoFsryvv_r_zA3Bngls</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>16194565</pqid></control><display><type>article</type><title>An immobilized whole yeast cell biocatalyst for enzymatic sucrose hydrolysis</title><source>Elsevier ScienceDirect Journals Complete</source><creator>Hasal, Pavel ; Vojtíšek, Vladimír ; Čejková, Alena ; Kleczek, Pavel ; Kofroňová, Olga</creator><creatorcontrib>Hasal, Pavel ; Vojtíšek, Vladimír ; Čejková, Alena ; Kleczek, Pavel ; Kofroňová, Olga</creatorcontrib><description>A novel granular immobilized biocatalyst with invertase activity was prepared by mutual covalent bonding of native bakers' yeast cells
Saccharomyces cerevisiae with polyethyleneimine and glutaraldehyde without the use of any solid carrier. The specific invertase activity of the biocatalyst was 300–1500 Ug
−1. The optimum pH value for the invertase activity was 4.6. The half-life of the invertase activity was 500–1000 h at reaction temperatures of 60–75°C. The activation energy of sucrose hydrolysis equaled 36.2 ± 5 kJ kmol
−1 at reaction temperatures below 65°C. The enzyme reaction was inhibited by substrate at concentrations above 1.0–1.5 mol l
−1, depending on the particle size. The biocatalyst was used for batch sucrose hydrolysis in laboratory-scale reactors at substrate concentrations of 10–70% (w/w), pH 4.6, and temperatures of 60–75°C. The specific productivity of the biocatalyst was 3–10 h
−1. The total biocatalyst productivity over the period of its lifetime was 2000–10,000 kg of sucrose hydrolysed per kilogram of the biocatalyst. The mechanical stability of the biocatalyst particles was quite satisfactory even during long-term operation in stirred reactors. The biocatalyst was stored at temperature +4°C for 1 year without appreciable loss of the invertase activity. The results of the biocatalyst exploration confirmed its applicability for enzymatic hydrolysis of even highly concentrated sucrose solutions under industrial conditions, especially at a high reaction temperature.</description><identifier>ISSN: 0141-0229</identifier><identifier>EISSN: 1879-0909</identifier><identifier>DOI: 10.1016/0141-0229(92)90070-5</identifier><identifier>CODEN: EMTED2</identifier><language>eng</language><publisher>Amsterdam: Elsevier Inc</publisher><subject>batch reactor ; beta -fructofuranosidase ; Biological and medical sciences ; bioreactors ; Biotechnology ; Fundamental and applied biological sciences. Psychology ; hydrolysis ; Immobilization of organelles and whole cells ; Immobilization techniques ; immobilized biocatalyst ; immobilized cells ; immobilized yeasts ; Invertase ; kinetics ; Methods. Procedures. Technologies ; Saccharomyces cerevisiae ; sucrose ; sucrose hydrolysis</subject><ispartof>Enzyme and microbial technology, 1992, Vol.14 (3), p.221-229</ispartof><rights>1992</rights><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c400t-712b04b1213a578efc30d8a41efe811ac1b4d8270bb71a42aec6844497d06d933</citedby><cites>FETCH-LOGICAL-c400t-712b04b1213a578efc30d8a41efe811ac1b4d8270bb71a42aec6844497d06d933</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0141-0229(92)90070-5$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,4021,27921,27922,27923,45993</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5227874$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Hasal, Pavel</creatorcontrib><creatorcontrib>Vojtíšek, Vladimír</creatorcontrib><creatorcontrib>Čejková, Alena</creatorcontrib><creatorcontrib>Kleczek, Pavel</creatorcontrib><creatorcontrib>Kofroňová, Olga</creatorcontrib><title>An immobilized whole yeast cell biocatalyst for enzymatic sucrose hydrolysis</title><title>Enzyme and microbial technology</title><description>A novel granular immobilized biocatalyst with invertase activity was prepared by mutual covalent bonding of native bakers' yeast cells
Saccharomyces cerevisiae with polyethyleneimine and glutaraldehyde without the use of any solid carrier. The specific invertase activity of the biocatalyst was 300–1500 Ug
−1. The optimum pH value for the invertase activity was 4.6. The half-life of the invertase activity was 500–1000 h at reaction temperatures of 60–75°C. The activation energy of sucrose hydrolysis equaled 36.2 ± 5 kJ kmol
−1 at reaction temperatures below 65°C. The enzyme reaction was inhibited by substrate at concentrations above 1.0–1.5 mol l
−1, depending on the particle size. The biocatalyst was used for batch sucrose hydrolysis in laboratory-scale reactors at substrate concentrations of 10–70% (w/w), pH 4.6, and temperatures of 60–75°C. The specific productivity of the biocatalyst was 3–10 h
−1. The total biocatalyst productivity over the period of its lifetime was 2000–10,000 kg of sucrose hydrolysed per kilogram of the biocatalyst. The mechanical stability of the biocatalyst particles was quite satisfactory even during long-term operation in stirred reactors. The biocatalyst was stored at temperature +4°C for 1 year without appreciable loss of the invertase activity. The results of the biocatalyst exploration confirmed its applicability for enzymatic hydrolysis of even highly concentrated sucrose solutions under industrial conditions, especially at a high reaction temperature.</description><subject>batch reactor</subject><subject>beta -fructofuranosidase</subject><subject>Biological and medical sciences</subject><subject>bioreactors</subject><subject>Biotechnology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>hydrolysis</subject><subject>Immobilization of organelles and whole cells</subject><subject>Immobilization techniques</subject><subject>immobilized biocatalyst</subject><subject>immobilized cells</subject><subject>immobilized yeasts</subject><subject>Invertase</subject><subject>kinetics</subject><subject>Methods. Procedures. Technologies</subject><subject>Saccharomyces cerevisiae</subject><subject>sucrose</subject><subject>sucrose hydrolysis</subject><issn>0141-0229</issn><issn>1879-0909</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LxDAQhoMouH78Aw89iOihOpNNm-YiLOIXLHjRc0jTKRtpG026SvfX27qyR08DM8-8887L2BnCNQLmN4ACU-BcXSp-pQAkpNkem2EhVQoK1D6b7ZBDdhTjO8DYEDBjy0WXuLb1pWvchqrke-UbSgYysU8sNU1SOm9Nb5phbNQ-JNRthtb0ziZxbYOPlKyGKvhx7uIJO6hNE-n0rx6zt4f717undPny-Hy3WKZWAPSpRF6CKJHj3GSyoNrOoSqMQKqpQDQWS1EVXEJZSjSCG7J5IYRQsoK8UvP5MbvY6n4E_7mm2OvWxcmt6civo8YclcjybATFFpycxkC1_giuNWHQCHqKTk-56CkXrbj-jU5Pa-d_-iZa09TBdNbF3W7GuSykGLHbLUbjr1-Ogo7WUWepcoFsryvv_r_zA3Bngls</recordid><startdate>1992</startdate><enddate>1992</enddate><creator>Hasal, Pavel</creator><creator>Vojtíšek, Vladimír</creator><creator>Čejková, Alena</creator><creator>Kleczek, Pavel</creator><creator>Kofroňová, Olga</creator><general>Elsevier Inc</general><general>Elsevier Science</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>M7N</scope><scope>P64</scope></search><sort><creationdate>1992</creationdate><title>An immobilized whole yeast cell biocatalyst for enzymatic sucrose hydrolysis</title><author>Hasal, Pavel ; Vojtíšek, Vladimír ; Čejková, Alena ; Kleczek, Pavel ; Kofroňová, Olga</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c400t-712b04b1213a578efc30d8a41efe811ac1b4d8270bb71a42aec6844497d06d933</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>batch reactor</topic><topic>beta -fructofuranosidase</topic><topic>Biological and medical sciences</topic><topic>bioreactors</topic><topic>Biotechnology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>hydrolysis</topic><topic>Immobilization of organelles and whole cells</topic><topic>Immobilization techniques</topic><topic>immobilized biocatalyst</topic><topic>immobilized cells</topic><topic>immobilized yeasts</topic><topic>Invertase</topic><topic>kinetics</topic><topic>Methods. Procedures. Technologies</topic><topic>Saccharomyces cerevisiae</topic><topic>sucrose</topic><topic>sucrose hydrolysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hasal, Pavel</creatorcontrib><creatorcontrib>Vojtíšek, Vladimír</creatorcontrib><creatorcontrib>Čejková, Alena</creatorcontrib><creatorcontrib>Kleczek, Pavel</creatorcontrib><creatorcontrib>Kofroňová, Olga</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</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>Algology Mycology and Protozoology Abstracts (Microbiology C)</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>Hasal, Pavel</au><au>Vojtíšek, Vladimír</au><au>Čejková, Alena</au><au>Kleczek, Pavel</au><au>Kofroňová, Olga</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An immobilized whole yeast cell biocatalyst for enzymatic sucrose hydrolysis</atitle><jtitle>Enzyme and microbial technology</jtitle><date>1992</date><risdate>1992</risdate><volume>14</volume><issue>3</issue><spage>221</spage><epage>229</epage><pages>221-229</pages><issn>0141-0229</issn><eissn>1879-0909</eissn><coden>EMTED2</coden><abstract>A novel granular immobilized biocatalyst with invertase activity was prepared by mutual covalent bonding of native bakers' yeast cells
Saccharomyces cerevisiae with polyethyleneimine and glutaraldehyde without the use of any solid carrier. The specific invertase activity of the biocatalyst was 300–1500 Ug
−1. The optimum pH value for the invertase activity was 4.6. The half-life of the invertase activity was 500–1000 h at reaction temperatures of 60–75°C. The activation energy of sucrose hydrolysis equaled 36.2 ± 5 kJ kmol
−1 at reaction temperatures below 65°C. The enzyme reaction was inhibited by substrate at concentrations above 1.0–1.5 mol l
−1, depending on the particle size. The biocatalyst was used for batch sucrose hydrolysis in laboratory-scale reactors at substrate concentrations of 10–70% (w/w), pH 4.6, and temperatures of 60–75°C. The specific productivity of the biocatalyst was 3–10 h
−1. The total biocatalyst productivity over the period of its lifetime was 2000–10,000 kg of sucrose hydrolysed per kilogram of the biocatalyst. The mechanical stability of the biocatalyst particles was quite satisfactory even during long-term operation in stirred reactors. The biocatalyst was stored at temperature +4°C for 1 year without appreciable loss of the invertase activity. The results of the biocatalyst exploration confirmed its applicability for enzymatic hydrolysis of even highly concentrated sucrose solutions under industrial conditions, especially at a high reaction temperature.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><doi>10.1016/0141-0229(92)90070-5</doi><tpages>9</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0141-0229 |
ispartof | Enzyme and microbial technology, 1992, Vol.14 (3), p.221-229 |
issn | 0141-0229 1879-0909 |
language | eng |
recordid | cdi_proquest_miscellaneous_16194565 |
source | Elsevier ScienceDirect Journals Complete |
subjects | batch reactor beta -fructofuranosidase Biological and medical sciences bioreactors Biotechnology Fundamental and applied biological sciences. Psychology hydrolysis Immobilization of organelles and whole cells Immobilization techniques immobilized biocatalyst immobilized cells immobilized yeasts Invertase kinetics Methods. Procedures. Technologies Saccharomyces cerevisiae sucrose sucrose hydrolysis |
title | An immobilized whole yeast cell biocatalyst for enzymatic sucrose hydrolysis |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-14T15%3A48%3A29IST&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=An%20immobilized%20whole%20yeast%20cell%20biocatalyst%20for%20enzymatic%20sucrose%20hydrolysis&rft.jtitle=Enzyme%20and%20microbial%20technology&rft.au=Hasal,%20Pavel&rft.date=1992&rft.volume=14&rft.issue=3&rft.spage=221&rft.epage=229&rft.pages=221-229&rft.issn=0141-0229&rft.eissn=1879-0909&rft.coden=EMTED2&rft_id=info:doi/10.1016/0141-0229(92)90070-5&rft_dat=%3Cproquest_cross%3E16194565%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=16194565&rft_id=info:pmid/&rft_els_id=0141022992900705&rfr_iscdi=true |